Semester 1 Flashcards

1
Q

Where is the thorax located?

A

Between the neck and abdomon

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2
Q

What does the thoracic skeleton consist of?

A

The sternum, ribs, costal cartilages and thoracic vertebrae

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3
Q

What is the main role of the thoracic skeleton?

A

It protects vital organs in chest and upper abdomen.
Contracts to assist inspiration.

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4
Q

What are the 2 main openings of the thorax?

A

The superior thoracic aperture found superiorly and the inferior thoracic aperture located inferiorly.

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5
Q

Which strucrures bound the superior thoracic aperture?

A

The bones of the upper thorax; manubrium of sternum, the first pair of ribs, and the body of the vertebra T1.

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6
Q

Which strucrures bound the inferior thoracic aperture?

A

Its almost completely bound by the diaphragm, separating it from the abdominal cavity.

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7
Q

Name some of the contents of the thorax?

A
  • Heart
  • Lungs
  • Oesophagus
  • Trachea
  • main bronchi
  • Thymus
  • Vagus and phrenic nerves
  • Sympathetic trunks and ganglia
  • Thoracic duct
  • Lymph nodes
  • Major systemic and pulmonary vasculature
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8
Q

Name the 3 parts of the sternum

A
  1. Superior part is the manubrium
  2. The middle and largest part is the body
  3. The inferior, smallest part is the xiphoid process
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9
Q

What is the sternal angle?

A

Junction of the manubrium and body

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10
Q

What is the jugular notch?

A

The depression on the superior surface of the manubrium

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11
Q

Which substance directly attaches the true ribs to the sternum?

A

Costal cartilage.

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12
Q

What is the role of the costal cartilage?

A

The elasticity of the thoracic cage and prevent various blows to the chest from fracturing the sternum and/or ribs.

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13
Q

What are articulations formed between the true ribs and the sternum?

A

Sternocostal joints

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14
Q

What is the name for the ribs directly attached to the sternum (1-7)?

A

True ribs

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15
Q

What is the name for the ribs indirectly attached to the sternum (8-10)?

A

False ribs/vertebrochondral ribs

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16
Q

What is the name for the ribs not attached to the sternum (11-12)?

A

Floating ribs/vertebral ribs

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17
Q

What is the ‘head’ of the rib?

A

A projection at the posterior end of the rib that contains a pair of articular facets

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18
Q

What is the name of the joint whereby the ribs articulate with the vertebrae?

A

A vertebrocostal joint.

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19
Q

What is the neck of the rib?

A

Constricted portion of a rib just lateral to the head.

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20
Q

What is the neck of the rib?

A

Constricted portion of a rib just lateral to the head.

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21
Q

What is the tubercle of the rib?

A

A knoblike structure on the posterior surface, where the neck joins the body.

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22
Q

Define the lateral costotransverse ligament

A

The nonarticular part of the tubercle attaches to the transverse process of a vertebra

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23
Q

Define the costal angle

A

A short distance beyond the tubercle, an abrupt change in the curvature of the shaft occurs.

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24
Q

Define the costal groove

A

The inner surface of the rib that protects the intercostal blood vessels and a small nerve.

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25
Q

Describe the articulation of the ribs with the thoracic vertebrae

A
  • The posterior portion of the rib connects to a thoracic vertebra by its head and the articular part of a tubercle.
  • The facet of the head fits into either a facet on the body of one vertebra (T1 only) or into the demifacets of two adjoining vertebrae.
  • The articular part of the tubercle articulates with the facet of the transverse process of the vertebra
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26
Q

Describe the articulation of the costochondral joint

A

The lateral end of the costal cartilage articulates with the sternal end of the rib.

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27
Q

Describe the articulation of the interveterbral joint

A

Adjacent verterbral bodies bound together by IV disc

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28
Q

Describe the articulation of the costoverterbral joint

A

Head of each rib with superior demi/costal facet of vertebral body.
Tubercle of rib with transverse process of vertebrae.

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29
Q

Describe the articulation of the interchondral joint

A

Between costal cartilage of 6th-9th ribs

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30
Q

Describe the articulation of the sternocostal joint

A

Articulation of the 1st costal cartilages with the manubrium of the sternum.
2nd-7th costal cartilages with the body of the sternum.

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31
Q

Describe the articulation of the sternoclavicular joint

A

Clavicle with manubrium of sternum and 1st costal cartilage.

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32
Q

Describe the articulation of the manubriosternal joint

A

Articulation of manubrium and body of sternum

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33
Q

Describe the articulation of the xiphoisternal joint

A

Articulation bewteen xiphoid process and body of sternum

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34
Q

What are the main muscles of the thorax?

A

-Diaphragm
-Intercostal muscles

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35
Q

What is the origin and insertion of the thorax?

A

Origin: Xiphoid process, inner surface lower 6 ribs, lumbar attachment via crura and arcuate ligaments.
Insertion: Large, trefoil-shaped central tendon

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36
Q

Which nerve supplies the thorax?

A

Left and right phrenic nerves C3-C5.

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37
Q

Describe the action of the diaphragm in inspiration

A

Inspiration starts with the 2 domes of the diaphragm flattening to bring muscle fibres into a position to pull down the central tendon. The central tendon then becomes fixed and continued muscular contraction lifts the ribs and sternum (bucket and pump handle action) to increase thoracic volume, decreasing pressure, drawing air in (atmospheric pressure greater than pulmonary pressure).

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38
Q

Which 3 sugroups make up the intercostal muscles?

A

-External
-Internal
-Innermost

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39
Q

Describe the 2 main functions of the intercostals

A

-Pull the ribs up/down to assist inspiration/expiration
-Fill the gaps between ribs, creating airtight cavity. Fibres run obliquely between adjacent ribs, the 3 layers at different angles.

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40
Q

Describe the action of the external intercostals apon the ribs?

A

External intercostal muscles pull the ribs upwards (upon contraction/inspiration) to increase the volume of the thorax.

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41
Q

Describe the action of the internal intercostals apon the ribs?

A

Internal intercostal muscles pull the ribs downwards (upon contraction/expiration) to decrease the volume of the thorax.

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42
Q

What is the role of accessory muscles in the thorax?

A

Recruited to increase ventilation by patients with laboured breathing.

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43
Q

What is the origin and insertion of the external intercostal muscles?

A

Origin: Inferior border of the rib
Insertion: Superior border of the rib

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44
Q

What is the origin and insertion of the internal intercostal muscles?

A

Origin: Superior border of the rib
Insertion: Inferior border of the rib

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45
Q

Which nerve supplies the intercostals?

A

Thoracic spinal nerves T2-T12

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46
Q

Describe the role of the levatores constorum

A

Elevate ribs in inspiration. 12 small muscles on either side of the thorax running between traverse process and ribs below.

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47
Q

Describe the role of the serratus posterior superior

A

Asssists inspiration.

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48
Q

Describe the role of the serratus posterior inferior

A

Assists expiration

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49
Q

Describe the role of the transverse thoracics?

A

Assists expiration

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50
Q

Describe the process of quiet inspiration

A
  • Contraction of the diaphragm flattens its domes
  • Volume of the thorax increased, which lowers intrapleural pressure and causes air to be drawn into the lungs
  • At the same time, the abdominal wall relaxes, allowing the abdominal contents to be displaced downwards as the diaphragm flattens.
  • The intercostal muscles can expand the ribcage by two movements:
  • Forward movement of the lower end of the sternum
  • Upward and outward movement of the ribs, as the external intercostal muscles contract.
  • The intercostal muscles mainly prevent deformation of the tissue between the ribs, which would otherwise lower the volume of the thoracic cage
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51
Q

Is quiet expiration an active or passive process?

A

Passive and there is no direct muscle action.
During inspiration, the lungs are expanded against their elastic recoil. This recoil is sufficient to drive air out of the lungs in expiration.

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52
Q

Describe the process of forced inspiration

A

In addition to the action of the diaphragm:
* Scalene muscles and sternocleidomastoids raise the ribs anteroposteriorly, producing movement at the manubriosternal joint.
* Intercostal muscles are more active and raise the ribs to a far greater extent than in quiet inspiration.
* The 12th rib, which is attached to quadratus lumborum, allows forcible downward movement of the diaphragm.
* Arching the back using erector spinae also increases thoracic volume.
* During respiratory distress, the scapulae are fixed by trapezius muscles. The rhomboid muscles and levator scapulae, pectoralis minor and serratus anterior raise the ribs. The arms can be fixed (e.g., by holding the back of a chair), allowing the use of pectoralis major.

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53
Q

Describe the process of forced expiration?

A

Elastic recoil of the lungs is reinforced by contraction of the muscles of the abdominal wall. This forces the abdominal contents against the diaphragm, displacing the diaphragm upwards
In addition, quadratus lumborum pulls the ribs down, adding to the force at which the abdominal contents are pushed against the diaphragm. Intercostal muscles prevent outward deformation of the tissue between the ribs.

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54
Q

Describe the pump and bucket handle mechanism

A
  • During respiration the anteroposterior, transverse and vertical diameters of the thorax change, resulting in changes in thoracic volume.
  • Vertical diameter changes are due to contraction and relaxation of the diaphragm.
  • Movement of the 2nd to 5th ribs during inspiration occurs about an axis along the rib neck through the costovertebral and costotransverse joints, causing their anterior ends to be raised (‘pump handle’ movement). Because the 1st rib is firmly attached to the manubrium, movement of its anterior end is slight: the longer 2nd to 5th ribs lift the body of the sternum upwards and forwards, resulting in bending of the manubriosternal joint and an increase in the anteroposterior diameter of the thorax.
  • In inspiration movement of the 8th to 10th ribs occurs about an axis through the costovertebral and sternocostal joints, causing the shaft of the rib to move outwards and upwards (‘bucket handle’ movement), widening the infrasternal angle to increase the transverse diameter of the thorax.
  • Ribs 11 and 12 have little influence on movement but provide firm attachment for the diaphragm.
  • During expiration reverse movements of the ribs and sternum occur, decreasing the anteroposterior and transverse diameters.
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55
Q

Describe the boundaries of the thorax

A

Bounded superiorly superior thoracic aperture
Bounded posteriorly by posterior thoracic aperture
Bounded laterally and posteriorly by ribcage and intercostal muscles
12 thoracic vertebrae posteriorly
Sternum anteriorly
Diaphragm inferiorly
Abdomon superiorly

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56
Q

What is the role of the sternocleidomastoids and scalenes?

A

Used for a more forceful inhalation, raise the ribs anteroposteriorly increasing intrathoracic volume.

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57
Q

What is the role of the abdominal muscles?

A

Used for a more forceful exhalation. Elastic recoil of the lungs is reinforced by contraction of the muscles of the abdominal wall; this forces the abdominal contents against the diaphragm, displacing the diaphragm upwards.

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58
Q

What is the role of the quadratus lumborum?

A

Attached to the 12th rib, allows forcible downward movement of the diaphragm.

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59
Q

What’s the role of errector spinae?

A

Arching the back to increase thoracic volume.

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60
Q

What is the role of trapezius muscles?

A

They fix the scapulae.

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61
Q

What’s the role of the rhomboid muscles, levator scapulae, pectoralis minor and serratus anterior?

A

They all raise the ribs/forced inspiration

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62
Q

Roughly give the size of the heart

A

The sized of a closed fist

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63
Q

Where does the heart rest?

A

Lies in the mediastinum, an anatomical region that extends from the sternum to the vertebral column, from the first rib to the diaphragm, and between the lungs

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64
Q

What is the base of the heart?

A

The base of the heart is opposite the apex and is its posterior aspect. It is formed by the atria of the heart, mostly the left atrium.

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65
Q

What is the apex of the heart?

A

The pointed apex is formed by the tip of the left ventricle and rests on the diaphragm. It is directed anteriorly, inferiorly, and to the left.

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66
Q

Which 3 veins does the right atrium recieve blood from?

A

The superior vena cava, inferior vena cava, and coronary sinus

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67
Q

What is the partition between the right and left atria called?

A

The interatrial septum

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68
Q

What is the partition between the right and left atria called?

A

The interatrial septum

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69
Q

What is the name of the valve between the right atria and ventricles?

A

Tricuspid Valve/Right Atrioventricular valve

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70
Q

Define the chordae tendineae

A

Tendon-like cords connected to the tricuspid and bicuspid valves, which in turn are connected to papillary muscles.

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71
Q

What is the partition between the right and left ventricles called?

A

Interventricular septum

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72
Q

Which major vessel is connected to the right ventricle?

A

Pulmonary artery- takes deoxygenated blood from the heart to the lungs via the pulmonary trunk.

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73
Q

Which major vessel suplies the left atrium?

A

The 4 Pulmonary veins

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74
Q

Name the valve that separates the left atrium and left ventricle

A

Bicuspid/mitral/atrioventricular valve

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75
Q

Which chamber of the heart has the thickest walls?

A

Left ventricle

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76
Q

How thick is the left ventricle?

A

10–15 mm

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77
Q

Which vessels are supplied by the left ventricle?

A
  • Blood passes from the left ventricle through the aortic valve (aortic semilunar valve) into the
    ascending aorta
  • Some of the blood in the aorta flows into the coronary arteries, which branch from the
    ascending aorta and carry blood to the heart wall.
  • Remainder of the blood passes into the arch of the aorta and descending aorta (thoracic aorta
    and abdominal aorta).
  • Branches of the arch of the aorta and descending aorta carry blood throughout the body.
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78
Q

Why do the atria have considerably thinner walls than the ventricles?

A

The atria deliver blood under less pressure into the adjacent ventricles. Because the ventricles pump blood under higher pressure over greater distances, their walls are thicker

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79
Q

Why is the muscular wall of the left ventricle considerably thicker than the right ventricle.

A

Although the right and left ventricles act as two separate pumps that simultaneously eject equal volumes of blood, the right side has a much smaller workload. It pumps blood a short distance to the lungs at lower pressure, and the resistance to blood flow is small.
The left ventricle pumps oxygenated blood great distances to all other parts of the body at higher pressure, and the resistance to blood flow is larger. Therefore, the left ventricle works much harder than the right ventricle to maintain the same rate of blood flow, so the walls are thicker to enable more forceful contractions, delivering blood under high pressure.

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80
Q

Define ‘pericardium’

A

The membrane that surrounds and protects the heart.

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81
Q

What are the 2 main parts of the pericardium?

A

The superficial fibrous pericardium and the deeper serous pericardium

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82
Q

Give the function of the fibrous pericardium

A

The fibrous pericardium prevents overstretching of the heart, provides protection, and anchors the heart in the mediastinum.
The fibrous pericardium near the apex of the heart is partially fused to the central tendon of the diaphragm and therefore aids movement of the diaphragm, as in deep breathing, facilitates the movement of blood by the heart.

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83
Q

Give the location of the fibrous pericardium

A

It resembles a bag that rests on and attaches to the diaphragm; its open end is fused to the connective tissues of the blood vessels entering and leaving the heart.

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84
Q

What is the composition of the fibrous pericardium

A

Composed of tough, inelastic, dense irregular connective tissue

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85
Q

Give the composition of the serous pericardium

A

Serous pericardium is a thinner, more delicate membrane that forms a double layer around the heart.
The outer parietal layer of the serous pericardium is fused to the fibrous pericardium. The inner visceral layer of the serous pericardium, which is also called the epicardium is one of the layers of the heart wall and adheres tightly to the surface of the heart.
* Between the parietal and visceral layers of the serous pericardium is a thin film of lubricating serous fluid, ‘pericardial fluid’.
* The space that contains the few millilitres of pericardial fluid is called the pericardial cavity.

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86
Q

What is the function of the pericardial fluid?

A

Reduces friction between the layers of the serous pericardium as the heart moves.

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87
Q

Give the 3 layers that make up the heart wall

A

The epicardium (external layer), the myocardium (middle layer), and the endocardium (inner layer).

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88
Q

Describe the epicardium

A

The epicardium is composed of two tissue layers. The outermost is called the visceral layer of the serous pericardium. This thin, transparent outer layer of the heart wall is composed of mesothelium. Beneath the mesothelium is a variable layer of delicate fibroelastic tissue and adipose tissue.
The adipose tissue predominates and becomes thickest over the ventricular surfaces, where it houses the major coronary and cardiac vessels of the heart. The epicardium imparts a smooth, slippery texture to the outermost surface of the heart. The epicardium contains blood vessels and lymphatics that supply the myocardium.

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89
Q

Describe the myocardium

A

The middle myocardium is responsible for the pumping action of the heart and is composed of cardiac muscle tissue. It makes up approximately 95% of the heart wall. The muscle fibers are wrapped and bundled with connective tissue sheaths composed of endomysium and perimysium. The cardiac muscle fibers are organized in bundles that swirl diagonally around the heart and generate the strong pumping actions of the heart.

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90
Q

Describe the endocardium

A

The innermost endocardium is a thin layer of endothelium overlying a thin layer of connective tissue. It provides a smooth lining for the chambers of the heart and covers the valves of the heart. The smooth endothelial lining minimizes the surface friction as blood passes through the heart. The
endocardium is continuous with the endothelial lining of the large blood vessels attached to the heart.

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91
Q

Describe the composition of the fibrous skeleton of the heart

A

The fibrous skeleton consists of 4 dense connective tissue rings that surround the valves of the heart, fuse with one another, and merge with the interventricular septum:
-Pulmonary fibrous ring
-Aortic fibrous ring
-Right atrioventricular fibrous ring
-Left atrioventricular fibrous ring

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92
Q

Give the function of the fibrous skeleton of the heart

A
  • In addition to forming a structural foundation for the heart valves, the fibrous skeleton prevents overstretching of the valves as blood passes through them.
  • It also serves as a point of insertion for bundles of cardiac muscle fibres and acts as an electrical insulator between the atria and ventricles.
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93
Q

Give the function of valves

A

The valves of the heart are structures which ensure blood flows in only one direction.

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94
Q

Describe the composition of valves

A

They are composed of connective tissue and endocardium (the inner layer of the heart).

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95
Q

List all the valves found in the heart

A
  • Atrioventricular valves: The tricuspid valve and mitral (bicuspid) valve. They are located between the atria and corresponding ventricle.
  • Semilunar valves: The pulmonary valve and aortic valve. They are located between the ventricles and their corresponding artery, and regulate the flow of blood leaving the heart.
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96
Q

Describe the mechanism behind the opening and closing of the atrioventricular valves

A
  • When an AV valve is open, the rounded ends of the cusps project into the ventricle.
  • When the ventricles are relaxed, the papillary muscles are relaxed, the chordae tendineae are
    slack, and blood moves from a higher pressure in the atria to a lower pressure in the ventricles
    through open AV valves
  • When the ventricles contract, the pressure of the blood drives the cusps upward until their edges
    meet and close the opening. At the same time, the papillary muscles contract, which pulls on and
    tightens the chordae tendineae. This prevents the valve cusps from everting (opening into the
    atria) in response to the high ventricular pressure. If the AV valves or chordae tendineae are damaged, blood may regurgitate into the atria when the ventricles contract.
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97
Q

Describe the mechinism behind the opening and closing of the semi-lunar valves

A

Made up of three crescent moon–shaped cusps.
* Each cusp attaches to the arterial wall by its convex outer margin.
* The SL valves allow ejection of blood from the heart into arteries but prevent backflow of blood into the ventricles. The free borders of the cusps project into the lumen of the artery.
* When the ventricles contract, pressure builds up within the chambers. The semilunar valves open when pressure in the ventricles exceeds the pressure in the arteries, permitting ejection of blood from the ventricles into the pulmonary trunk and aorta.
* As the ventricles relax, blood starts to flow back toward the heart. Arteriole pressure exceeds ventricular pressure. This backflowing blood fills the valve cusps, which causes the free edges of the semilunar valves to contact each other tightly and close the opening between the ventricle and artery.

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98
Q

Which vessels does the left coronary artery branch into?

A
  • Circumflex artery
  • Left Anterior Descending artery (LAD)
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99
Q

What do the left coronary arteries supply?

A
  • Circumflex artery - supplies blood to the left atrium, side and back of the left ventricle
  • Left Anterior Descending artery (LAD) - supplies the front and bottom of the left ventricle and the front of the septum
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100
Q

What does the right coronary artery branch into?

A
  • Right marginal artery
  • Posterior descending artery
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101
Q

What does the right artery supply?

A
  • Right atrium, right ventricle, bottom portion of both ventricles and back of the septum
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102
Q

Describe ‘Collateral Circulation’

A
  • A network of tiny blood vessels, and, under normal conditions, not open.
  • When the coronary arteries narrow to the point that blood flow to the heart muscle is limited (coronary artery disease), collateral vessels may enlarge and become active. This allows blood to flow around the blocked artery to another artery nearby or to the same artery past the blockage, protecting the heart tissue from injury.
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103
Q

Give features of the autorhythmic fibres

A
  • a network of specialised cardiac muscle fibres which are self-excitable.
  • generate action potentials that trigger heart contractions.
  • during embryonic development, only about 1% of the cardiac muscle fibres become autorhythmic fibres
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104
Q

Give functions of the autorhythmic fibres

A
  1. They act as a pacemaker, setting the rhythm of electrical excitation that causes contraction of the heart.
  2. They form the cardiac conduction system, a network of specialized cardiac muscle fibres that provide a path for each cycle of cardiac excitation to progress through the heart. The conduction system ensures that cardiac chambers become stimulated to contract in a coordinated manner, which makes the heart an effective pump. Problems with autorhythmic fibres can result in arrhythmias (abnormal rhythms) in which the heart beats irregularly, too fast, or too slow.
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105
Q

Describe the process of cardiac excitation

A
  1. Cardiac excitation begins in the sinoatrial (SA) node, located in the right atrial wall just inferior and lateral to the opening of the superior vena cava. SA node cells do not have a stable resting potential. Rather, they repeatedly depolarize to threshold spontaneously. The spontaneous depolarization is a pacemaker potential. When the pacemaker potential reaches threshold, it triggers an action potential. Each action potential from the SA node propagates throughout both atria via gap junctions in the intercalated discs of atrial muscle fibers. Following the action potential, the two atria contract at the same time.
  2. By conducting along atrial muscle fibers, the action potential reaches the atrioventricular (AV) node, located in the interatrial septum, just anterior to the opening of the coronary sinus. At the AV node, the action potential slows considerably as a result of various differences in cell structure in the AV node. This delay provides time for the atria to empty their blood into the ventricles.
  3. From the AV node, the action potential enters the atrioventricular (AV) bundle (also known as the bundle of His). This bundle is the only site where action potentials can conduct from the atria to the ventricles. (Elsewhere, the fibrous skeleton of the heart electrically insulates the atria from the ventricles.) The atrioventricular bundle (bundle of His) is a continuation of the specialised tissue of the AV node, and serves to transmit the electrical impulse from the AV node to the Purkinje fibres of the ventricles.
    It descends down the membranous part of the interventricular septum, before dividing into two main bundles:
    * Right bundle branch - conducts the impulse to the Purkinje fibres of the right ventricle
    * Left bundle branch - conducts the impulse to the Purkinje fibres of the left ventricle
    * The Purkinje fibres (sub-endocardial plexus of conduction cells) are a network of specialised cells. They are abundant with glycogen and have extensive gap junctions. These cells are located in the subendocardial surface of the ventricular walls and are able to rapidly transmit cardiac action potentials from the atrioventricular bundle to the myocardium of the ventricles.
  4. This rapid conduction allows coordinated ventricular contraction (ventricular systole) and blood is moved from the right and left ventricles to the pulmonary artery and aorta respectively.
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106
Q

Which factors do cardiac output depend on?

A

Heartrate
Stroke volume

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107
Q

What can cause a change in heart rate?

A

Exercise
Exessive bleeding
Increase bp/increase hr

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108
Q

Which factors are involved in the regulation of heartrate?

A

Autonomic nervous system
Hormones released by adrenal medullae (epinephrine and norepinephrine)

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109
Q

Where is the cardiovascular centre located?

A

Medulla oblongata

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110
Q

Describe the role of the cardiovascular centre

A

This region of the brain stem receives input from a variety of sensory receptors and from higher brain centres, such as the limbic system and cerebral cortex. The cardiovascular centre then directs appropriate output by increasing or decreasing the frequency of nerve impulses in both the sympathetic and parasympathetic branches of the ANS to increase or decrease heartrate respectively.

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111
Q

Describe how heart rate is regulated by the autonomic nervous system.

A

-A wave of electrical excitation spreads out from the sinoatrial node (SAN) across both atria, causing them to contract.
-A layer of non-conductive tissue prevents the wave crossing to the ventricles.
-The wave of excitation enters the atrioventricular node (AVN).
-The atrioventricular node, conveys a wave of electrical excitation between the ventricles along the Purkyne tissue muscle fibres, collectively making up the bundle of His.
-The bundle of His conducts the wave through the atrioventricular septum to the base of the ventricles, where the bundle branches into smaller fibres of Purkyne tissue.
-The wave of excitation is released from the Purkyne tissue, causing the ventricles to contract quickly at the same time, from the bottom of the heart upwards.

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112
Q

How do chemoreceptors control heartrate?

A

-When blood has a high concentration of carbon dioxide, the pH is lowered.
-Chemoreceptors detect this pH change and increase the frequency of nervous impulses to the centre in the medulla oblongata that increases heart rate.
-This centre increases the frequency of impulses via the sympathetic nervous system to the sinoatrial node. This increases the rate of increases the rate of production of electrical waves by the sinoatrial node and therefore increases the heart rate.
-The increased blood flow that this causes leads to more carbon dioxide being removed by the lungs and so the carbon dioxide concentration of the blood returns to normal
-As a consequence the pH of blood rises to normal and the chemoreceptors in the wall of caratoid arteries and aorta reduce the frequency of nerve impulses to the medulla oblongata.
-The medulla oblongata reduces the frequency of impulses to the sinoatrial node, therefore leading to reduction in heart rate.

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113
Q

How does exercise affect cardiac output?

A

-Increased muscular activity
-More carbon dioxide produced by tissues by increased respiration
-Blood pH lowered
-Chemical receptors in carotid arteries increase frequency of impulses to medulla oblongata.
-Centre in medulla oblongata that speeds heart rate, increases frequency of impulses to SA node via the sympathetic nervous system.
-SA node increases heart rate.
-Increased blood blow removed carbon dioxide faster.

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114
Q

How do baroreceptors control heart rate when blood pressure is too high?

A

Pressure receptors transmit more nervous impulses to the centre in the medulla oblongata that decreases heart rate. This centre sends impulses via the parasympathetic nervous system to the sinoatrial node of the heart which leads to decrease in heart rate.

115
Q

Suppose the parasympathetic nerve connections from the medulla oblongata to the sinoatrial node were out. Suggest what might happen if a persons blood pressure increases above normal

A

Blood pressure remains high because the parasympathetic system is unable to transit nerve impulses to the SA node, which decreases heart rate and so lowers blood pressure.

116
Q

The nerve connecting the carotid artery to the medulla oblongata of a person is cut. This person then undertakes some strenuous exercise. Suggest what might happen to the persons heart rate?

A

Heart rate remains as it was before taking exercise, blood pressure increases and carbon dioxide concentration of blood rises (lowering pH). The changes are detected by pressure and chemical receptors in the wall of the carotid arteries. As the nerve from here to the medulla oblongata is cut, no nerve impulse can be sent to centres that control heart rate.

117
Q

The nerve connecting the carotid artery to the medulla oblongata of a person is cut. This person then undertakes some strenuous exercise. Suggest what might happen to the persons carbon dioxide concentration?

A

Blood CO2 concentration increased as a result of increased respiration during exercise.

118
Q

Describe how ECGs relate to Conducting systems

A
  • In a typical record, three clearly recognizable waves appear with each heartbeat
  • The first, called the P wave, is a small upward deflection on the ECG. The P wave represents atrial depolarization, which spreads from the SA node through contractile fibres in both atria.
  • The second wave, called the QRS complex, begins as a downward deflection, continues as a large, upright, triangular wave, and ends as a downward wave. The QRS complex represents rapid ventricular depolarization, as the action potential spreads through ventricular contractile fibers.
  • The third wave is a dome-shaped upward deflection called the T wave. It indicates ventricular repolarization and occurs just as the ventricles are starting to relax. The T wave is smaller and wider than the QRS complex because repolarization occurs more slowly than depolarization.
  • During the plateau period of steady depolarization, the ECG tracing is flat.
119
Q

Define ‘systole’

A

The period of contraction that the heart undergoes while it pumps blood into circulation

120
Q

Define ‘diastole’

A

The period of relaxation that occurs as the chambers fill with blood

121
Q

Describe how ECGs relate to the cardiac cycle

A
  1. A cardiac action potential arises in the SA node. It propagates throughout the atrial muscle and down to the AV node in about 0.03 sec. As the atrial contractile fibres depolarize, the P wave appears in the ECG.
  2. After the P wave begins, the atria contract (atrial systole). Conduction of the action potential slows at the AV node because the fibres there have much smaller diameters and fewer gap junctions. The resulting 0.1-sec delay gives the atria time to contract, thus adding to the volume of blood in the ventricles, before ventricular systole begins.
  3. The action potential propagates rapidly again after entering the AV bundle. About 0.2 sec after onset of the P wave, it has propagated through the bundle branches, Purkinje fibres, and the entire ventricular myocardium. Depolarization progresses down the septum, upward from the apex, and outward from the endocardial surface, producing the QRS complex. At the same time, atrial repolarization is occurring, but it is not usually evident in an ECG because the larger QRS complex masks it.
  4. Contraction of ventricular contractile fibres (ventricular systole) begins shortly after the QRS complex appears and continues during the S–T segment. As contraction proceeds from the apex toward the base of the heart, blood is squeezed upward toward the semilunar valves.
  5. Repolarization of ventricular contractile fibres begins at the apex and spreads throughout the ventricular myocardium. This produces the T wave in the ECG about 0.4 sec after the onset of the P wave.
  6. Shortly after the T wave begins, the ventricles start to relax (ventricular diastole). By 0.6 sec, ventricular repolarization is complete and ventricular contractile fibres are relaxed.
122
Q

Describe atrial systole

A
  • During atrial systole, which lasts about 0.1 sec, the atria are contracting. At the same time, the ventricles are relaxed.
  • Depolarization of the SA node causes atrial depolarization, marked by the P wave in the ECG.
  • Atrial depolarization causes atrial systole. As the atria contract, they exert pressure on the blood within, which forces blood through the open AV valves into the ventricles.
  • Atrial systole contributes a final 25 mL of blood to the volume already in each ventricle. The end of atrial systole is also the end of ventricular diastole. Thus, each ventricle contains about 130 mL at the end of diastole. This blood volume is called the end-diastolic volume (EDV).
  • The QRS complex in the ECG marks the onset of ventricular depolarization.
123
Q

Describe ventricular systole

A
  • During ventricular systole, which lasts about 0.3 sec, the ventricles are contracting. At the same time, the atria are relaxed in atrial diastole.
    Ventricular depolarization causes ventricular systole. As ventricular systole begins, pressure rises inside the ventricles and pushes blood up against the AV valves, forcing them shut. For about 0.05 seconds, both the SL and AV valves are closed. This is the period of isovolumetric contraction.
  • Continued contraction of the ventricles causes pressure inside the chambers to rise sharply. When left ventricular pressure surpasses aortic pressure at about 80 mmHg and right ventricular pressure rises above the pressure in the pulmonary trunk, both SL valves open. At this point, ejection of blood from the heart begins. The period when the SL valves are open is ventricular ejection and lasts for about 0.25 sec. The pressure in the left ventricle continues to rise to about 120 mmHg, and the pressure in the right ventricle climbs to about 25–30 mmHg.
  • The left ventricle ejects about 70 mL of blood into the aorta and the right ventricle ejects the same volume of blood into the pulmonary trunk. The volume remaining in each ventricle at the end of systole, about 60 mL, is the end-systolic volume (ESV). * The T wave in the ECG marks the onset of ventricular repolarization.
124
Q

How do you calculate stroke volume?

A

Stroke volume, the volume ejected per beat from each ventricle, equals end-diastolic volume minus end-systolic volume: SV = EDV − ESV. At rest, the stroke volume is about 130 mL − 60 mL = 70 mL (a little more than 2 oz).

125
Q

Describe diastole

A
  • During the relaxation period, which lasts about 0.4 sec, the atria and the ventricles are both relaxed. As the heart beats faster and faster, the relaxation period becomes shorter and shorter, whereas the durations of atrial systole and ventricular systole shorten only slightly.
  • Ventricular repolarization causes ventricular diastole. As the ventricles relax, pressure within the chambers falls, and blood in the aorta and pulmonary trunk begins to flow backward toward the regions of lower pressure in the ventricles. Backflowing blood catches in the valve cusps and closes the SL valves. The aortic valve closes at a pressure of about 100 mmHg. Rebound of blood off the closed cusps of the aortic valve produces the dicrotic wave on the aortic pressure curve. After the SL valves close, there is a brief interval when ventricular blood volume does not change because all 4 valves are closed. This is the period of isovolumetric relaxation.
  • As the ventricles continue to relax, the pressure falls quickly. When ventricular pressure drops below atrial pressure, the AV valves open, and ventricular filling begins. The major part of ventricular filling occurs just after the AV valves open. Blood that has been flowing into and building up in the atria during ventricular systole then rushes rapidly into the ventricles. At the end of the relaxation period, the ventricles are about three-quarters full. The P wave appears in the ECG, signaling the start of another cardiac cycle.
126
Q

Define cardiac output

A

Cardiac output (CO) is the volume of blood ejected from the left ventricle (or the right ventricle) into the aorta (or pulmonary trunk) each minute.

127
Q

How is cardiac ouput calculated

A
  • CO=SV×HR
128
Q

Define End Systolic Volume (ESV)

A

The volume of blood in the ventricles at the end of systole. It is the lowest volume of blood in the ventricles at any point of the cardiac cycle.

129
Q

What are the main factors that affect ESV

A

Afterload
Contractibility of the heart

130
Q

Define End Diastolic Volume (EDV)

A

The volume of blood in the ventricles at the end of diastole.

131
Q

Describe the anatomical locations position of the conducting system of the heart

A

Sinoatrial Node in right atrium.
Atrioventricular node between right and left atria and ventricles (Interatrioventricular septum)
Bundle of His between AV node and bundle branches
Right and left bundle branches in interventricular septum
Purkinje fibres in endocardium

132
Q

Define ‘Lung volume’

A

The volume of gas held in the lungs.

133
Q

How are lung volumes measured?

A

Spirometre

134
Q

Give the 4 lung volumes

A

Tidal Volume
Inspiratory Reserve Volume
Expiratory Reserve Volume
Residual Volume

135
Q

Define tidal volume

A

Volume of air breathed in and out in a single breath

136
Q

Define Inspiratory Reserve Volume

A

Volume of air breathed in by a maximum inspiration at the end of a normal inspiration

137
Q

Define Expiratory Reserve Volume

A

Volume of air that can be expelled by a maximum effort at the end of a normal expiration

138
Q

Define Residual Volume

A

Volume of air remaining in lungs at the end of maximum expiration.

139
Q

What are pulmonary capacities?

A

A combination of 2 or more volumes.

140
Q

Define Inspiratory Capacity and give the calculation

A

IC= TV+IRV
Volume of air breathed in by a maximum inspiration at the end of a normal expiration

141
Q

Define Functional Residual Capacity and give the calculation

A

FRC= ERV+RV
Volume of air remaining in the lungs at the end of a normal expiration. Acts as a buffer against extreme changes in alveolar gas levels with each breath.

142
Q

Define Vital Capacity and give the calculation

A

VC= IRV+TV+ERV
Volume of air that can be breathed in by a maximum inspiration following a maximum expiration.

143
Q

Define Total Lung Capacity

A

TLC=VC+RV
The total volume of air that can be held by the lungs.
Only a fraction of TLC is used in normal breathing.

144
Q

After exhalation, the lungs are not completely emptied of air, why is this?

A

This is useful physiologically, as a completely deflated lung requires significantly more energy to inflate it than one in which the alveoli have not completely collapsed. Even following a maximum respiratory effort (forced expiration), some air remains within the lungs.

145
Q

Why is there still a residual volume?

A

This occurs because as the expiratory muscles contract during forced expiration, all the structures within the lungs (including the airways) are compressed by the positive intrapleural pressure. Consequently, the smaller airways collapse before the alveoli empty completely, meaning some air
remains within the lungs; this is known as the residual volume (RV).

146
Q

Describe what happens in quiet breathing after the tidal volume has been expired

A
  • Pressure outside the chest is equal to pressure inside the alveoli (i.e., atmospheric pressure).
  • Elastic forces tending to collapse the lung are balanced by the elastic recoil trying to expand the chest.
  • This creates a subatmospheric (negative) pressure in the intrapleural space.
  • The lung volume at this point is known as functional residual capacity (FRC).
147
Q

Describe how Residual Volume and Functional Residual Capacity can be measured

A

Nitrogen washout, helium dilution and plethysmography

148
Q

How can disease affect lung volumes?

A

Disease affects lung volumes in specific patterns, depending on the pathological processes.

149
Q

What are the 3 types of lung disease

A

Obstructive, restrictive or mixed

150
Q

What is an obstructive disorder

A

This group of disorders is characterized by obstruction of normal air flow caused by airway narrowing, which if not reversed, leads to hyperinflation of the lungs as air is trapped behind closed airways.
An example of an obstructive lung disease where a patient develops gas trapping and hyperinflation is chronic obstructive pulmonary disease (COPD).

151
Q

How do obstructive disorders affect lung volumes?

A
  • The RV is increased as gas that is trapped cannot leave the lung, and the RV:total lung capacity (TLC) ratio increases.
  • In patients with severe obstruction, air trapping can be so extensive that vital capacity is decreased.
152
Q

What is a restrictive disorder?

A

Restrictive disorders result in stiffer lungs that cannot expand to normal volumes. An example of a restrictive lung disorder is Idiopathic pulmonary fibrosis.

153
Q

How do restrictive disorders affect lung volumes?

A

All the subdivisions of volume are decreased and the RV:TLC ratio will be normal or increased (where vital capacity has decreased more quickly than RV).

154
Q

Define FEV1 (forced expiratory volume in 1 second)

A

FEV1 is the volume of air expelled in the first second of a forced expiration, starting from full inspiration.

155
Q

Define FVC (the forced vital capacity)

A

FVC is a measure of total lung volume exhaled; the patient is asked to exhale with maximal effort after a full inspiration.

156
Q

How can FEV1 and FVC be measured

A

Spirometre

157
Q

Which factors affect FEV1 and FVC

A

Height, age and sex of the patient.

158
Q

Explain the FEV1:FVC ratio

A

The FEV1:FVC ratio is a more useful measurement than FEV1 or FVC alone. FEV1 is 80% of FVC in normal subjects. The FEV1:FVC ratio is an excellent measure of airway limitation and allows us to differentiate obstructive from restrictive lung disease

159
Q

How is the FEV1:FVC ratio affected in obstructive disorders?

A
  • High intrathoracic pressures generated by forced expiration cause premature closure of the
    airways with trapping of air in the chest
  • FEV1 is reduced much more than FVC
  • FEV1:FVC ratio is reduced (< 80%)
160
Q

How is the FEV1:FVC ratio affected in restrictive disorders?

A
  • Both FEV1 and FVC are reduced, often in proportion to each other
  • FEV1:FVC ratio is normal or increased (> 80%)
161
Q

What does the upper respiratory system include?

A

The upper respiratory system includes the nose, nasal cavity, pharynx, and associated structures

162
Q

What does the lower respiratory system include?

A

The lower respiratory system includes the larynx, trachea, bronchi, and lungs.

163
Q

Define ‘pulmonary ventilation’

A

Breathing- the inhalation and exhalation of air and involves the exchange of air betrween the atmosphere and the alveoli of the lungs. Inhalation permits oxygen to enter the lungs and exhalation permits carbon dioxide to leave the lungs.

164
Q

Define ‘External pulmonary respiration’

A

The exchange of gases between the alveoli of the lungs and the blood in pulmonary capillaries acorss the respiratory membrane. In the process, pulmonary capillary blood gains oxygen and loses carbon dioxide.

165
Q

Define Internal pulmonary respiration

A

Internal respiration is the exchange of gases between blood in systemic capillaries and tissue cells. In this step the blood loses oxygen and gains carbon dioxide. Within cells, the metabolic reactions that consume oxygen and give off carbon dioxide duiring the production of ATP are termed cellular respiration.

166
Q

What are the 2 fundamental parts of the respiratory system

A

-The conducting zone
-The respiratory zone

167
Q

Describe the conducting zone

A

The conducting zone consists of a series of interconnecting cavities and tubes both outside and within the lungs. These include the nose, nasal cavity, pharynx, larynx, trachea, bronchi, bronchioles, and terminal bronchioles; their function is to filter, warm, and moisten air and conduct it into the lungs.

168
Q

Describe the respiratory zone

A

The respiratory zone consists of tubes and tissues within the lungs where gas exchange occurs. These include the respiratory bronchioles, alveolar ducts, alveolar sacs, and alveoli and are the main sites of gas exchange between air and blood.

169
Q

Describe the gross structure of the lungs and pleura

A
  • The lungs extend from the diaphragm to just slightly superior to the clavicles and lie against the ribs anteriorly and posteriorly
  • The broad inferior portion of the lung, the base, is concave and fits over the convex area of the diaphragm.
  • The narrow superior portion of the lung is the apex.
    *The surface of the lung lying against the ribs, the costal surface, matches the rounded curvature of the ribs.
  • The mediastinal (medial) surface of each lung contains a region, the hilum, through which bronchi, pulmonary blood vessels, lymphatic vessels, and nerves enter and exit
  • These structures are held together by the pleura and connective tissue and constitute the root of the lung.
  • Medially, the left lung also contains a concavity, the cardiac notch, in which the apex of the heart lies.
  • Due to the space occupied by the heart, the left lung is about 10% smaller than the right lung.
  • Although the right lung is thicker and broader, it is also somewhat shorter than the left lung because the diaphragm is higher on the right side, accommodating the liver that lies inferior to it.
  • The oblique fissure divides the left lung into two lobes. The oblique and horizontal fissures divide the right lung into three lobes.
  • The lungs almost fill the thorax
  • The apex of the lungs lies superior to the medial third of the clavicles, and this is the only area that can be palpated.
  • The anterior, lateral, and posterior surfaces of the lungs lie against the ribs. The base of the lungs extends from the sixth costal cartilage anteriorly to the spinous process of the tenth thoracic vertebra posteriorly.
  • The pleura extends about 5 cm (2 in.) below the base from the sixth costal cartilage anteriorly to the twelfth rib posteriorly.
170
Q

What does the hilum (root) of the lung consist of?

A
  • Bronchi
  • Vessels: pulmonary artery and vein
  • Nerves
  • Lymph nodes and lymphatic vessels
  • Pulmonary ligament.
171
Q

Describe the oblique fissures

A
  • One or two fissures divide each lung into sections called lobes
  • Both lungs have an oblique fissure, which extends inferiorly and anteriorly; the right lung also has a horizontal fissure.
  • The oblique fissure in the left lung separates the superior lobe from the inferior lobe.
  • In the right lung, the superior part of the oblique fissure separates the superior lobe from the inferior lobe; the inferior part of the oblique fissure separates the inferior lobe from the middle lobe, which is bordered superiorly by the horizontal fissure.
172
Q

Describe the lobar bronchi

A

*Each lobe receives its own lobar bronchus. Thus, the right main bronchus gives rise to three lobar bronchi called the superior, middle, and inferior lobar bronchi, and the left main bronchus gives rise to superior and inferior lobar bronchi.

173
Q

Describe the segmental bronchi

A

*Within the lung, the lobar bronchi give rise to the segmental bronchi, which are constant in both origin and distribution—there are 10 segmental bronchi in each lung. The portion of lung tissue that each segmental (tertiary) bronchus supplies is called a bronchopulmonary segment.

174
Q

What is the pleural membrane (pleura)

A

Each lung is enclosed and protected by a double-layered serous membrane.

175
Q

What is the paritial pleura?

A

The superficial layer lining the wall of the thoracic cavity.

176
Q

What is the visceral pleura?

A

The deep layer, covers the lungs themselves.

177
Q

What is the visceral pleura?

A

The deep layer, covers the lungs themselves.

178
Q

What is the pleural cavity?

A

A small space between the visceral and parietal pleurae which contains a small amount of lubricating fluid secreted by the membranes.
Separate pleural cavities surround the left and right lungs.

179
Q

Give the function of the pleaural fluid

A

Pleural fluid reduces friction between the membranes, allowing them to slide easily over one another during breathing.
Pleural fluid also causes the two membranes to adhere to one another, a phenomenon called surface tension.

180
Q

Define atmospheric pressure (Patm)

A

Pressure at the entrance of the respiratory tract.

181
Q

Define alveolar pressure (PA)

A

Pressure inside the lungs.

182
Q

Explain the mechansim of respiration in relation to pressure

A

Pressure differences in the lungs generate air flow.
Respiratory muscles generate these pressure differences.
If PA = Patm, no air flow occurs
If PA<Patm, air flows into the lungs
If PA>Patm, air flows out of the lungs

183
Q

Explain Boyle’s Law

A

Boyle’s Law states that at a fixed temperature, the pressure and volume of an ideal gas are inversely proportional, so as volume of air within the lungs increases, the pressure decreases.
Atmospheric pressure is always the same, therefore the alveolar pressure needs to change to achieve airflow.
When the diaphragm flattens, thoracic volume increases, intrapleural pressure decreases, so air flows into the lungs.
In expiration, relaxation of muscles of the chest wall allows the elastic recoil of the lungs to cause contraction of the lungs, reducing thoracic volume and increasing intrapleural pressure and thus expulsion of gas.

184
Q

Describe the process of inspiration

A

-The external intercostal muscles contract, whilst the internal intercostal muscles relax
-The ribs are pulled upwards and outwards, increasing the volume of the thorax.
-The diaphragm muscles contract, causing it to flatten, also increasing the volume of the thorax.
-The increased volume of the thorax results in reduced pressure in the lungs.
-Atmospheric pressure is now greater than pulmonary pressure, so air is forced into the lungs.

185
Q

Describe the process of expiration

A

-The internal intercostal muscles contract, whilst the external intercostal muscles relax
-The ribs are pulled downwards and inwards, decreasing the volume of the thorax.
-The diaphragm muscles relax, so it’s pushed up again by the contents of the abdomen that were compressed during inspiration, decreasing the volume of the thorax.
-The decreased volume of the thorax results in increased pressure in the lungs.
-Pulmonary pressure is now greater than atmospheric pressure, so air is forced out of the lungs.

186
Q

Give the surface markings of the lungs

A

The apices of the lung extend above the level of the medial third of the clavicles.
* The lower borders of the lung are:
* T6 - mid-clavicular line
* T8 - mid-axillary line
* T10 - posteriorly
* The lower borders of the pleura are:
* T8 - mid-clavicular line
* T10 - mid-axillary line
* T12 - posteriorly
* The upper lobe is in front of the lower lobe and thus the area of lung behind the anterior aspect of the chest wall is mainly the upper lobe; in the right lung the
middle lobe also contributes significantly to the anterior aspect (between T4 and T6 anteriorly). From the posterior aspect, the chest wall encloses the lower lobes
of each lung.
* In the right lung the oblique fissure runs from the spinal process of T3 posteriorly to the level of T6 anteriorly; The transverse fissure is at T4.
* Left lung has upper and lower lobes only. The middle lobe is replaced by a small segment called the lingula

187
Q

Give the surface markings of the lungs

A

The apices of the lung extend above the level of the medial third of the clavicles.
* The lower borders of the lung are:
* T6 - mid-clavicular line
* T8 - mid-axillary line
* T10 - posteriorly
* The lower borders of the pleura are:
* T8 - mid-clavicular line
* T10 - mid-axillary line
* T12 - posteriorly
* The upper lobe is in front of the lower lobe and thus the area of lung behind the anterior aspect of the chest wall is mainly the upper lobe; in the right lung the
middle lobe also contributes significantly to the anterior aspect (between T4 and T6 anteriorly). From the posterior aspect, the chest wall encloses the lower lobes
of each lung.
* In the right lung the oblique fissure runs from the spinal process of T3 posteriorly to the level of T6 anteriorly; The transverse fissure is at T4.
* Left lung has upper and lower lobes only. The middle lobe is replaced by a small segment called the lingula

188
Q

Give examples of accessory muscles of respiration, describing how they support with breathing

A

The sternocleidomastoids and scalenes may be used for a more forceful inhalation, raise the ribs anteroposteriorly increasing intrathoracic volume.
The abdominal muscles may be used for a more forceful exhalation. Elastic recoil of the lungs is reinforced by contraction of the muscles of the abdominal wall; this forces the abdominal contents against the diaphragm, displacing the diaphragm upwards.
Intercostal muscles are more active and raise the ribs to a far greater extent than in quiet inspiration
The 12th rib, which is attached to quadratus lumborum, allows forcible downward movement of the diaphragm.
Arching the back using erector spinae also increases thoracic volume.
Scapulae are fixed by trapezius muscles.
The rhomboid muscles and levator scapulae, pectoralis minor and serratus anterior raise the ribs. The arms can be fixed (e.g., by holding the back of a chair), allowing the use of pectoralis major.
Levatores constorum- Elevate ribs in inspiration. 12 small muscles on either side of the thorax running between traverse process and ribs below.
Serratus posterior superior- Help inspiration.
Serratus posterior inferior- Assist expiration.
Transverse thoracics- Assist expiration, lie on inner surface of anterior thoracic wall running from superior surface xiphoid process, sternum and costal cartilage.

188
Q

Give examples of accessory muscles of respiration, describing how they support with breathing

A

The sternocleidomastoids and scalenes may be used for a more forceful inhalation, raise the ribs anteroposteriorly increasing intrathoracic volume.
The abdominal muscles may be used for a more forceful exhalation. Elastic recoil of the lungs is reinforced by contraction of the muscles of the abdominal wall; this forces the abdominal contents against the diaphragm, displacing the diaphragm upwards.
Intercostal muscles are more active and raise the ribs to a far greater extent than in quiet inspiration
The 12th rib, which is attached to quadratus lumborum, allows forcible downward movement of the diaphragm.
Arching the back using erector spinae also increases thoracic volume.
Scapulae are fixed by trapezius muscles.
The rhomboid muscles and levator scapulae, pectoralis minor and serratus anterior raise the ribs. The arms can be fixed (e.g., by holding the back of a chair), allowing the use of pectoralis major.
Levatores constorum- Elevate ribs in inspiration. 12 small muscles on either side of the thorax running between traverse process and ribs below.
Serratus posterior superior- Help inspiration.
Serratus posterior inferior- Assist expiration.
Transverse thoracics- Assist expiration, lie on inner surface of anterior thoracic wall running from superior surface xiphoid process, sternum and costal cartilage.

189
Q

Describe the structure of the nose

A

The lateral wall of the nasal cavity consists of bony ridges called conchae or turbinates which provide a large surface area covered in highly vascularized mucous membrane to warm and humidify inspired air.
* Under each turbinate, there is a groove or meatus.
* The paranasal air sinuses (frontal, sphenoid, ethmoid and maxillary) drain into these meatuses via small ostia, or openings.

190
Q

Describe the gross structure of the pharynx

A
  • The pharynx extends from the base of the skull to the inferior border of the cricoid cartilage,
    where it is continuous anteriorly with the trachea and posteriorly with the oesophagus. It is
    described as being divided into three parts: the nasopharynx, oropharynx and laryngopharynx,
    which open anteriorly into the nose, mouth and larynx, respectively
  • The pharynx is part of both the respiratory and gastrointestinal systems.
  • The nasopharynx is situated above the soft palate and opens anteriorly into the nasal cavities at
    the choanae (posterior nares).
  • During swallowing, the nasopharynx is cut off from the oropharynx by the soft palate. The
    nasopharynx contains the opening of the eustachian canal (pharyngotympanic or auditory tube)
    and the adenoids, which lie beneath the epithelium of its posterior wall.
191
Q

Describe the gross structure of the pharynx

A
  • The pharynx extends from the base of the skull to the inferior border of the cricoid cartilage,
    where it is continuous anteriorly with the trachea and posteriorly with the oesophagus. It is
    described as being divided into three parts: the nasopharynx (Ciliated pseudostratified columnar epithelium), oropharynx (Nonkeratinized stratified squamous epithelium) and laryngopharynx(Nonkeratinized stratified squamous epithelium), which open anteriorly into the nose, mouth and larynx, respectively
  • The pharynx is part of both the respiratory and gastrointestinal systems.
  • The nasopharynx is situated above the soft palate and opens anteriorly into the nasal cavities at
    the choanae (posterior nares).
  • During swallowing, the nasopharynx is cut off from the oropharynx by the soft palate. The
    nasopharynx contains the opening of the eustachian canal (pharyngotympanic or auditory tube)
    and the adenoids, which lie beneath the epithelium of its posterior wall.
192
Q

Describe the structure of the larynx

A

The larynx is continuous with the trachea at its inferior end. At its superior end, it is attached to the U-shaped hyoid bone and lies below the epiglottis of the tongue. The larynx consists of a cartilaginous skeleton linked by a number of membranes. This cartilaginous skeleton comprises the epiglottis, thyroid, arytenoid and cricoid cartilages.
Made of Nonkeratinized stratified squamous epithelium above vocal folds and Ciliated pseudostratified columnar epithelium below.

193
Q

Give functions of the larynx

A
  1. As an open valve, to allow air to pass when breathing.
  2. Protection of the trachea and bronchi during swallowing. The vocal folds close, the epiglottis is pushed back covering the opening to the larynx, and the larynx is pulled upwards and forwards beneath the tongue (preventing aspiration).
  3. Speech production (phonation).
194
Q

Describe the structure of the trachea

A

The trachea is a cartilaginous and membranous tube of about 10 cm in length. It extends from the
larynx to its bifurcation at the carina (at the level of the fourth or fifth thoracic vertebra). The trachea is approximately 2.5 cm in diameter and is supported by C-shaped rings of hyaline cartilage. The rings are completed posteriorly by the trachealis muscle.
Made of Ciliated pseudostratified columnar epithelium

195
Q

Give the important relations of the trachea within the neck

A
  1. The thyroid gland, which straddles the trachea, with its two lobes positioned laterally, and its
    isthmus anterior to the trachea with the inferior thyroid veins.
  2. The common carotid arteries, which lie lateral to the trachea.
  3. The oesophagus, which lies directly behind the trachea, and the recurrent laryngeal nerve, which
    lies between these two structures.
196
Q

Describe the struture of the respiratory tree (bronchi)

A
  • Inside the thorax, the trachea divides into the left and right primary bronchi at the carina.
  • The right main bronchus is shorter and more vertical than the left (for this reason, inhaled foreign bodies are more likely to pass into the right lung).
  • The primary bronchi within each lung divide into secondary or lobar bronchi.
  • The lobar bronchi divide again into tertiary or segmental bronchi.
  • The airways continue to divide, always splitting into two daughter airways of progressively smaller calibre until eventually forming bronchioles.
    Bronchi made of Ciliated pseudostratified columnar epithelium
197
Q

Give the location and function of the conducting zone

A

Airways proximal to the respiratory bronchioles. Involved in air movement by bulk flow to the end respiratory units.

198
Q

Give the location and function of the respiratory zone

A

Airways distal to the terminal bronchiole
Involved in gaseous exchange.

199
Q

Describe the structure of the acnius

A

The acinus is the part of the airway involved in gaseous exchange. The acinus consists of:
* Respiratory bronchioles, leading to the alveolar ducts.
* Alveolar ducts, opening into two or three alveolar sacs, which in turn open into several alveoli.
Multiple acini are grouped together and surrounded by parenchymal tissue, forming a lung lobule. Lobules are separated by interlobular septa.

200
Q

What is the blood air interface?

A
  • The blood–air interface is a term that describes the site at which gaseous exchange takes place within the lung.
  • Average surface area of the alveolar–capillary membrane = 50–100 m2.
  • Average thickness of alveolar–capillary membrane = 0.4 mm.
    Short diffusion distance for efficient gas exchange.
201
Q

Describe the structure of alveoli

A
  • The alveoli are microscopic blind-ending air pouches forming the distal termination of the respiratory tract; there are 150–400 million in each normal lung. The alveoli open into alveolar sacs and then into alveolar ducts.
  • Simple squamous epithelium, 1 squamous cell thick- very thin, short diffusion distance
  • Most gaseous exchange occurs in the alveoli. Because alveoli are so numerous, they provide the majority of lung volume and surface area. The majority of alveoli open into the alveolar sacs.
  • Communication between adjacent alveoli is possible through perforations in the alveolar wall, called pores of Kohn.
  • The alveoli are lined with type I and type II pneumocytes, which sit on a basement membrane.
  • Type I pneumocytes are structural, whereas type II pneumocytes produce surfactant.
202
Q

What is the function of alveolar macrophages?

A
  • The most numerous of all cells in the lung are the alveolar macrophages (dust cells), which drift through the alveolar lumens and the connective tissue between them clearing up debris through phagocytosis.
  • These macrophages “eat” the dust particles that escape from mucus in the higher parts of the respiratory tract, as well as other debris that is not trapped and cleared out by your mucus.
  • If your lungs are infected or bleeding, the macrophages also function to phagocytize bacteria and loose blood cells.
  • At the end of each day, as many as 100 million of these alveolar macrophages will expire as they ride up the mucociliary escalator to be swallowed at the esophagus and digested.
203
Q

What is Collateral Ventilation?

A

Provides alternate pathways for airflow upon obstruction.

204
Q

What are the interalveolar pores of Kohn?

A

The interalveolar pores of Kohn are epithelial-lined openings between adjacent alveoli
The pores of Kohn are usually filled with fluid and only open in response to a high pressure gradient across them. The fluid may contain alveolar lining fluid, components of surfactant, and macrophages.
There are between 13 and 21 pores in each alveolus

205
Q

What are the bronchoalveolar canals of Lambert?

A

The bronchoalveolar canals of Lambert are communications that reached from respiratory bronchioles to the alvelar ducts. They have a muscular wall with possible regional airflow control.

206
Q

What are the interbronchiolar channels of Martin?

A

The interbronchiolar channels of Martin have a diameter of 30 μm and are found between respiratory bronchioles and terminal bronchioles

207
Q

Describe Nonkeratinized stratified squamous epithelium

A
  • Consists of cells arranged in layers upon a basal membrane.
  • Only one layer is in contact with the basement membrane; while the other layers are adhered
    to one another to maintain structural integrity.
  • This type of epithelium is well suited to areas in the body subject to constant abrasion, as it
    is the thickest layer.
  • Additionally, this layer can be sequentially sloughed off and replaced before the basement membrane is exposed.
  • Non-keratinised surfaces must be kept moist by bodily secretions to prevent them from
    drying out.
208
Q

Describe Ciliated pseudostratified columnar epithelium

A
  • Pseudostratified columnar epithelia are tissues formed by a single layer of cells
    that give the appearance of being made from multiple layers, especially when seen in cross section. The nuclei of these epithelial cells are at different levels leading to the illusion of being stratified. However, this tissue is made of a single layer of cells and each cell is in
    contact with the basement membrane.
  • The coordinated action of cilia on longer columnar cells facing the lumen moves the mucus along with the particulate matter away from the lung.
209
Q

Describe Golblet Cells

A
  • a specialized type of epithelial cell that secrete mucins, which are significant components of mucus
  • most often found in the respiratory and gastrointestinal tracts, where they make up part of the surface epithelium. The secretion of mucus in these tracts lubricates and protects the lining of the organs
  • The increased activity or number of goblet cells has been associated with some diseases.
210
Q

Describe club/clara cells

A
  • Nonciliated bronchiolar epithelial cells found in the mucosa of the terminal bronchioles
  • Secrete a club cell secretory protein which has antioxidant and immune-modulatory functions
211
Q

Describe the structure of bronchioles

A
  • The epithelium here is ciliated and cuboidal but contains some Clara cells, which are non-ciliated and secrete proteinaceous fluid. Bronchioles contain no cartilage, meaning these airways must be kept open by radial traction, and there are no glands in the submucosa. The smooth-muscle layer is prominent. Adjusting the tone of the smooth-muscle layer alters airway diameter, enabling
    resistance to air flow to be effectively controlled.
    Made of Ciliated simple columnar epithelium.
212
Q

Describe the structure of respiratory bronchioles

A

The respiratory bronchioles are lined by ciliated cuboidal epithelium, which is surrounded by smooth muscle. Clara cells are present within the walls of the respiratory bronchioles. Goblet cells are absent but there are a few alveoli in the walls; thus, the respiratory bronchiole is a site for gaseous exchange.

213
Q

Describe the physical defence system of the lungs

A
  • Filtering at the nasopharynx
  • Swallowing
  • Irritant C-fibre nerve endings (receptors stimulated which leads to contraction of the smooth muscle)
  • Cough reflex
  • Mucociliary clearance
214
Q

Describe the humoral defence system of the lungs

A
  • Antimicrobial peptides (short protein structures, antibacterial, e.g. lysozymes)
  • Surfactant (plays a role in defence, e.g. SpA)
  • Immunoglobulins ( contained in mucus secretions, directed against specific antigens)
  • Complement (high concentration during inflammation, propagates inflammatory response)
  • Antiproteases (type of enzyme, breaks down destructive proteases released from e.g. neutrophils)
215
Q

Give 2 examples of cellular defence of the lungs

A

Alveolar macrophages
Neutrophils

216
Q

Give the function of alevolar macropahes

A
  • Ingest bacteria by phagocytosis
  • Initiate and amplify inflammatory response
217
Q

Give the function of neutrophils

A
  • Predominant cells recruited in the acute inflammatory response
  • Emigrate from intravascular space to alveolar lumen, and here intracellular killing of bacteria takes place ( 2 mechanisms, oxidative and non-oxidative)
218
Q

Define the Mucociliary Escalator

A

“Mucociliary clearance is an innate defense mechanism that protects the pulmonary system from the harmful consequences of inhaled agents, including those of biological, chemical, and physical
nature. Ciliated cells, which line the surface epithelium of the airways, provide the force necessary for mucociliary clearance by the coordinated beating of their cilia.”

219
Q

Describe the 2 layers of the mucus film

A
  1. Periciliary fluid (sol) layer about 6 μm deep, immediately adjacent to the surface of the epithelium. The mucus here is hydrated by epithelial cells. This reduces its viscosity and allows movement of the cilia.
  2. Superficial gel layer about 5–10 μm deep. This is a relatively viscous layer forming a sticky blanket, which traps particles.
220
Q

Describe the role of the cilia

A
  • The cilia beat synchronously at 1000–1500 strokes per minute. Coordinated movement causes the superficial gel layer, together with trapped particles, to be continually transported towards the mouth at 1–3 cm/min. The mucus and particles reach the trachea and larynx where they are swallowed or expectorated.
221
Q

Which factors inhibit mucociliary clearance?

A
  • Tobacco smoke
  • Cold air
  • Drugs e.g. general anaesthetic, so implications for this following surgery
    Cystic Fibrosis – ineffective mucociliary clearance
222
Q

Define the ‘cough reflex’

A

The cough reflex is an important defence mechanism which clears the airways of irritants by forcefully expelling air from the respiratory tract.

223
Q

Describe the inspiratory phase of the cough reflex

A

Irritation of cough receptors causes the vocal cords to open more widely, allowing more air to enter the lungs. The external intercostal muscles and diaphragm then contract causing expansion of the chest cavity, facilitating movement of air into the lungs, and increasing intra-thoracic pressure.

224
Q

Describe the compression phase of the cough reflex

A

The epiglottis and vocal cords close, trapping the air within the lungs. There is expiration against the closed epiglottis, causing a further increase in intra-thoracic pressure.

225
Q

Describe the expiratory phase of the cough reflex

A

The internal intercostal muscles and abdominal muscles contract to depress the thoracic cavity. The vocal cords relax, and the epiglottis opens. This releases the pressure from the lungs and causes air and the irritant to be rapidly expelled.

226
Q

Briefly describe the cough reflex arc

A

-Receptors: mechanical/chemical
-Afferent nerves
-Reflex Arc: cough centre: NTS medulla
-Efferent nerves
-Expiratory muscles: cough

227
Q

Describe the sensory afferent pathway of the cough reflex arc

A
  • The cough reflex arc is initiated by irritation of cough receptors, for example, mechanoreceptors
    or chemoreceptors. Irritants are detected by these receptors and they send sensory
    information to afferent nerves. Receptors are found in the trachea, main carina, branching
    points of large airways, and more distal smaller airways; also, they are present in the pharynx.
228
Q

Describe the central pathway of the cough reflex arc

A

Sensory information travels to the nucleus tractus solitarius (NTS) of the medulla. The vagus
nerve then synapses with motor neurons, delivering information to effector muscles and
causing the cough reflex to occur.

229
Q

Describe the motor efferent pathway of the cough reflex arc

A
  • Various respiratory muscles contract to allow initiation of the cough reflex.
  • The diaphragm contracts to become flattened which increases the thoracic cavity space
  • The laryngeal muscles contract to close the vocal cords
  • The external intercostal muscles contract to change the space available in the thoracic cavity
  • Rectus abdominis contracts to depress the rib cage and decrease space in the thoracic cavity
230
Q

Describe the muscocillary escalator and the role it plays in pulmonary defence (12 marks)

A

Mucociliary clearance deals with a lot of the large particles trapped in the bronchi and bronchioles and debris brought up by alveolar macrophages.
* Respiratory epithelium is covered by a layer of mucus secreted by goblet cells and submucosal glands.
* The mucus film is divided into two layers
* Periciliary fluid (sol) layer immediately adjacent to the surface of the epithelium. The mucus here is hydrated by epithelial cells. This reduces its viscosity and allows movement of the cilia.
* Superficial gel layer, a relatively viscous layer forming a sticky blanket, which traps particles.
* Coordinated movement of the cilia causes the superficial gel layer, together with trapped particles, to be continually transported towards the mouth
* The mucus and particles reach the trachea and larynx where they are swallowed or expectorated.

231
Q

Give the 3 processes of gaseous exchange

A
  • Pulmonary ventilation
  • External respiration
  • Internal respiration
232
Q

Describe external respiration

A
  • diffusion of O2 from air in the alveoli of the lungs to blood in pulmonary capillaries and the diffusion of CO2 in the opposite direction
  • deoxygenated blood (depleted of some O2) coming from the right side of the heart is converted into oxygenated blood (saturated with O2) that returns to the left side of the heart
  • blood flows through the pulmonary capillaries, picks up O2 from alveolar air and unloads CO2 into alveolar air
  • each gas diffuses independently from the area where its partial pressure is higher to the area where its partial pressure is lower.
233
Q

Describe the saturation values of external respiration

A
  • O2 diffuses from alveolar air, where its partial pressure is 105 mmHg, into the blood in pulmonary capillaries, where PO2 is only 40 mmHg in a resting person.
  • If you have been exercising, the PO2 will be even lower because contracting muscle fibers are using more O2. Diffusion continues until the PO2 of pulmonary capillary blood increases to match the PO2 of alveolar air, 105 mmHg.
  • Because blood leaving pulmonary capillaries near alveolar air spaces mixes with a small volume of blood that has flowed through conducting portions of the respiratory system, where gas exchange does not occur, the PO2 of blood in the pulmonary veins is slightly less than the PO2 in pulmonary capillaries, about 100 mmHg.
  • While O2 is diffusing from alveolar air into deoxygenated blood, CO2 is diffusing in the opposite direction. The PCO2 of deoxygenated blood is 45 mmHg in a resting person, and the PCO2 of alveolar air is 40 mmHg. Because of this difference in PCO2, carbon dioxide diffuses from deoxygenated blood into the alveoli until the PCO2 of the blood decreases to 40 mmHg.
    Exhalation keeps alveolar PCO2 at 40 mmHg. Oxygenated blood returning to the left side of the heart in the pulmonary veins thus has a PCO2 of 40 mmHg.
234
Q

Describe internal respiration

A
  • The left ventricle pumps oxygenated blood into the aorta and through the systemic arteries to systemic capillaries.
  • The exchange of O2 and CO2 between systemic capillaries and tissue cells is called internal respiration or systemic gas exchange.
  • As O2 leaves the bloodstream, oxygenated blood is converted into deoxygenated blood. Unlike external respiration, which occurs only in the lungs, internal respiration occurs in tissues throughout the body.
235
Q

Describe the saturation values of internal respiration

A
  • The PO2 of blood pumped into systemic capillaries is higher (100 mmHg) than the PO2 in
    tissue cells (40 mmHg at rest) because the cells constantly use O2 to produce ATP. Due to this
    pressure difference, oxygen diffuses out of the capillaries into tissue cells and blood PO2
    drops to 40 mmHg by the time the blood exits systemic capillaries.
  • CO2 diffuses in the opposite direction. Because tissue cells are constantly producing CO2, the
    PCO2 of cells (45 mmHg at rest) is higher than that of systemic capillary blood (40 mmHg). As
    a result, CO2 diffuses from tissue cells through interstitial fluid into systemic capillaries until
    the PCO2 in the blood increases to 45 mmHg. The deoxygenated blood then returns to the
    heart and is pumped to the lungs for another cycle of external respiration.
236
Q

Describe the composition of proteins

A

Proteins are complex macromolecules (polymers). They have high molecular weight and are made up of structural units (monomers) called amino acids.
Amino acids are the protein’s building units. They are organic compounds made up of hydrogen, oxygen, carbon and nitrogen atoms. Amino acids are made up of a basic group (amino group NH2), an acidic group (carboxyl group COOH), a hydrogen atom, and a terminal group R which differs from one amino acid to another.
* Amino group, carboxyl group, R group (changes)
* The combination of two amino acids is called a dipeptide compound, and the protein chain formed of several amino acids is called a polypeptide.

237
Q

How much oxygen is transported in blood plasma?

A

1.5% (due to the relative insolubility of oxygen in water)

238
Q

How much oxygen is transported in red blood cells/haemoglobin?

A

98.5%

239
Q

Describe the structure of haemoglobin

A
  • Haemoglobin is a globular protein which is an oxygen-carrying pigment found in vast quantities in red blood cells
  • It has a quaternary structure as there are four polypeptide chains. These chains or subunits are globin proteins (two α–globins and two β–globins) and each subunit has a prosthetic haem group
  • The four globin subunits are held together by disulphide bonds and arranged so that their hydrophobic R groups are facing inwards (helping preserve the three-dimensional spherical
    shape) and the hydrophilic R groups are facing outwards (helping maintain its solubility)
  • The arrangements of the R groups is important to the functioning of haemoglobin. If changes occur to the sequence of amino acids in the subunits this can result in the properties of haemoglobin changing.
  • The prosthetic haem group contains an iron II ion (Fe2+) which is able to reversibly combine with an oxygen molecule forming oxyhaemoglobin and results in the haemoglobin appearing
    bright red
  • Each haemoglobin with the four haem groups can therefore carry four oxygen molecules (eight oxygen atoms)
240
Q

What is the function of haemoglobin?

A

Haemoglobin is responsible for binding oxygen in the lung and transporting the oxygen to tissue to be used in aerobic metabolic pathways
As oxygen is not very soluble in water and haemoglobin is, oxygen can be carried more efficiently around the body when bound to the haemoglobin

241
Q

Give the function of the ferrous group

A
  • The presence of the haem group (and Fe2+) enables small molecules like oxygen to be bound more easily because as each oxygen molecule binds it alters the quaternary structure (due to alterations in
    the tertiary structure) of the protein which causes haemoglobin to have a higher affinity for the subsequent oxygen molecules and they bind more easily
  • The existence of the iron II ion (Fe2+) in the prosthetic haem group also allows oxygen to reversibly bind as none of the amino acids that make up the polypeptide chains in haemoglobin are well suited to binding with oxygen
242
Q

Describe the affinity of haemoglobin for carbon monxide compared to oxygen

A
  • The affinity of haemoglobin for carbon monoxide is 245-fold higher than that for oxygen Therefore, haemoglobin will preferentially bind irreversably to carbon monoxide over oxygen following an exposure.
  • This decreases the oxygen carrying capacity of the blood and alters the dissociation curve of oxyhaemoglobin.
    As a result, the rate at which oxygen is delivered to cells is reduced, interfering with cellular respiration and causing tissue hypoxia.
243
Q

Describe the relatishsp between haemoglobin and the partial pressure of oxygen

A

The higher the PO2, the more O2 combines with Hb.

244
Q

Give the 3 ways carbon dioxide is transported throughout the body

A

-Dissolved in blood - 7%
-Carbamino compounds - 23%
-Bicarbonate ions – 70%

245
Q

Describe the transport of carbon dioxide dissolved in the blood

A

CO2 is dissolved in blood plasma. On reaching the lungs, it diffuses into alveolar air and is exhaled.

246
Q

Describe the transport of carbon dioxide in carbamino compounds

A

CO2 combines with the amino groups of amino acids and proteins in blood to form carbamino compounds.
Because the most prevalent protein in blood is haemoglobin (inside red blood cells), most of the CO2 transported in this manner is bound to haemoglobin.
The main CO2 binding sites are the terminal amino acids in the two alpha and two beta globin chains.
Haemoglobin that has bound CO2 is termed carbaminohaemoglobin (Hb–CO2).
The formation of carbaminohaemoglobin is greatly influenced by PCO2. For example, in tissue capillaries
PCO2 is relatively high, which promotes formation of carbaminohaemoglobin. But in pulmonary capillaries,
PCO2 is relatively low, and the CO2 readily splits apart from globin and enters the alveoli by diffusion.

247
Q

Describe the transport of carbon dioxide in bicarbinate ions

A

As CO2 diffuses into systemic capillaries and enters red blood cells, it reacts with water in the presence of the enzyme carbonic anhydrase (CA) to form carbonic acid, which dissociates into H+ and HCO3−:
Thus, as blood picks up CO2, HCO3− accumulates inside RBCs. Some HCO3− moves out into the blood plasma, down its concentration gradient.
In exchange, chloride ions (Cl−) move from plasma into the RBCs. This exchange of negative ions, which maintains the electrical balance between blood plasma and RBC cytosol, is known as the chloride shift.
The net effect of these reactions is that CO2 is removed from tissue cells and transported in blood plasma as HCO3−. As blood passes through pulmonary capillaries in the lungs, all of these reactions reverse and CO2 is exhaled.

248
Q

Describe and explain the shape of an oxygen dissociation curve

A
  • When the PO2 is high, haemoglobin binds with large amounts of O2 and is almost 100% saturated. When PO2 is low, haemoglobin is only partially saturated. In other words, the greater the PO2, the more O2 will bind to haemoglobin, until all the available haemoglobin molecules are saturated.
  • In pulmonary capillaries, where PO2 is high, a lot of O2 binds to haemoglobin (has high affinity for oxygen). In tissue capillaries, where the PO2 is lower, haemoglobin does not hold as much O2, and the dissolved O2 is unloaded via diffusion into tissue cells (hb has low affinity for oxygen)
  • Note that haemoglobin is still 75% saturated with O2 at a PO2 of 40 mmHg, the average PO2 of tissue cells in a person at rest, only 25% of the available O2 unloads from haemoglobin and is used by tissue cells under resting conditions.
  • When the PO2 is between 60 and 100 mmHg, haemoglobin is 90% or more saturated with O2 , thus, blood picks up a nearly full load of O2 from the lungs even when the PO2 of alveolar air is as low as 60 mmHg. The Hb–PO2 curve explains why people can still perform well when they have certain cardiac and pulmonary diseases, even though PO2 may drop as low as 60 mmHg.
  • Note also in the curve that at a considerably lower PO2 of 40 mmHg, haemoglobin is still 75% saturated with O2. However, oxygen saturation of Hb drops to 35% at 20 mmHg.
  • Between 40 and 20 mmHg, large amounts of O2 are released from haemoglobin in response to only small decreases in PO2. In active tissues such as contracting muscles, PO2 may drop well below 40 mmHg. Then, a large percentage of the O2 is released from haemoglobin, providing more O2 to
    metabolically active tissues.
249
Q

GIve factors which affect the affinity of haemoglobin for oxygen

A

Acidity
Partial pressure of Carbon Dioxide
Temperature
BPG

250
Q

Explain how acidity affects haemoglobin affinity

A
  • When pH decreases (CO2 conc increases), the entire oxygen–haemoglobin dissociation curve shifts to the right; at any given PO2, Hb is less saturated with O2, a change termed the Bohr effect.
  • The Bohr effect works both ways: An increase in H+ in blood causes O2 to unload from haemoglobin, and the binding of O2 to haemoglobin causes unloading of H+ from haemoglobin.
  • The explanation for the Bohr effect is that haemoglobin can act as a buffer for hydrogen ions (H+). But when H+ ions bind to amino acids in haemoglobin, they alter its structure slightly, decreasing its oxygen-carrying capacity.
  • Thus, lowered pH drives O2 off haemoglobin, making more O2 available for tissue cells. By contrast, elevated pH increases the affinity of haemoglobin for O2 and shifts the oxygen–haemoglobin dissociation curve to the left.
251
Q

Describe how concentration of CO2 affects haemoglobin affinity

A

CO2 also can bind to haemoglobin, and the effect is similar to that of H+ (shifting the curve to the right). As PCO2 rises, haemoglobin releases O2 more readily (lower affinity).
* PCO2 and pH are related factors because low blood pH (acidity) results from high PCO2. As CO2 enters the blood, much of it is temporarily converted to carbonic acid (H2CO3), a reaction catalyzed by an enzyme in red blood cells called carbonic anhydrase (CA):
* The carbonic acid thus formed in red blood cells dissociates into hydrogen ions and bicarbonate ions. As the H+ concentration increases, pH decreases. Thus, an increased PCO2 produces a more acidic environment, which helps release O2 from haemoglobin. During exercise, lactic acid—a by-product of anaerobic metabolism within muscles—also decreases blood pH. Decreased PCO2 (and elevated pH) shifts the saturation curve to the left

252
Q

Describe how temperature affects affinity of haemoglobin

A
  • As temperature increases, so does the amount of O2 released from haemoglobin.
  • Heat is a by-product of the metabolic reactions of all cells, and the heat released by contracting muscle fibres tends to raise body temperature.
  • Metabolically active cells require more O2 and liberate more acids and heat.
  • The acids and heat in turn promote release of O2 from oxyhaemoglobin.
  • Fever produces a similar result. In contrast, during hypothermia (lowered body temperature) cellular metabolism slows, the need for O2 is reduced, and more O2 remains bound to haemoglobin (a shift to the left in the saturation curve).
253
Q

Describe how temperature affects affinity of haemoglobin

A
  • As temperature increases, so does the amount of O2 released from haemoglobin.
  • Heat is a by-product of the metabolic reactions of all cells, and the heat released by contracting muscle fibres tends to raise body temperature.
  • Metabolically active cells require more O2 and liberate more acids and heat.
  • The acids and heat in turn promote release of O2 from oxyhaemoglobin.
  • Fever produces a similar result. In contrast, during hypothermia (lowered body temperature) cellular metabolism slows, the need for O2 is reduced, and more O2 remains bound to haemoglobin (a shift to the left in the saturation curve).
254
Q

Describe how BPG affects affinity of haemoglobin

A
  • A substance found in red blood cells called 2,3-bisphosphoglycerate (BPG) decreases the affinity of
    haemoglobin for O2 and thus helps unload O2 from haemoglobin.
  • BPG is formed in red blood cells when they break down glucose to produce ATP in a process called
    glycolysis
  • When BPG combines with haemoglobin by binding to the terminal amino groups of the two beta globin chains, the haemoglobin binds O2 less tightly at the haem group sites. The greater the level of BPG, the more O2 is unloaded from haemoglobin. Certain hormones, such as thyroxine, human growth hormone, epinephrine, norepinephrine, and testosterone, increase the formation of BPG.
255
Q

Give the normal values for arteriole blood gases

A
  • pH: 7.35 – 7.45
  • pO2: 10 – 14kPa
  • pCO2: 4.5 – 6kPa
  • Base excess (BE): -2 – 2 mmol/l
  • HCO3: 22 – 26 mmol/l
  • SaO2 = 95-100%
256
Q

Define ‘oxygen uptake’

A

Oxygen uptake (VO2) is the amount of oxygen that the body takes up and utilizes.

257
Q

How is oxygen uptake measured?

A

Oxygen uptake can be measured by gas analysis of the oxygen content of inspired air vs. the oxygen content of expired air.
During exercise at a constant workload, VO2 increases exponentially at the start of exercise until it reaches the point at which oxygen supply matches oxygen demand and then it plateaus, this plateau is termed steady-state.

258
Q

Define ‘maximal oxygen uptake’

A

Maximal oxygen uptake (VO2max) is the maximal amount of oxygen that the body can uptake and
utilize and is the gold standard measure of exercise capacity. VO2max is the point at which oxygen
uptake plateaus and shows no further increase in response to additional workload.

259
Q

Which factors can affect VO2 max?

A

Gender
Height
Weight
Lung function
Fitness level
Activity they are performing. VO2max is exercise-specific and is greater for activities involving large muscle groups.

260
Q

Define ‘Global Oxygen Delivery’

A

Global oxygen delivery (DO2) is the total amount of oxygen delivered to the tissues in the entire body per minute, regardless of the distribution of blood flow. It is the product of total blood flow or cardiac output (CO) and the oxygen content of arterial blood and is usually expressed in ml O2/min.

261
Q

How is oxygen delivery calculated

A

Oxygen Delivery (mL O2/min) = CaO2 x CO

262
Q

How is carbon dioxide transported around the body (6 marks)

A

Under normal resting conditions, each 100 mL of deoxygenated blood contains the equivalent of 53 mL of gaseous CO2, which is transported in the blood in three main forms.
Dissolved in plasma 7%
Combined with globin carbaminoglobin 23%
Dissolved in plasma as bicarbonate ions 70%
Carbon dioxide plus water in presence of carbonic anhydrase forms carbonic acid dissociates into hydrogen ions

263
Q

Define ‘homeostasis’

A

“Homeostasis is the state of steady internal chemical and physical conditions maintained by living systems.”

264
Q

What is a chemoreceptor?

A
  • Cell that responds to chemical compounds to give an impulse to a sensory nerve, Two sets of chemoreceptors
  • Oxygen receptors which are in the peripheral nervous system
  • Carbon dioxide receptors which are found both peripherally and centrally
265
Q

What is a mechanoreceptor?

A
  • Mechanoreceptors are sensory receptors that respond to mechanical deformation of the receptor or surrounding tissue.
266
Q

What are stretch receptors?

A

Respond to the stretching of muscles by giving impulses to the central nervous system (CNS)

267
Q

What are proprioreceptors?

A

Cells that monitor body changes brought about by muscular movement to give an impulse to the central nervous system to co-ordinate movement.

268
Q

What are juxtacapillary receptors?

A

Cells that cause an increase in breathing rate as reflex response, thought to be involved in the sensation of dyspnea.

269
Q

What is a nociceptor?

A

Cells that respond to a pain stimulus by giving impulses to the central nervous system.

270
Q

Define nucleus

A

Nucleus is a collection of neuronal cell bodies within the central nervous system.
The neurons in one nucleus usually have roughly similar connections and functions.
Nuclei are connected to other nuclei by tracts, the bundles (fascicles) of axons (nerve fibers) extending from the cell bodies.

271
Q

Describe the Pneumotaxic Centre

A
  • is in the upper aspect of the pons
  • controls the fine tuning of respiratory rate and depth.
  • sends signals inferiorly and can influence the VRG (expiratory centre)and DRG (inspiratory centre)
  • Inhibits inspiration, which allows for the transition from inspiration to expiration.
  • It decreases tidal volume.
  • Transitioning occurs as a response to stimulus from peripheral receptors
272
Q

Describe the Apneustic Centre

A
  • controls prolonged breathing
  • receives peripheral stimulus from stretch receptors
  • sends signals to the VRG and DRG to trigger inspiration
  • It increases tidal volume
  • If there is damage to the Pneumotaxic Centre the DRG and VRG would only receive signals from the Apneustic Centre,it cannot inhibit transition from inspiration to expiration, and undergoes prolonged inspiration called apneustic breathing
273
Q

Describe the Dorsal Respiratory Group DRG (inspiratory)

A
  • is located in medial aspect within the medulla
  • Has two functions
    o Receives peripheral stimulus signals from the stretch receptors, proprioceptors,
    Juxtacapillary receptors, and both central and peripheral chemoreceptors.
    o Sends signals to the external intercostals and diaphragm to cause inspiration
274
Q

Describe the Ventral Respiratory Group VRG (expiratory)

A

Is in the anterior aspect of the medulla
o Controls expiration via sending expiratory signals

275
Q

What do chemoreceptors respond to?

A
  • Chemoreceptors monitor blood gas tensions, PaCO2, PaO2 and pH, and help keep minute volume appropriate to the metabolic demands of the body. Therefore, chemoreceptors respond to:
    *Hypercapnia
    *Hypoxia
    *Acidosis.
  • The most important factor controlling the rate and depth of breathing is the effect of carbon dioxide on the central chemoreceptors.
276
Q

Describe the role of central chemoreceptors

A

o 80% of the drive for ventilation is a result of stimulation of the central chemoreceptors.
o When they are inactivated, respiration ceases.
o These receptors are readily depressed by drugs (e.g., opiates and barbiturates).
o respond to hydrogen ion concentration within the surrounding brain tissue and cerebrospinal fluid (CSF) and low partial pr0essure of oxygen (less than 60mmHg)
* Raised hydrogen ion concentration increases ventilation.
* Lowered hydrogen ion concentration decreases ventilation.
* Increase in pCO2 levels leads to increased carbonic acid in CSF. This leads to increase in protons in CSF. Central chemoreceptors are stimulated, leads to increased ventilation and increase in blood pH, bringing it back to normal level.

277
Q

Describe the location of central chemoreceptors

A

o located in the brainstem on the ventrolateral surface of the medulla
o they are anatomically separate from the medullary respiratory control centre.

278
Q

Describe the role of peripheral chemorecptors

A

Stimulation of peripheral chemoreceptors
has both cardiovascular and respiratory effects. Of the two receptor groups, the carotid bodies have the greatest effect on respiration.

279
Q

Describe the location of peripheral chemoreceptors

A

Carotid sinus and aortic arch

280
Q

What are peripheral chemorecptors sensitive to?

A

PaO2
*PaCO2
*pH
*Blood flow
*Temperature.

281
Q

Describe the carotid bodies

A
  • The carotid bodies contain two different types of cells. Type I and Type II cells
  • There is a rich blood supply to the carotid bodies (blood flow per mass of tissue far exceeds that to the brain); venous blood flow, therefore, remains saturated with oxygen.
  • It is believed that type I (glomus) cells are activated by hypoxia and release transmitter substances that stimulate afferents to the brainstem.
282
Q

List stimuli that increase breathing rate and depth

A

Voluntary hyperventilation
Increase in arterial blood PCO2 above 40 mmHg/H+
Decrease in arterial blood PO2 from 105 mmHg to 50mmHg
Increased activity of propriorecpetors
Increased body temperature
Prolonged pain
Decreased blood pressure
Stretching of anal sphincter

283
Q

List stimuli that decrease breathing rate/depth

A

Voluntary hypoventilation
Decrease in arterial blood PCO2 below 40mmHg/H+
Decrease in arterial blood PO2 below 50 mmHg
Decreased activity of propriorecetors
Decrease in body temperature/sudden cold stimulus (causes apnea)
Severe pain (causes apnea)
Increase in blood pressure
Irritation of phharynx/larynx (causes apnea)