Jackson 1 Flashcards

1
Q

Lungs Regulate

A

blood pH

ventilation rate affects amount of CO2 in plasma

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2
Q

Lungs Provide microbial defense by means of

A

epithelial secretions –

lymphoid tissue in tract –

coughing and sneezing reflexes –

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3
Q

Lungs

6. Activate (or inactivate)

A

chemical messengers in blood –

e.g. convert angiotensin I to angiotensin II

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4
Q

Lungs 7. Defend against

A

blood clots – small blood clots get trapped in narrow vessels in lungs and are dissolved

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5
Q

Components and zones of the respiratory system

A

airways – series of tubes needed to exchange air between lungs and environment

lungs – site of gas exchange between air and blood

mechanical aids – skeletal muscles used to vary the volume of the thoracic cavity

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6
Q

upper airway – structures are

A

outside of the thoracic cavity

mouth/nose → pharynx → larynx → top of trachea

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7
Q
  1. conducting zone –
A

in thoracic cavity, but no gas exchange occurs

trachea → primary bronchi → secondary bronchi → tertiary bronchioles → bronchioles → terminal bronchioles

trachea and bronchi include cartilaginous rings and mucous glands –

bronchioles lose cartilage and glands, but add smooth muscle

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8
Q

respiratory zone – structures where

A

gas exchange can occur

respiratory bronchioles → alveolar ducts → alveolar sacs

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9
Q

respiratory bronchioles very

A

thin-walled; have alveoli in walls

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10
Q

Branching creates

A

parallel airways to maintain airflow and minimize increasing resistance to airflow. Compare this set-up to one in which multiple tubes simply become narrower.

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11
Q

Air is warmed and moistened – heat and water vapor are

A

exchanged with the blood in airway walls

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12
Q

Conducting zone protects against

A

microbes

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13
Q

goblet cells secrete mucus which can

A

trap airborne particles and pathogens;

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14
Q

cilia on epithelial cells move

A

mucus upwards to pharynx where it can be swallowed or expelled

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15
Q

Closed pneumothorax:

A

Pleural cavity pressure less than ATM

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16
Q

Open pneumothorax:

A

pleural cavity pressure = atm

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17
Q

tension pneumothorax:

A

pleural cavity pressure > ATM

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18
Q

Cystic fibrosis is a disease that

A

impairs the normal function of the conducting zone

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19
Q

Cystic fibrosis: mutation in genetic code for

A

Cl- channel reduces the amount of Na+ and Cl- secreted across the epithelium into mucus. This leads to there being less water in the mucus (due to osmosis)→ mucus is thick and dry

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20
Q

Cystic fibrosis: consequences of abnormal mucus -

A

infectious agents are trapped, but not expelled; airways are obstructed

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21
Q

Airflow is regulated by

A

bronchiolar smooth muscle

22
Q

——- in alveoli provides time for exchange –

A

low rate of bloodflow

23
Q

Microbial defense is provided by

A

pulmonary macrophage

24
Q

Type I –

A

epithelial; gas exchange surface

25
Q

Type II –

A

secrete surfactant

26
Q

Macrophages – are considered the

A

3rd alveoli cells??

27
Q

alveolar sacs are

A

~0.5 μm in diameter

28
Q

distance between alveolus and capillary

A

≈ 0.2 μm

29
Q

Respiratory gases are small non-polar molecules that diffuse down a “concentration” gradient - diffuse easily through plasma membranes, less easily through

A

body fluids

30
Q

CO2 solubility = 77 mmol/L;

A

77 mmol/L;

31
Q

O2 solubility =

A

2.2 mmol/L

32
Q

Intrapleural fluid fills sacs (—– thick

A

10 – 20 μm thick)

33
Q

Air flow is a function of the

A

pressure gradient and the resistance to flow within the airways

34
Q

F =

A

ΔP/R
In the respiratory system, the pressure difference (ΔP) of concern is the difference between gas pressure in the lung/alveoli and atmospheric pressure (Palv - Patm )

35
Q

If Palv < Patm, air flows

A

into lung (inspiration)

36
Q

If Palv > Patm, air flows

A

out of lung (expiration)

37
Q

Alveolar pressure changes in response to

A

changing the volume of the lungs according to Boyle’s Law

(P1 V1 = P2 V2 ),

38
Q

transpulmonary (Ptp) =

A

Palv - Pip (Pip = interpleural pressure)

39
Q

diaphragm contracts →

A

lowers floor of cavity → increases volume - inhale

40
Q

external intercostals contract →

A

raise ribcage → increase volume - inhale

41
Q

diaphragm relaxes →

A

raises floor of cavity → reduces volume - exhale.

42
Q

external intercostals relax /internal intercostals contract→

A

lower ribcage → reduces volume - exhale

43
Q

Palv equal Patm

A

between breaths (no air is moving)

44
Q

Pip below

A

atmospheric pressure between breaths

45
Q

Ptp = Palv – Pip;

A

lungs remain expanded
lungs tend to recoil inward –

chest wall tends to recoil outward –

net result is Pip is always subatmospheric

46
Q

During inspiration – diaphragm

A

contracts → thorax expands

47
Q

During inspiration:

Pip becomes

A

more negative

48
Q

During inspiration: Ptp

A

increases so lung volume increases and air flows in until Palv = Patm

49
Q

During expiration - diaphragm

A

relaxes → thorax compresses

50
Q

During expiration: Pip becomes

A

less negative

51
Q

During expiration: Ptp

A

decreases so lung volume decreases and air flows out until Palv = Patm