Respiratory System Flashcards

1
Q

What is the upper and lower respiratory tract made up of?

A

Upper: nasal cavity, pharynx, nasopharynx, oropharynx, laryngopharynx, larynx

Lower: trachea, bronchi, bronchioles, alveolar sacs, alveoli

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2
Q

Describe the functions of upper respiratory tract?

A

Nasal cavity: air inhaled, warmed, humidified as it moves through nasal cavity
Scroll-shaped bones: nasal conchae protrude forming spaces where air passes, allows air to humidify, warm and be cleaned before entering lungs.
Epithelial cilia + mucous membrane: servo mucous and other glands produce mucous and cilia traps where unwanted large particles are coughed or swallowed.

Pharynx: connects nasal and oral cavities to larynx and oesophagus
Epiglottis: stays up so air can pass, when eating it closes and folds, covers larynx entrance (so food/liquid doesn’t enter trachea)

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3
Q

What is the pleura and pleural cavity

A

Pleura: a closed sac of serous membrane (contains serous fluid one for each lung).

Parietal pleura: the outer layer of pleura
Visceral pleura: the inner layer

Helps keep things lubricated to stop friction (which would result in inflammation)

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4
Q

What are the divisions and processes of lower respiratory tract

A

Air moves down trachea to conducting zone (bronchi,bronchioles, terminal bronchioles) no alveoli in this zone so no gas exchange.

  • Alveoli (large SA) has two types of cells Type I (squamous, covers 90% permits gas exchange with capillaries)
    Type II (cuboidal, 10% produce surfactant)
    Macrophages line alveolar surface to phagocytose particles.
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5
Q

What protection does the lungs have

A

Epithelial lining (respiratory epithelium): has goblet cells and cilia (line from nasal cavity to largest bronchioles), this dusts other particles and are disposed to mucous layer/wafted towards pharynx where its coughed or swallowed.

At alveolar level goblet and cilia impede gas exchange so infection relies on antibodies and phagocytes.

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6
Q

Muscles used when breathing

A

Intercostal muscles: 11 pairs occupies spaces between 12 pairs of ribs two layers internal/external.
External IM: extend downwards and forward from lower border of rib to upper in inspiration
Internal IM: extend downwards and backwards from lower border of ribs to upper (crosses EIM fibres at right angles) used in active expiration eg exercise.

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7
Q

What are the functions of diaphragm and accessory muscles

A

Diaphragm: dome-shaped muscle supplied by phrenic nerve (separates thoracic and abdominal cavities, forms floor of thoracic and roof of abdominal).

Accessory muscles forced inspiration: assisted by STERNOCLEIDOMASTOID and scalene muscles, linking cervical vertebrae to first two ribs increasing ribcage expansion. Muscles contract pulling ribcage upwards.

Forced expiration: contraction of internal IM pull ribcage down and in compressing lungs aiding exhalation. (Rectus abdominis muscle sometimes used compression of abdominal organs increases pressure on diaphragm helping force air out of lungs.

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8
Q

What is the cycle of breathing

A

Inspiration: EIM (lifts ribcage up and out) and diaphragm contract simultaneously enlarges thoracic cavity in all directions. Perital pleura and visceral (PP) stuck to diaphragm is pulled out along with EIM (since the pleuras are held by negative intrapleural pressure) also causing lung tissue to be pulled up out and down towards diaphragm, causes negative pressure in thoracic cavity (venous return to heart this is called respiratory pump). Active process lasts 2 secs.

Expiration: EIM and diaphragm down and in as they relax causing elastic recoil of lungs increasing pressure in lungs to expel air. Lung still contains air to prevent complete collapse by intact pleura. Passive process lasts 3 secs.

Pause: everything relaxed respiration cycle paused (allows body to rest)

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9
Q

What are the physiological variables affecting breathing

A

Elasticity: amount of stretch lung has and ability to return to og shape

Compliance: how easy it is to stretch in first place (if diseased lungs r stiff making Work of Breathing (WOK) harder:

Airway resistance: how easy it is for air to move through airway

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10
Q

What is the role of surfactant

A

Produced by Type II alveolar cells (pneumocytes) reduces friction decreases surface tension so it’s easier for alveoli to expand and contract. Detergent like properties.

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11
Q

What is tidal volume

A

The amount of air that moves into lung in one single respiratory cycle

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12
Q

What is functional residual capacity

A

Amount of air left in lungs at end of expiration (required or else lungs will stick together causing collapse of lung)

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13
Q

What is inspiratory reserve volume

A

Extra volume of air one and above normal tidal volume that can be inhaled into lungs during maximal inspiration (tested using spirometer)

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14
Q

What is inspiratory capacity

A

Maximum amount of air inspired (both tidal and inspiratory reserve vol)

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15
Q

What is peak expiratory flow

A

Measured with peak flow meter generally between (400-700L/min) depends on dips meter of larger airways if constricted peak flow decreases. Regular in ppl with asthma.

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16
Q

Describe the process of gas diffusion

A

O2 enters plasma and dissolves, enters RBC and binds to Hb continues until fully saturated.

17
Q

How is Carbon Dioxide transported

A

Through a chemical reaction
CO2 + H2O — H2CO3 — HCO3- + H+
This is the major buffer body system the respiratory system controls these levels, kidney controls bicarbonate levels.
If breathing too slow and CO2 removal decreased equilibrium moves to the right increasing H+ ions, causes include narcotic overdose, head injury. (Acidosis)

Breathing fast CO2 removal increased equilibrium moves to left decreasing H+ ions, causes include anxiety, pain, low O2.

18
Q

Why does acid/base levels need to be balanced in the body?

A

Acidosis pH < 7.35 proteins won’t function properly and if drops further proteins denature

Alkalosis > 7.45 drop in ionised calcium (promotes binding calcium to albumin) affects function of muscles and nerves
£

19
Q

How do central and peripheral respiratory centres affect pH

A

Central chemoreceptors: brainstem neurone identify change in pH, reflected of CO2 in blood, respiration regulated to maintain stable pH.

Peripheral chemoreceptors: in carotid and aortic bodies of large arteries above heart, sensitive to partial pressure of CO2 and low arterial pO2.