Respiratory System Flashcards

(25 cards)

1
Q

Cellular respiration

A

Aerobic muscle respiration:

  • C6H12O6 + 6O2 = 6CO2 = 6H2O
  • 36 ADP = 36 ATP

Anaerobic muscle respiration:

  • C6H12O6 = 2C3H6O3 (lactic acid)
  • oxygen debt.
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2
Q

Feed forward

A

Breathing rate increases before muscles need more oxygen

Deciding to exercise/run is enough to trigger this

Measuring HBO/Hb (oxygenated vs non oxygenated) ration blood oxygen level dependent in the brain centres controlled breathing: feed forward can be observed

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3
Q

Breathing

A

Inhalation requires energy - volume increases and opens up the lungs and pressure goes down so air comes in (as there is less pressure inside then outside the lungs).

Exhalation normally passive - rib cage and longs collapse, that puts pressure on the air inside and it exits the lungs

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4
Q

The pleura

A

Keeps the lungs open at all times so they don’t collapse

  • visceral pleura (inner layer) stuck tightly to the lungs
  • parietal pleura lines the inside of the chest cavity
  • pleura cavity
  • pleura fluid

Intrapleural pressure is always negative - the lungs stay inflated within the chest cavity:

  • elasticity of the lungs inwards
  • elasticity of the thoracic wall - outwards
  • functional residual capacity: the volume at which the pull of the chest is equal and opposite to the inward pull of the lungs
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5
Q

Breathing route

A
  • Nasal or oral cavity
  • trachaea
  • bronchi
  • secondary bronchii
  • tertiary bronchii
  • smaller bronchii (20-30 orders of branching in total)
  • bronchioles
  • terminal bronchioles
  • respiratory bronchioles
  • alveoli
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6
Q

Surfactant and lung compliance

A

Surfactant keeps the lungs moist and stops the alveoli from sticking together

Surfactant increases polmonary compliance, the ability of the lungs to expand

Bigger alveoli expand more slowly due to surfactant more spread out

All alveoli in the lungs expand at eh same rate. Bigger: rise in surface tension = slower expansion

Surfactant reduces surface tension more readily when the alveoli are smaller because the surfactant is more concentrated

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7
Q

Airway conductance

A

Airway resistance = combined resistance of individual airways

Combined radii increases due to the large number of small tubes

Overall the resistance is decreased in the alveoli

Thin film of water lining the alveoli, useful for gas exchange, but hydrogen bonds between water molecules would pull the walls of the alveoli inwards - collapse
- So there is a increase in muscular work required to inflate the lungs

Would tend to collapse the alveoli, making them useless for gas exchange
- pulmonary surfactant and Laplace’s law

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8
Q

Laplace’s las: pulmonary surfactant

A

Pressure to collapse an alveolus is directly proportional to the surface tension and inversely proportional to the radius of the alveolus

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9
Q

Partial pressure

A

The tendency of a particular type of molecule to diffuse from one area to another is given by the difference in density

Gaseous mixture: pressure of one type of molecule depends on its density

Pressure exerted by each type of gas molecules adds up - density of a single type of gas is called partial pressure

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10
Q

Physical limitations to gas exchange

A

Exchange occurs when gas levels (diffusion potential) are not in equilibrium - there is a diffusion gradient

The rate at which the gradient decays, which is specified by the equation time

The amount of gas available in the high potential medium, and the amount that can be absorbed bey the low potential medium

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11
Q

What happens in alveolar air?

A

Alveolar air has a lot of water vapour

Diffusion across membrane into the haemoglobin

Difference in partial pressure: alveolar air - oxygen = 100mmHg and CO2 = 40mmHg (not the same as in atmospheric air)

In pulmonary capillaries (prior to gas exchange) - O = 40mmHg and CO2 = 45mmHg

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12
Q

Haemoglobin

A

Haemoglobin (Hb) is a tetra Eric protein of 2 alpha and 2 beta subunits, each with a haeme co-factor

Haeme group contains a ferrous ion (Fe2+) that allows the haeme group to reversible bind to O2

Each subunit associates with a haeme group - each haeme group can associates with one oxygen = so each haemoglobin can associate with 4 oxygens

Affinity of O2 is controlled by the chemical environment and by co-operative interactions between protein-globin subunits

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13
Q

Factors that can influence partial pressure of oxygen

A
  • pH: changes the shape of proteins (haemoglobin is protein)
  • CO2: liked to pH in water and competes with oxygen for haemoglobin
  • temperature
  • 2,3-BPG or 2,3-DPG: metabolic intermediate in the glycolysis pathway - in anaerobic respiration (lactic acid will influence the pH).
  • Cl- ions
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14
Q

Control of breathing

A
  • medulla oblong at and Pons coordinate breathing

- aortic and carotid pH sensors also relay information to the brain stem

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15
Q

Neural control of breathing: generation and control of rhythmic behaviour

A
  • central areas
  • central pattern generators (CPG)
  • afferent pathways (central and peripheral chemoreceptors, mechanoreceptors and higher brain centres)
  • effrontery pathways (muscle control)

Detection of CO2 in the brainstem

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16
Q

Consequences of departures of O2, CO2 and pH from their set point

A
  • hypoxia: low levels of oxygen - reduced metabolism (sleepy)
  • hyperopia: high levels of oxygen - can lead to tissue damage
  • hypocapnia: low CO2 - suppression of gas exchange
  • hypercapnia: excess CO2, panic and sensations of drowning
  • acidosis: low pH - cramps and other metabolic disturbances
  • alkalosis: high pH - insufficient oxygen to tissues, when low pH haemoglobin gives up oxygen more readily to tissues
17
Q

Carbon dioxide

A

CO2 dissolves in water - forms carbonic acid - dissociates to give protons and bicarbonate ions

This process is catalysed by carbonic anhydrase

The haemoglobin hinds H+ to act as a proton buffer, and also binds CO2 in the carbamino reaction
Chloride shift: removal of bicarbonate ions from the red blood cell could change the electrical balance (negative charges being removed), so chloride ions come in to balance this. When there is enough CO2 to initiate O2 binding to haemoglobin there will be an increase in chloride ion concentration within the red blood cel. Chloride ion is another signal to the haemoglobin to release more oxygen

18
Q

The Haldane effect

A

Describes the phenomenon by which binding of oxygen to haemoglobin promoters the release of carbon dioxide

19
Q

How is CO2 transported in the blood?

A
  1. Bicarbonate (HCO3) - 60%
  2. Carbamino-haemoglobin - 30%
  3. Dissolved in the plasma - 10%
20
Q

Myoglobin

A

Found in big muscles

Stores oxygen and has a higher affinity for oxygen

It’s only made of one subunit (however haemoglobin is co-operative).

21
Q

Emphysema

A

Chronic long term disease.

Walls of the alveoli damaged.

Caused by the the release of the enzyme alpha-1-anti-trypsin due to irritants

Heart has to work harder to achieve gas exchange due to being full of mucus (increases diffusion distance) and destroyed alveoli - eventually heart failure

Destruction of alveoli means less surface area for gas exchange

22
Q

Oedema

A

Fluid in interstitial space

Increases diffusion distance

Arterial pressure of CO2 may be normal due to high CO2 solubility

Caused: some forms of heart failure and pneumonia

HAPE: high altitude pulmonary oedema

Lower air pressure at high altitudes. Hypoxic. Can lead to pulmonary vasoconstriction (pulmonary hypertension). Increased permeability of vascular epithelium

23
Q

Reduced ventilation - asthma

A

Increased airway resistance, decreases airway ventilation

24
Q

Chronic Obstructive Pulmonary Disease (COPD)

A

Chronic bronchitis and emphysema usually both present (asthma)

Causes (irritants):

  • cigarette smoke
  • cystic fibrosis
  • some pollutants can also cause it

Permanent damage to airway - chronic

Symptoms:

  • cough - productive cough (comes and goes at first, a lot of sputum coughed up)
  • breathlessness and wheezing
  • chest infections much more common
25
Sickle cell anaemia
Anaemia - not getting enough oxygen around. Cause by not enough iron. Beta subunit in the haemoglobin is the problem in sickle cell disease Mutation in 6th amino acid (one base pair). Autosomal recessive (single locus mutation) Formation of haemoglobin S (HbS) - when oxygenated it keeps its shape. When deoxygenated it loses its normal shape and becomes a sickle red blood cell. Damage to RBC membrane and blocks blood vessels, which cause pain, serious infections and organ damage Offered resistance to malaria