Basic Respiratory Physiology Flashcards

1
Q

What neural areas make us breathe?

A

In the brainstem the respiratory centre (pons and medulla) drives respiratory muscle activity dependent on the neural inputs they receive

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2
Q

Why do we need to breathe?

A

Adequate ventilation must be maintained to keep neutral pH range to allow optimal cellular function

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3
Q

What changes blood pH most from ventilation?

A

PaCO2 is the most important ABG affecting ventilation. Increased PaCO2 levels will drive ventilation (e.g. increasing tidal volume or increasing respiratory rate) which blows off the excess CO2 and returns PaCO2 (and therefore blood pH) back to baseline

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4
Q

What are the stages of breathing?

A
  1. At rest
  2. During inspiration
  3. End inspiration
  4. During expiration
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5
Q

Describe the “at rest” stage of breathing

A

The barometric pressure at the mouth is 0 (PB), the pressure in the lungs (alveolar pressure PA) is 0, and the intrapleural pressure (Ppl) is negative. Therefore, there is no airflow as PB = PA

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6
Q

Describe the “during inspiration” stage of breathing

A
  1. Inspiratory muscles contract
  2. Thoracic cage expands
  3. Lungs expand (increasing lung volume)
  4. Intrapleural and intraalveolar pressure decreases
  5. Air flows into the lungs because the pressure in the alveoli is less than the pressure at the mouth
    Therefore, there is airflow inwards as PA < PB
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7
Q

Describe the “end inspiration” stage of breathing

A

When the intraalveolar pressure equals the mouth (barometric/atmospheric) pressure, airflow ceases (as PA = PB again)

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8
Q

Describe the “during expiration” stage of breathing

A
  1. Respiratory muscles relax
  2. Lungs passively recoil (to FRC)
  3. Alveolar pressure rises (becomes positive) compared to mouth pressure
  4. Gas therefore moves towards the mouth
    Therefore, there is airflow outwards as PA > PB
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9
Q

Total/minute ventilation equation

A

(VE) = Vt x RR (e.g. VE = 500ml x 12 breaths/min = 6000mL (or 6L/min). This shows the mass movement of gas in/out of lungs

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10
Q

Define alveolar ventilation (VA)

A

VA is the amount of fresh gas getting to the alveoli

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11
Q

Define the anatomic dead space (VD)

A

Gas in the conducting airwards (from nose to terminal bronchioles) is called anatomic dead space (VD) and is about 150mL (VA = (VT – VD) x RR) so normal alveolar ventilation is approx 4.2L/min. Low alveolar ventilation will result in increase PaCO2 and decreased PaO2

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12
Q

What affects the distribution of ventilation?

A
  1. Pressure gradients in the lungs (affecting lung compliance)
  2. Lung volume at which you breathe in from (i.e. FRC)
  3. Flow rate
  4. Pattern of breathing
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13
Q

Define lung compliance

A

The change in volume produced by a change in pressure (C = ΔV/ ΔP). Low lung compliance makes it harder to inflate (stiff), whereas high lung compliance makes it easier to inflate

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14
Q

What structures make up the mucociliary clearance (MCC) apparatus?

A

MUCUS: provides mechanical, biological and chemical barrier to inhaled material. 100-250ml produced per day by bronchial submucosal glands (larger airways) and goblet cells (bronchial epithelium).
CILIA: moves particles caught in the mucus to pharynx for swallowing

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15
Q

What increases MCC ability?

A

Exercise, the environment (less inhaled particles), and medications (ventolin)

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16
Q

What decreases MCC ability?

A

Higher age, sleeping, respiratory disease, medications (anaesthesia, opiates) and smoking

17
Q

MCC dysfunction: Smoking

A
  • Increases mucus production
  • Increases viscosity of mucus
  • Decreases ciliary movement/beat frequency
  • Cilial destruction
  • Alveolar macrophage dysfunction
18
Q

MCC dysfunction: Chronic bronchitis

A
  • Increases size and number of secretory cells
  • Increases volume of mucus
19
Q

What is the function of a cough?

A

To assist in the removal of material from the central airways (either inhaled or produced in the airways). It is used if the volume of mucus is too large for normal MCC or if the MCC is damaged

20
Q

What is alveolar clearance?

A

This deals with small particles (e.g. asbestos, tobacco smoke, virus) that reach the alveoli. As there are no cilia in the alveoli, alternative mechanisms are used. Deposit via sedimentation/diffusion, and these particles are engulfed by macrophages, which migrate to smaller airways to be removed by MCC/lymphatic system (taking 1-3 days)