Chapter 23, Lecture 3
Intrapleural Pressure ( P_{ip} )
- Pleural cavity between parietal & visceral pleura contains thin serous fluid ➔ creates surface tension
- Surface tension forms a partial vacuum ➔ P{ip} always < atmospheric pressure ( P{atm}=760\,\text{mmHg} )
• At rest: P_{ip}\approx 756\,\text{mmHg} ( −4 mmHg ) - Negative P_{ip} mechanically couples lung to thoracic wall; lungs follow chest movements
Pressure Changes During Quiet Breathing
- Boyle’s law: P \propto \dfrac{1}{V} (in closed system)
Inhalation
- Muscles: diaphragm + external intercostals contract ➔ thoracic volume ↑
- Parietal pleura pulled outward ➔ lungs & alveoli expand
- Alveolar pressure falls to P_{alv}=758\,\text{mmHg}
- Gradient: 760 \rightarrow 758\,\text{mmHg} ➔ air flows in
- P_{ip} remains negative
- Deep inhalation recruits scalenes & sternocleidomastoid
Exhalation
- Muscles relax; elastic recoil shrinks thoracic volume
- Alveolar volume ↓ ➔ P_{alv}=762\,\text{mmHg}
- Gradient: 762 \rightarrow 760\,\text{mmHg} ➔ air flows out
- Forced exhalation uses internal intercostals & abdominal muscles
Factors Affecting Ventilation (besides pressure gradient)
- Surface tension of alveolar fluid
- Water molecules tend to collapse alveoli
- Type II cells secrete surfactant ➔ lowers tension, keeps alveoli open
- Surfactant deficiency → neonatal respiratory distress syndrome
- Lung compliance (ease of expansion)
- Depends on elasticity + surface tension
- Low compliance: scar tissue, edema, surfactant lack, muscle paralysis, thoracic arthritis
- Airway resistance (diameter of bronchioles)
- Bronchoconstriction ↑ resistance, ↓ airflow (parasymp, cold air, inflammation, mucus)
- Bronchodilation ↓ resistance, ↑ airflow (symp, epinephrine → EpiPen)
- Airflow ∝ \dfrac{\Delta P}{R}
Clinical Connection
- Pneumothorax = air in pleural cavity (trauma or spontaneous)
• Eliminates negative P_{ip} ➔ lung collapses - COPD/obstructive disease: ↑ airway resistance; patients expend up to 25 % of energy on breathing