L18: Capillary And Lymphatic Function Flashcards

1
Q

2 main mechanisms in which substance cross capillary wall

A
  1. Diffusion (passive)
    - concentration gradient
    - surface area
  2. Filtration (passive)
    - Hydrostatic force + Oncotic force
    - k ([Pc + πi] - [Pi + πc])
    - k: filtration constant (permeability x SA)
    - filtration (sum = +ve), absorption (sum = -ve)
  3. main driving force out: Pc (since πi: low 0.1-5 mmHg)
    —> arterial + venous pressure
    —> post:pre-capillary resistance

—> Pc = [(Rv/Ra)xPa + Pv] / 1+(Rv/Ra) (no need to rmb)
—> Pa↑: ↑Pc (↑P gradient from artery to capillary —> more blood into capillary)
—> Pv↑: ↑Pc (↓P gradient from capillary to vein —> more blood stay in capillary)
—> Ra↑: ***↓Pc (more difficult for blood to go from artery to capillary —> less blood in capillary)
—> Rv↑: ↑Pc (more difficult for blood to go from capillary to vein —> more blood in capillary)

  1. main driving force back in: πc: 25 mmHg (since Pi low: +1 mmHg or even negative)
    —> colloid osmotic pressure (non-diffusable large molecules)
    —> plasma protein —> draw water back into capillary
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2
Q

Starling’s hypothesis (NOT Starling’s law)

A
  • Arterial end: Pc high —> net filtration
  • Venous end: Pc low —> net reabsorption
  • πc remain the same throughout
  • amounts of fluid filtered = amount of fluid reabsorbed
  • true for most tissue
  • some tissue only filtration: renal glomerulus (high Pc)
  • some tissue only absorption: lung (low Pc)
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3
Q

Congestive heart failure and Starvation / Nephrosis

A
Heart fail to pump out blood
—> Residual volume of heart ↑
—> Right atrial pressure ↑
—> venous return ↓
—> venous pressure ↑
—> capillary pressure ↑
—> capillary filtration ↑
—> oedema
Starvation / Nephrosis:
↓ plasma protein synthesis / ↑ plasma protein lost in urine
—> ↓ πc
—> ↓ reabsorption
—> filtration > reabsorption
—> oedema
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4
Q

Lymphatics

A
  • slow lymph flow (2-4L/day)
  • clear excess fluid, protein, lipid, foreign material
  • blind ends in interstitial space
  • series of chambers with valves
  • edges of epithelial cells not joined but freely overlap
  • ↑ interstitial pressure allow valve to open
  • ↑ lymphatic pressure close clave and trap fluid
  • presence of fluid stretch wall —> contract and propel to next chamber
  • 25 mmHg during contraction, 0 mmHg when not contracting
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