The Microcirculation (31) Flashcards

1
Q

What is the passage of microcirculation?

A

arteriole–>capillaries–>venule

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2
Q

What is the overall aim of the cardiovascular system?

A

ensuring adequate blood flow through the capillaries

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3
Q

What is blood flow rate?

A
  • volume of blood passing through a vessel per unit time

- Q (flow rate) = Pressure gradient / Resistance

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4
Q

What is the pressure gradient in terms of blood flow to the capillaries?

A

pressure at the start of the arteriole - pressure at the end of the arteriole
(pressure A- pressure B)
N.B. inc. pressure gradient–> inc. flow rate

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5
Q

What is resistance in terms of blood flow?

A

hindrance to blood flow due to friction between moving fluid and stationary vascular walls
R= 8Ln/ pi x r^4

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6
Q

What happens to blood flow rate when you increase resistance?

A

blood flow rate decreases

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7
Q

What vessels have the biggest influence on resistance?

A

arterioles

bc biggest pressure gradient

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8
Q

Why is blood flow determined only by resistance?

A

as pressure gradient is basically just mean arteriole pressure, as venule pressure is so low–>0
so flow= MAP/resistance

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9
Q

Why is it important that vessels are normally partially constricted?

A

‘vascular tone’
so that it can contract further OR dilate
(if it was totally dilated or totally contracted, you would remove a method of controlling blood flow)

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10
Q

What happens to resistance and blood flow in vasoconstriction?

A

dec. radius
inc. resistance
dec. blood flow

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11
Q

What happens to resistance and blood flow in vasodilation?

A

inc. radius
dec. resistance
inc. blood flow

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12
Q

What are the 2 distinct functions of the arterioles?

A
  1. matching blood flow to the metabolic needs of specific tissues via local/intrinsic controls (momentary needs)
  2. helping regulating systemic arterial blood pressure via extrinsic controls (nerves or blood), centrally coordinated
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13
Q

How does active hyperaemia work?

A
  • chemoreceptors in tissues detect inc. CO2 etc…–> directly causes smooth muscle contraction/relaxation
  • vasodilation increases blood flow to active tissue
    e. g. in skeletal muscle
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14
Q

How does myogenic auto regulation work?

A

if tissue doesn’t need inc. blood flow–> detects inc. stretch (due to inc. BP) —> causes vasoconstriction of arterioles ensuring that blood doesn’t overly flow into particular tissue

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15
Q

What happens to arterioles when blood temperature decreases?

A

vasoconstriction to preserve temp.

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16
Q

What is an equation for blood pressure across the whole circulation?

A

BP= Q X TPR

blood pressure= cardiac output X total peripheral resistance

17
Q

How does the brain regulate arterial blood pressure via neurones?

A

e. g. if there is blood loss detected
- -> cardiovascular control centre in medulla
- -> vasoconstriction
- -> dec. blood flow to specific organs (brain always takes priority, so blood flow preserved here)

18
Q

How does the brain regulate arterial blood pressure via hormones?

A

vasopressin/ADH, angiotensin 2, adrenaline/noradrenaline

–> all cause vasoconstriction

19
Q

What is the purpose of capillary exchange?

A

to deliver metabolic substrates to the cells of the organism
- highly branched (max. SA)
- thin cell width (min. diffusion distance
^ enhance diffusion - Fick’s Law

20
Q

Why is capillary density important?

A
  • depends on how active tissue is
  • dec. diffusion distance and inc. SA
  • highly metabolically active tissues have denser capillary networks
    e. g. brain, skeletal muscle and lungs (to enable proximity to alveoli)
21
Q

What are the types of capillaries?

A
  • continuous (small, water-filled gap junctions)
  • fenestrated (larger holes)
  • discontinuous (less common, but found in liver)
22
Q

What is bulk flow?

A

a certain volume of protein-free plasma filters out of the capillary (bc hydrostatic pushing force), mixes w/ surrounding interstitial fluid and is reabsorbed (bc oncotic pulling force of proteins)

23
Q

What is Starling’s hypothesis in terms of hydrostatic/oncotic forces?

A

there is a balance between hydrostatic pressure pushing it out and oncotic pressure drawing it back in

24
Q

How do the pressure changes in capillaries affect fluid movement?

A
  • if pressure inside capillary > pressure in interstitial fluid–> ultrafiltration
  • if inward driving pressure > outward pressures across the capillary–> reabsorption (bc oncotic pressure is constant but hydrostatic dec.)
25
Q

Why do we need the lymphatic system?

A

net loss of fluid out of capillaries bc ultrafiltration is more effective than reabsorption

26
Q

What type of capillary structure is the blood brain barrier?

A

continuous

allows brain to have tight control over what enters