5 - Microcirculation Flashcards

1
Q

What is being referred to by “exchange vessels” and “resistance vessels”?

A

Exchange vessels - capillaries

Resistance vessels - arterioles

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2
Q

Capillaries will be able to do its function of exchange due to (3)

A
  1. Physical structure
  2. Large number of capillaries
  3. Surface Area
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3
Q

The “stopcocks” because they control the blood flow through the particular capillary that each one guards?

A

Precapillary sphincters

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4
Q

Role of arterioles

A

Important in changing blood pressure occurring throughout the vascular system

Pressure drop so capillaries will not burst

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5
Q

Precapillary Sphincters when tissue metab increases

A

When tissue metab increases, the local metabolic changes -> relaxation of precap sphincters -> increasing the number of open capillaries

When there is an inc in metab activity, tissues will be using a lot of O2 that’s why PO2 dec, PCO2 inc, pH dec bc of this you have:
>Relaxation of precap sphincters = allowing more blood to enter capillaries
>Number of open cap inc

When metabolic changes/tissue activity is dec, precap sphincters contracting -> constriction -> less blood flow towards capillaries

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6
Q

Transport mechanisms

A
  1. Diffusion
    - For transporting gases like O2 and CO2 and other lipid soluble substances (e.g. steroid hormones)
  2. Bulk flow
    - small molecules, electrolytes, water
    - due to presence of intercellular/slit-like gaps/clefts
  3. Vesicles
    - how macromolecules are transported -e.g. proteins
  4. Actin Transport
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7
Q
DIFFUSION
>effect of:
1. Concentration gradient
2. SA for exchange
3. Diffusion distance
4. Permeability of capillary wall to the diffusing substance
A
  1. Directly proportional
  2. Directly
  3. Inversely
  4. Directly
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8
Q

Components of microcirculation

A
Arterioles
Capillaries
Venules
Metarteriole(thoroughfare channel)
Precapillary sphincters
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9
Q

Precapillary sphincters
>Yes or no?
1. Innervated
2. Have a high degree of myogenic tone
3. Sensitive to local metabolic changes (PO2, PCO2, pH)
4. Referred to as stopcocks. Explain your answer.

A
  1. NOT innervated
  2. Yes
  3. Yes
  4. Yes. Only way to control blood flow to the particular capillary that they are guarding
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10
Q

Importance of extensive capillary branching in diffusion

A

Good so if ever specific tissues need more blood supply, they have a higher number of capillaries

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11
Q

How exchangeable proteins are transported

A

Vesicular transport

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12
Q

What happens when you have an increase in metabolic activity?

A

If you have inc in metab activity = less O2, inc in CO2…
First there’s relaxation of precap sphincters and arteriolar vasodilation
Relaxation of PCS -> inc open capillaries -> SA for exchange higher, diffusion distance will be smaller
Through arteriolar vasodilation -> delivery of O2 will be more efficient -> conc grad of O2 and CO2 across cap wall will be greater
And those in the red box will be favoring exchange of matls bet blood and tissues

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13
Q

Starling forces

A
  1. Capillary hydrostatic pressure (Pc)
    - Pressure when your blood reaches capillaries
    - Favors filtration
  2. Osmotic force due to plasma protein concentration (pi c)
    - aka Oncotic pressure due to plasma proteins)
    - Due to presence of plasma proteins within your blood
    - Pushes fluid in
  3. Interstitial fluid hydrostatic pressure (P IF)
  4. Osmotic force due to interstitial protein concentration

Significance: Net Filtration Pressure -Net difference between the forces that favor filtration versus forces that inhibit filtration
= Pc + pi IF - P IF - pi c

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14
Q
Which of the following mechanisms is most important quantitatively for the exchange of electrolytes across capillaries?
A. Bulk flow
B. Diffusion
C. Osmosis
D. Vesicular Transport
A

A

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15
Q

Which of the following can increase the rate of oxygen diffusion from blood to tissue?
A. Arteriolar vasodilation
B. Decreased arteriolar PO2
C. Increased tissue PO2
D. Decreased number of flowing capillaries

A

A

***B & C: affecting conc gradient; D. Affected: SA (dec)

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16
Q

The lymphatic system has lymphatic vessels which collect lymph from loose connective tissue. It has pumps and valves.

A

False. No pumps BUT ONLY VALVES

17
Q

How much excess tissue fluid is returned to the blood vessels via the lymphatic system?

A

2-4 L per day

18
Q

Initial lymphatics

A
  • Another term for lymph capillaries
  • Has an intimate relationship with your systemic blood capillaries
  • Found on skin, genitourinary, respiratory, gastrointestinal tract
19
Q

2 phases of lymph capillaries

A

A. Expansion Phase

  • overlap of endothelial cells will open (aka primary lymph valves) due to pressure within interstitial fluid > P within lymphatics and allow fluids to get in
  • Beyond initial lymphatics, there’s collecting lymphatics to make sure blood flow in capillaries is one way.
  1. Compression Phase
    - P within lymphatic vessel > P in interstitium
    - increase in P w/in lymphatics will force 2’ lymph valves to open
20
Q

Resting CO is _ per minute? Day?

A

5-6 L/min; 7200 L/day

21
Q

When does edema occur

A

When too much interstitial fluid accumulates

22
Q

What changes in the ff will result to edema formation?
1. Plasma protein concentration

  1. Permeability of capillary walls
  2. Venous pressure/capillary hydrostatic P
  3. Lymph vessels
A
  1. Reduced
  2. Increased
  3. Increased
  4. Blockage
23
Q

A patient treated for hypertension w/ an arterial vasodilator develops peripheral edema. The most likely cause of this edema is:

A. Dec capillary hydrostatic pressure
B. Dec capillary filtration constant
C. Increased postcapillary/precapillary resistance ratio
D. Reduced venous pressure

A

C

A. Dec capillary hydrostatic pressure
True but doesn’t answer this q
B. Dec capillary filtration constant
B also; filtration constant is the SA and the permeability of capillaries true but doesn’t explain edema
C. Increased postcapillary/precapillary resistance ratio
D. Reduced venous pressure
Will not explain edema; but true

24
Q

How do precapillary sphincters regulate microcirculation?

A

Active contraction of VSMs regulate precapillary resistance which controls capillary blood flow.

Inc P grad = inc blood flow; if inc resistance = dec blood flow

25
Q

How do tissue metabolites regulate microcirculation?

A
  1. Myogenic activity
    Inc blood flow -> VSMCs stretched -> opening of nonselective cation esp Ca2+ channel -> VSMCs contract -> constriction
    (Intrinsic mode of control of activity)
  2. Local and chemical humoral factors
    >Factors may also contribute to osmolality
    >Chemical changes directly act on VSMCs
    >Factors causing vasodilation:

A. Dec PO2 (-> Dec [ATP]i -> inc adenosine release -> inc PGI2 release -> inc NO release)

B. Inc PCO2 (-> dec pHo)

C. Dec pH (-> dec pHo)

D. Inc [K+]o(Transient hyperpolarization -> Closes voltage-gated Ca2+ channels)

E. Inc [Lactic Acid]o (-> probably dec pHo)

F. Dec [ATP]i (Opens K ATP channels)

G. Inc [ATP]o (Activates purinergic receptors P2Y)

H. Inc [ADP]p (Activates purinergic receptors P2Y)

I. Inc [Adenosine]o (Activates adenosine receptor A2)

26
Q

The endothelium of capillary beds secrete vasoactive compounds that regulate microcirculation. Determine the effect of these compounds:

  1. NO
  2. EDCF1 & EDCF2
  3. ET
  4. PGI2
  5. EDHF
A
  1. Vasodilator
  2. Vasoconstrictors
  3. Vasoconstrictor
  4. Vasodilator
  5. Vasodilator
27
Q

True or False. Large fluctuations in systemic arterial pressure will automatically damage your system.

A

False! Autoregulation will try to compensate for the great changes. (Intrinsic which happens within your blood vessels)

Myogenic mech: BP inc -> blood flow inc -> smooth ms contract due to stretching of smooth ms cells

Metabolic mech: Autoregulation due to local and humoral factors mentioned

28
Q

This factor is very important in angiogenesis.

A

Autoregulation

29
Q

Angiogenesis promoters or inhibitors?

  1. Endostatin
  2. VEGF
  3. ANGPT1
  4. ANGPT2
  5. Angiostatin
  6. FGF
A
  1. Inhibitor
  2. Promoter
  3. Promoter
  4. Inhibitor
  5. Inhibitor
  6. Promoter