autonomic control of the cardiovascular system Flashcards

1
Q

control of CVS

A
  • extrinsic: neurohumoral control
  • intrinsic: mechanosensitivity autocrine
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2
Q

mean arterial pressure

A

slides

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3
Q

mechanism

A

Activation of neurons in the CVS occurs by multiple processes.

convergence- one neuron influenced by many

divergence- many neutrons influenced by one neuron

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4
Q

excitatory and inhibitory potentials

A

Excitatory and inhibitory potentials occur during activation of single
neural inputs.

Excitatory Post-Synaptic
Potential (EPSP)
Depolarizes the target neuron

Inhibitory Post-Synaptic
Potential (IPSP)
Hyperpolarizes the target
neuron

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5
Q

heart rate regulation

A

Autonomic nervous system primary controller of heart rate
* Both divisions (sympathetic and parasympathetic) influence
sinoatrial node activity

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6
Q

sympathetic pathway (heart rate regulation)

A
  • Response to stimulation begins slowly, as:
    (i) nerve terminals slowly release norepinephrine
    (ii) downstream effects mediated by relatively slow second
    messenger system involving production of cAMP
  • Response decays gradually, as nerve terminals take
    up only ~70% of released norepinephrine, with
    remainder carried away by blood
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7
Q

parasympathetic pathway (heart rate regulation)

A
  • Rapid response to stimulation, as:
    (i) nerve terminals rapidly release acetylcholine
    (ii) downstream effects mediated by specialised
    acetylcholine-regulated K+ channels directly coupled to
    muscarinic receptors to which acetylcholine binds
  • Rapid decay, as SA and AV nodes rich in cholinesterase, an
    enzyme that quickly hydrolyses acetylcholine
  • Rapid response and decay allow beat-by-beat control of SA
    and AV node function
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8
Q

resting heart rate

A

Resting rate determined primarily by parasympathetic activity
* Parasympathetic effects stronger than sympathetic effects

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9
Q

stroke volume regulation

A

Stroke volume determined by:
Contractility:
- Regulated by sympathetic and parasympathetic activity
- Sympathetic activity: Increases stroke volume by
increasing magnitude and rate of force generation
(as well as rate of relaxation)

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10
Q

reflex regulation of blood pressure

A

Arterial Baroreceptors:
- Stretch receptors in the carotid sinuses and the aortic arch
- Stretch increases receptor firing, inhibiting sympathetic
outflow from pressor region (depressor effect)

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11
Q

arteries

A
  • Systemic arteries have thick walls with three layers:
  • Intima: Single layer of endothelial cells acting as a
    metabolically active barrier between blood and vessel wall
  • Media: Thickest layer, composed of elastin (elasticity),
    collagen (strength), and vascular smooth muscle
    (contraction)
  • Adventitia: Layer of connective tissue containing nerves,
    lymphatics and blood supply to vessel wall
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12
Q

arterioles

A

Arterioles regulate rate and distribution of blood flow
* Composed of endothelium and smooth muscle, arranged in
rings around the vessel, allowing large changes in vessel
diameter (vasoconstriction or vasodilation)

  • Arterioles regulate rate and distribution of blood flow
  • Under dual control: intrinsic (local conditions surrounding the
    blood vessels) and extrinsic (nervous system input)
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13
Q

extrinsic control of blood flow

A
  • Two sources of extrinsic (nervous system) control of flow:
    (i) Sympathetic Regulation
    (ii) Hormonal Regulation
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14
Q

sympathetic regulation (extrinsic control of blood flow)

A
  • Under similar control as blood pressure
    through regions in cerebral medulla
    that influence vessel tone
  • Stimulation of pressor region
    causes sympathetic outflow,
    resulting in vasoconstriction
  • Stimulation of depressor region
    causes inhibition of pressor region,
    resulting in vasodilation
  • cerebral medulla influences vessel tone
  • influenced by neural impulses and by blood concentration of carbon dioxide and oxygen
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15
Q

sympathetic regulation of vessels

A
  • Sympathetic nerve terminal releases neurotransmitters,
    neuropeptides, and other molecules which act on the
    vascular smooth muscle cells and to cause vasoconstriction
    or vasodilation
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16
Q

signalling molecules and response in sympathetic regulation

A

Norephinephrine (NE) –vasoconstriction

ATP —vasoconstriction

Neuropeptide Y —-vasoconstriction

Vasoactive intestinal peptide (VIP)—- vasodilation

Nitric Oxide —-vasodilation

17
Q

hormonal regulation (extrinsic control of blood flow)

A
  • Two sources of extrinsic (nervous system) control of flow:
    (ii) Hormonal Regulation
  • Epinephrine / norepinephrine released by the adrenal
    medulla influences arteriole tone
  • Low epinephrine concentration dilates arterioles
    (-adrenergic), high concentration constricts arterioles
    (-adrenergic), while norepinephrine only causes constriction
18
Q

balance of intrinsic/extrinsic control

A

Dual control of peripheral vessels allows direction of blood flow
to areas with greatest need

  • In some tissue effects fixed, in others balance is adjusted based
    on activity:
    a) In brain and heart (vital structures with limited tolerance for
    reduced blood flow), intrinsic mechanisms are dominant
    b) In skin (important for homeostasis), extrinsic vascular
    control is dominant
    c) In skeletal muscle (in which there can be large changes in
    metabolic activity), intrinsic and extrinsic mechanisms
    interact, allowing tuned response to changes in activity
19
Q

ageing

A

Ageing alters function of parasympathetic and sympathetic inputs to the
intracardiac nervous system.

Changes in cardiac function with ageing occur as a result of tissue and
cellular-level changes.

20
Q

pathological conditions

A

Pathological conditions result in a changes in both neuronal
and myocardial tissue functions.

Pathological disruption of cardiac function often results in predictable
physiological changes.