Autonomic Pharmacology Flashcards

1
Q

peripheral nervous system subdivisions

A

afferent (sensory) and efferent (motor)

  • efferent divided into somatic nervous system (under conscious control) and autonomic nervous system (automatic)
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2
Q

dominant tone

A

either SNS or PSNS is more dominant in an organ system - sympathetic dugs may be more effective in a certain organ

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3
Q

terms used to indicate PSNS

A
  • cholinergic (acetylcholine)
  • muscarinic (muscarinic receptors)
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4
Q

terms used to indicate SNS

A

adrenergic (adrenaline)

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5
Q

PS nerves originate from

A

craniosacral

  • originate from the top (cranio) and bottom (sacral) regions of the spinal cord
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6
Q

SNS nerves originate from

A

thoracolumbar

  • middle (thoracic and lumbar) regions of the spinal cord
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7
Q

PS usually have ____ preganglionic and ____ postganglionic fibers

A

longer; shorter

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8
Q

why dont we see more ganglionic blocking drugs

A

because we want more selectivity - wanna affect either the sympathetic or parasympathetic nervous system - not both - wanna go downstream right to the target organ

  • instead, we target postganglionic receptors on target organs because it gives us more selectivity
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9
Q

____ is the neurotransmitter released at the ganglia in both PS and SNS

A

acetylcholine

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10
Q

receptors at the ganglia

A

nicotinic receptors

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11
Q

acetylcholine is synthesized from

A

Acetyl CoA and Choline

  • stored in synaptic vesicles
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12
Q

adrenal medulla

A
  • part of the sympathetic nervous system
  • releases epinephrine (80%) and norepinephrine (20%)
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13
Q

catecholamines

A

dopamine, epinephrine, norepinephrine, serotonin

  • made from tyrosine
  • tyrosine –> dopa –> dopamine –> norepinephrine –> epinephrine
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14
Q

2 types of cholinergic receptors

A
  • NICOTINIC [Nm (muscle) and Nn (neurologic - ganglia)]
  • MUSCARINIC (M1… M5)
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15
Q

Adrenergic receptor division

A
  • alpha 1 (1a, 1b, 1d) and 2 (2a, 2b, 2c)
  • beta 1,2,3
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16
Q

receptors in the PSNS are referred to as

A

Muscarinic

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17
Q

M1, M3, M5 receptors

A
  • usually causing contraction
  • G-protein coupled (Gq - stimulatory)
  • G-protein (Gq) –> phospholipase C –> IP3 –> DAG –> Ca2+ –> smooth muscle contraction
18
Q

M2, M4

A
  • inhibitory
  • G-protein coupled (Gi)
  • Gi –> reduced adenylate cyclase –> reduced cAMP –> reduced calcium channels –> reduced heart rate
19
Q

effects of a muscarinic agonist

A
  • decreased HR, contraction
  • bronchoconstriction
  • relaxed sphincters of GI and bladder
  • contracted walls of GI (to move food along)
  • increased secretion (salivary, respiratory, tears)
20
Q

example of coordinated action

A

bladder and urination

  • M3 in bladder wall contracts
  • M3 in sphincter relaxes
21
Q

anti-cholinergic drugs

A

blocking cholinergic receptors

  • side effect: M receptors important in the CNS (imp. in cognitive function) - so blocking cholinergic receptors in the brain can affect cognitive function
22
Q

ways to stimulate M receptors

A
  • direct: using an agonist
  • indirect: acetycholinesterase inhibitors (increase the concentration of ACh) - revrsible/irreversible
23
Q

3 types of chemical rxn that can occur when cholinesterase is bound (acetylcholinesterase inhibitors)

A
  • acetylation: rapid recovery of enzyme (physiological modulation of acetylcholine breakdown)
  • carbamylation: slower recovery of enzyme (reversible acetylcholinesterase inhibitors - neostigmine)
  • phosphorylation: no recovery of enzyme (covalent reaction - irreversible inhibition - nerve gases)
24
Q

excessive cholinergic response

A
  • increased secretions (drooling, tearing, clogged airways)
  • bronchoconstriction (difficulty breathing)
  • reduced heart rate (decreased endurance)
  • increased GI motility (nausea, vomiting, diarrhea)
  • contraction of bladder, relaxation of sphincters (urination)
25
parasympatholytics
block parasympathetic responses - aka anticholinergics/ anti-muscarinics - accomplished by antagonism of M receptors (blocking muscarinic receptors) - eg. atropine
26
atropine uses
- intubation (drying up secretions - make it easier to insert tube) - ophthalmology (dilate pupils) - asthma (bronchodilation) - antidote
27
atropine side effects
- dry mouth - tachycardia - constipation - difficulty urinating
28
alpha-1 function
constriction of smooth muscles - location: sphincters, blood vessels (vasoconstriction) - G protein --> IP3 --> increased Ca2+ --> contraction
29
alpha-2 function
function: when bound, inhibits of presynaptic release of norepinephrine
30
beta-1 function
- stimulates the heart (increases heart rate, AV conduction, contractility) - G-protein --> adenylate cyclase --> cAMP --> Ca2+ channels (L-type Ca2+ channel increase contractility) --> increased heart rate and contractility - stimulate renin release in the kidney, leading to increased blood pressure
31
organs only innervated by SNS
liver, kidney, uterus
32
Beta-2 function
relaxation of smooth muscles - lungs (bronchodilation) - blood vessels in SKELETAL muscle (vasodilation) - relaxation of walls in GI tract, bladder, uterus - mediate glucose release by liver (gluconeogenesis or glycogenolysis) - G-protein coupled --> AC--> cAMP --> bronchodilation
33
coordination of alpha 1 and beta 1 receptors
alpha 1 are receptors in the body core - beta 1 are in skeletal muscle - alpha 1 receptors cause contraction of blood vessels to move blood from the core into the periphery (skeletal muscle) during a sympathetic response - allows to increase oxygenation of skeletal muscle
34
bladder and urination in SNS
- B-2 in bladder wall causes relaxation - alpha-1 in sphincter causes constriction
35
sympathomimetics
drugs that mimic stimulation of sympathetic nervous system - by directly activating adrenergic receptors (eg. norepinephrine, adrenaline) - by increasing the amount of sympathetic neurotransmitter in the synapse
36
how to increase the amount of neurotransmitter in the synapse
- increase NT release - inhibit reuptake of NT (reuptake pumps) - inhibit metabolism of NT (MAO inhibitors: monoamine oxidase breaks down catecholamines) - nonselective
37
sympatholytics
drugs that block or reduce sympathetic activity - by directly blocking adrenergic receptors (propanolol) - by decreasing the amount of sympathetic neurotransmitter in the synapse (clonidine)
38
how to decrease the amount of sympathetic neurotransmitter in the synapse
- alpha 2 agonists (inhibit NT release into synapse) - block B-1 receptors
39
2 sets of muscles in the eye
iris + ciliary - 2 diff sets of iris muscle: circular (sphincter - M3, M2 receptors) and radial (longitudinal - alpha-1 receptors)
40