general autonomic nervous system pharmacology topic Flashcards

receptors: classify the cholinoceptors/adrenoceptors located in the ANS and state (a) where each type is found and (b) the signaling systems they each employ

1
Q

2 types of membrane bound acetylcholine receptors

A

muscarinic, nicotinic

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2
Q

location of nicotinic receptors

A

all autonomic ganglia in nervous system (between pre and post ganglion); if blockaded at rest, constipation and (if at rest), increased heart rate - if during exercise, heart rate increases but less effect

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3
Q

stimulation of nicotinic receptors

A

nicotine or acetylcholine

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4
Q

what type of channel is nicotinic receptor

A

type 1 (ionotropic): ion-channel linked receptor (fastest mode of transmission)

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5
Q

location of muscarinic receptors

A

all effector organs innovated by post ganglionic PSNS fibres and in post ganglionic SNS for sweat glands

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6
Q

stimulation of muscarinic receptors

A

muscarine or acetylcholine

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7
Q

what type is muscarinic receptor

A

type 2: G-protein coupled (slightly slower)

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8
Q

5 sub types of muscarinic cholinoreceptors (M1, 2 and 3 are most important)

A

M1 (neural; forebrain - learning and memory), M2 (cardiac; brain - inhibitory autoreceptors), M3 (exocrine and smooth muscle e.g. lungs; hypothalamus - food intake); [M4 (periphery; prejunctional nerve endings - inhibitory for dopamine in Parkinson’s), M5 (striatal dopamine release)]

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9
Q

location of adrenoceptors

A

all effector organs innervated by post ganglionic SNS fibres (except sweat glands)

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10
Q

stimulation of adrenoceptors

A

noradrenaline or adrenaline

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11
Q

what is type 2 adrenoceptor

A

G-protein coupled

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12
Q

sub types of adrenoceptors

A

a1, a2, B1, B2

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13
Q

in pharmacology, what are receptors classified as

A

drug targets

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14
Q

3 pharmacology questions for drugs (e.g. acetylcholine for stomach)

A

what is the drug target (normally muscarinic or adrenoceptor as localised at tissue), where is the drug target (gastric smooth muscle, parietal cell, endocrine cell), what is end result of interaction (contraction or increased secretion)

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