ANS pharma chapter 1 Katzung Flashcards

1
Q

motor portion has 2 subdivisions

A

sympathetic ANS and Parasympathetic ANS

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

enteric ANS Is a semiautonomous part of GIT

A

neuronal cell bodies are located in myenteric(Auerbach plexus) and the sub muscous plexus ( Meissner)..send motor+sensory input to PS+S nervous system and receive output from them

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

cranial nerve 3,7,9,10 and sacral segments of the spinal cord

A

sympathetic cholinergic fibers,2 paravertebral chains that lie along the sides of the spinal column in both thorax and abdomen

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

difference between pre and post ganglionic fibres

A

pre ganglionic sympathetic fibers are short,post ganglionic fibres are long.

opp is true for for parasympathetic system

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

2 paravertebral chains that are located in the anterior aspect of abdominal aorta,

A

opp will be true for parasympathetic system

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

muscarinic receptors on the endothelium of blood vessels,

A

some presynaptic receptors on nerve ending

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

adrenoceptors on apocrine sweat glands

A

alpha 2 and beta adrenoceptors in vlood vessels

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Acetylcholine

A

primary transmitter in all autonomic ganglia, and at the synapses bw primary postganglionic neurons and their effector cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

primary transmitter

A

somatic(voluntary) skeletal muscle neuromuscular junction

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

SYNTHESIS AND STORAGE

A

synthesized by ChAT(Choline Acetyl Transferase) and Choline——-

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

inhibited by hemicholinium

A

transport of choline into nerve terminal

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

inhibited by vesamicol

A

vesicle-associated transport

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Release

A

Entry of Ca associated w triggeringvof an interaction between SNARE proteins including vSNARE(Vesicle associated membrane proteins, synaptobrevin,synaptotagmin) and tSNARE associated w nerve terminals(SNAP25,syntaxin)
DOCKING,INFLUX,FUSION,OPENING and RELEASE

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Botulinum

A

Enter botulinum toxin enters cholinergic nerve alters synaptobrevin to counter the release process

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Nor Epinephrine

A

primary transmitter at the primary transmitter at the sympathetic postganglionic neuron effector cell synapses in most
eccrine sweat glands and vasodilation in skeletal muscles that release acetylcholine choline

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

in kidneys

A

vasodilator in skeletal muscles,norepinephrine is a vasoconstrictor

17
Q

synthesis of dopamine and epinephrine

A

tyrosine to tyrosine hydroxylase
DOPA(dihydroxyphenylalanine)
dehydroxylated to depamine and hydroxylated to norepinephrine.

decarboxylated to dopamine
and(inside the vesicle)hydroxylated to norepinephrine.

18
Q

tyrosine hydroxylase

A

can be inhibited by metyrosine

19
Q

norepinephrine and dopamine are transported into vesicles by

A

vesicular monoamine transporter

20
Q

MAO

A

present on mitochondria,inactivates a portion of dopamine and norepinephrine in the cytoplasm.

21
Q

MAO inhibitors

A

may inc the stores of transmitters and other amines in their nerve endings,VMAT can be inhibited by reserpine. resulting in depletion of nerve endings

22
Q

INHIBITION OF COMT

A

USEFUL IN PARKINSON’S

23
Q

hypertension

A

Drugs that
block norepinephrine synthesis (eg, metyrosine) or catecholamine
storage (eg, reserpine) or release (eg, guanethidine) were used in
treatment of several diseases (eg,

24
Q

transmitter vesicles that contain other transmitter molecules in addition to the
primary agents (acetylcholine or norepinephrine) previously
described.

A
ATP (adenosine triphosphate), enkephalins, vasoac-
tive intestinal peptide, neuropeptide Y, substance P, neuro-
tensin, somatostatin, and others. Their main role in autonomic
function appears
25
NICOTINIC receptors—These receptors are located on Na+ -K+ ion channels and respond to acetylcholine and nicotine, another acetylcholine mimic
but not to muscarine) by opening the channel. The 2 major nicotinic subtypes are located in ganglia and in skeletal muscle end plates.
26
(
receptors—These are located on vascular smooth muscle, presynaptic nerve terminals, blood platelets, fat cells (lipocytes), and neurons in the brain. Alpha receptors are further divided into 2 major types, α1 and α2.
27
Beta receptors
These 2 subtypes constitute different families and use different G-coupling receptors—These receptors are located on most types of smooth, cardiac, some presynaptic nerve terminals, and lipocytes. Beta receptors are divided into 3 major subtypes, β1, β2, and β3.(similar used g protein coupled receptor)
28
``` Dopamine (D, DA) receptors are a subclass of adrenoceptors but with rather different distribution and function. Dopamine ``` receptors are especially important in the renal and splanchnic ves- sels and in the brain.
the D1 subtype appears to be the most important dopamine receptor on peripheral effector cells. D2 receptors are found on presynaptic nerve terminals. D1, D2, and other types of dopamine receptors also occur in the CNS.
29
example, both the pupil and, at rest, the | sinoatrial node are dominated by the parasympathetic system(.100–110/min)
system. Thus, blockade of both systems, with removal of the dominant PANS and nondominant SANS effects, result in mydriasis and tachycardia.
30
2 feedback loops are present: the autonomic nervous sys- tem loop and the hormonal loop. Each major loop has several components. In the neuronal loop, sensory input to the vasomotor center is via affer- ent fibers in the ninth and tenth cranial (PANS) nerves.
On the efferent side, the sympathetic nervous system directly influences 4 major variables: ``` peripheral vascular resistance, heart rate, contractile force, and venous tone. The parasympathetic nervous system directly influences heart rate. In addition, angiotensin II directly increases peripheral vascular resistance (not shown), and sympathetic nervous system discharge directly increases renin secretion (not shown). Because these control mechanisms have evolved to maintain normal blood pressure, the net feedback effect of each ```
31
present: the autonomic nervous sys- tem loop and the hormonal loop. Each major loop has several components. In the neuronal loop, sensory input to the vasomotor center is via affer- ent fibers in the ninth and tenth cranial (PANS) nerves. On the efferent side, the sympathetic nervous system directly influences 4 major variables: peripheral vascular resistance, heart rate, contractile force, and venous tone.
parasympathetic nervous system directly influences heart rate. In addition, angiotensin II directly increases peripheral vascular resistance and sympathetic nervous system discharge directly increases renin secretion. Because these control mechanisms have evolved to maintain normal blood pressure, the net feedback effect of each loop is negative; feedback tends to compensate for the change in arterial blood pressure that evoked the response.
32
peripheral vascular resistance, venous tone, heart rate, and cardiac force are increased by norepinephrine released from sympathetic nerves. This ANS response can be blocked with ganglion-blocking drugs such as hexamethonium.
These compensatory responses may be large enough to overcome some of the actions of drugs. For example, the chronic treatment of hypertension with a vasodilator such as hydralazine will be unsuccessful if compensatory tachycardia (via the baroreceptor reflex) and salt and water retention (via the renin system response) are not prevented through the use of additional drugs.
33
The pupil, discussed previously, is under reciprocal control by the SANS (via α receptors on the pupillary dilator muscle) and the PANS (via muscarinic receptors on the pupillary constrictor).
ciliary muscle, which controls accommodation, is under primary control of muscarinic receptors innervated by the PANS,