ANS pharma chapter 1 Katzung Flashcards
motor portion has 2 subdivisions
sympathetic ANS and Parasympathetic ANS
enteric ANS Is a semiautonomous part of GIT
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
cranial nerve 3,7,9,10 and sacral segments of the spinal cord
sympathetic cholinergic fibers,2 paravertebral chains that lie along the sides of the spinal column in both thorax and abdomen
difference between pre and post ganglionic fibres
pre ganglionic sympathetic fibers are short,post ganglionic fibres are long.
opp is true for for parasympathetic system
2 paravertebral chains that are located in the anterior aspect of abdominal aorta,
opp will be true for parasympathetic system
muscarinic receptors on the endothelium of blood vessels,
some presynaptic receptors on nerve ending
adrenoceptors on apocrine sweat glands
alpha 2 and beta adrenoceptors in vlood vessels
Acetylcholine
primary transmitter in all autonomic ganglia, and at the synapses bw primary postganglionic neurons and their effector cells
primary transmitter
somatic(voluntary) skeletal muscle neuromuscular junction
SYNTHESIS AND STORAGE
synthesized by ChAT(Choline Acetyl Transferase) and Choline——-
inhibited by hemicholinium
transport of choline into nerve terminal
inhibited by vesamicol
vesicle-associated transport
Release
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
Botulinum
Enter botulinum toxin enters cholinergic nerve alters synaptobrevin to counter the release process
Nor Epinephrine
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
in kidneys
vasodilator in skeletal muscles,norepinephrine is a vasoconstrictor
synthesis of dopamine and epinephrine
tyrosine to tyrosine hydroxylase
DOPA(dihydroxyphenylalanine)
dehydroxylated to depamine and hydroxylated to norepinephrine.
decarboxylated to dopamine
and(inside the vesicle)hydroxylated to norepinephrine.
tyrosine hydroxylase
can be inhibited by metyrosine
norepinephrine and dopamine are transported into vesicles by
vesicular monoamine transporter
MAO
present on mitochondria,inactivates a portion of dopamine and norepinephrine in the cytoplasm.
MAO inhibitors
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
INHIBITION OF COMT
USEFUL IN PARKINSON’S
hypertension
Drugs that
block norepinephrine synthesis (eg, metyrosine) or catecholamine
storage (eg, reserpine) or release (eg, guanethidine) were used in
treatment of several diseases (eg,
transmitter vesicles that contain other transmitter molecules in addition to the
primary agents (acetylcholine or norepinephrine) previously
described.
ATP (adenosine triphosphate), enkephalins, vasoac- tive intestinal peptide, neuropeptide Y, substance P, neuro- tensin, somatostatin, and others. Their main role in autonomic function appears