ANS A&P Flashcards
how many spinal nerves are there
31
A1 and V1 stimulation increases
PLC activity (Gq)
B1, 2, and 3 stimulation increases
adenylate cyclase activity (Gs)
A2, M2, M4, D2 receptor decreases
adenylate cyclase activity (Gi)
heart SNS and PSNS receptors and effects
SNS: B1–> positive inotropic, chronotropic, and dromotropic effects
PSNS: M2–> negative inotropic, chronotropic, and dromotropic effects
lung SNS and PSNS receptors and effects
SNS: B2–> bronchodilation
PSNS: M3–> bronchoconstriciton, gland secretions
GI tract SNS and PSNS receptors and effects
SNS: a1 –> vasoconstriction, sphincter contraction
PSNS: M3 –> increased Gi motility, sphincter relaxation, increased gland secretion
glands SNS and PSNS receptors and effects
SNS: a1 –> increased sweating and decreased pancreatic activity
PSNS: M1, M3 –>increased salivation, increased lacrimation, increased pancreatic activity
urinary tract SNS and PSNS receptors and effects
SNS: a1, b2 –>bladder sphincter contraction, increased renin secretion
PSNS: M3 –> bladder sphincter relaxation
skin SNS and PSNS receptors and effects
SNS: a1 –> vasoconstriction
PSNS: —–
skeletal muscle SNS and PSNS receptors and effects
SNS: B2 –> vasodilation
PSNS: ——-
pupils SNS and PSNS receptors and effects
SNS: a1–> dilation (mydriasis)
PSNS: M3 –> constriction (miosis)
intrinsic muscles of the eye (smooth muscles) include (3)
ciliary muscle, sphincter pupillae, dilator pupillae
A2 stimulation can produce these effects (3)
produce anti shivering effect
inhibit insulin release (which creates hyperglycemia)
promotes platelet aggregation
physiologic effect of A2 receptor stimulation for the following organs/effector sites
vasculature
renal tubules
pancreas
platelets
salivary glands
Gi tract
vasculature: constricts
renal tubules: inhibit ADH (diuresis)
pancreas: decreases insulin release
platelets: increases aggregation
salivary glands: dry mouth
Gi tract: decreased gut motility
in VSMC, cAMP inhibits ___________ which produces these two effects
inhibits myosin light chain kinase
vasodilation and decreased SVR result
PDE3 inhibitors are useful in the following clinical situations (4)
BB induced myocardial depression
acute HF
unresponsiveness to IV catecholamines
any time increased inotropy with reduced after load would be desirable.
how many molecules of ATP can be produced from 1 mole of glucose
38
rate limiting step in catecholamine synthesis
tyrosine hydroxylase
stimulation of which presynaptic adrenergic receptor augments NE release? stops it?
augments: B2
stops: A2
catecholamines are removed from synaptic cleft via what 3 mechanisms?
- reuptake into presynaptic nerve
- reuptake into extra neural tissue
- diffusion away from synaptic cleft
what 2 enzymes metabolize NE in the liver and kidney
MAO and COMT
major metabolite of dopamine
homovanillic acid (HVA)
Ach synthesis in presynaptic nerve terminal
- acetyl coenzyme A is produced in mitochondria and released into the cytoplasm
- choline is transported from the blood to the cytoplasm of the nerve terminal
- in the presence of choline aminotransferase, choline and acetyl coa are combined to form acetylcholine, which is then packaged into vescicles
byproducts of Ach metabolism
choline, which diffuses into circulation
acetate, acetate, which diffuses away from synaptic cleft
what is another name for true cholinesterase
acetylcholinesterase (AchE)
compare and contrast SNS and PSNS:
preganglionic fiber length
postganglionic receptor types
target organs
anatomical origin of SNS fibers
(origin, location on SC, where cell bodies arise from)
thoracolumbar region, mainly T1-L3
cell bodies arise from interomediolateral horn of SC and axons exit via ventral roots, aka lateral horn/rexeds lamina 7
anatomical origin of PSNS fibers
craniosacral
CN 3, 7, 9, 10
S2-S4
SNS ganglia compared to PSNS ganglia location
SNS ganglia are near SC (sympathetic chain) while PSNS ganglia are near or inside tissue effector/organ
SNS pre to post ganglionic ratio versus PSNS
SNS: 30:1, post synaptic amplification contributes to mass response
PSNS: 1:1 or 3:1, precise control of each effector organ