Acetylcholine Synthesis, Release & Metabolism Flashcards
Select the true statements regarding acetylcholine. (Select 3.)

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—– is the primary transmitter in the parasympathetic nervous system
Acetylcholine
Acetylcholine is the primary transmitter in the parasympathetic nervous system. It stimulates which 3 different receptor types in the body?
Nicotinic type N
Nicotinic type M
Muscarinic
Nicotinic type N receptors are found in —–.
PNS ganglia
SNS ganglia
Central nervous system
Nicotinic type M receptors are found at the —–.
Neuromuscular junction
Muscarinic receptors found in the —– effector organs and in the —–.
Postganglionic PNS effector organs
Central nervous system
Note that nicotinic receptors are —–, while muscarinic receptors are linked to —–.
ion channels
G- proteins
—– starts the process of Ach synthesis
Choline
Choline is transported from the —– into the —– of the nerve terminal
blood into the cytoplasm
—– is produced in the mitochondria and released to the cytoplasm.
Acetyl Coenzyme A
In the presence of the enzyme —–, choline and acetyl CoA are joined to form acetylcholine (Ach).
Choline acetyltransferase (ChAT)
Acetylcholine is packaged into —–.
vesicles
The —– initiates Ach release
Action potential
The action potential depolarizes the —– terminal
nerve terminal
Voltage-gated —– channels open
Ca+2 channels
Voltage gated Ca+2 channels open and allow an influx of —– into the nerve terminal
Ca+2
—– is required for Ach vesicles to fuse with the nerve terminal
Ca+2
Ca+2 is required for Ach vesicles to fuse with the nerve terminal and release Ach via —– into the synaptic cleft.
exocytosis
—– is an antagonist of Ca+2 at the presynaptic nerve terminal
Mg +2
Mg +2 is an antagonist of Ca+2 at the presynaptic nerve terminal. This explains why Mg +2 can cause —– weakness
muscle weakness
Mg +2 is an antagonist of Ca+2 at the presynaptic nerve terminal. This explains why Mg +2 can cause muscle weakness or how it acts synergistically with which drugs?
neuromuscular blockers
Unlike norepinephrine, Ach is not —–
Ach is not reused
Unlike norepinephrine, Ach is not reused and there is no —- mechanism
uptake mechanism
Ach must be rapidly —– to allow precise control of the effector organs
metabolized
