acetylcholine

—acetylcholinic /euh seet'l koh lin"ik, euh set'-, as'i tl-/, adj.

/euh seet'l koh"leen, euh set'-, as'i tl-/, n.

1. Biochem. the acetic acid ester of choline, C₇H₁₇NO₃, released and hydrolyzed during nerve conduction and causing muscle action by transmitting nerve impulses across synapses.

2. Pharm. this substance used in its chloride form in eye surgery. Abbr.: ACh

[1905-10; ACETYL + CHOLINE]

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Ester of choline and acetic acid, a neurotransmitter active at many nerve synapses and at the motor end plate of vertebrate voluntary muscles.

It affects several of the body's systems, including the cardiovascular system (decreases heart rate and contraction strength, dilates blood vessels), gastrointestinal system (increases peristalsis in the stomach and amplitude of digestive contractions), and urinary system (decreases bladder capacity, increases voluntary voiding pressure). It also affects the respiratory system and stimulates secretion by all glands that receive parasympathetic nerve impulses (see autonomic nervous system). It is important in memory and learning and is deficient in the brains of those with late-stage Alzheimer disease.

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▪ chemical compound

      (ACh), an ester of choline and acetic acid that is the transmitter (neurotransmitter) substance at many neural, or nerve, synapses and at the motor end plate of vertebrate muscles (see end-plate potential). When a nerve impulse arrives at the nerve ending, ACh, which is stored there in vesicles, is released and combines with a receptor molecule in the postsynaptic membrane or the end-plate membrane (end-plate potential) of a muscle fibre. This bonding changes the permeability of the membrane, and a change in the nature of a generator potential results. The effects of successive nerve impulses accumulate if they arrive at a sufficiently high frequency. The ACh is destroyed by an enzyme, acetylcholinesterase, and thus is effective only briefly. Inhibitors of the enzyme, however, prolong the lifetime of ACh itself.

      ACh affects a number of body systems including the cardiovascular system by acting as a vasodilator, by decreasing cardiac rate, and by decreasing cardiac contraction; the gastrointestinal system by such activities as increasing peristalsis in the stomach and by increasing the amplitude of digestive contractions; and the urinary tract by such actions as decreasing the capacity of the bladder and increasing the voluntary voiding pressure. It also affects the respiratory system and stimulates secretion by all glands that receive parasympathetic nerve impulses.

 ACh was first isolated around 1914; its functional significance was first established in about 1921 by Otto Loewi (Loewi, Otto), a German physiologist and later (1936) Nobel laureate. Loewi demonstrated that ACh is the substance liberated when the vagus nerve is stimulated, causing slowing of the heartbeat. Subsequently he and others showed that ACh is also liberated as a transmitter at the motor end plate of striated (voluntary) muscles of vertebrates, and it has since been identified as a transmitter at many neural synapses and in many invertebrate systems as well.

      ACh is also known to play an important role in memory and learning and is in abnormally short supply in the brains of those with Alzheimer's disease (Alzheimer disease).

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