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anticholinesterase

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anticholinesterase /an·ti·cho·lin·es·ter·ase/ (-ko″lin-es´ter-ās) cholinesterase inhibitor.
an·ti·cho·lin·es·ter·ase (nt-kl-nst-rs, -rz, nt-)
n.
A substance that inhibits the activity of cholinesterases, including acetylcholinesterase.

anticholinesterase
[an′tikol′ənes′tərās]
a drug that inhibits or inactivates the action of acetylcholinesterase. Drugs of this class cause acetylcholine to accumulate at the junctions of various cholinergic nerve fibers and their effector sites or organs, allowing potentially continuous stimulation of cholinergic fibers throughout the central and peripheral nervous systems. Anticholinesterases include physostigmine salicylate, neostigmine, edrophonium, and pyridostigmine. Neostigmine and pyridostigmine are prescribed in the treatment of myasthenia gravis; edrophonium in the diagnosis of myasthenia gravis and the treatment of overdose of curariform drugs. Many agricultural insecticides have been developed from anticholinesterases; these are the highly toxic chemicals called organophosphates. Nerve gases developed as potential chemical warfare agents contain potent, irreversible forms of anticholinesterase.

anticholinesterase (an´tīkō´lines´-trās),
n a drug or chemical that inhibits or inactivates the enzyme cholinesterase, resulting in the actions produced by the accumulation of acetylcholine at cholinergic sites.

anticholinesterase
a drug that inhibits the enzyme acetylcholinesterase, thereby potentiating the action of acetylcholine at postsynaptic membrane receptors in the parasympathetic nervous system.

anticholinesterase
Pharmacology An agent–eg, certain nerve gases, which blocks nerve impulses by inhibiting anticholinesterase Examples Insecticides–eg, parathion, and nerve gas agents–eg, sarin, soman, tabun; AChEs can be reversible or irreversible Action Eyes–hyperemia and pupillary constriction, GI tract—↑ GI contractions and secretion of gastric acid


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Myasthenia Autoimmune Muscle weakness Anticholinesterase gravis (12) attack against and fatigue, agents such as the cells at the including Mestinon junction of weakness of the (pyridostigmine), nerves and eye muscles.
2002) but is below the threshold for cholinesterase inhibition (Das and Barone 1999); the in vivo CPF metabolite, CPF oxon, is the active agent that produces irreversible anticholinesterase actions and is three orders of magnitude more potent than CPF itself in inhibiting cholinesterase (Das and Barone 1999).
Anticholineserases Guttmann and Walsh[21] reported that the anticholinesterase drug prostigmine elicited spontaneous erections and ejaculations when intrathecally administered to 134 men with SCI.
 
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