1987Military MedicineRequires access

Antagonistic Effects of Scopolamine and Atropine on the Physostigmine Response in Man

David S. Janowsky, S. Craig Risch, Michael G. Ziegler, J. Christian Gillin

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Abstract

A series of preclinical studies suggest that scopolamine may be a better antidote for centrally acting cholinesterase inhibitor toxicity than is atropine. The current experiment was designed to compare the antagonistic effects on centrally mediated cholinergic symptoms in man of scopolamine and atropine, using noncentrally acting methscopolamine as a reference compound. Scopolamine, but not atropine, significantly antagonized physostigmine's behavioral, neuroendocrine, and cardiovascular effects. Scopolamine may thus be a preferred treatment for centrally mediated cholinesterase inhibitor-induced symptoms.

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What this paper is about

A series of preclinical studies suggest that scopolamine may be a better antidote for centrally acting cholinesterase inhibitor toxicity than is atropine. The current experiment was designed to compare the antagonistic effects on centrally mediated cholinergic symptoms in man of scopolamine and atropine, using noncentrally acting methscopolamine as a reference compound. Scopolamine, but not atropine, significantly antagonized physostigmine's behavioral, neuroendocrine, and cardiovascular effects. Scopolamine may thus be a preferred treatment for centrally mediated cholinesterase inhibitor-induced symptoms.

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Available abstract

A series of preclinical studies suggest that scopolamine may be a better antidote for centrally acting cholinesterase inhibitor toxicity than is atropine. The current experiment was designed to compare the antagonistic effects on centrally mediated cholinergic symptoms in man of scopolamine and atropine, using noncentrally acting methscopolamine as a reference compound. Scopolamine, but not atropine, significantly antagonized physostigmine's behavioral, neuroendocrine, and cardiovascular effects. Scopolamine may thus be a preferred treatment for centrally mediated cholinesterase inhibitor-induced symptoms.

Key concepts: Physostigmine, Atropine, Cholinesterase, Scopolamine, Parasympatholytic, Cholinergic, Pharmacology, Antidote

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