Effects of subacute pyridostigmine administration on mammalian skeletal muscle function. (Reannouncement with new availability information)
Abstract
The subacute effects of pyridostigmine bromide were investigated on the contractile properties of rat extensor digitorum longus (EDL) and diaphragm muscles. The cholinesterase inhibitor was delivered via subcutaneously implanted osmotic minipumps (Alzet) at 9 microns g h-1 (low dose) or 60 micro g h-1 (high dose). Animals receiving high-dose pyridostigmine pumps exhibited marked alterations in muscle properties within the first day of exposure that persisted for the remaining 13 days. With 0.1 Hz stimulation, EDL twitch tensions of treated animals were elevated relative to control. Repetitive stimulation at frequencies > 1 Hz led a use-dependent depression in the amplitude of successive twitches during the train. Recovery from pyridostigmine was essentially complete by 1 day of withdrawal. Rats implanted with low-dose pyridostigmine pumps showed little or no alteration of in vivo twitch tensions during the entire 14 days of treatment. Diaphragm and EDL muscles excised from pyridostigmine-treated rats and tested in vitro showed no significant alterations in twitch and tetanic tensions and displayed the same sensitivity as muscles of control animals to subsequent pyridostigmine exposures. In the presence of atropine, subacutely administered pyridostigmine protected rats from two LD5O doses of the irreversible cholinesterase inhibitor, soman. In the absence of atropine, themore »
- Authors:
- Publication Date:
- Research Org.:
- Army Medical Research Inst. of Chemical Defense, Aberdeen Proving Ground, MD (United States)
- OSTI Identifier:
- 166865
- Report Number(s):
- AD-A-250686/3/XAB; USAMRICD-P-89-069
TRN: 53520627
- Resource Type:
- Technical Report
- Resource Relation:
- Other Information: PBD: 1992
- Country of Publication:
- United States
- Language:
- English
- Subject:
- 45 MILITARY TECHNOLOGY, WEAPONRY, AND NATIONAL DEFENSE; 56 BIOLOGY AND MEDICINE, APPLIED STUDIES; CHEMICAL WARFARE AGENTS; TOXICITY; PREVENTIVE MEDICINE; BROMIDES; THERAPEUTIC USES; CHOLINESTERASE
Citation Formats
Adler, M, Deshpande, S S, Foster, R E, Maxwell, D M, and Albuquerque, E X. Effects of subacute pyridostigmine administration on mammalian skeletal muscle function. (Reannouncement with new availability information). United States: N. p., 1992.
Web.
Adler, M, Deshpande, S S, Foster, R E, Maxwell, D M, & Albuquerque, E X. Effects of subacute pyridostigmine administration on mammalian skeletal muscle function. (Reannouncement with new availability information). United States.
Adler, M, Deshpande, S S, Foster, R E, Maxwell, D M, and Albuquerque, E X. 1992.
"Effects of subacute pyridostigmine administration on mammalian skeletal muscle function. (Reannouncement with new availability information)". United States.
@article{osti_166865,
title = {Effects of subacute pyridostigmine administration on mammalian skeletal muscle function. (Reannouncement with new availability information)},
author = {Adler, M and Deshpande, S S and Foster, R E and Maxwell, D M and Albuquerque, E X},
abstractNote = {The subacute effects of pyridostigmine bromide were investigated on the contractile properties of rat extensor digitorum longus (EDL) and diaphragm muscles. The cholinesterase inhibitor was delivered via subcutaneously implanted osmotic minipumps (Alzet) at 9 microns g h-1 (low dose) or 60 micro g h-1 (high dose). Animals receiving high-dose pyridostigmine pumps exhibited marked alterations in muscle properties within the first day of exposure that persisted for the remaining 13 days. With 0.1 Hz stimulation, EDL twitch tensions of treated animals were elevated relative to control. Repetitive stimulation at frequencies > 1 Hz led a use-dependent depression in the amplitude of successive twitches during the train. Recovery from pyridostigmine was essentially complete by 1 day of withdrawal. Rats implanted with low-dose pyridostigmine pumps showed little or no alteration of in vivo twitch tensions during the entire 14 days of treatment. Diaphragm and EDL muscles excised from pyridostigmine-treated rats and tested in vitro showed no significant alterations in twitch and tetanic tensions and displayed the same sensitivity as muscles of control animals to subsequent pyridostigmine exposures. In the presence of atropine, subacutely administered pyridostigmine protected rats from two LD5O doses of the irreversible cholinesterase inhibitor, soman. In the absence of atropine, the LD50 of soman was not altered by subacute pyridostigmine treatment. Extensor digitorum longus; diaphragm; twitch tension; ACh release; subacute; Alzet pumps; tolerance; anticholinesterase; pyridostigmine; soman.},
doi = {},
url = {https://www.osti.gov/biblio/166865},
journal = {},
number = ,
volume = ,
place = {United States},
year = {Thu Dec 31 00:00:00 EST 1992},
month = {Thu Dec 31 00:00:00 EST 1992}
}