Effects of a carbamate, BPMC, on the central cholinergic functions and behavior of mice
O-sec-butylphenyl methylcarbamate (BPMC), an anticholinesterase carbamate, was injected once (100mg/kg, s.c.) or repeatedly (50mg/kg/day for 10 days) into mice. Animals were examined for their behavior and for parameters of cholinergic activity in the forebrain. Mice that received only a single inje...
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Published in | Japanese journal of veterinary science Vol. 51; no. 4; pp. 789 - 795 |
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Main Authors | , , , |
Format | Journal Article |
Language | English Japanese |
Published |
Japan
JAPANESE SOCIETY OF VETERINARY SCIENCE
01.08.1989
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Subjects | |
Online Access | Get full text |
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Summary: | O-sec-butylphenyl methylcarbamate (BPMC), an anticholinesterase carbamate, was injected once (100mg/kg, s.c.) or repeatedly (50mg/kg/day for 10 days) into mice. Animals were examined for their behavior and for parameters of cholinergic activity in the forebrain. Mice that received only a single injection exhibited reduced ambulation, hypothermia, and impairment of rotarod performance for up to 3 hr after a single injection. BPMC increased levels of acetylcholine (ACh) in the forebrain for up to 6 hr, and decreased acetylcholinesterase (AChE) activity for up to 24 hr. Both high-affinity choline uptake (HACU) and binding of [3H] quinuclidinyl benzilate (QNB) were reduced 20 min after a single injection without any effect on choline acetyltransferase (ChAT) activity. In behavioral tests conducted 10 min prior to the daily injections, rotarod performance and ambulation were slightly impaired for a few days before and after cessation of injection. Repeated treatment decreased HACU and binding of [3H] QNB for 24 hr after the final injection without any changes in levels of ACh content, AChE activity and ChAT activity. BPMC may reversibly impair cholinergic functions through effects not only on AChE activity but also on HACU and binding of [3H] QNB. |
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Bibliography: | L70 9202174 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0021-5295 1881-1442 |
DOI: | 10.1292/jvms1939.51.789 |