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Chronic treatment with cholinesterase inhibitors increases [alpha]2-adrenoceptors in rat brain

dc.contributor.authorHollingsworth, Peggie J.en_US
dc.date.accessioned2006-04-07T20:13:29Z
dc.date.available2006-04-07T20:13:29Z
dc.date.issued1988-08-24en_US
dc.identifier.citationHollingsworth, Peggie J. (1988/08/24)."Chronic treatment with cholinesterase inhibitors increases [alpha]2-adrenoceptors in rat brain." European Journal of Pharmacology 153(2-3): 167-173. <http://hdl.handle.net/2027.42/27177>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6T1J-4746BGV-TT/2/d632306c58051db9c95500bd59c957d1en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/27177
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=2846316&dopt=citationen_US
dc.description.abstractThe specific binding of [3H]clonidine to [alpha]2-adrenoceptorson neural membranes isolated from various brain areas was determined with rats treated for 7-14 days with the cholinesterase inhibitors neostigmine, triorthocresyl phosphate (TOCP), diisopropylfluorophosphate (DFP) and paraoxon, or with vihicle. Treatment with all four inhibitors increased the number of clonidine binding sites in various brain areas. In those areas which demonstrated significant increases in [3H]clonidine binding, there was also a significant inhibition of acetylcholinesterase activity. The possibility is discussed that increases in brain [alpha]2-adrenoceptors are related to the alterations in mood seen in individuals chronically exposed to organophosphorus cholinesterase inhibitors.en_US
dc.format.extent579789 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleChronic treatment with cholinesterase inhibitors increases [alpha]2-adrenoceptors in rat brainen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPharmacy and Pharmacologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Pharmacology, The University of Michigan Medical School, Ann Arbor, MI 48109, U.S.A.en_US
dc.identifier.pmid2846316en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/27177/1/0000175.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0014-2999(88)90603-6en_US
dc.identifier.sourceEuropean Journal of Pharmacologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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