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Central muscle relaxant effects of diazepam

dc.contributor.authorHudson, Roy D.en_US
dc.contributor.authorWolpert, Mary K.en_US
dc.date.accessioned2006-04-17T15:08:17Z
dc.date.available2006-04-17T15:08:17Z
dc.date.issued1970-09en_US
dc.identifier.citationHudson, R. D., Wolpert, Mary K. (1970/09)."Central muscle relaxant effects of diazepam." Neuropharmacology 9(5): 481-484. <http://hdl.handle.net/2027.42/32707>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6T0C-477XHDT-9/2/a4b98a620e037a57e1a1dd783b48513fen_US
dc.identifier.urihttps://hdl.handle.net/2027.42/32707
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=5477433&dopt=citationen_US
dc.description.abstractMotor depressant effects of diazepam were studied in the intact, decerebrate and high spinal cat. Diazepam (0[middle dot]125-16 mg/kg i.v.) produced a depression of both the patellar and linguomandibular reflexes in the intact cat. In the high spinal (C1) cat only the linguomandibular reflex was depressed. Facilitation and inhibition of the patellar reflex elicited in both intact and high spinal (C1) cats were reduced by diazepam. No depression was observed in the in vivo neuromuscular preparation of the tibialis anticus muscle. Small doses of diazepam (0[middle dot]125 mg/kg i.v.) abolished the rigidity of the mid-collicular decerebrate cat.Mean arterial blood pressure was initially depressed in all animals (0[middle dot]125-2 mg/kg) with an intact medullary vasomotor outflow. Larger doses (4-16 mg/kg) tended to return the blood pressure toward control levels.The present study presents evidence for both a brain stem reticular and a spinal cord site of action of diazepam on motor systems. Possible mechanisms of action of diazepam on motor systems are discussed.en_US
dc.format.extent937447 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleCentral muscle relaxant effects of diazepamen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPsychiatryen_US
dc.subject.hlbsecondlevelNeurosciencesen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Pharmacology, The University of Michigan, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationotherSection of Neuroscience, Division of Biological and Medical Sciences, Brown University, Providence, Rhode Island, USAen_US
dc.identifier.pmid5477433en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/32707/1/0000074.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0028-3908(70)90021-3en_US
dc.identifier.sourceNeuropharmacologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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