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Tetrahydroaminoacridine (THA) reduces voltage-dependent calcium currents in rat sensory neurons

dc.contributor.authorKelly, Kevin M.en_US
dc.contributor.authorGross, Robert A.en_US
dc.contributor.authorMacdonald, Robert L.en_US
dc.date.accessioned2006-04-10T14:31:00Z
dc.date.available2006-04-10T14:31:00Z
dc.date.issued1991-11-11en_US
dc.identifier.citationKelly, Kevin M., Gross, Robert A., Macdonald, Robert L. (1991/11/11)."Tetrahydroaminoacridine (THA) reduces voltage-dependent calcium currents in rat sensory neurons." Neuroscience Letters 132(2): 247-250. <http://hdl.handle.net/2027.42/29032>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6T0G-485RNMY-1N2/2/782df544975a1fc79042e4eb48ee0867en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/29032
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=1784428&dopt=citationen_US
dc.description.abstractTetrahydroaminoacridine (THA) is a centrally active anticholinesterase that also interacts with neuronal K+ and Na+ channels and cardiac Ca2+ channels. The effects of THA on neuronal voltage-dependent Ca2+ channels are not known. We tested the effects of THA (25 nM-250 [mu]M) on the Ca2+ current components of acutely dissociated rat nodose ganglion and dorsal root ganglion (DRG) neurons using the whole cell patch clamp recording technique. THA reduced the low-threshold (T) and high-threshold (N/L) Ca2+ current components in a concentration-dependent manner (IC50 [congruent with] 125 [mu]M for T; [congruent with] 80 [mu]M for (N/L). Minimal current reduction was seen below ~ 10 [mu]M. Our results show that THA reduces voltage-dependent Ca2+ currents in rodent sensory neurons suggesting another means by which THA may affect Ca2+-dependent physiologic processes.en_US
dc.format.extent366209 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleTetrahydroaminoacridine (THA) reduces voltage-dependent calcium currents in rat sensory neuronsen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbsecondlevelPsychologyen_US
dc.subject.hlbsecondlevelNeurosciencesen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbtoplevelSocial Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Neurology, University of Michigan Medical Center, Ann Arbor, Michigan 48109, U.S.A.en_US
dc.contributor.affiliationumDepartment of Neurology, University of Michigan Medical Center, Ann Arbor, Michigan 48109, U.S.A.en_US
dc.contributor.affiliationumDepartment of Physiology, University of Michigan Medical Center, Ann Arbor, Michigan 48109, U.S.A.; Department of Neurology, University of Michigan Medical Center, Ann Arbor, Michigan 48109, U.S.A.en_US
dc.identifier.pmid1784428en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/29032/1/0000064.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0304-3940(91)90312-Hen_US
dc.identifier.sourceNeuroscience Lettersen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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