Opioid peptides decrease calcium-dependent action potential duration of mouse dorsal root ganglion neurons in cell culture
dc.contributor.author | Werz, Mary Ann | en_US |
dc.contributor.author | Macdonald, Robert L. | en_US |
dc.date.accessioned | 2006-04-07T17:52:11Z | |
dc.date.available | 2006-04-07T17:52:11Z | |
dc.date.issued | 1982-05-06 | en_US |
dc.identifier.citation | Werz, Mary Ann, Macdonald, Robert L. (1982/05/06)."Opioid peptides decrease calcium-dependent action potential duration of mouse dorsal root ganglion neurons in cell culture." Brain Research 239(1): 315-321. <http://hdl.handle.net/2027.42/23986> | en_US |
dc.identifier.uri | http://www.sciencedirect.com/science/article/B6SYR-4847RP4-10Y/2/e92ded9400c5974c43d587504729ae19 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/23986 | |
dc.identifier.uri | http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=7093688&dopt=citation | en_US |
dc.description.abstract | We investigated opioid peptide actions on somatic calcium-dependent action potentials of dorsal root ganglion (DRG) neurons grown in primary dissociated cell culture. We report that leucine-enkephalin decreased the duration and amplitude of DRG somatic calcium-dependent action potentials. The opioid peptide action was dose-dependent over 20 nM to 5 [mu]M and was antagonized by naloxone, consistent with mediation by opiate receptors. Thus, DRG neuron membranes have opiate receptors which act to decrease calcium influx. It is likely, therefore, that opiate receptors on the somata of DRG neurons in culture are functionally similar to opiate receptors on primary afferent terminals. | en_US |
dc.format.extent | 420575 bytes | |
dc.format.extent | 3118 bytes | |
dc.format.mimetype | application/pdf | |
dc.format.mimetype | text/plain | |
dc.language.iso | en_US | |
dc.publisher | Elsevier | en_US |
dc.title | Opioid peptides decrease calcium-dependent action potential duration of mouse dorsal root ganglion neurons in cell culture | en_US |
dc.type | Article | en_US |
dc.rights.robots | IndexNoFollow | en_US |
dc.subject.hlbsecondlevel | Public Health | en_US |
dc.subject.hlbsecondlevel | Neurosciences | en_US |
dc.subject.hlbsecondlevel | Molecular, Cellular and Developmental Biology | en_US |
dc.subject.hlbtoplevel | Science | en_US |
dc.subject.hlbtoplevel | Health Sciences | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.contributor.affiliationum | Neurosciences Program, University of Michigan Medical Center, Neuroscience Laboratory Building, 1103 E. Huron, Ann Arbor, MI 48109, U.S.A. | en_US |
dc.contributor.affiliationum | Department of Neurology, University of Michigan Medical Center, Neuroscience Laboratory Building, 1103 E. Huron, Ann Arbor, MI 48109, U.S.A. | en_US |
dc.identifier.pmid | 7093688 | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/23986/1/0000235.pdf | en_US |
dc.identifier.doi | http://dx.doi.org/10.1016/0006-8993(82)90859-9 | en_US |
dc.identifier.source | Brain Research | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
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