Ca2+, histamine antagonists and relaxation to electrical impulses in dog coronary artery
dc.contributor.author | Gantzos, Robin D. | en_US |
dc.contributor.author | Ebeigbe, Anthony B. | en_US |
dc.contributor.author | Clinton Webb, R. | en_US |
dc.date.accessioned | 2006-04-07T18:42:37Z | |
dc.date.available | 2006-04-07T18:42:37Z | |
dc.date.issued | 1983-05-06 | en_US |
dc.identifier.citation | Gantzos, Robin D., Ebeigbe, Anthony B., Clinton Webb, R. (1983/05/06)."Ca2+, histamine antagonists and relaxation to electrical impulses in dog coronary artery." European Journal of Pharmacology 89(3-4): 287-291. <http://hdl.handle.net/2027.42/25219> | en_US |
dc.identifier.uri | http://www.sciencedirect.com/science/article/B6T1J-47463BT-5B/2/ad554db8bc7161e9c3ae2a8f38ea7a50 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/25219 | |
dc.identifier.uri | http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=6873165&dopt=citation | en_US |
dc.description.abstract | Isolated dog coronary arteries relax in response to electrical stimulation (0.1-8.0 Hz, 9 V, 1.0 ms) following contraction induced by serotonin. Cimetidine, metiamide and ranitidine inhibited this relaxation. The relaxation was not blocked by pyrilamine. Reducing the concentration of Ca+ (0.1 mM) decreased the rate of relaxation whereas relaxation was more rapid when the Ca2+ concentration was increased (3.2 mM). These results suggest that relaxation to electrical stimulation is modulated by Ca2+ and by the H2-subclass of histamine receptors. | en_US |
dc.format.extent | 350465 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 | Ca2+, histamine antagonists and relaxation to electrical impulses in dog coronary artery | en_US |
dc.type | Article | en_US |
dc.rights.robots | IndexNoFollow | en_US |
dc.subject.hlbsecondlevel | Pharmacy and Pharmacology | en_US |
dc.subject.hlbtoplevel | Health Sciences | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.contributor.affiliationum | Department of Physiology, University of Michigan, Ann Arbor, Michigan 48109, U.S.A. | en_US |
dc.contributor.affiliationum | Department of Physiology, University of Michigan, Ann Arbor, Michigan 48109, U.S.A. | en_US |
dc.contributor.affiliationum | Department of Physiology, University of Michigan, Ann Arbor, Michigan 48109, U.S.A. | en_US |
dc.identifier.pmid | 6873165 | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/25219/1/0000659.pdf | en_US |
dc.identifier.doi | http://dx.doi.org/10.1016/0014-2999(83)90508-3 | en_US |
dc.identifier.source | European Journal of Pharmacology | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
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