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dc.contributor.authorÖztürk, Yusuf
dc.contributor.authorAltınkurt, Onur
dc.contributor.authorYıldızoğulları, N
dc.contributor.authorAltan, Vecdi Melih
dc.date.accessioned2019-10-18T18:44:22Z
dc.date.available2019-10-18T18:44:22Z
dc.date.issued1990
dc.identifier.issn0022-3573
dc.identifier.urihttps://hdl.handle.net/11421/10601
dc.descriptionWOS: A1990EP02800014en_US
dc.descriptionPubMed ID: 1983153en_US
dc.description.abstractVerapamil, nifedipine, phentolamine, tolazoline, gentamicin and neomycin inhibited calcium-induced contractions of K+-depolarized duodenum of the rat by shifting the concentration-response curves to the right. Non-competitive inhibitions were observed with trifluoperazine, lidoflazine, procaine and tetracaine. Lanthanum behaved as a partial agonist in this preparation, while nitroprusside was ineffective. Contraction times in the presence of the antagonists and recovery time of the Ca2+ responses after the removal of the antagonists from the bathing medium were evaluated. From the findings, it is suggested that the contraction time and the time required for tissue recovery after removal of a Ca2+ antagonist are parameters making K+-depolarized rat duodenum a potential tool for the evaluation of the pharmacological effects of Ca2+ antagonists.en_US
dc.language.isoengen_US
dc.publisherRoyal Pharmaceutical Soc Great Britainen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleEvaluation of Contraction Time and Recovery Period as a Parameter in the Calcium Antagonistic Action on the K+-Depolarized Rat Duodenumen_US
dc.typeotheren_US
dc.relation.journalJournal of Pharmacy and Pharmacologyen_US
dc.contributor.departmentAnadolu Üniversitesien_US
dc.contributor.authorIDOZTURK, Yusuf/0000-0002-9488-0891en_US
dc.identifier.volume42en_US
dc.identifier.issue12en_US
dc.identifier.startpage874en_US
dc.identifier.endpage877en_US
dc.relation.publicationcategoryDiğeren_US
dc.contributor.institutionauthorÖztürk, Yusuf


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