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dc.contributor.authorAltınkurt, Onur
dc.contributor.authorÖztürk, Yusuf
dc.date.accessioned2019-10-18T19:02:36Z
dc.date.available2019-10-18T19:02:36Z
dc.date.issued1990
dc.identifier.issn0196-9781
dc.identifier.urihttps://dx.doi.org/10.1016/0196-9781(90)90107-G
dc.identifier.urihttps://hdl.handle.net/11421/10723
dc.descriptionPubMed: 2160652en_US
dc.description.abstractPharmacological properties of the bradykinin receptors in the isolated rat duodenum were investigated by examining the relaxant and contractile responses to bradykinin and [des-Arg9]-bradykinin, an agonist of B1 receptors. A specific desensitization and de novo formation for B1 receptors were observed. Changes in medium pH caused a decrease in the responses to bradykinin and [des-Arg9]-bradykinin of rat duodenum. Urea incubation in test tube inhibited the responses to bradykinin and [des-Arg9]-bradykinin of rat duodenum, while urea in bathing medium was ineffective. These findings strongly suggested that (a) ionic bonds are important in the interaction between bradykinin and its receptors, and (b) B2 receptors in rat duodenum are different from those in guinea pig ileumen_US
dc.language.isoengen_US
dc.relation.isversionof10.1016/0196-9781(90)90107-Gen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectB1 And B2 Receptorsen_US
dc.subjectBradykininen_US
dc.subject[Des-Arg9]-Bradykininen_US
dc.titleBradykinin receptors in isolated rat duodenumen_US
dc.typearticleen_US
dc.relation.journalPeptidesen_US
dc.contributor.departmentAnadolu Üniversitesien_US
dc.identifier.volume11en_US
dc.identifier.issue1en_US
dc.identifier.startpage39en_US
dc.identifier.endpage44en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.contributor.institutionauthorÖztürk, Yusuf


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