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Characterization of angiotensin II antagonism displayed by SK-1080, a novel nonpeptide AT1-receptor antagonist.

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dc.contributor.authorLee, SH-
dc.contributor.authorJung, YS-
dc.contributor.authorLee, BH-
dc.contributor.authorYun, SI-
dc.contributor.authorYoo, SE-
dc.contributor.authorShin, HS-
dc.date.accessioned2011-09-02-
dc.date.available2011-09-02-
dc.date.issued1999-
dc.identifier.issn0160-2446-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/3994-
dc.description.abstractThe pharmacologic profile of SK-1080, a nonpeptide AT1-selective angiotensin-receptor antagonist, was investigated by receptor-binding studies, functional in vitro assays with rabbit and rat aorta, and in vivo experiments in pithed rats. SK-1080 inhibited the specific binding of [125I]-[Sar1, Ile8]-angiotensin II to human recombinant AT1 receptor with a 12-fold greater potency than losartan [median inhibitory concentration (IC50): 1.01 and 12.3 nM, respectively], but it did not inhibit the binding of [125I]-CGP 42112A to human recombinant AT2 receptor (IC50: >10 microM for both). The Hill coefficient for the competition curve of SK-1080 against AT1 receptor was not significantly different from unity (0.96). Scatchard analysis showed that SK-1080 interacted with human recombinant AT1 receptor in a competitive manner, as with losartan. In functional studies with rat and rabbit aorta, SK-1080 competitively inhibited the contractile response to angiotensin II (pKB values: 9.97 and 9.51, respectively) with 15-25% decrease in the maximal contractile responses, unlike losartan, which showed competitive antagonism without any change in the maximal contractile responses to angiotensin II (pA2 values, 8.02 and 7.59, respectively). In pithed rats, SK-1080 (i.v.) induced a nonparallel right shift in the dose-pressor response curve to angiotensin II (ID50, 0.07 mg/kg) with a dose-dependent reduction in the maximal responses; this antagonistic effect was approximately 25 times more potent than losartan (ID50, 1.74 mg/kg), which showed competitive antagonism. SK-1080 did not alter the responses induced by other agonists such as norepinephrine, KCI, and vasopressin in isolated rabbit aorta and pithed rats. These results suggest that SK-1080 is a highly potent AT1-selective angiotensin II-receptor antagonist with a mode of insurmountable antagonism.-
dc.language.isoen-
dc.subject.MESHAngiotensin II-
dc.subject.MESHAngiotensin Receptor Antagonists-
dc.subject.MESHAnimals-
dc.subject.MESHAntihypertensive Agents-
dc.subject.MESHAorta, Thoracic-
dc.subject.MESHBinding, Competitive-
dc.subject.MESHBlood Pressure-
dc.subject.MESHDecerebrate State-
dc.subject.MESHDiastole-
dc.subject.MESHDose-Response Relationship, Drug-
dc.subject.MESHHeart Rate-
dc.subject.MESHImidazoles-
dc.subject.MESHLosartan-
dc.subject.MESHMale-
dc.subject.MESHMuscle Contraction-
dc.subject.MESHPyridines-
dc.subject.MESHRabbits-
dc.subject.MESHRadioligand Assay-
dc.subject.MESHRats-
dc.subject.MESHRats, Sprague-Dawley-
dc.subject.MESHReceptor, Angiotensin, Type 1-
dc.subject.MESHReceptor, Angiotensin, Type 2-
dc.subject.MESHReceptors, Angiotensin-
dc.subject.MESHSensitivity and Specificity-
dc.subject.MESHTetrazoles-
dc.titleCharacterization of angiotensin II antagonism displayed by SK-1080, a novel nonpeptide AT1-receptor antagonist.-
dc.typeArticle-
dc.identifier.pmid10069670-
dc.identifier.urlhttp://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?issn=0160-2446&volume=33&issue=3&spage=367-
dc.contributor.affiliatedAuthor이, 수환-
dc.contributor.affiliatedAuthor정, 이숙-
dc.type.localJournal Papers-
dc.citation.titleJournal of cardiovascular pharmacology-
dc.citation.volume33-
dc.citation.number3-
dc.citation.date1999-
dc.citation.startPage367-
dc.citation.endPage374-
dc.identifier.bibliographicCitationJournal of cardiovascular pharmacology, 33(3). : 367-374, 1999-
dc.identifier.eissn1533-4023-
dc.relation.journalidJ001602446-
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Journal Papers > School of Medicine / Graduate School of Medicine > Physiology
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