dc.creatorMorales, M. A.
dc.creatorSilva, A.
dc.creatorBrito, G.
dc.creatorBustamante, S.
dc.creatorPonce, H.
dc.creatorPaeile, C.
dc.date.accessioned2018-12-20T14:34:27Z
dc.date.available2018-12-20T14:34:27Z
dc.date.created2018-12-20T14:34:27Z
dc.date.issued1995
dc.identifierGeneral Pharmacology, Volumen 26, Issue 2, 2018, Pages 425-430
dc.identifier03063623
dc.identifier10.1016/0306-3623(94)00166-K
dc.identifierhttp://repositorio.uchile.cl/handle/2250/156549
dc.description.abstract1. 1. A novel vasorelaxant effect of clonixinate of l-lysine (Clx), analgesic and anti-inflammatory, was studied in rat aortic rings. 2. 2. Clx completely relaxed aortic rings contracted by KCl 70 mM and together with its analog flunixin exhibited lesser potency but equal efficacy than verapamil. In comparison, indomethacin, which is a more potent cyclo-oxygenase inhibitor relaxed only about 40% of the maximal contraction of aortic rings. 3. 3. Furthermore, Clx antagonized Ca2+ dependent aortic contraction and BAY K-8644 induced aortic contraction suggesting its calcium antagonist character. 4. 4. From these results it can be concluded that the hypotensive effect seen in rats in vivo after Clx i.v. injection arises because of vasodilatory effect of Clx and gives further support to the proposal that the pharmacological mechanism of action of Clx should be calcium antagonism. © 1995.
dc.languageen
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
dc.sourceGeneral Pharmacology
dc.subjectBAY K-8644
dc.subjectcalcium antagonists
dc.subjectClonixin
dc.subjectflunixin
dc.subjectrat aorta
dc.titleVasorelaxant effect of the analgesic clonixin on rat aorta
dc.typeArtículos de revistas


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