Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/134001
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dc.titleThe roles of α2-adrenoceptors in the nucleus reticularis gigantocellularis and vagal mechanism in the cardiovascular suppressive effects of guanabenz in the rat
dc.contributor.authorLim, H.C.
dc.contributor.authorChan, S.H.H.
dc.date.accessioned2016-12-20T08:42:24Z
dc.date.available2016-12-20T08:42:24Z
dc.date.issued1986-01-02
dc.identifier.citationLim, H.C., Chan, S.H.H. (1986-01-02). The roles of α2-adrenoceptors in the nucleus reticularis gigantocellularis and vagal mechanism in the cardiovascular suppressive effects of guanabenz in the rat. Neuroscience Letters 63 (1) : 45-50. ScholarBank@NUS Repository.
dc.identifier.issn03043940
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/134001
dc.description.abstractIn pentobarbital-anesthetized rats, pretreatment with yohimbine (10 μg), which was microinjected into the bilateral nucleus reticularis gigantocellularis (NRGC), significantly antagonized the reduction in arterial pressure, and the force and rate of heart contraction normally promoted by systemic administration of guanabenz (10 μg/kg, i.v.). At the same time, the vasodepressive as well as negative inotropic and chronotropic effects of direct application of guanabenz (500 ng) into the NRGC were attenuated by bilateral cervical vagotomy or atropine sulfate (1 mg/kg, i.v.). We conclude that guanabenz may promote antihypertension by activating the α2-adrenoceptors in the NRGC, which in turn elicits cardiovascular suppression by at least facilitating the vagal outflows to the heart. © 1986.
dc.subjectα2-adrenoceptor
dc.subjectbradycardia
dc.subjectguanabenz
dc.subjectheart contractility reduction
dc.subjectnucleus reticularis gigantocellularis
dc.subjectrat
dc.subjectvagal mechanism hypotension
dc.typeArticle
dc.contributor.departmentPHYSIOLOGY
dc.description.sourcetitleNeuroscience Letters
dc.description.volume63
dc.description.issue1
dc.description.page45-50
dc.description.codenNELED
dc.identifier.isiutNOT_IN_WOS
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