Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/11224
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dc.contributor.authorPhillips, P Aen
dc.contributor.authorWiddop, Robert Een
dc.contributor.authorChai, Syn Yen
dc.contributor.authorKelly, Jen
dc.contributor.authorMooser, Ven
dc.contributor.authorTrinder, Den
dc.contributor.authorJohnston, Colin Ien
dc.date.accessioned2015-05-16T00:48:46Z
dc.date.available2015-05-16T00:48:46Z
dc.date.issued1990-04-01en
dc.identifier.citationClinical and Experimental Pharmacology & Physiology; 17(4): 321-5en
dc.identifier.govdoc2140739en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/11224en
dc.description.abstract1. Anaesthetized male Sprague-Dawley rats underwent unilateral nodose ganglionectomy or sham operation. 2. One week later hindbrain V1 vasopressin binding site density was assessed by in vitro autoradiography with the selective V1 antagonist radioligand [125I] [d(CH2)5, Sar7]AVP. 3. Specific binding was observed in the nodose ganglion, nucleus tractus solitarius (NTS), area postrema, and inferior olive. Only binding in the medial subnucleus of the NTS was reduced by ipsilateral nodose ganglionectomy. 4. These findings are consistent with V1 vasopressin receptors occurring presynaptically on vagal primary viscerosensory afferent fibres. 5. Such receptors may be involved in the effect of AVP on blood pressure and/or the baroreflex.en
dc.language.isoenen
dc.subject.otherAnimalsen
dc.subject.otherGanglionectomyen
dc.subject.otherMaleen
dc.subject.otherMedulla Oblongata.metabolismen
dc.subject.otherNodose Ganglion.physiologyen
dc.subject.otherRatsen
dc.subject.otherRats, Inbred Strainsen
dc.subject.otherReceptors, Angiotensin.metabolismen
dc.subject.otherReceptors, Vasopressinen
dc.subject.otherRhombencephalon.metabolismen
dc.subject.otherVagus Nerve.physiologyen
dc.subject.otherVasopressins.metabolismen
dc.titleReduced V1 vasopressin binding in the rat nucleus solitarii after nodose ganglionectomy.en
dc.typeJournal Articleen
dc.identifier.journaltitleClinical and Experimental Pharmacology & Physiologyen
dc.identifier.affiliationDepartment of Medicine, University of Melbourne, Austin Hospital, Heidelberg, Victoria, Australiaen
dc.description.pages321-5en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/2140739en
dc.type.austinJournal Articleen
item.grantfulltextnone-
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
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