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dc.contributor.authorBagchi, Sovan-
dc.contributor.authorDeshpande, Shripad B-
dc.date.accessioned2013-11-22T08:43:34Z-
dc.date.available2013-11-22T08:43:34Z-
dc.date.issued2000-09-
dc.identifier.issn0975-1009 (Online); 0019-5189 (Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/24055-
dc.description881-886en_US
dc.description.abstractThe present study was undertaken to determine the afferent and efferent pathways involved in the phenyldiguanide (PDG)-induced reflex response in rats. Intravenous (iv) injection of PDG (10 μg/kg), produced hypotension, bradycardia and apnea over a period of time. Bilateral vagotomy abolished the PDG-induced reflex changes. Atropine (2 mg/kg;iv) blocked only the bradycardiac response produced by PDG, while prazosin (0.5 mg/kg; iv) blocked the hypotensive response, and bilateral vagotomy in these animals abolished the apneic response. In separate series of experiments, intrapericardial injection of lignocaine abolished the hypotensive and bradycardiac responses evoked by PDG in artificially ventilated rats. The results reveal that the PDG-induced reflex is mediated through vagal afferents originating from the heart and efferents involve three different pathways. The bradycardiac response was through the muscarinic receptors, the hypotension is mediated through α1 adrenoceptors and the apnea presumably through the spinal motoneurones supplying the respiratory muscles.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJEB Vol.38(09) [September 2000]en_US
dc.titlePhenyldiguanide activates cardiac receptors to produce responses by involving three different efferent pathways in anaesthetized ratsen_US
dc.typeArticleen_US
Appears in Collections:IJEB Vol.38(09) [September 2000]

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