Angiotensin II in the paraventricular nucleus stimulates sympathetic outflow to the cardiovascular system and make vasopressin release in rat. (6th October 2016)

• Record Type: Journal Article
• Authors: Khanmoradi, Mehrangiz; Nasimi, Ali
• Is Part Of: Neuroscience letters. Volume 632(2016)
• Page Start: 98
• Page End: 103
• Publication Date: 2016-10-06
• Subjects: Paraventricular nucleus -- PVN -- Arterial pressure -- Angiotensin II -- Vasopressin -- Hexamethonium; Neurology -- Periodicals; Neurology -- Periodicals; Research -- Periodicals; Neurologie -- Périodiques; Neuroanatomie -- Périodiques; Neuropharmacologie -- Périodiques; Neurophysiologie -- Périodiques; Neurology; Periodicals; Electronic journals; 617.48
• DOI: 10.1016/j.neulet.2016.08.040
• Languages: English
• ISSNs: 0304-3940

Abstract

Highlights: Ang II microinjected into the PVN increases arterial pressure by sympathoexcitation. Ang II microinjected into the PVN increases arterial pressure by increasing vasopressin release. Correlated neurons' firings were explored. Abstract: The hypothalamic paraventricular nucleus (PVN) plays essential roles in neuroendocrine and autonomic functions, including cardiovascular regulation. It was shown that microinjection of angiotensin II (AngII) into the PVN produced a pressor response. In this study, we explored the probable mechanisms of this pressor response. AngII was microinjected into the PVN and cardiovascular responses were recorded. Then, the responses were re-tested after systemic injection of a ganglionic blocker, Hexamethonium, or a vasopressin V1 receptor blocker. Hexamethonium pretreatment (i.v.) greatly and significantly attenuated the pressor response to AngII, with no significant effect on heart rate, indicating that the sympathetic system is involved in the cardiovascular effect of AngII in the PVN. Systemic pretreatment (i.v.) with V1 antagonist greatly and significantly attenuated the pressor response to AngII, with no significant effect on heart rate, indicating that vasopressin release is involved in the cardiovascular effect of AngII in the PVN. Overall, we found that AngII microinjected into the PVN produced a pressor response mediated by the sympathetic system and vasopressin release, indicating that other than circulating AngII, endogenous AngII of the PVN increases the vasopressin release from the PVN.