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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

RAPID STIMULATION OF SODIUM INTAKE COMBINING ALDOSTERONE INTO THE 4TH VENTRICLE AND THE BLOCKADE OF THE LATERAL PARABRACHIAL NUCLEUS

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Author(s):
Gasparini, S. ; Melo, M. R. ; Leite, G. F. ; Nascimento, P. A. ; Andrade-Franze, G. M. F. ; Menani, J. V. ; Colombari, E.
Total Authors: 7
Document type: Journal article
Source: Neuroscience; v. 346, p. 94-101, MAR 27 2017.
Web of Science Citations: 1
Abstract

Chronic infusion of aldosterone into the 4th ventricle (4th V) induces robust daily sodium intake, whereas acute injection of aldosterone into the 4th V produces no sodium intake. The inhibitory mechanism of the lateral para-brachial nucleus (LPBN) restrains sodium intake induced by different natriorexigenic stimuli and might affect the acute response to aldosterone into the 4th V. In the present study, 1.8% NaCl and water intake was tested in rats treated with acute injections of aldosterone into the 4th V combined with the blockade of the inhibitory mechanisms with injections of moxonidine (alpha(2) adrenergic/imidazoline agonist) or methy-sergide (a serotonergic antagonist) into the LPBN. Male Holtzman rats with stainless steel cannulas implanted in the 4th V and bilaterally in the LPBN were used. Aldosterone (250 or 500 ng) into the 4th V combined with vehicle into the LPBN induced no 1.8% NaClintake compared to control (1.5 +/- 1.1 and 1.1 +/- 0.4, respectively, vs. vehicle into 4th V: 1.0 +/- 0.5 ml/2 h). However, aldosterone (250 or 500 ng) into the 4th V combined with moxonidine (0.5 nmol) into the LPBN induced strong ingestion of 1.8% NaCl (12.7 +/- 4.6 and 17.6 +/- 3.7 ml/2 h, respectively). Aldosterone (250 ng) into the 4th V combined with methysergide (4 mu g) into the LPBN also induced 1.8% NaCl intake (17.6 +/- 5.4 ml/2 h). These data suggest that the inhibitory mechanisms of the LPBN counteract the facilitation of sodium intake produced by aldosterone injected into the 4th, restraining sodium intake in this condition. (C) 2017 IBRO. Published by Elsevier Ltd. All rights reserved. (AU)

FAPESP's process: 13/00026-0 - Characterization of aldosterone action on hindbrain on the hydroeletrolytic control and cardiovascular regulation
Grantee:Silvia Gasparini
Support Opportunities: Scholarships in Brazil - Post-Doctoral
FAPESP's process: 15/23467-7 - Experimental pathophysiology: role of central mechanisms of the cardiovascular and respiratory control changes induced by experimental hypertension and obesity
Grantee:Eduardo Colombari
Support Opportunities: Research Projects - Thematic Grants
FAPESP's process: 11/50770-1 - Neural mechanisms involved of hydroelectrolytic balance and cardiorespiratory control
Grantee:José Vanderlei Menani
Support Opportunities: Research Projects - Thematic Grants