Enhanced central response to dehydration in mice lacking angiotensin AT1a receptors

Author:

Morris Mariana1,Means Shelia1,Oliverio Michael I.2,Coffman Thomas M.2

Affiliation:

1. Department of Pharmacology and Toxicology, Wright State University School of Medicine, Dayton, Ohio 45401;

2. Department of Medicine, Duke University, Winston-Salem; and Veterans Affairs Medical Center, Durham, North Carolina 27705

Abstract

The objective was to determine the central nervous system (CNS) responses to dehydration (c-Fos and vasopressin mRNA) in mice lacking the ANG AT1a receptor [ANG AT1a knockout (KO)]. Control and AT1a KO mice were dehydrated for 24 or 48 h. Baseline plasma vasopressin (VP) was not different between the groups; however, the response to dehydration was attenuated in AT1a KO (24 ± 11 vs. 10.6 ± 2.7 pg/ml). Dehydration produced similar increases in plasma osmolality and depletion of posterior pituitary VP content. Neuronal activation was observed as increases in c-Fos protein and VP mRNA. The supraoptic responses were not different between groups. In the paraventricular nucleus (PVN), c-Fos-positive neurons (57.4 ± 10.7 vs. 98.4 ± 7.4 c-Fos cells/PVN, control vs. AT1aKO) and VP mRNA levels (1.0 ± 0.1 vs. 1.4 ± 0.1 μCi, control vs. AT1a KO) were increased with greater responses in AT1a KO. A comparison of 1- to 2-day water deprivation showed that plasma VP, brain c-Fos, and VP mRNA returned toward control on day 2, although plasma osmolality remained high. Data demonstrate that AT1a KO mice show a dichotomous response to dehydration, reduced for plasma VP and enhanced for PVN c-Fos protein and VP mRNA. The results illustrate the importance of ANG AT1a receptors in the regulation of osmotic and endocrine balance.

Publisher

American Physiological Society

Subject

Physiology (medical),Physiology

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