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Central angiotensin-(1-7) increases osmotic thirst.
- Source :
-
Experimental physiology [Exp Physiol] 2017 Nov 01; Vol. 102 (11), pp. 1397-1404. Date of Electronic Publication: 2017 Oct 04. - Publication Year :
- 2017
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Abstract
- New Findings: What is the central question of this study? The central goal of this study was to understand the effects of central angiotensin-(1-7) on basal and osmotically stimulated water intake in rats. What is the main finding and its importance? This study demonstrated that central administration of angiotensin-(1-7) did not induce thirst in basal conditions but increased water intake after osmotic stimulation, such as water deprivation and salt loading. These results indicate a new function for this peptide, which, in turn, allows for future research on the mechanisms through which angiotensin-(1-7) influences osmotic thirst. Angiotensin-(1-7) [Ang-(1-7)] is generated by type 2 angiotensin-converting enzyme (ACE2) and binds to the MAS receptor. Although it is well known that Ang-(1-7) functionally antagonizes the effects of the classical renin-angiotensin system in several situations, the role of Ang-(1-7) in hydromineral homeostasis is not clear. The aim of this study was to assess the role of Ang-(1-7) on neuroendocrine responses to hyperosmolality in rats. Male Wistar rats were divided into the following three groups: control; 24 h of water deprivation (WD); and 24 h of salt loading (SL; 1.8% NaCl). Intracerebroventricular (i.c.v.) injections of Ang-(1-7) or vehicle were given to assess water intake and plasma concentration of vasopressin. Additionally, the brains from control and WD groups were collected to evaluate gene expression in the subfornical organ (SFO), paraventricular nucleus (PVN) and supraoptic nucleus (SON). It was found that i.c.v. Ang-(1-7) did not change water and salt intake in control rats; however, Ang-(1-7) increased water intake after WD and SL, with no change in salt intake. Plasma vasopressin was not changed by i.c.v. Ang-(1-7) in control or WD rats. Moreover, WD increased Mas gene expression in the SON and PVN, with no changes in Ace2 mRNA levels. In conclusion, Ang-(1-7) increases thirst after osmotic stimuli, indicating that a previous sensitization to its action is necessary. This finding is consistent with the increased Mas gene expression in the PVN and SON after water deprivation.<br /> (© 2017 The Authors. Experimental Physiology © 2017 The Physiological Society.)
- Subjects :
- Angiotensin-Converting Enzyme 2
Animals
Injections, Intraventricular
Male
Paraventricular Hypothalamic Nucleus metabolism
Peptidyl-Dipeptidase A genetics
Peptidyl-Dipeptidase A metabolism
Proto-Oncogene Mas
Proto-Oncogene Proteins genetics
Proto-Oncogene Proteins metabolism
Rats, Wistar
Receptors, G-Protein-Coupled genetics
Receptors, G-Protein-Coupled metabolism
Sodium Chloride administration & dosage
Subfornical Organ metabolism
Supraoptic Nucleus metabolism
Up-Regulation
Vasopressins blood
Water Deprivation
Angiotensin I administration & dosage
Drinking drug effects
Osmotic Pressure
Paraventricular Hypothalamic Nucleus drug effects
Peptide Fragments administration & dosage
Subfornical Organ drug effects
Supraoptic Nucleus drug effects
Thirst drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1469-445X
- Volume :
- 102
- Issue :
- 11
- Database :
- MEDLINE
- Journal :
- Experimental physiology
- Publication Type :
- Academic Journal
- Accession number :
- 28833692
- Full Text :
- https://doi.org/10.1113/EP086417