ArticleAmerican journal of physiology. Regulatory, integrative and comparative physiology2014
Properly timed exposure to central ANG II prevents behavioral sensitization and changes in angiotensin receptor expression.
Article in American journal of physiology. Regulatory, integrative and comparative physiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed, 7 citations in OpenAlex.
- A microstructural analysis of sodium and water intake in male and female rats.Physiology & behavior · 2026Article
- Fluid transitions.Neuropharmacology · 2024Review
- The anti-dipsogenic and anti-natriorexigenic effects of estradiol, but not the anti-pressor effect, are lost in aged female rats.Physiological reports · 2021Article
- Associative learning contributes to the increased water intake observed after daily injections of angiotensin II.Physiology & behavior · 2017Article
- Angiotensin II (de)sensitization: Fluid intake studies with implications for cardiovascular control.Physiology & behavior · 2016Review
- Divergent effects of ERα and ERβ on fluid intake by female rats are not dependent on concomitant changes in AT1R expression or body weight.American journal of physiology. Regulatory, integrative and comparative physiology · 2016Article
- Activation of G protein-coupled estrogen receptor 1 (GPER-1) decreases fluid intake in female rats.Hormones and behavior · 2015Article
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Authors and funding
5 authors at 2 institutions in 1 country.
Funding
Abstract
Previous studies show that the angiotensin type 1 receptor (AT1R) is susceptible to rapid desensitization, but that more chronic treatments that stimulate ANG II lead to sensitization of several responses. It is unclear, however, if the processes of desensitization and sensitization interact. To test for differences in AT1R expression associated with single or repeated injections of ANG II, we measured AT1R mRNA in nuclei that control fluid intake of rats given ANG II either in a single injection or divided into three injections spaced 20 min apart. Rats given a single injection of ANG II had more AT1R mRNA in the subfornical organ (SFO) and the periventricular tissue surrounding the anteroventral third ventricle (AV3V) than did controls. The effect was not observed, however, when the same cumulative dose of ANG II was divided into multiple injections. Behavioral tests found that single daily injections of ANG II sensitized the dipsogenic response to ANG II, but a daily regimen of four injections did not cause sensitization. Analysis of (125)I-Sar(1)-ANG II binding revealed a paradoxical decrease in binding in the caudal AV3V and dorsal median preoptic nucleus after 5 days of single daily injections of ANG II; however, this effect was absent in rats treated for 5 days with four daily ANG II injections. Taken together, these data suggest that a desensitizing treatment regimen prevents behavior- and receptor-level effects of repeated daily ANG II.
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