Divergent effects of ERα and ERβ on fluid intake by female rats are not dependent on concomitant changes in AT1R expression or body weight

Jessica Santollo, Anikó Marshall, Kathleen S. Curtis, Robert C. Speth, Stewart D. Clark, Derek Daniels

Research output: Contribution to journalArticlepeer-review

13 Scopus citations


Estradiol (E2) decreases both water and saline intakes by female rats. The ERα and ERβ subtypes are expressed in areas of the brain that control fluid intake; however, the role that these receptors play in E2’s antidipsogenic and antinatriorexigenic effects have not been examined. Accordingly, we tested the hypothesis that activation of ERα and ERβ decreases water and saline intakes by female rats. We found a divergence in E2’s inhibitory effect on intake: activation of ERα decreased water intake, whereas activation of ERβ decreased saline intake. E2 decreases expression of the angiotensin II type 1 receptor (AT1R), a receptor with known relevance to water and salt intakes, in multiple areas of the brain where ERα and ERβ are differentially expressed. Therefore, we tested for agonist-induced changes in AT1R mRNA expression by RT-PCR and protein expression by analyzing receptor binding to test the hypothesis that the divergent effects of these ER subtypes are mediated by region-specific changes in AT1R expression. Although we found no changes in AT1R mRNA or binding in areas of the brain known to control fluid intake associated with agonist treatment, the experimental results replicate and extend previous findings that body weight changes mediate alterations in AT1R expression in distinct brain regions. Together, the results reveal selective effects of ER subtypes on ingestive behaviors, advancing our understanding of E2’s inhibitory role in the controls of fluid intake by female rats.

Original languageEnglish
Pages (from-to)R14-R23
JournalAmerican Journal of Physiology - Regulatory Integrative and Comparative Physiology
Issue number1
StatePublished - Jul 2016

Bibliographical note

Funding Information:
This work was supported by National Institutes of Health Grants HL- 091911 to D. Daniels, DK-098841 to J. Santollo, HL-113905 and Pilot Award from the Translational Technologies Component of the Georgetown, Howard Universities Center for Clinical and Translational Science UL1TR000101 to R. C. Speth, and DA-024754 to S. D. Clark and a grant from OCAST (HR12-196) to K. S. Curtis.

Publisher Copyright:
© 2016 the American Physiological Society.


  • Angiotensin II type 1 receptor
  • Brain
  • Drinking microstructure
  • Estrogen
  • Estrogen receptors
  • Fluid balance
  • Water intake

ASJC Scopus subject areas

  • Medicine (all)


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