Abstract
Previous in vivo and in vitro studies demonstrate that the angiotensin type 1 receptor rapidly desensitizes after exposure to angiotensin II (AngII). Behaviorally, this likely underlies the reduced drinking observed after acute repeated central injections of AngII. To date, this phenomenon has been studied exclusively in male subjects. Because there are sex differences in the dipsogenic potency of AngII, we hypothesized that sex differences also exist in desensitization caused by AngII. As expected, when male rats were pretreated with AngII, they drank less water after a test injection of AngII than did rats pretreated with vehicle. Intact cycling female rats, however, drank similar amounts of water after AngII regardless of the pretreatment. To probe the mechanism underlying this sex difference, we tested the role of gonadal hormones in adult and developing rats. Gonadectomy in adults did not produce a male-like propensity for desensitization of water intake in female rats, nor did it produce a female-like response in male rats. To test if neonatal brain masculinization generated a male-like responsiveness, female pups were treated at birth with vehicle, testosterone propionate (TP), or dihydrotestosterone (DHT). When tested as adults, TPtreated female rats showed a male-like desensitization after repeated AngII that was not found in vehicle- or DHT-treated rats. Together, these data reveal a striking sex difference in the behavioral response to elevated AngII that is mediated by organizational effects of gonadal hormones and provide an example of one of the many ways that sex influences the renin-angiotensinaldosterone system.
| Original language | English |
|---|---|
| Pages (from-to) | 676-684 |
| Number of pages | 9 |
| Journal | Endocrinology |
| Volume | 159 |
| Issue number | 2 |
| DOIs | |
| State | Published - Feb 2018 |
Bibliographical note
Publisher Copyright:© 2018 Endocrine Society.
Funding
Financial Support: This work was supported by National Institutes of Health Grants HL091911 and DK107500 (to D.D.) and DK098841 (to J.S.).
| Funders | Funder number |
|---|---|
| National Institutes of Health (NIH) | HL091911, DK107500 |
| National Institute of Diabetes and Digestive and Kidney Diseases | F32DK098841 |
ASJC Scopus subject areas
- Endocrinology