Chronic intracerebroventricular infusion of angiotensin II causes dose- and sex-dependent effects on intake behaviors and energy homeostasis in C57BL/6J mice

Author:

Oliveira Vanessa1,Reho John J.12,Balapattabi Kirthikaa1ORCID,Ritter McKenzie L.1,Mathieu Natalia M.1,Opichka Megan A.1ORCID,Lu Ko-Ting1,Grobe Connie C.3,Silva Sebastião D.1,Wackman Kelsey K.1,Nakagawa Pablo14,Segar Jeffrey L.134,Sigmund Curt D.145ORCID,Grobe Justin L.12456ORCID

Affiliation:

1. Department of Physiology, Medical College of Wisconsin, Milwaukee, Wisconsin

2. Comprehensive Rodent Metabolic Phenotyping Core, Medical College of Wisconsin, Milwaukee, Wisconsin

3. Department of Pediatrics, Medical College of Wisconsin, Milwaukee, Wisconsin

4. Cardiovascular Research Center, Medical College of Wisconsin, Milwaukee, Wisconsin

5. Neuroscience Research Center, Medical College of Wisconsin, Milwaukee, Wisconsin

6. Department of Biomedical Engineering, Medical College of Wisconsin, Milwaukee, Wisconsin

Abstract

The renin-angiotensin system (RAS) within the brain is implicated in the control of fluid and electrolyte balance, autonomic functions, blood pressure, and energy expenditure. Mouse models are increasingly used to explore these mechanisms; however, sex and dose dependencies of effects elicited by chronic intracerebroventricular (ICV) angiotensin II (ANG II) infusion have not been carefully established in this species. To examine the interactions among sex, body mass, and ICV ANG II on ingestive behaviors and energy balance, young adult C57BL/6J mice of both sexes were studied in a multiplexed metabolic phenotyping system (Promethion) during chronic infusion of ANG II (0, 5, 20, or 50 ng/h). At these infusion rates, ANG II caused accelerating dose-dependent increases in drinking and total energy expenditure in male mice, but female mice exhibited a complex biphasic response with maximum responses at 5 ng/h. Body mass differences did not account for sex-dependent differences in drinking behavior or total energy expenditure. In contrast, resting metabolic rate was similarly increased by ICV ANG II in a dose-dependent manner in both sexes after correction for body mass. We conclude that chronic ICV ANG II stimulates water intake, resting, and total energy expenditure in male C57BL/6J mice following straightforward accelerating dose-dependent kinetics, but female C57BL/6J mice exhibit complex biphasic responses to ICV ANG II. Furthermore, control of resting metabolic rate by ANG II is dissociable from mechanisms controlling fluid intake and total energy expenditure. Future studies of the sex dependency of ANG II within the brain of mice must be designed to carefully consider the biphasic responses that occur in females.

Funder

Children's Hospital of Wisconsin Research Institute

HHS | NIH | National Center for Advancing Translational Sciences

HHS | NIH | National Heart, Lung, and Blood Institute

American Heart Association

American Physiological Society

HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases

Publisher

American Physiological Society

Subject

Physiology (medical),Physiology

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