The Role of Mediobasal Hypothalamic PACAP in the Control of Body Weight and Metabolism

Author:

Bozadjieva-Kramer Nadejda1,Ross Rachel A234,Johnson David Q5,Fenselau Henning3678,Haggerty David L9,Atwood Brady9,Lowell Bradford34,Flak Jonathan N5910ORCID

Affiliation:

1. Department of Surgery, University of Michigan, Ann Arbor, MI, USA

2. Albert Einstein College of Medicine, Bronx, NY, USA

3. Beth Israel Deaconess Medical Center, Boston, MA, USA

4. Harvard Medical School, Boston, MA, USA

5. Indiana Biosciences Research Institute, Diabetes Research Center, Indianapolis, IN, USA

6. Synaptic Transmission in Energy Homeostasis Group, Max Planck Institute for Metabolism Research, Cologne, Germany

7. Center for Endocrinology, Diabetes and Preventive Medicine (CEDP), University Hospital Cologne, Cologne, Germany

8. Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases (CECAD) and Center of Molecular Medicine Cologne (CMMC), University of Cologne, Cologne, Germany

9. Indiana University School of Medicine, Pharmacology and Toxicology, Indianapolis, IN, USA

10. Department of Internal Medicine, Division of Metabolism, Endocrinology, and Diabetes, University of Michigan, Ann Arbor, MI, USA

Abstract

Abstract Body energy homeostasis results from balancing energy intake and energy expenditure. Central nervous system administration of pituitary adenylate cyclase activating polypeptide (PACAP) dramatically alters metabolic function, but the physiologic mechanism of this neuropeptide remains poorly defined. PACAP is expressed in the mediobasal hypothalamus (MBH), a brain area essential for energy balance. Ventromedial hypothalamic nucleus (VMN) neurons contain, by far, the largest and most dense population of PACAP in the medial hypothalamus. This region is involved in coordinating the sympathetic nervous system in response to metabolic cues in order to re-establish energy homeostasis. Additionally, the metabolic cue of leptin signaling in the VMN regulates PACAP expression. We hypothesized that PACAP may play a role in the various effector systems of energy homeostasis, and tested its role by using VMN-directed, but MBH encompassing, adeno-associated virus (AAVCre) injections to ablate Adcyap1 (gene coding for PACAP) in mice (Adcyap1MBHKO mice). Adcyap1MBHKO mice rapidly gained body weight and adiposity, becoming hyperinsulinemic and hyperglycemic. Adcyap1MBHKO mice exhibited decreased oxygen consumption (VO2), without changes in activity. These effects appear to be due at least in part to brown adipose tissue (BAT) dysfunction, and we show that PACAP-expressing cells in the MBH can stimulate BAT thermogenesis. While we observed disruption of glucose clearance during hyperinsulinemic/euglycemic clamp studies in obese Adcyap1MBHKO mice, these parameters were normal prior to the onset of obesity. Thus, MBH PACAP plays important roles in the regulation of metabolic rate and energy balance through multiple effector systems on multiple time scales, which highlight the diverse set of functions for PACAP in overall energy homeostasis.

Funder

National Institutes of Health

American Diabetes Association

Publisher

The Endocrine Society

Subject

Endocrinology

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