Chemogenetic Excitation of Ventromedial Hypothalamic Steroidogenic Factor 1 (SF1) Neurons Increases Muscle Thermogenesis in Mice

Author:

Watts Christina A.1ORCID,Smith Jordan2ORCID,Giacomino Roman3ORCID,Walter Dinah3,Jang Guensu3,Malik Aalia3,Harvey Nicholas3,Novak Colleen M.134ORCID

Affiliation:

1. School of Biomedical Sciences, Kent State University, Kent, OH 44242, USA

2. College of Public Health, Kent State University, Kent, OH 44242, USA

3. Department of Biological Sciences, Kent State University, Kent, OH 44242, USA

4. Brain Health Research Institute, Kent State University, Kent, OH 44242, USA

Abstract

Allostatic adaptations to a perceived threat are crucial for survival and may tap into mechanisms serving the homeostatic control of energy balance. We previously established that exposure to predator odor (PO) in rats significantly increases skeletal muscle thermogenesis and energy expenditure (EE). Evidence highlights steroidogenic factor 1 (SF1) cells within the central and dorsomedial ventromedial hypothalamus (c/dmVMH) as a modulator of both energy homeostasis and defensive behavior. However, the brain mechanism driving elevated EE and muscle thermogenesis during PO exposure has yet to be elucidated. To assess the ability of SF1 neurons of the c/dmVMH to induce muscle thermogenesis, we used the combined technology of chemogenetics, transgenic mice, temperature transponders, and indirect calorimetry. Here, we evaluate EE and muscle thermogenesis in SF1-Cre mice exposed to PO (ferret odor) compared to transgenic and viral controls. We detected significant increases in muscle temperature, EE, and oxygen consumption following the chemogenetic stimulation of SF1 cells. However, there were no detectable changes in muscle temperature in response to PO in either the presence or absence of chemogenetic stimulation. While the specific role of the VMH SF1 cells in PO-induced thermogenesis remains uncertain, these data establish a supporting role for SF1 neurons in the induction of muscle thermogenesis and EE similar to what is seen after predator threats.

Funder

National Institute of Health

Kent State University Department of Biological Sciences Research Committee Open Access Publishing Fund

Publisher

MDPI AG

Reference62 articles.

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