Neural Mechanisms Underlying Central Induction of Skeletal Muscle Thermogenesis

NIH RePORTER · NIH · R15 · $447,126 · view on reporter.nih.gov ↗

Abstract

Neural Mechanisms Underlying Central Induction of Skeletal Muscle Thermogenesis Though individual health and the US health-care system as a whole suffer from the deleterious consequences of obesity, weight loss and maintenance have proven difficult for the majority of people. Developing methods to increase energy expenditure would ease this process. We have found that exposing rats to the odor of their natural predator (ferret) provokes a rapid and robust rise in skeletal muscle (gastrocnemius) temperature, with a corresponding increase in energy expenditure. Here, we probe the most likely brain and muscle mediators of this response. First, we will use a chemogenetic tool we developed to target neurons expressing steroidogenic factor 1 (SF-1) in the dorsomedial/central subregions of the ventromedial hypothalamus (dmVMH), specifically predicting that inhibition of this cell population will decrease the ability of predator odor to induce muscle thermogenesis in rats. Second, we will investigate the most probable mechanism underlying the thermogenic induction at the level of the skeletal myocyte, namely sarcolipin uncoupling of sarco/endoplasmic reticulum ATPase (SERCA) Ca2+ cycling. We will determine if predator odor exposure suppresses SERCA Ca2+ transport relative to ATPase activity, while increasing sarcolipin expression. We also predict that, since unilateral sympathetic neural (lumbar sympathetic nerve) surgical denervation inhibits the ability of predator odor to induce thermogenesis in the denervated gastrocnemius muscle relative to the contralateral (intact) muscle, SERCA uncoupling and sarcolipin expression will similarly be altered in the denervated muscle compared to the intact muscle in the same rat. These studies will demonstrate the roles of brain SF-1 neurons and muscle SERCA uncoupling in central induction of skeletal muscle non-shivering thermogenesis. Altogether, we will establish multiple components of this brain-muscle thermogenic pathway as viable targets to counter weight gain, while engaging undergraduate students in research.

Key facts

NIH application ID
9880531
Project number
1R15DK121246-01A1
Recipient
KENT STATE UNIVERSITY
Principal Investigator
Colleen M Novak
Activity code
R15
Funding institute
NIH
Fiscal year
2020
Award amount
$447,126
Award type
1
Project period
2020-03-01 → 2024-05-31