Muscle nonshivering thermogenesis in a feral mammal

Sci Rep. 2019 Apr 23;9(1):6378. doi: 10.1038/s41598-019-42756-z.

Abstract

Muscle nonshivering thermogenesis (NST) was recently suggested to play an important role in thermoregulation of species lacking brown adipose tissue (BAT). The mechanism, which is independent of muscle contractions, produces heat based on the activity of an ATPase pump in the sarcoplasmic reticulum (SERCA1a) and is controlled by the protein sarcolipin. To evaluate whether muscle NST could indeed play an important role in thermoregulation in species lacking BAT, we investigated the thermogenic capacities of newborn wild boar piglets. During cold exposure over the first 5 days of life, total heat production was improved while shivering intensity decreased, indicating an increasing contribution of NST. Sampling skeletal muscle tissue for analyses of SERCA activity as well as gene expression of SERCA1a and sarcolipin, we found an age-related increase in all three variables as well as in body temperature. Hence, the improved thermogenesis during the development of wild boars is not due to shivering but explained by the observed increase in SERCA activity. Our results suggest that muscle NST may be the primary mechanism of heat production during cold stress in large mammals lacking BAT, strengthening the hypothesis that muscle NST has likely played an important role in the evolution of endothermy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Wild / genetics
  • Animals, Wild / physiology*
  • Body Temperature / genetics
  • Body Temperature / physiology
  • Cold Temperature
  • Gene Expression Regulation
  • Muscle Proteins / genetics
  • Muscle Proteins / metabolism
  • Muscle, Skeletal / physiology*
  • Proteolipids / genetics
  • Proteolipids / metabolism
  • Regression Analysis
  • Sarcoplasmic Reticulum Calcium-Transporting ATPases / genetics
  • Sarcoplasmic Reticulum Calcium-Transporting ATPases / metabolism
  • Sus scrofa / genetics
  • Sus scrofa / physiology*
  • Thermogenesis / genetics
  • Thermogenesis / physiology*

Substances

  • Muscle Proteins
  • Proteolipids
  • sarcolipin
  • Sarcoplasmic Reticulum Calcium-Transporting ATPases

Associated data

  • figshare/10.6084/m9.figshare.6839591