Cargando…

Muscle nonshivering thermogenesis in a feral mammal

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Nowack, Julia, Vetter, Sebastian G., Stalder, Gabrielle, Painer, Johanna, Kral, Maria, Smith, Steve, Le, Minh Hien, Jurcevic, Perica, Bieber, Claudia, Arnold, Walter, Ruf, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6476883/
https://www.ncbi.nlm.nih.gov/pubmed/31011179
http://dx.doi.org/10.1038/s41598-019-42756-z
_version_ 1783412952302354432
author Nowack, Julia
Vetter, Sebastian G.
Stalder, Gabrielle
Painer, Johanna
Kral, Maria
Smith, Steve
Le, Minh Hien
Jurcevic, Perica
Bieber, Claudia
Arnold, Walter
Ruf, Thomas
author_facet Nowack, Julia
Vetter, Sebastian G.
Stalder, Gabrielle
Painer, Johanna
Kral, Maria
Smith, Steve
Le, Minh Hien
Jurcevic, Perica
Bieber, Claudia
Arnold, Walter
Ruf, Thomas
author_sort Nowack, Julia
collection PubMed
description 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.
format Online
Article
Text
id pubmed-6476883
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-64768832019-05-02 Muscle nonshivering thermogenesis in a feral mammal Nowack, Julia Vetter, Sebastian G. Stalder, Gabrielle Painer, Johanna Kral, Maria Smith, Steve Le, Minh Hien Jurcevic, Perica Bieber, Claudia Arnold, Walter Ruf, Thomas Sci Rep Article 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. Nature Publishing Group UK 2019-04-23 /pmc/articles/PMC6476883/ /pubmed/31011179 http://dx.doi.org/10.1038/s41598-019-42756-z Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Nowack, Julia
Vetter, Sebastian G.
Stalder, Gabrielle
Painer, Johanna
Kral, Maria
Smith, Steve
Le, Minh Hien
Jurcevic, Perica
Bieber, Claudia
Arnold, Walter
Ruf, Thomas
Muscle nonshivering thermogenesis in a feral mammal
title Muscle nonshivering thermogenesis in a feral mammal
title_full Muscle nonshivering thermogenesis in a feral mammal
title_fullStr Muscle nonshivering thermogenesis in a feral mammal
title_full_unstemmed Muscle nonshivering thermogenesis in a feral mammal
title_short Muscle nonshivering thermogenesis in a feral mammal
title_sort muscle nonshivering thermogenesis in a feral mammal
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6476883/
https://www.ncbi.nlm.nih.gov/pubmed/31011179
http://dx.doi.org/10.1038/s41598-019-42756-z
work_keys_str_mv AT nowackjulia musclenonshiveringthermogenesisinaferalmammal
AT vettersebastiang musclenonshiveringthermogenesisinaferalmammal
AT staldergabrielle musclenonshiveringthermogenesisinaferalmammal
AT painerjohanna musclenonshiveringthermogenesisinaferalmammal
AT kralmaria musclenonshiveringthermogenesisinaferalmammal
AT smithsteve musclenonshiveringthermogenesisinaferalmammal
AT leminhhien musclenonshiveringthermogenesisinaferalmammal
AT jurcevicperica musclenonshiveringthermogenesisinaferalmammal
AT bieberclaudia musclenonshiveringthermogenesisinaferalmammal
AT arnoldwalter musclenonshiveringthermogenesisinaferalmammal
AT rufthomas musclenonshiveringthermogenesisinaferalmammal