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Pronounced expression of the lipolytic inhibitor G0/G1 Switch Gene 2 (G0S2) in adipose tissue from brown bears (Ursus arctos) prior to hibernation

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Standard

Pronounced expression of the lipolytic inhibitor G0/G1 Switch Gene 2 (G0S2) in adipose tissue from brown bears (Ursus arctos) prior to hibernation. / Jessen, Niels; Nielsen, Thomas S; Vendelbo, Mikkel H; Viggers, Rikke; Støen, Ole-Gunnar; Evans, Alina; Frøbert, Ole.

I: Physiological Reports, Bind 4, Nr. 8, e12781, 04.2016, s. 1-7.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Jessen, N, Nielsen, TS, Vendelbo, MH, Viggers, R, Støen, O-G, Evans, A & Frøbert, O 2016, 'Pronounced expression of the lipolytic inhibitor G0/G1 Switch Gene 2 (G0S2) in adipose tissue from brown bears (Ursus arctos) prior to hibernation', Physiological Reports, bind 4, nr. 8, e12781, s. 1-7. https://doi.org/10.14814/phy2.12781

APA

Jessen, N., Nielsen, T. S., Vendelbo, M. H., Viggers, R., Støen, O-G., Evans, A., & Frøbert, O. (2016). Pronounced expression of the lipolytic inhibitor G0/G1 Switch Gene 2 (G0S2) in adipose tissue from brown bears (Ursus arctos) prior to hibernation. Physiological Reports, 4(8), 1-7. [e12781]. https://doi.org/10.14814/phy2.12781

Vancouver

Jessen N, Nielsen TS, Vendelbo MH, Viggers R, Støen O-G, Evans A o.a. Pronounced expression of the lipolytic inhibitor G0/G1 Switch Gene 2 (G0S2) in adipose tissue from brown bears (Ursus arctos) prior to hibernation. Physiological Reports. 2016 apr;4(8):1-7. e12781. https://doi.org/10.14814/phy2.12781

Author

Jessen, Niels ; Nielsen, Thomas S ; Vendelbo, Mikkel H ; Viggers, Rikke ; Støen, Ole-Gunnar ; Evans, Alina ; Frøbert, Ole. / Pronounced expression of the lipolytic inhibitor G0/G1 Switch Gene 2 (G0S2) in adipose tissue from brown bears (Ursus arctos) prior to hibernation. I: Physiological Reports. 2016 ; Bind 4, Nr. 8. s. 1-7.

Bibtex

@article{6d72344b94eb4cbbb4117b24b43a7123,
title = "Pronounced expression of the lipolytic inhibitor G0/G1 Switch Gene 2 (G0S2) in adipose tissue from brown bears (Ursus arctos) prior to hibernation",
abstract = "Prior to hibernation, the brown bear (Ursus arctos) exhibits unparalleled weight gain. Unlike humans, weight gain in bears is associated with lower levels of circulating free fatty acids (FFA) and increased insulin sensitivity. Understanding how free-ranging brown bears suppress lipolysis when gaining weight may therefore provide novel insight toward the development of human therapies. Blood and subcutaneous adipose tissue were collected from immobilized free-ranging brown bears (fitted with GPS-collars) during hibernation in winter and from the same bears during the active period in summer in Dalarna, Sweden. The expression of lipid droplet-associated proteins in adipose tissue was examined under the hypothesis that bears suppress lipolysis during summer while gaining weight by increased expression of negative regulators of lipolysis. Adipose triglyceride lipase (ATGL) expression did not differ between seasons, but in contrast, the expression of ATGL coactivator Comparative gene identification-58 (CGI-58) was lower in summer. In addition, the expression of the negative regulators of lipolysis, G0S2 and cell-death inducing DNA fragmentation factor-a-like effector (CIDE)C markedly increased during summer. Free-ranging brown bears display potent upregulation of inhibitors of lipolysis in adipose tissue during summer. This is a potential mechanism for increased insulin sensitivity during weight gain and G0S2 may serve as a target to modulate insulin sensitivity.",
keywords = "Adaptation, Physiological, Adipose Tissue, Animals, Blotting, Western, Cell Cycle Proteins, Fatty Acids, Nonesterified, Female, Hibernation, Insulin Resistance, Lipolysis, Male, Ursidae, Journal Article, Research Support, Non-U.S. Gov't",
author = "Niels Jessen and Nielsen, {Thomas S} and Vendelbo, {Mikkel H} and Rikke Viggers and Ole-Gunnar St{\o}en and Alina Evans and Ole Fr{\o}bert",
note = "{\circledC} 2016 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of the American Physiological Society and The Physiological Society.",
year = "2016",
month = "4",
doi = "10.14814/phy2.12781",
language = "English",
volume = "4",
pages = "1--7",
journal = "Physiological Reports",
issn = "2051-817X",
publisher = "Wiley Periodicals, Inc.",
number = "8",

}

RIS

TY - JOUR

T1 - Pronounced expression of the lipolytic inhibitor G0/G1 Switch Gene 2 (G0S2) in adipose tissue from brown bears (Ursus arctos) prior to hibernation

AU - Jessen, Niels

AU - Nielsen, Thomas S

AU - Vendelbo, Mikkel H

AU - Viggers, Rikke

AU - Støen, Ole-Gunnar

AU - Evans, Alina

AU - Frøbert, Ole

N1 - © 2016 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of the American Physiological Society and The Physiological Society.

PY - 2016/4

Y1 - 2016/4

N2 - Prior to hibernation, the brown bear (Ursus arctos) exhibits unparalleled weight gain. Unlike humans, weight gain in bears is associated with lower levels of circulating free fatty acids (FFA) and increased insulin sensitivity. Understanding how free-ranging brown bears suppress lipolysis when gaining weight may therefore provide novel insight toward the development of human therapies. Blood and subcutaneous adipose tissue were collected from immobilized free-ranging brown bears (fitted with GPS-collars) during hibernation in winter and from the same bears during the active period in summer in Dalarna, Sweden. The expression of lipid droplet-associated proteins in adipose tissue was examined under the hypothesis that bears suppress lipolysis during summer while gaining weight by increased expression of negative regulators of lipolysis. Adipose triglyceride lipase (ATGL) expression did not differ between seasons, but in contrast, the expression of ATGL coactivator Comparative gene identification-58 (CGI-58) was lower in summer. In addition, the expression of the negative regulators of lipolysis, G0S2 and cell-death inducing DNA fragmentation factor-a-like effector (CIDE)C markedly increased during summer. Free-ranging brown bears display potent upregulation of inhibitors of lipolysis in adipose tissue during summer. This is a potential mechanism for increased insulin sensitivity during weight gain and G0S2 may serve as a target to modulate insulin sensitivity.

AB - Prior to hibernation, the brown bear (Ursus arctos) exhibits unparalleled weight gain. Unlike humans, weight gain in bears is associated with lower levels of circulating free fatty acids (FFA) and increased insulin sensitivity. Understanding how free-ranging brown bears suppress lipolysis when gaining weight may therefore provide novel insight toward the development of human therapies. Blood and subcutaneous adipose tissue were collected from immobilized free-ranging brown bears (fitted with GPS-collars) during hibernation in winter and from the same bears during the active period in summer in Dalarna, Sweden. The expression of lipid droplet-associated proteins in adipose tissue was examined under the hypothesis that bears suppress lipolysis during summer while gaining weight by increased expression of negative regulators of lipolysis. Adipose triglyceride lipase (ATGL) expression did not differ between seasons, but in contrast, the expression of ATGL coactivator Comparative gene identification-58 (CGI-58) was lower in summer. In addition, the expression of the negative regulators of lipolysis, G0S2 and cell-death inducing DNA fragmentation factor-a-like effector (CIDE)C markedly increased during summer. Free-ranging brown bears display potent upregulation of inhibitors of lipolysis in adipose tissue during summer. This is a potential mechanism for increased insulin sensitivity during weight gain and G0S2 may serve as a target to modulate insulin sensitivity.

KW - Adaptation, Physiological

KW - Adipose Tissue

KW - Animals

KW - Blotting, Western

KW - Cell Cycle Proteins

KW - Fatty Acids, Nonesterified

KW - Female

KW - Hibernation

KW - Insulin Resistance

KW - Lipolysis

KW - Male

KW - Ursidae

KW - Journal Article

KW - Research Support, Non-U.S. Gov't

U2 - 10.14814/phy2.12781

DO - 10.14814/phy2.12781

M3 - Journal article

C2 - 27117803

VL - 4

SP - 1

EP - 7

JO - Physiological Reports

JF - Physiological Reports

SN - 2051-817X

IS - 8

M1 - e12781

ER -

ID: 166158434