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Inhibition of Lipolysis in the Novel Transgenic Quail Model Overexpressing G(0)/G(1) Switch Gene 2 in the Adipose Tissue during Feed Restriction

In addition to the issue of obesity in humans, the production of low-fat meat from domestic animals is important in the agricultural industry to satisfy consumer demand. Understanding the regulation of lipolysis in adipose tissue could advance our knowledge to potentially solve both issues. Although...

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Autores principales: Shin, Sangsu, Choi, Young Min, Han, Jae Yong, Lee, Kichoon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4071008/
https://www.ncbi.nlm.nih.gov/pubmed/24964090
http://dx.doi.org/10.1371/journal.pone.0100905
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author Shin, Sangsu
Choi, Young Min
Han, Jae Yong
Lee, Kichoon
author_facet Shin, Sangsu
Choi, Young Min
Han, Jae Yong
Lee, Kichoon
author_sort Shin, Sangsu
collection PubMed
description In addition to the issue of obesity in humans, the production of low-fat meat from domestic animals is important in the agricultural industry to satisfy consumer demand. Understanding the regulation of lipolysis in adipose tissue could advance our knowledge to potentially solve both issues. Although the G(0)/G(1) switch gene 2 (G0S2) was recently identified as an inhibitor of adipose triglyceride lipase (ATGL) in vitro, its role in vivo has not been fully clarified. This study was conducted to investigate the role of G0S2 gene in vivo by using two independent transgenic quail lines during different energy conditions. Unexpectedly, G0S2 overexpression had a negligible effect on plasma NEFA concentration, fat cell size and fat pad weight under ad libitum feeding condition when adipose lipolytic activity is minimal. A two-week feed restriction in non-transgenic quail expectedly caused increased plasma NEFA concentration and dramatically reduced fat cell size and fat pad weight. Contrary, G0S2 overexpression under a feed restriction resulted in a significantly less elevation of plasma NEFA concentration and smaller reductions in fat pad weights and fat cell size compared to non-transgenic quail, demonstrating inhibition of lipolysis and resistance to loss of fat by G0S2. Excessive G0S2 inhibits lipolysis in vivo during active lipolytic conditions, such as food restriction and fasting, suggesting G0S2 as a potential target for treatment of obesity. In addition, transgenic quail are novel models for studying lipid metabolism and mechanisms of obesity.
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spelling pubmed-40710082014-06-27 Inhibition of Lipolysis in the Novel Transgenic Quail Model Overexpressing G(0)/G(1) Switch Gene 2 in the Adipose Tissue during Feed Restriction Shin, Sangsu Choi, Young Min Han, Jae Yong Lee, Kichoon PLoS One Research Article In addition to the issue of obesity in humans, the production of low-fat meat from domestic animals is important in the agricultural industry to satisfy consumer demand. Understanding the regulation of lipolysis in adipose tissue could advance our knowledge to potentially solve both issues. Although the G(0)/G(1) switch gene 2 (G0S2) was recently identified as an inhibitor of adipose triglyceride lipase (ATGL) in vitro, its role in vivo has not been fully clarified. This study was conducted to investigate the role of G0S2 gene in vivo by using two independent transgenic quail lines during different energy conditions. Unexpectedly, G0S2 overexpression had a negligible effect on plasma NEFA concentration, fat cell size and fat pad weight under ad libitum feeding condition when adipose lipolytic activity is minimal. A two-week feed restriction in non-transgenic quail expectedly caused increased plasma NEFA concentration and dramatically reduced fat cell size and fat pad weight. Contrary, G0S2 overexpression under a feed restriction resulted in a significantly less elevation of plasma NEFA concentration and smaller reductions in fat pad weights and fat cell size compared to non-transgenic quail, demonstrating inhibition of lipolysis and resistance to loss of fat by G0S2. Excessive G0S2 inhibits lipolysis in vivo during active lipolytic conditions, such as food restriction and fasting, suggesting G0S2 as a potential target for treatment of obesity. In addition, transgenic quail are novel models for studying lipid metabolism and mechanisms of obesity. Public Library of Science 2014-06-25 /pmc/articles/PMC4071008/ /pubmed/24964090 http://dx.doi.org/10.1371/journal.pone.0100905 Text en © 2014 Shin et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Shin, Sangsu
Choi, Young Min
Han, Jae Yong
Lee, Kichoon
Inhibition of Lipolysis in the Novel Transgenic Quail Model Overexpressing G(0)/G(1) Switch Gene 2 in the Adipose Tissue during Feed Restriction
title Inhibition of Lipolysis in the Novel Transgenic Quail Model Overexpressing G(0)/G(1) Switch Gene 2 in the Adipose Tissue during Feed Restriction
title_full Inhibition of Lipolysis in the Novel Transgenic Quail Model Overexpressing G(0)/G(1) Switch Gene 2 in the Adipose Tissue during Feed Restriction
title_fullStr Inhibition of Lipolysis in the Novel Transgenic Quail Model Overexpressing G(0)/G(1) Switch Gene 2 in the Adipose Tissue during Feed Restriction
title_full_unstemmed Inhibition of Lipolysis in the Novel Transgenic Quail Model Overexpressing G(0)/G(1) Switch Gene 2 in the Adipose Tissue during Feed Restriction
title_short Inhibition of Lipolysis in the Novel Transgenic Quail Model Overexpressing G(0)/G(1) Switch Gene 2 in the Adipose Tissue during Feed Restriction
title_sort inhibition of lipolysis in the novel transgenic quail model overexpressing g(0)/g(1) switch gene 2 in the adipose tissue during feed restriction
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4071008/
https://www.ncbi.nlm.nih.gov/pubmed/24964090
http://dx.doi.org/10.1371/journal.pone.0100905
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