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Reducing insulin via conditional partial gene ablation in adults reverses diet-induced weight gain

Excess circulating insulin is associated with obesity in humans and in animal models. However, the physiologic causality of hyperinsulinemia in adult obesity has rightfully been questioned because of the absence of clear evidence that weight loss can be induced by acutely reversing diet-induced hype...

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Autores principales: Page, Melissa M., Skovsø, Søs, Cen, Haoning, Chiu, Amy P., Dionne, Derek A., Hutchinson, Daria F., Lim, Gareth E., Szabat, Marta, Flibotte, Stephane, Sinha, Sunita, Nislow, Corey, Rodrigues, Brian, Johnson, James D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Federation of American Societies for Experimental Biology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5892722/
https://www.ncbi.nlm.nih.gov/pubmed/29122848
http://dx.doi.org/10.1096/fj.201700518R
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author Page, Melissa M.
Skovsø, Søs
Cen, Haoning
Chiu, Amy P.
Dionne, Derek A.
Hutchinson, Daria F.
Lim, Gareth E.
Szabat, Marta
Flibotte, Stephane
Sinha, Sunita
Nislow, Corey
Rodrigues, Brian
Johnson, James D.
author_facet Page, Melissa M.
Skovsø, Søs
Cen, Haoning
Chiu, Amy P.
Dionne, Derek A.
Hutchinson, Daria F.
Lim, Gareth E.
Szabat, Marta
Flibotte, Stephane
Sinha, Sunita
Nislow, Corey
Rodrigues, Brian
Johnson, James D.
author_sort Page, Melissa M.
collection PubMed
description Excess circulating insulin is associated with obesity in humans and in animal models. However, the physiologic causality of hyperinsulinemia in adult obesity has rightfully been questioned because of the absence of clear evidence that weight loss can be induced by acutely reversing diet-induced hyperinsulinemia. Herein, we describe the consequences of inducible, partial insulin gene deletion in a mouse model in which animals have already been made obese by consuming a high-fat diet. A modest reduction in insulin production/secretion was sufficient to cause significant weight loss within 5 wk, with a specific effect on visceral adipose tissue. This result was associated with a reduction in the protein abundance of the lipodystrophy gene polymerase I and transcript release factor (Ptrf; Cavin) in gonadal adipose tissue. RNAseq analysis showed that reduced insulin and weight loss also associated with a signature of reduced innate immunity. This study demonstrates that changes in circulating insulin that are too fine to adversely affect glucose homeostasis nonetheless exert control over adiposity.—Page, M. M., Skovsø, S., Cen, H., Chiu, A. P., Dionne, D. A., Hutchinson, D. F., Lim, G. E., Szabat, M., Flibotte, S., Sinha, S., Nislow, C., Rodrigues, B., Johnson, J. D. Reducing insulin via conditional partial gene ablation in adults reverses diet-induced weight gain.
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spelling pubmed-58927222018-04-13 Reducing insulin via conditional partial gene ablation in adults reverses diet-induced weight gain Page, Melissa M. Skovsø, Søs Cen, Haoning Chiu, Amy P. Dionne, Derek A. Hutchinson, Daria F. Lim, Gareth E. Szabat, Marta Flibotte, Stephane Sinha, Sunita Nislow, Corey Rodrigues, Brian Johnson, James D. FASEB J Research Excess circulating insulin is associated with obesity in humans and in animal models. However, the physiologic causality of hyperinsulinemia in adult obesity has rightfully been questioned because of the absence of clear evidence that weight loss can be induced by acutely reversing diet-induced hyperinsulinemia. Herein, we describe the consequences of inducible, partial insulin gene deletion in a mouse model in which animals have already been made obese by consuming a high-fat diet. A modest reduction in insulin production/secretion was sufficient to cause significant weight loss within 5 wk, with a specific effect on visceral adipose tissue. This result was associated with a reduction in the protein abundance of the lipodystrophy gene polymerase I and transcript release factor (Ptrf; Cavin) in gonadal adipose tissue. RNAseq analysis showed that reduced insulin and weight loss also associated with a signature of reduced innate immunity. This study demonstrates that changes in circulating insulin that are too fine to adversely affect glucose homeostasis nonetheless exert control over adiposity.—Page, M. M., Skovsø, S., Cen, H., Chiu, A. P., Dionne, D. A., Hutchinson, D. F., Lim, G. E., Szabat, M., Flibotte, S., Sinha, S., Nislow, C., Rodrigues, B., Johnson, J. D. Reducing insulin via conditional partial gene ablation in adults reverses diet-induced weight gain. Federation of American Societies for Experimental Biology 2018-03 2017-11-16 /pmc/articles/PMC5892722/ /pubmed/29122848 http://dx.doi.org/10.1096/fj.201700518R Text en © The Author(s) http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0) (http://creativecommons.org/licenses/by-nc/4.0/) which permits noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Page, Melissa M.
Skovsø, Søs
Cen, Haoning
Chiu, Amy P.
Dionne, Derek A.
Hutchinson, Daria F.
Lim, Gareth E.
Szabat, Marta
Flibotte, Stephane
Sinha, Sunita
Nislow, Corey
Rodrigues, Brian
Johnson, James D.
Reducing insulin via conditional partial gene ablation in adults reverses diet-induced weight gain
title Reducing insulin via conditional partial gene ablation in adults reverses diet-induced weight gain
title_full Reducing insulin via conditional partial gene ablation in adults reverses diet-induced weight gain
title_fullStr Reducing insulin via conditional partial gene ablation in adults reverses diet-induced weight gain
title_full_unstemmed Reducing insulin via conditional partial gene ablation in adults reverses diet-induced weight gain
title_short Reducing insulin via conditional partial gene ablation in adults reverses diet-induced weight gain
title_sort reducing insulin via conditional partial gene ablation in adults reverses diet-induced weight gain
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5892722/
https://www.ncbi.nlm.nih.gov/pubmed/29122848
http://dx.doi.org/10.1096/fj.201700518R
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