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Changes in adipose tissue lipolysis gene expression and insulin sensitivity after weight loss
OBJECTIVE: Insulin resistance is a major pathophysiological link between obesity and its metabolic complications. Weight loss (WL) is an effective tool to prevent obesity-related diseases; however, the mechanisms of an improvement in insulin sensitivity (IS) after weight-reducing interventions are n...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bioscientifica Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6993275/ https://www.ncbi.nlm.nih.gov/pubmed/31905163 http://dx.doi.org/10.1530/EC-19-0507 |
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author | Karczewska-Kupczewska, Monika Nikołajuk, Agnieszka Majewski, Radosław Filarski, Remigiusz Stefanowicz, Magdalena Matulewicz, Natalia Strączkowski, Marek |
author_facet | Karczewska-Kupczewska, Monika Nikołajuk, Agnieszka Majewski, Radosław Filarski, Remigiusz Stefanowicz, Magdalena Matulewicz, Natalia Strączkowski, Marek |
author_sort | Karczewska-Kupczewska, Monika |
collection | PubMed |
description | OBJECTIVE: Insulin resistance is a major pathophysiological link between obesity and its metabolic complications. Weight loss (WL) is an effective tool to prevent obesity-related diseases; however, the mechanisms of an improvement in insulin sensitivity (IS) after weight-reducing interventions are not completely understood. The aim of the present study was to analyze the relationships between IS and adipose tissue (AT) expression of the genes involved in the regulation of lipolysis in obese subjects after WL. METHODS: Fifty-two obese subjects underwent weight-reducing dietary intervention program. The control group comprised 20 normal-weight subjects, examined at baseline only. Hyperinsulinemic-euglycemic clamp and s.c. AT biopsy with subsequent gene expression analysis were performed before and after the program. RESULTS: AT expression of genes encoding lipases (PNPLA2, LIPE and MGLL) and lipid-droplet proteins enhancing (ABHD5) and inhibiting lipolysis (PLIN1 and CIDEA) were decreased in obese individuals in comparison with normal-weight individuals. The group of 38 obese participants completed dietary intervention program and clamp studies, which resulted in a significant WL and an improvement in mean IS. However, in nine subjects from this group IS did not improve in response to WL. AT expression of PNPLA2, LIPE and PLIN1 increased only in the group without IS improvement. CONCLUSIONS: Excessive lipolysis may prevent an improvement in IS during WL. The change in AT PNPLA2 and LIPE expression was a negative predictor of the change in IS after WL. |
format | Online Article Text |
id | pubmed-6993275 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Bioscientifica Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-69932752020-02-03 Changes in adipose tissue lipolysis gene expression and insulin sensitivity after weight loss Karczewska-Kupczewska, Monika Nikołajuk, Agnieszka Majewski, Radosław Filarski, Remigiusz Stefanowicz, Magdalena Matulewicz, Natalia Strączkowski, Marek Endocr Connect Research OBJECTIVE: Insulin resistance is a major pathophysiological link between obesity and its metabolic complications. Weight loss (WL) is an effective tool to prevent obesity-related diseases; however, the mechanisms of an improvement in insulin sensitivity (IS) after weight-reducing interventions are not completely understood. The aim of the present study was to analyze the relationships between IS and adipose tissue (AT) expression of the genes involved in the regulation of lipolysis in obese subjects after WL. METHODS: Fifty-two obese subjects underwent weight-reducing dietary intervention program. The control group comprised 20 normal-weight subjects, examined at baseline only. Hyperinsulinemic-euglycemic clamp and s.c. AT biopsy with subsequent gene expression analysis were performed before and after the program. RESULTS: AT expression of genes encoding lipases (PNPLA2, LIPE and MGLL) and lipid-droplet proteins enhancing (ABHD5) and inhibiting lipolysis (PLIN1 and CIDEA) were decreased in obese individuals in comparison with normal-weight individuals. The group of 38 obese participants completed dietary intervention program and clamp studies, which resulted in a significant WL and an improvement in mean IS. However, in nine subjects from this group IS did not improve in response to WL. AT expression of PNPLA2, LIPE and PLIN1 increased only in the group without IS improvement. CONCLUSIONS: Excessive lipolysis may prevent an improvement in IS during WL. The change in AT PNPLA2 and LIPE expression was a negative predictor of the change in IS after WL. Bioscientifica Ltd 2019-12-22 /pmc/articles/PMC6993275/ /pubmed/31905163 http://dx.doi.org/10.1530/EC-19-0507 Text en © 2020 The authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (http://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Research Karczewska-Kupczewska, Monika Nikołajuk, Agnieszka Majewski, Radosław Filarski, Remigiusz Stefanowicz, Magdalena Matulewicz, Natalia Strączkowski, Marek Changes in adipose tissue lipolysis gene expression and insulin sensitivity after weight loss |
title | Changes in adipose tissue lipolysis gene expression and insulin sensitivity after weight loss |
title_full | Changes in adipose tissue lipolysis gene expression and insulin sensitivity after weight loss |
title_fullStr | Changes in adipose tissue lipolysis gene expression and insulin sensitivity after weight loss |
title_full_unstemmed | Changes in adipose tissue lipolysis gene expression and insulin sensitivity after weight loss |
title_short | Changes in adipose tissue lipolysis gene expression and insulin sensitivity after weight loss |
title_sort | changes in adipose tissue lipolysis gene expression and insulin sensitivity after weight loss |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6993275/ https://www.ncbi.nlm.nih.gov/pubmed/31905163 http://dx.doi.org/10.1530/EC-19-0507 |
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