Literature DB >> 23928404

Adipose tissue and liver expression of SIRT1, 3, and 6 increase after extensive weight loss in morbid obesity.

Alexander R Moschen1, Verena Wieser, Romana R Gerner, Alexandra Bichler, Barbara Enrich, Patrizia Moser, Christoph F Ebenbichler, Susanne Kaser, Herbert Tilg.   

Abstract

BACKGROUND & AIMS: Severe obesity is associated with a state of chronic inflammation. Sirtuins (SIRT) are a family of conserved enzymes which are able to affect many metabolic and inflammatory pathways thereby potentially improving health and increasing lifespan.
METHODS: We investigated the effect of weight loss on subcutaneous adipose tissue and liver mRNA and immunohistochemical expression of SIRT1, SIRT3, and SIRT6. Twenty-nine severely obese patients undergoing laparoscopic adjustable gastric banding (LAGB) were studied. Tissue samples were collected before and 6months after LAGB surgery. Tissue mRNA expression levels of SIRT1, SIRT3, and SIRT6 were correlated with clinical, biochemical, and histological parameters. In vitro, we studied sirtuin expression in native and stimulated monocytes, adipocytes, and hepatocytes.
RESULTS: SIRT1, SIRT3, and SIRT6 mRNA expression was higher in the subcutaneous adipose tissue than in the liver. Weight loss resulted in a significant induction of SIRT1, SIRT3, and SIRT6 expression in the subcutaneous adipose tissue. In the liver, a significant increase after weight loss was observed, particularly for SIRT3 and SIRT6 mRNA expression; immunohistochemically, SIRT1 and SIRT3 expression was upregulated. Endotoxin and tumor necrosis factor-alpha suppressed SIRT1, SIRT3, and SIRT6 expression in human monocytes. The same stimuli suppressed total sirtuin deacetylase activity again, mainly in monocytes and less in adipocytes and hepatocytes.
CONCLUSIONS: The relative abundance of adipose tissue mRNA expression of certain sirtuins exceeds its expression in the liver. Extensive weight loss increases sirtuin expression significantly both in adipose tissue and liver, probably as a consequence of reduced inflammation.
Copyright © 2013 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Insulin resistance; Metabolism; NAFLD; SIRT1; SIRT3; SIRT6

Mesh:

Substances:

Year:  2013        PMID: 23928404     DOI: 10.1016/j.jhep.2013.07.027

Source DB:  PubMed          Journal:  J Hepatol        ISSN: 0168-8278            Impact factor:   25.083


  33 in total

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Journal:  Obes Surg       Date:  2018-11       Impact factor: 4.129

2.  Reduced SIRT1 and SIRT2 expression promotes adipogenesis of human visceral adipose stem cells and associates with accumulation of visceral fat in human obesity.

Authors:  Sebastio Perrini; Stefania Porro; Pasquale Nigro; Angelo Cignarelli; Cristina Caccioppoli; Valentina Annamaria Genchi; Gennaro Martines; Michele De Fazio; Palma Capuano; Annalisa Natalicchio; Luigi Laviola; Francesco Giorgino
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3.  SIRT1 and SIRT7 expression in adipose tissues of obese and normal-weight individuals is regulated by microRNAs but not by methylation status.

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Journal:  Int J Obes (Lond)       Date:  2016-08-02       Impact factor: 5.095

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Journal:  Bioessays       Date:  2017-03-15       Impact factor: 4.345

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Review 6.  Sirtuins-Mediated System-Level Regulation of Mammalian Tissues at the Interface between Metabolism and Cell Cycle: A Systematic Review.

Authors:  Parcival Maissan; Eva J Mooij; Matteo Barberis
Journal:  Biology (Basel)       Date:  2021-03-04

7.  Circulating SIRT1 Increases After Intragastric Balloon Fat Loss in Obese Patients.

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8.  Changes in human sirtuin 6 gene promoter methylation during aging.

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Journal:  Biomed Rep       Date:  2014-03-31

Review 9.  Dysmetabolic adipose tissue in obesity: morphological and functional characteristics of adipose stem cells and mature adipocytes in healthy and unhealthy obese subjects.

Authors:  S Porro; V A Genchi; A Cignarelli; A Natalicchio; L Laviola; F Giorgino; S Perrini
Journal:  J Endocrinol Invest       Date:  2020-11-03       Impact factor: 4.256

10.  Resveratrol attenuates microvascular inflammation in sepsis via SIRT-1-Induced modulation of adhesion molecules in ob/ob mice.

Authors:  Xianfeng Wang; Nancy L Buechler; Barbara K Yoza; Charles E McCall; Vidula T Vachharajani
Journal:  Obesity (Silver Spring)       Date:  2015-05-09       Impact factor: 5.002

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