Resveratrol suppresses PAI-1 gene expression in a human in vitro model of inflamed adipose tissue |
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Author: | Zagotta, Ivana1; Dimova, Elitsa Y.2; Funcke, Jan-Bernd1; |
Organizations: |
1Division of Pediatric Endocrinology and Diabetes, Department of Pediatrics and Adolescent Medicine, Ulm University Medical Center, Eythstraße 24, 89075 Ulm, Germany 2Department of Biochemistry and Biocenter Oulu, University of Oulu, P.O.B. 3000, 90014 Oulu, Finland |
Format: | article |
Version: | published version |
Access: | open |
Online Access: | PDF Full Text (PDF, 2.1 MB) |
Persistent link: | http://urn.fi/urn:nbn:fi-fe201703152188 |
Language: | English |
Published: |
Hindawi,
2013
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Publish Date: | 2017-03-15 |
Description: |
AbstractIncreased plasminogen activator inhibitor-1 (PAI-1) levels are associated with a number of pathophysiological complications; among them is obesity. Resveratrol was proposed to improve obesity-related health problems, but the effect of resveratrol on PAI-1 gene expression in obesity is not completely understood. In this study, we used SGBS adipocytes and a model of human adipose tissue inflammation to examine the effects of resveratrol on the production of PAI-1. Treatment of SGBS adipocytes with resveratrol reduced PAI-1 mRNA and protein in a time- and concentration-dependent manner. Further experiments showed that obesity-associated inflammatory conditions lead to the upregulation of PAI-1 gene expression which was antagonized by resveratrol. Although signaling via PI3K, Sirt1, AMPK, ROS, and Nrf2 appeared to play a significant role in the modulation of PAI-1 gene expression under noninflammatory conditions, those signaling components were not involved in mediating the resveratrol effects on PAI-1 production under inflammatory conditions. Instead, we demonstrate that the resveratrol effects on PAI-1 induction under inflammatory conditions were mediated via inhibition of the NFκB pathway. Together, resveratrol can act as NFκB inhibitor in adipocytes and thus the subsequently reduced PAI-1 expression in inflamed adipose tissue might provide a new insight towards novel treatment options of obesity. see all
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Series: |
Oxidative medicine and cellular longevity |
ISSN: | 1942-0900 |
ISSN-E: | 1942-0994 |
ISSN-L: | 1942-0900 |
Volume: | 2013 |
Article number: | 793525 |
DOI: | 10.1155/2013/793525 |
OADOI: | https://oadoi.org/10.1155/2013/793525 |
Type of Publication: |
A1 Journal article – refereed |
Field of Science: |
1182 Biochemistry, cell and molecular biology |
Subjects: | |
Funding: |
PFP was
funded by aMargarete vonWrangell scholarship financed by
the Baden-Wuerttemberg Ministry of Science, Research and
Arts; the European Social Fund; and Ulm University. Ivana
Zagotta is funded by the International Graduate School in
Molecular Medicine Ulm. This study was in part supported
by the Research Training Group GRK 1041 “Molecular Diabetology
and Endocrinology inMedicine” to Pamela Fischer-
Posovszky and Martin Wabitsch and the foundation “Das
zuckerkranke Kind” to Pamela Fischer-Posovszky. Work in
the Thomas Kietzmann lab is supported by grants from the
Biocenter Oulu, Academy of Finland, and Sigrid Juselius
Foundation. |
Copyright information: |
Copyright © 2013 Ivana Zagotta et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
https://creativecommons.org/licenses/by/3.0/ |