Mitochondrial function and oxidative stress in white adipose tissue in a rat model of PCOS: effect of SGLT2 inhibition

Highlights 1. Androgen excess in PCOS model is associated with decreased markers of mitochondrial content in both subcutaneous and visceral white adipose tissue. 2. Androgen excess in PCOS model is associated with increased frequency of small adipocytes in subcutaneous white adipose tissue while dec...

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Main Authors: Jacob E. Pruett, Steven J. Everman, Ngoc H. Hoang, Faridah Salau, Lucy C. Taylor, Kristin S. Edwards, Jonathan P. Hosler, Alexandra M. Huffman, Damian G. Romero, Licy L. Yanes Cardozo
Format: Article
Language:English
Published: BMC 2022-08-01
Series:Biology of Sex Differences
Subjects:
Online Access:https://doi.org/10.1186/s13293-022-00455-x
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author Jacob E. Pruett
Steven J. Everman
Ngoc H. Hoang
Faridah Salau
Lucy C. Taylor
Kristin S. Edwards
Jonathan P. Hosler
Alexandra M. Huffman
Damian G. Romero
Licy L. Yanes Cardozo
author_facet Jacob E. Pruett
Steven J. Everman
Ngoc H. Hoang
Faridah Salau
Lucy C. Taylor
Kristin S. Edwards
Jonathan P. Hosler
Alexandra M. Huffman
Damian G. Romero
Licy L. Yanes Cardozo
author_sort Jacob E. Pruett
collection DOAJ
description Highlights 1. Androgen excess in PCOS model is associated with decreased markers of mitochondrial content in both subcutaneous and visceral white adipose tissue. 2. Androgen excess in PCOS model is associated with increased frequency of small adipocytes in subcutaneous white adipose tissue while decreasing frequency of small adipocytes in visceral white adipose tissue. 3. SGLT2 inhibition did not modify markers of mitochondrial content or oxidative stress in either subcutaneous or visceral white adipose tissue in PCOS model. 4. SGLT2 inhibition increased frequency of small adipocytes in both subcutaneous and visceral white adipose tissue in control rats; however, SGLT2 inhibition only increased frequency of small adipocytes in visceral white adipose tissue in PCOS model.
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spelling doaj.art-1fa16c82e76e4c35adfc865f1a25a9d92022-12-22T02:15:08ZengBMCBiology of Sex Differences2042-64102022-08-0113111710.1186/s13293-022-00455-xMitochondrial function and oxidative stress in white adipose tissue in a rat model of PCOS: effect of SGLT2 inhibitionJacob E. Pruett0Steven J. Everman1Ngoc H. Hoang2Faridah Salau3Lucy C. Taylor4Kristin S. Edwards5Jonathan P. Hosler6Alexandra M. Huffman7Damian G. Romero8Licy L. Yanes Cardozo9Department of Cell and Molecular Biology, University of Mississippi Medical CenterDepartment of Cell and Molecular Biology, University of Mississippi Medical CenterDepartment of Cell and Molecular Biology, University of Mississippi Medical CenterDepartment of Cell and Molecular Biology, University of Mississippi Medical CenterDepartment of Cell and Molecular Biology, University of Mississippi Medical CenterDepartment of Cell and Molecular Biology, University of Mississippi Medical CenterDepartment of Cell and Molecular Biology, University of Mississippi Medical CenterDepartment of Cell and Molecular Biology, University of Mississippi Medical CenterDepartment of Cell and Molecular Biology, University of Mississippi Medical CenterDepartment of Cell and Molecular Biology, University of Mississippi Medical CenterHighlights 1. Androgen excess in PCOS model is associated with decreased markers of mitochondrial content in both subcutaneous and visceral white adipose tissue. 2. Androgen excess in PCOS model is associated with increased frequency of small adipocytes in subcutaneous white adipose tissue while decreasing frequency of small adipocytes in visceral white adipose tissue. 3. SGLT2 inhibition did not modify markers of mitochondrial content or oxidative stress in either subcutaneous or visceral white adipose tissue in PCOS model. 4. SGLT2 inhibition increased frequency of small adipocytes in both subcutaneous and visceral white adipose tissue in control rats; however, SGLT2 inhibition only increased frequency of small adipocytes in visceral white adipose tissue in PCOS model.https://doi.org/10.1186/s13293-022-00455-xPolycystic ovary syndromeAndrogensMitochondrial dysfunctionWhite adipose tissueSodium–glucose cotransporter-2
spellingShingle Jacob E. Pruett
Steven J. Everman
Ngoc H. Hoang
Faridah Salau
Lucy C. Taylor
Kristin S. Edwards
Jonathan P. Hosler
Alexandra M. Huffman
Damian G. Romero
Licy L. Yanes Cardozo
Mitochondrial function and oxidative stress in white adipose tissue in a rat model of PCOS: effect of SGLT2 inhibition
Biology of Sex Differences
Polycystic ovary syndrome
Androgens
Mitochondrial dysfunction
White adipose tissue
Sodium–glucose cotransporter-2
title Mitochondrial function and oxidative stress in white adipose tissue in a rat model of PCOS: effect of SGLT2 inhibition
title_full Mitochondrial function and oxidative stress in white adipose tissue in a rat model of PCOS: effect of SGLT2 inhibition
title_fullStr Mitochondrial function and oxidative stress in white adipose tissue in a rat model of PCOS: effect of SGLT2 inhibition
title_full_unstemmed Mitochondrial function and oxidative stress in white adipose tissue in a rat model of PCOS: effect of SGLT2 inhibition
title_short Mitochondrial function and oxidative stress in white adipose tissue in a rat model of PCOS: effect of SGLT2 inhibition
title_sort mitochondrial function and oxidative stress in white adipose tissue in a rat model of pcos effect of sglt2 inhibition
topic Polycystic ovary syndrome
Androgens
Mitochondrial dysfunction
White adipose tissue
Sodium–glucose cotransporter-2
url https://doi.org/10.1186/s13293-022-00455-x
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