Metformin delays the decline in thermogenic function of brown adipose tissue in a mouse model of Hutchinson-Gilford progeria syndrome

Brown adipose tissue (BAT) is the primary site for non-shivering thermogenesis in the body and plays a crucial role in maintaining core body temperature. However, its function gradually declines with age. To mitigate the age-related decline in BAT thermogenic capacity, we treated progeroid mice with...

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Main Authors: Xin Xiang, Yuyue Feng, Hongcheng Li, Wenbo Li, Jia Li, Zhu Xia, Hua Pang, Zhengjie Wang
Format: Article
Language:English
Published: Elsevier 2025-03-01
Series:Experimental Gerontology
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Online Access:http://www.sciencedirect.com/science/article/pii/S0531556525000300
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author Xin Xiang
Yuyue Feng
Hongcheng Li
Wenbo Li
Jia Li
Zhu Xia
Hua Pang
Zhengjie Wang
author_facet Xin Xiang
Yuyue Feng
Hongcheng Li
Wenbo Li
Jia Li
Zhu Xia
Hua Pang
Zhengjie Wang
author_sort Xin Xiang
collection DOAJ
description Brown adipose tissue (BAT) is the primary site for non-shivering thermogenesis in the body and plays a crucial role in maintaining core body temperature. However, its function gradually declines with age. To mitigate the age-related decline in BAT thermogenic capacity, we treated progeroid mice with metformin to investigate the potential mechanisms by which metformin can slow the reduction in BAT thermogenic function. We found that progeroid mice, after receiving metformin treatment, showed significant improvement in the senescent state of brown adipocytes through the activation of SIRT1, and effectively reduced mitochondrial oxidative stress. Additionally, metformin slowed the age-related decline in UCP1 expression levels in brown adipose tissue, thereby maintaining the thermogenic capacity of the progeroid mice. Moreover, metformin reduced inflammatory responses around senescent cells, further improving the overall senescent state of the tissue. These findings suggest that metformin can slow down the aging process in brown adipose tissue by targeting SIRT1, thereby enhancing its thermogenic capacity.
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institution Kabale University
issn 1873-6815
language English
publishDate 2025-03-01
publisher Elsevier
record_format Article
series Experimental Gerontology
spelling doaj-art-565cff3a3c9540ad8985e54a1b2f478d2025-02-07T04:46:51ZengElsevierExperimental Gerontology1873-68152025-03-01201112702Metformin delays the decline in thermogenic function of brown adipose tissue in a mouse model of Hutchinson-Gilford progeria syndromeXin Xiang0Yuyue Feng1Hongcheng Li2Wenbo Li3Jia Li4Zhu Xia5Hua Pang6Zhengjie Wang7Department of Nuclear Medicine, the First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, ChinaDepartment of Nuclear Medicine, the First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, ChinaDepartment of Nuclear Medicine, the First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, ChinaDepartment of Nuclear Medicine, the First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, ChinaDepartment of Nuclear Medicine, the First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, ChinaDepartment of Nuclear Medicine, the First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, ChinaCorresponding authors at: Department of Nuclear Medicine, the First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China.; Department of Nuclear Medicine, the First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, ChinaCorresponding authors at: Department of Nuclear Medicine, the First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China.; Department of Nuclear Medicine, the First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, ChinaBrown adipose tissue (BAT) is the primary site for non-shivering thermogenesis in the body and plays a crucial role in maintaining core body temperature. However, its function gradually declines with age. To mitigate the age-related decline in BAT thermogenic capacity, we treated progeroid mice with metformin to investigate the potential mechanisms by which metformin can slow the reduction in BAT thermogenic function. We found that progeroid mice, after receiving metformin treatment, showed significant improvement in the senescent state of brown adipocytes through the activation of SIRT1, and effectively reduced mitochondrial oxidative stress. Additionally, metformin slowed the age-related decline in UCP1 expression levels in brown adipose tissue, thereby maintaining the thermogenic capacity of the progeroid mice. Moreover, metformin reduced inflammatory responses around senescent cells, further improving the overall senescent state of the tissue. These findings suggest that metformin can slow down the aging process in brown adipose tissue by targeting SIRT1, thereby enhancing its thermogenic capacity.http://www.sciencedirect.com/science/article/pii/S0531556525000300Brown adipose tissueMetforminSIRT1SenescenceThermogenic function
spellingShingle Xin Xiang
Yuyue Feng
Hongcheng Li
Wenbo Li
Jia Li
Zhu Xia
Hua Pang
Zhengjie Wang
Metformin delays the decline in thermogenic function of brown adipose tissue in a mouse model of Hutchinson-Gilford progeria syndrome
Experimental Gerontology
Brown adipose tissue
Metformin
SIRT1
Senescence
Thermogenic function
title Metformin delays the decline in thermogenic function of brown adipose tissue in a mouse model of Hutchinson-Gilford progeria syndrome
title_full Metformin delays the decline in thermogenic function of brown adipose tissue in a mouse model of Hutchinson-Gilford progeria syndrome
title_fullStr Metformin delays the decline in thermogenic function of brown adipose tissue in a mouse model of Hutchinson-Gilford progeria syndrome
title_full_unstemmed Metformin delays the decline in thermogenic function of brown adipose tissue in a mouse model of Hutchinson-Gilford progeria syndrome
title_short Metformin delays the decline in thermogenic function of brown adipose tissue in a mouse model of Hutchinson-Gilford progeria syndrome
title_sort metformin delays the decline in thermogenic function of brown adipose tissue in a mouse model of hutchinson gilford progeria syndrome
topic Brown adipose tissue
Metformin
SIRT1
Senescence
Thermogenic function
url http://www.sciencedirect.com/science/article/pii/S0531556525000300
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