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Inguinal Fat Compensates Whole Body Metabolic Functionality in Partially Lipodystrophic Mice with Reduced PPARγ Expression

Title: Inguinal Fat Compensates Whole Body Metabolic Functionality in Partially Lipodystrophic Mice with Reduced PPARγ Expression
Authors: Cherng-Shyang Chang; Shang-Shiuan Yu; Li-Chun Ho; Shu-Hsin Chao; Ting-Yu Chou; Ai-Ning Shao; Ling-Zhen Kao; Chia-Yu Chang; Yu-Hsin Chen; Ming-Shan Wu; Pei-Jane Tsai; Nobuyo Maeda; Yau-Sheng Tsai
Source: International Journal of Molecular Sciences ; Volume 24 ; Issue 4 ; Pages: 3904
Publisher Information: Multidisciplinary Digital Publishing Institute
Publication Year: 2023
Collection: MDPI Open Access Publishing
Subject Terms: PPARγ; partial lipodystrophy; insulin sensitivity; fat depot; adipose tissue flexibility; inguinal fat-dependence index
Subject Geographic: agris
Description: Peroxisome proliferator-activated receptor γ (PPARγ) gene mutations in humans and mice lead to whole-body insulin resistance and partial lipodystrophy. It is unclear whether preserved fat depots in partial lipodystrophy are beneficial for whole-body metabolic homeostasis. We analyzed the insulin response and expression of metabolic genes in the preserved fat depots of PpargC/- mice, a familial partial lipodystrophy type 3 (FPLD3) mouse model resulting from a 75% decrease in Pparg transcripts. Perigonadal fat of PpargC/- mice in the basal state showed dramatic decreases in adipose tissue mass and insulin sensitivity, whereas inguinal fat showed compensatory increases. Preservation of inguinal fat metabolic ability and flexibility was reflected by the normal expression of metabolic genes in the basal or fasting/refeeding states. The high nutrient load further increased insulin sensitivity in inguinal fat, but the expression of metabolic genes became dysregulated. Inguinal fat removal resulted in further impairment of whole-body insulin sensitivity in PpargC/- mice. Conversely, the compensatory increase in insulin sensitivity of the inguinal fat in PpargC/- mice diminished as activation of PPARγ by its agonists restored insulin sensitivity and metabolic ability of perigonadal fat. Together, we demonstrated that inguinal fat of PpargC/- mice plays a compensatory role in combating perigonadal fat abnormalities.
Document Type: text
File Description: application/pdf
Language: English
Relation: Molecular Endocrinology and Metabolism; https://dx.doi.org/10.3390/ijms24043904
DOI: 10.3390/ijms24043904
Availability: https://doi.org/10.3390/ijms24043904
Rights: https://creativecommons.org/licenses/by/4.0/
Accession Number: edsbas.3C19A7B
Database: BASE