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Delayed body development with reduced triglycerides levels in leptin transgenic pigs.

Authors :
Qing, Yubo
Jamal, Muhammad Ameen
Shi, Dejia
Zhao, Sumei
Xu, Kaixiang
Jiao, Deling
Zhao, Heng
Li, Honghui
Jia, Baoyu
Wang, Haizhen
Zhao, Hong-Ye
Wei, Hong-Jiang
Source :
Transgenic Research; Feb2022, Vol. 31 Issue 1, p59-72, 14p
Publication Year :
2022

Abstract

Leptin is a well-known adipokine that plays critical role in adiposity. To further investigate the role of leptin in adiposity, we utilized leptin overexpressing transgenic pigs and evaluated the effect of leptin on growth and development, fat deposition, and lipid metabolism at tissue and cell level. Leptin transgenic pigs were produced and divided into two groups: elevated leptin expression (leptin (+)) and normal leptin expression group (control). Results indicated that leptin (+) pigs had elevated leptin protein and mRNA expression levels and exhibited sluggish growth and development followed by decreased subcutaneous fat thickness, low serum triglycerides, saturated, unsaturated fatty acids and high cholesterol esters (p < 0.05). There were differences in the lipid metabolism related genes at different fat depots, including upregulation of PPARγ, AGPAT6, PLIN2, HSL and ATGL in subcutaneous, PPARγ in perirenal, and FAT/CD36 and PLIN2 in mesenteric adipose tissues and downregulation of AGPAT6 and ATGL in perirenal and AGPAT6 in mesenteric adipose tissues (p < 0.05). Additionally, in-vitro cultured leptin (+) preadipocytes exhibited upregulation of PPARγ, FAT/CD36, ACACA, AGPAT, PLIN2, ATGL and HSL as compared to control (p < 0.05). These findings suggested that homeostasis imbalance in lipolysis and lipogenesis at adipose tissue and adipocytes levels led to low subcutaneous fat depots in leptin overexpression pigs. These pigs can act as model for obesity and related metabolic disorder. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09628819
Volume :
31
Issue :
1
Database :
Complementary Index
Journal :
Transgenic Research
Publication Type :
Academic Journal
Accession number :
155105684
Full Text :
https://doi.org/10.1007/s11248-021-00288-1