Estrogen restores disordered lipid metabolism in visceral fat of prediabetic mice

Su-Huan Liu; Zhao-Shui Shangguan; Paiziliya Maitiaximu; Zhi-Peng Li; Xin-Xin Chen; Can-Dong Li

doi:10.4239/wjd.v15.i5.988

Estrogen restores disordered lipid metabolism in visceral fat of prediabetic mice

World J Diabetes. 2024 May 15;15(5):988-1000. doi: 10.4239/wjd.v15.i5.988.

Authors

Su-Huan Liu^{1

2}, Zhao-Shui Shangguan², Paiziliya Maitiaximu², Zhi-Peng Li², Xin-Xin Chen², Can-Dong Li³

Affiliations

¹ Research Base of Chinese Medicine Syndrome, Fujian University of Traditional Chinese Medicine, Fuzhou 350122, Fujian Province, China.
² Research Center for Translational Medicine, The First Affiliated Hospital of Xiamen University, School of Medicine, Xiamen University, Xiamen 361003, Fujian Province, China.
³ Research Base of Chinese Medicine Syndrome, Fujian University of Traditional Chinese Medicine, Fuzhou 350122, Fujian Province, China. fjzylcd@126.com.

Abstract

Background: Visceral obesity is increasingly prevalent among adolescents and young adults and is commonly recognized as a risk factor for type 2 diabetes. Estrogen [17β-estradiol (E2)] is known to offer protection against obesity via diverse me-chanisms, while its specific effects on visceral adipose tissue (VAT) remain to be fully elucidated.

Aim: To investigate the impact of E2 on the gene expression profile within VAT of a mouse model of prediabetes.

Methods: Metabolic parameters were collected, encompassing body weight, weights of visceral and subcutaneous adipose tissues (VAT and SAT), random blood glucose levels, glucose tolerance, insulin tolerance, and overall body composition. The gene expression profiles of VAT were quantified utilizing the Whole Mouse Genome Oligo Microarray and subsequently analyzed through Agilent Feature Extraction software. Functional and pathway analyses were conducted employing Gene Ontology and Kyoto Encyclopedia of Genes and Genomes analyses, respectively.

Results: Feeding a high-fat diet (HFD) moderately increased the weights of both VAT and SAT, but this increase was mitigated by the protective effect of endogenous E2. Conversely, ovariectomy (OVX) led to a significant increase in VAT weight and the VAT/SAT weight ratio, and this increase was also reversed with E2 treatment. Notably, OVX diminished the expression of genes involved in lipid metabolism compared to HFD feeding alone, signaling a widespread reduction in lipid metabolic activity, which was completely counteracted by E2 administration. This study provides a comprehensive insight into E2's local and direct protective effects against visceral adiposity in VAT at the gene level.

Conclusion: In conclusion, the present study demonstrated that the HFD-induced over-nutritional challenge disrupted the gene expression profile of visceral fat, leading to a universally decreased lipid metabolic status in E2 deficient mice. E2 treatment effectively reversed this condition, shedding light on the mechanistic role and therapeutic potential of E2 in combating visceral obesity.

Keywords: Energy metabolism; Estrogen; Obesity, Visceral adiposity; Type 2 diabetes.