Abstract

Background: White adipose tissue (WAT) browning confers beneficial effects on metabolic diseases. However, visceral adipose tissue (VAT) is not as susceptible to browning as subcutaneous adipose tissue (SAT). Aim: Interpreting the heterogeneity of VAT and SAT in brown remodeling and provide promising lipid targets to promote WAT browning. Methods: We first investigated the effects of β3-adrenergic stimulation by CL316,243 on systemic metabolism. Then, high-coverage targeted lipidomics approach with multiple reaction monitoring (MRM) was utilized to provide extensive detection of lipid metabolites in VAT and SAT. Results: CL316,243 notably ameliorated the systemic metabolism and induced brown remodeling of SAT but browning resistance of VAT. Comprehensive lipidomics analysis revealed browning heterogeneity of VAT and SAT with more dramatic alteration of lipid classes and species in VAT rather than SAT, though VAT is resistant to browning. Adrenergic stimulation differentially affected glycerides content in VAT and SAT and boosted the abundance of more glycerophospholipids species in VAT than in SAT. Besides, CL316,243 increased sphingolipids in VAT without changes in SAT, meanwhile, elevated cardiolipin species more prominently in VAT than in SAT. Conclusions: We demonstrated the browning heterogeneity of WAT and identified potential lipid biomarkers which may provide lipid targets for overcoming VAT browning resistance.

Highlights

  • White adipose tissue (WAT) and brown adipose tissue (BAT), two general types of adipose tissue, are critical for maintenance of metabolic homeostasis

  • We identified some species of cardiolipin as previous observations mitochondrial cardiolipin composition in diverse eukaryotes the important potential biomarkers of WAT browning, especially C72:8 (18:2) and C72:7 (18:2)

  • WAT browning has been proposed as a promising therapeutic approach against obesity; visceral adipose tissue (VAT), the most pathogenic adipose tissue, is less susceptible to browning than subcutaneous adipose tissue (SAT) evidenced by our current study

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Summary

Introduction

White adipose tissue (WAT) and brown adipose tissue (BAT), two general types of adipose tissue, are critical for maintenance of metabolic homeostasis. WAT is typically classified as subcutaneous adipose tissue (SAT) and visceral adipose tissue (VAT) [1]. White adipose tissue (WAT) browning confers beneficial effects on metabolic diseases. Aim: Interpreting the heterogeneity of VAT and SAT in brown remodeling and provide promising lipid targets to promote WAT browning. Results: CL316,243 notably ameliorated the systemic metabolism and induced brown remodeling of SAT but browning resistance of VAT. Comprehensive lipidomics analysis revealed browning heterogeneity of VAT and SAT with more dramatic alteration of lipid classes and species in VAT rather than SAT, though VAT is resistant to browning. Conclusions: We demonstrated the browning heterogeneity of WAT and identified potential lipid biomarkers which may provide lipid targets for overcoming VAT browning resistance

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