Kinin B1 receptor deficiency promotes enhanced adipose tissue thermogenic response to β3-adrenergic stimulation

Inflamm Res. 2024 Sep;73(9):1565-1579. doi: 10.1007/s00011-024-01917-1. Epub 2024 Jul 17.

Abstract

Objective and design: Kinin B1 receptor (B1R) has a key role in adipocytes to protect against obesity and glycemic metabolism, thus becoming a potential target for regulation of energy metabolism and adipose tissue thermogenesis.

Material or subjects: Kinin B1 knockout mice (B1KO) were subjected to acute induction with CL 316,243 and chronic cold exposure.

Methods: Metabolic and histological analyses, gene and protein expression and RNA-seq were performed on interscapular brown adipose tissue (iBAT) and inguinal white adipose tissue (iWAT) of mice.

Results: B1KO mice, under acute effect of CL 316,243, exhibited increased energy expenditure and upregulated thermogenic genes in iWAT. They were also protected from chronic cold, showing enhanced non-shivering thermogenesis with increased iBAT mass (~ 90%) and recruitment of beige adipocytes in iWAT (~ 50%). Positive modulation of thermogenic and electron transport chain genes, reaching a 14.5-fold increase for Ucp1 in iWAT. RNA-seq revealed activation of the insulin signaling pathways for iBAT and oxidative phosphorylation, tricarboxylic acid cycle, and browning pathways for iWAT.

Conclusion: B1R deficiency induced metabolic and gene expression alterations in adipose tissue, activating thermogenic pathways and increasing energy metabolism. B1R antagonists emerge as promising therapeutic targets for regulating obesity and associated metabolic disorders, such as inflammation and diabetes.

Keywords: Adipocyte; Adipose tissue; Kinins; Metabolic diseases; Metabolism; Thermogenesis.

MeSH terms

  • Adipose Tissue, Brown* / drug effects
  • Adipose Tissue, Brown* / metabolism
  • Adipose Tissue, White* / drug effects
  • Adipose Tissue, White* / metabolism
  • Adrenergic beta-3 Receptor Agonists / pharmacology
  • Animals
  • Cold Temperature
  • Dioxoles* / pharmacology
  • Energy Metabolism / drug effects
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout*
  • Receptor, Bradykinin B1* / genetics
  • Receptor, Bradykinin B1* / metabolism
  • Receptors, Adrenergic, beta-3 / genetics
  • Receptors, Adrenergic, beta-3 / metabolism
  • Thermogenesis* / drug effects
  • Thiazoles / pharmacology
  • Uncoupling Protein 1 / genetics
  • Uncoupling Protein 1 / metabolism

Substances

  • Adrenergic beta-3 Receptor Agonists
  • Dioxoles
  • disodium (R,R)-5-(2-((2-(3-chlorophenyl)-2-hydroxyethyl)-amino)propyl)-1,3-benzodioxole-2,3-dicarboxylate
  • Receptor, Bradykinin B1
  • Receptors, Adrenergic, beta-3
  • Thiazoles
  • Uncoupling Protein 1
  • Adrb3 protein, mouse