Fenugreek attenuates obesity-induced inflammation and improves insulin resistance through downregulation of iRhom2/TACE

Life Sci. 2020 Oct 1:258:118222. doi: 10.1016/j.lfs.2020.118222. Epub 2020 Aug 6.

Abstract

Aims: We previously reported that fenugreek-derived 4-hydroxyisoleucine ameliorates insulin resistance via regulation of TNF-α converting enzyme (TACE) expression. In the present study, we further investigate the effects and mechanisms of fenugreek on obesity-induced inflammation and insulin signaling in the high-fat diet (HFD)-challenged obese mice.

Main methods: After 12 weeks of HFD intervention, mice were treated with the low or high dosages of fenugreek. Serum levels of glucose, insulin, lipid profile, inflammation cytokines, and adipokines were detected. Macrophage infiltration and adipose tissue morphology were observed. Western blot was conducted to investigate the expressions of inactive rhomboid 2 (iRhom2) and TACE as well as other signaling pathways in subcutaneous adipose tissue.

Key findings: We showed that fenugreek significantly suppressed body weight gain and fat accumulation in HFD-challenged obese mice. Meanwhile, fasting glucose, insulin, and HOMA-IR in fenugreek-treated mice were remarkably decreased, which were properly explained by fenugreek-induced activation of the insulin receptor signaling pathway. Moreover, the anti-inflammatory properties of fenugreek were shown by the decrease of systemic and local expressions of pro-inflammatory cytokines as well as reduced macrophage infiltration into adipose tissue. Additionally, fenugreek markedly deactivated NF-κB and JNK pathways. Finally, we demonstrated that fenugreek strikingly repressed the transcriptions and expressions of iRhom2 and TACE.

Significance: Fenugreek shows an encouraging and promising property in ameliorating insulin resistance and suppressing inflammation in obesity, which might be realized by fenugreek-mediated inhibition of iRhom2/TACE axis-facilitated TNF-α release from adipocytes.

Keywords: Fenugreek; Inflammation; Insulin resistance; Obesity; TACE; iRhom2.

MeSH terms

  • ADAM17 Protein / antagonists & inhibitors*
  • ADAM17 Protein / blood
  • Animals
  • Carrier Proteins / antagonists & inhibitors*
  • Carrier Proteins / blood
  • Dose-Response Relationship, Drug
  • Down-Regulation / drug effects
  • Down-Regulation / physiology
  • Inflammation / blood
  • Inflammation / drug therapy
  • Inflammation Mediators / antagonists & inhibitors*
  • Inflammation Mediators / blood
  • Insulin Resistance / physiology*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Obesity / blood
  • Obesity / drug therapy*
  • Plant Extracts / isolation & purification
  • Plant Extracts / pharmacology
  • Plant Extracts / therapeutic use
  • Seeds
  • Trigonella*

Substances

  • Carrier Proteins
  • Inflammation Mediators
  • Plant Extracts
  • iRhom2 protein, mouse
  • ADAM17 Protein
  • Adam17 protein, mouse