Liraglutide improved inflammation via mediating IL-23/Th-17 pathway in obese diabetic mice with psoriasiform skin

J Dermatolog Treat. 2021 Nov;32(7):745-751. doi: 10.1080/09546634.2019.1708853. Epub 2020 Jan 3.

Abstract

Objectives: The purpose of this study was to investigate the effect of liraglutide on obesity diabetic mice with psoriasiform skin inflammation.

Methods: Wild-type mice and db/db mice were randomly divided into five groups (n = 6): including the control group which received Vaseline, the imiquimod (IMQ)-induction group and the liraglutide-treatment group. The advanced treatment with liraglutide (0.3 mg/kg/d) for 4 weeks before IMQ induced psoriatic skin inflammation in the db/db + IMQ + Lira group. Basic parameters of diabetes, PASI, histopathology of skin, the expression of IL-17A, IL-23, IL-22, and TNF-α in the skin of back were measured.

Results: After IMQ induction, the psoriatic skin inflammation and pathological changes in the db/db + IMQ group were more serious than those in the WT + IMQ group. The glucose metabolism and insulin resistance of in the db/db + IMQ + Lira group were significantly improved, Psoriasis Area and Severity Index (PASI) was significantly reduced, and the protein and mRNA expressions of IL-23, IL-17, IL-22, and TNF-α in the back skin tissues were decreased.

Conclusions: Liraglutide can improve psoriasis skin lesions of obese diabetic mice, and the mechanism may be related to the inhibition of the expression of IL-23, IL-17, IL-22, and TNF-α through the IL-23/Th-17 pathway.

Keywords: Diabetes; glucagon-like peptide-1; inflammation; liraglutide; psoriasis.

MeSH terms

  • Animals
  • Diabetes Mellitus, Experimental / complications
  • Disease Models, Animal
  • Inflammation
  • Interleukin-17*
  • Interleukin-23*
  • Liraglutide* / therapeutic use
  • Mice
  • Mice, Obese
  • Obesity / complications
  • Psoriasis* / drug therapy
  • Skin

Substances

  • Interleukin-17
  • Interleukin-23
  • Liraglutide