Abstract | OBJECTIVES: 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.
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Authors | Pin Chen, Lu Lin, Xiangjin Xu, Zhenting Zhang, Wei Cai, Zhulin Shao, Shengping Chen, Xiangqi Chen, Qiaoling Weng |
Journal | The Journal of dermatological treatment
(J Dermatolog Treat)
Vol. 32
Issue 7
Pg. 745-751
(Nov 2021)
ISSN: 1471-1753 [Electronic] England |
PMID | 31868553
(Publication Type: Journal Article)
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Chemical References |
- Interleukin-17
- Interleukin-23
- Liraglutide
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Topics |
- 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
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