[Tacrolimus down-regulates the mRNA levels of IL-17 and IL-23 in the muscle tissues of mice with experimental autoimmune myositis]

Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2017 Feb;33(2):206-9.
[Article in Chinese]

Abstract

Objective: To measure the expression levels of interleukin-17( IL-17) and IL-23 mRNAs in the muscle tissue of the mice with experimental autoimmune myositis( EAM),and investigate the impact of tacrolimus( TAC) treatment on the mRNA levels of IL-17 and IL-23 and its therapeutic effect in EAM mice.

Methods: Fifteen female BALB / c mice were divided randomly into three groups,a normal control group,an EAM model group and a TAC-treated group. HE staining was used to observe the pathological changes for evaluating muscle inflammation of EAM mice. The expression levels of IL-17 and IL-23 mRNAs in the muscle tissues were measured by real-time fluorescence quantitative PCR. Then the correlations between the pathological changes and the expressions of IL-17 and IL-23 mRNAs were analyzed by Pearson methods.

Results: Compared with the normal controls,the mRNA levels of IL-17 and IL-23 were significantly up-regulated in the EAM model group,and they were down-regulated obviously after TAC treatment. Moreover,the mRNA levels of IL-17 and IL-23 had a significantly positive correlation with the pathological score of the muscle tissues. Compared with the EAM model group,the pathological score of the muscle tissues decreased in the TAC-treated group.

Conclusion: TAC can down-regulate mRNA levels of IL-17 and IL-23 in the EAM mice.

MeSH terms

  • Animals
  • Down-Regulation
  • Female
  • Immunosuppressive Agents / pharmacology*
  • Interleukin-17 / genetics
  • Interleukin-17 / metabolism*
  • Interleukin-23 / genetics
  • Interleukin-23 / metabolism*
  • Mice
  • Mice, Inbred BALB C
  • Muscle, Skeletal / metabolism*
  • Nervous System Autoimmune Disease, Experimental / metabolism*
  • RNA, Messenger / metabolism*
  • Random Allocation
  • Tacrolimus / pharmacology*

Substances

  • Immunosuppressive Agents
  • Interleukin-17
  • Interleukin-23
  • RNA, Messenger
  • Tacrolimus