Swertiamarin attenuates carbon tetrachloride (CCl4)-induced liver injury and inflammation in rats by regulating the TLR4 signaling pathway

  • Tao Wu Huazhong University of Science and Technology, Tongji Medical College, Puai Hospital, Department of Pharmacy
  • Qianrui Zhang General Hospital of the Yangtze River Shipping, Department of Pharmacy
  • Hongping Song Huazhong University of Science and Technology, Tongji Medical College, Puai Hospital, Department of Pharmacy
Keywords: Swertiamarin/effects, Carbon tetrachloride, Inflammation, TLR4, NF-κB

Abstract

The aim of the present study is to illustrate the effects of swertiamarin (STM), a natural iridoid from herbal medicines, on hepatic inflammation induced by carbon tetrachloride (CCl4) in rats. Male Sprague Dawley rats were exposed to CCl4 with or without STM co-administration for 8 weeks. Our results revealed that STM administration (100 and 200 mg/kg b.w.) significantly attenuated inflammation in livers of CCl4-treated rats. STM remarkably reduced the production of interleukin-1β (IL-1β), interleukin-6 (IL-6), tumor necrosis factor alpha (TNF-α), macrophage inflammatory protein-1a (MIP1α), and monocyte chemotactic protein-1 (MCP-1) in liver tissue of CCl4-treated rats. In addition, STM treatment downregulated connective tissue growth factor (CTGF) and ser307pIRS-1 expression, which was induced by CCl4 exposure. In the process of exploring the anti-inflammatory mechanisms of STM action, we demonstrated that STM significantly inhibited Toll-like receptor 4 (TLR4) and nuclear factor kappa B (NF-κB) p65 expression in the liver. In conclusion, these results suggested that the inhibition of CCl4-induced inflammation by STM was, at least in part, due to its regulation of the TLR4 /NF-κB signaling pathway.

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Published
2018-12-20
How to Cite
Wu, T., Zhang, Q., & Song, H. (2018). Swertiamarin attenuates carbon tetrachloride (CCl4)-induced liver injury and inflammation in rats by regulating the TLR4 signaling pathway. Brazilian Journal of Pharmaceutical Sciences, 54(4), e17449. https://doi.org/10.1590/s2175-97902018000417449
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Articles