Frontiers in Pharmacology (Apr 2023)

Licorice extract inhibits the cGAS-STING pathway and protects against non-alcoholic steatohepatitis

  • Wei Luo,
  • Wei Luo,
  • Wei Luo,
  • Guang Xu,
  • Guang Xu,
  • Guang Xu,
  • Zheng Song,
  • Zheng Song,
  • Wenqing Mu,
  • Wenqing Mu,
  • Wenqing Mu,
  • Jincai Wen,
  • Jincai Wen,
  • Siwen Hui,
  • Siwen Hui,
  • Jia Zhao,
  • Jia Zhao,
  • Jia Zhao,
  • Xiaoyan Zhan,
  • Xiaoyan Zhan,
  • Zhaofang Bai,
  • Zhaofang Bai,
  • Xiaohe Xiao,
  • Xiaohe Xiao,
  • Xiaohe Xiao

DOI
https://doi.org/10.3389/fphar.2023.1160445
Journal volume & issue
Vol. 14

Abstract

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Background: Inflammation and fibrosis are typical symptoms of non-alcoholic steatohepatitis (NASH), which is one of the most common chronic liver diseases. The cGAS-STING signaling pathway has been implicated in the progression of NASH, and targeting this pathway may represent a new therapeutic strategy. Licorice is a widely used herb with anti-inflammatory and liver-protective properties. In this study, we assessed the effect of licorice extract on the cGAS-STING pathway.Methods: Bone marrow-derived macrophages (BMDMs) were treated with licorice extract and then stimulated with HT-DNA, 2'3'-cGAMP, or other agonists to activate the cGAS-STING pathway. Quantitative real-time PCR and western blot were conducted to analyze whether licorice extract could affect the cGAS-STING pathway. Methionine and choline-deficient diet (MCD) was used to induce NASH in mice, which were treated with licorice extract (500 mg/kg) by gavage and/or c-176 (15 mg/kg) by intraperitoneal injection every 2 days. After 6 weeks of treatment, histological analysis of liver tissue was performed, along with measurements of plasma biochemical parameters.Results: Licorice extract inhibits cGAS-STING pathway activation. Mechanistically, it might function by inhibiting the oligomerization of STING. Treatment with licorice extract reduced inflammation and fibrosis in MCD diet-induced NASH mice models. Furthermore, we found that the therapeutic effect of combination treatment with licorice extract and C-176 (STING inhibitor) on the pathology and fibrosis of MCD diet-induced NASH models was similar to that of licorice extract or C-176 administered alone.Conclusion: Licorice extract can inhibit the cGAS-STING pathway and improve hepatic inflammation and fibrosis in NASH mice models. It strongly suggests that licorice extract may be a candidate therapeutic for NASH.

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