Molecules (Jan 2023)

Hepatoprotective Effect of a New FFAR1 Agonist—N-Alkylated Isobornylamine

  • Darya Pon`kina,
  • Sergey Kuranov,
  • Mikhail Khvostov,
  • Nataliya Zhukova,
  • Yulia Meshkova,
  • Mariya Marenina,
  • Olga Luzina,
  • Tatyana Tolstikova,
  • Nariman Salakhutdinov

DOI
https://doi.org/10.3390/molecules28010396
Journal volume & issue
Vol. 28, no. 1
p. 396

Abstract

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Free fatty acid receptor-1 (FFAR1) is one of the possible therapeutic targets in the search for new hepatoprotective drugs. FFAR1 agonists were found to have hypolipidemic, antifibrotic, anti-inflammatory, antiproliferative and antioxidant effects in addition to hypoglycemic action. In this work, we conducted a study of the hepatoprotective effect of the compound QS-528 (previously discovered as an agonist of FFAR1) at doses of 60, 90, 120 and 150 mg/kg on carbon tetrachloride (CCl4)-induced liver injury. At the end of the experiment, a biochemical blood assay demonstrated that the introduction of QS-528 dose-dependently reduces the levels of liver enzymes (AST, ALT and ALKP). Histological and morphometric studies of animals’ livers treated with QS-528 at doses of 120 and 150 mg/kg showed a decrease in degenerative/necrotic changes in hepatocytes and an increase in the regenerative activity of the liver. In addition, no toxicity at a single oral dose of 1000 mg/kg and an increase in HepG2 cell viability in vitro were found. Thus, the compound QS-528 was found to exhibit a hepatoprotective effect against CCl4-induced toxic liver damage.

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