Synthesis of Bis-Chalcones and Evaluation of Its Effect on Peroxide-Induced Cell Death and Lipopolysaccharide-Induced Cytokine Production

Molecules. 2023 Aug 30;28(17):6354. doi: 10.3390/molecules28176354.

Abstract

Plant secondary metabolites are important sources of biologically active compounds with wide pharmacological potentials. Among the different classes, the chalcones form integral pharmacologically active agents. Natural chalcones and bis-chalcones exhibit high antioxidant and anti-inflammatory properties in various experiments. Studies are also underway to explore more biologically active bis-chalcones by chemical synthesis of these compounds. In this study, the effects of six synthetic bis-chalcones were evaluated in intestinal epithelial cells (IEC-6); further, the anti-inflammatory potentials were studied in lipopolysaccharide-induced cytokine production in macrophages. The synthesized bis-chalcones differ from each other first of all by the nature of the aromatic cores (functional group substitution, and their position) and by the size of a central alicycle. The exposure of IEC-6 cells to peroxide radicals reduced the cell viability; however, pre-treatment with the bis-chalcones improved the cell viability in these cells. The mechanism of action was observed to be the increased levels of glutathione and antioxidant enzyme activities. Further, these bis-chalcones also inhibited the LPS-stimulation-induced inflammatory cytokine production in RAW 264.7 macrophages. Overall, the present study indicated the cytoprotective and anti-inflammatory abilities of synthetic bis-chalcones.

Keywords: anti-inflammatory activity; antioxidant activity; bis-chalcones; cytoprotection; peroxide toxicity.

MeSH terms

  • Antioxidants* / pharmacology
  • Cell Death
  • Chalcones* / pharmacology
  • Cytokines
  • Lipopolysaccharides / pharmacology
  • Peroxides

Substances

  • Antioxidants
  • Chalcones
  • Lipopolysaccharides
  • Peroxides
  • Cytokines

Grants and funding

This research was funded by Researchers Supporting Project Number (RSP2023R11), King Saud University, Riyadh, Saudi Arabia.