Design, synthesis, and evaluation of mono‐carbonyl analogues of curcumin (MCACs) as potential antioxidants against periodontitis. (18th February 2021)

• Record Type: Journal Article
• Authors: Zhao, Ya; Zheng, Zhiwei; Zhang, Menghan; Wang, Yi; Hu, Rongdang; Lin, Weijia; Huang, Chenyang; Xu, Chuchu; Wu, Jianzhang; Deng, Hui
• Is Part Of: Journal of periodontal research. Volume 56:Number 4(2021)
• Page Start: 656
• Page End: 666
• Publication Date: 2021-02-18
• Subjects: Antioxidants -- Curcumin -- Mono‐carbonyl analogues of curcumin (MCACs) -- Nuclear factor erythroid 2‐related factor 2 (Nrf2) -- periodontal disease; Periodontics -- Periodicals; 617.632
• DOI: 10.1111/jre.12862
• Languages: English
• ISSNs: 0022-3484

Abstract

Abstract: Background and objective: The application of curcumin is limited by its instability. Mono‐carbonyl analogues of curcumin (MCACs) are structurally stable, yet the intermediate bridging ketones in their skeletons account for increased toxicity. This study aimed to synthesize and screen MCACs that exhibit low cytotoxicity and high antioxidant ability, and the effects of MCACs on experimental periodontitis were also investigated. Materials and methods: The cytotoxicity of MCACs on MC3 T3‐E1 was determined by MTT assay. The antioxidant capacity was investigated by the cell viability against H2 O2 ‐induced damage and the level of reactive oxygen species (ROS) and malondialdehyde (MDA). The localization and protein expression of nuclear factor erythroid 2‐related factor 2 (Nrf2) and heme oxygenase‐1 (HO‐1) was detected by immunofluorescence and western blot, respectively. In addition, MCAC was intragastrically administrated in rats with ligature‐induced experimental periodontitis. The effects were assessed by bone resorption, as well as the immunohistology staining of inflammatory and oxidative stress markers. Results: MCACs with cyclopentanone and containing pyrone showed lower toxicity than natural curcumin were synthesized (1A ‐10A, 1H ‐10H ), among which, 1A exhibited the most potent cytoprotective effect against H2 O2 ‐induced damage. Such effects could be explained by the reduced MDA and ROS level, possibly through the nucleus translocation of Nrf2 and the induction of HO‐1. Micro‐CT results further indicated that 1A significantly reduced bone loss, along with an increased level of Nrf2 and HO‐1, and decreased TNF‐α and IL‐1β. Conclusion: The present study has synthesized a novel antioxidant MCAC 1A with good biosafety and stability. MCAC 1A could serve as a host response modulator with preventive and protective effects on periodontitis.