4.5 Article

Pro-inflammatory cytokine molecules from Boswellia serrate suppresses lipopolysaccharides induced inflammation demonstrated in an in-vivo zebrafish larval model

Journal

MOLECULAR BIOLOGY REPORTS
Volume 49, Issue 8, Pages 7425-7435

Publisher

SPRINGER
DOI: 10.1007/s11033-022-07544-5

Keywords

Boswellia serrata; Anti-inflammation; Zebrafish model; Pro-inflammatory cytokines; Acetyl-11-keto-boswellic; 11-keto-beta-boswellic acid

Funding

  1. King Saud University, Riyadh, Saudi Arabia [RSP2022R414]

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The study found that Boswellia serrata extract has antioxidant and anti-inflammatory properties, and can protect against LPS-induced inflammation in zebrafish larvae. It also inhibits the expression of specific inflammatory genes.
Background Boswellia serrate is an ancient and highly valued ayurvedic herb. Its extracts have been used in medicine for centuries to treat a wide variety of chronic inflammatory diseases. However, the mechanism by which B. serrata hydro alcoholic extract inhibited pro-inflammatory cytokines in zebrafish (Danio rerio) larvae with LPS-induced inflammation remained unknown. Methods LC-MS analysis was used to investigate the extract's phytochemical components. To determine the toxicity of B. serrata extract, cytotoxicity and embryo toxicity tests were performed. The in-vivo zebrafish larvae model was used to evaluate the antioxidant and anti-inflammatory activity of B. serrata extract. Results According to an in silico study using molecular docking and ADMET, the compounds acetyl-11-keto-boswellic and 11-keto-beta-boswellic acid present in the extract had higher binding affinity for the inflammatory specific receptor, and it is predicted to be an orally active molecule. In both in-vitro L6 cells and in-vivo zebrafish larvae, 160 mu g/mL concentration of extract caused a high rate of lethality. The extract was found to have a protective effect against LPS-induced inflammation at concentrations ranged between 10 and 80 mu g/mL. In zebrafish larvae, 80 mu g/mL of treatment significantly lowered the level of intracellular ROS, apoptosis, lipid peroxidation, and nitric oxide. Similarly, zebrafish larvae treated with B. serrata extract (80 mu g/mL) showed an increased anti-inflammatory activity by lowering inflammatory specific gene expression (iNOS, TNF-alpha, COX-2, and IL-1). Conclusions Overall, our findings suggest that B. serrata can act as a potent redox scavenger against LPS-induced inflammation in zebrafish larvae and an inhibitor of specific inflammatory genes.

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