Insights into the radioprotective efficacy of Pterocarpus santalinus L. aqueous extract

• Published in: Fitoterapia 2024-07, Vol.176, p.105986, Article 105986
• Main Authors: Ghali, E.N. Hanuma Kumar, Sandopu, Sravan Kumar, Maurya, Dharmendra Kumar, Meriga, Balaji
• Format: Article
• Language: English
• Subjects: Antioxidant; Flavonoid; Immunomodulatory; Polyphenols; Radioprotection
• ISSN: 0367-326X
• DOI: 10.1016/j.fitote.2024.105986

In the present study, we have attempted a comprehensive assessment of the possible radioprotective efficacy of Pterocarpus santalinus aqueous extract (PSAE). All the studied models were gamma-irradiated with prior treatment with PSAE. First, the content of total phenols (4.061 μg/mg gallic acid equivalents), flavonoids (6.616 μg/mg quercetin equivalents), and tannins (0.008 mg/L of PSAE) were determined spectrophotometrically. Second, UHPLC-HRMS analysis was performed to identify the possible radioprotectors. Of those, santalins A & B are known for their usage as natural color in foods and alcoholic beverages identified in PSAE. Treatment was well tolerated with no side effects from PSAE. Later, it was shown that radiation-induced lethality significantly amended in PSAE-treated spleen lymphocytes as evidenced by reduced elevated levels of ROS and lipid peroxidation, restored total thiols and GSH: GSSG, inhibited DNA DSBs and cell death. Furthermore, an immunomodulation study was carried out because radiation exposure induces an inflammatory response. Our study shows that PSAE suppressed concanavalin A-induced T-cell proliferation as evidenced by CFSE dye dilution and CD69 antibody staining methods. Taken together, the current study explored the protective efficacy of PSAE from gamma radiation-inflicted injuries and hence we recommend PSAE as a potent radioprotective formulation. [Display omitted] •P. santalinus aqueous extract (PSAE) possesses in vitro radioprotective activity.•Quercetin, Rutin, and Apigenin were the major compounds detected in the PSAE.•PSAE protected spleen lymphocytes from DNA damage and cell death.•PSAE suppressed concanavalin A-induced T-cell proliferation.