Nguyen Hue Thi, Hoa-Tran Thi Nguyen, Tran Huy Quang, Nguyen Thuy Thi Thu
Phenikaa University Nano Institute (PHENA), Phenikaa University, Hanoi, 12116, Vietnam.
Faculty of Biomedical Sciences, Phenikaa University, Hanoi, 12116, Vietnam.
Chem Biodivers. 2025 Feb;22(2):e202400986. doi: 10.1002/cbdv.202400986. Epub 2024 Nov 12.
Although berberine (BBR) is well known as an active constituent in traditional medicines used in the treatment of gastrointestinal diseases, its potential against viral gastroenteritis has not been specifically reported. This study aims to investigate the antiviral activity of BBR against rotavirus and evaluate its cytotoxicity and pharmacological efficacies, including antioxidant and anti-inflammatory activities in vitro. Using ultraviolet-visible absorption spectroscopy, the saturation concentration of BBR was determined as 2261 μg/mL, indicating that BBR is a poor water-soluble compound. The inhibition rate of nitric oxide (NO) production of BBR solution at a concentration of 283 μg/mL was similar to that of Cardamonin 0.3 μM with a cell viability of 92.46±0.35 %, revealing the anti-inflammatory activity of BBR. The cytotoxicity of the BBR solution depended on its concentration, whereby the 50 % cytotoxicity concentration (CC) of BBR after 96 h exposure was 664 μg/mL. Investigation of cytopathic effects (CPEs) of MA104 cells treated with BBR and BBR-incubated rotavirus indicates that BBR could effectively inhibit the replication of rotavirus. CPEs were not observed in the cells inoculated with rotavirus (100TCID) which was pre-incubated with BBR for 96 hours at a BBR concentration of 283 μg/mL. Therefore, the study provides reliable results to demonstrate the ability of BBR to inhibit the replication of rotavirus.
尽管小檗碱(BBR)作为治疗胃肠道疾病的传统药物中的一种活性成分广为人知,但其对病毒性肠胃炎的潜在作用尚未有具体报道。本研究旨在探究BBR对轮状病毒的抗病毒活性,并评估其细胞毒性和药理功效,包括体外抗氧化和抗炎活性。采用紫外可见吸收光谱法,测定BBR的饱和浓度为2261μg/mL,表明BBR是一种水溶性较差的化合物。浓度为283μg/mL的BBR溶液对一氧化氮(NO)生成的抑制率与0.3μM小豆蔻明相似,细胞活力为92.46±0.35%,揭示了BBR的抗炎活性。BBR溶液的细胞毒性取决于其浓度,96小时暴露后BBR的50%细胞毒性浓度(CC)为664μg/mL。对用BBR处理的MA104细胞和经BBR孵育的轮状病毒的细胞病变效应(CPE)进行研究表明,BBR可有效抑制轮状病毒的复制。在接种了轮状病毒(100TCID)的细胞中未观察到CPE,该轮状病毒在283μg/mL的BBR浓度下预先与BBR孵育96小时。因此,该研究提供了可靠的结果来证明BBR抑制轮状病毒复制的能力。