Jairaman Chitra, Alehaideb Zeyad I, Yacoob Syed Ali Mohamed, Alghamdi Sahar S, Suliman Rasha S, Venkataraman Anuradha, Alghanem Bandar, Sivanesan Senthilkumar, Vijayaraghavan Rajagopalan, Rameshbabu Saranya, Pari Shree Mukilan, Matou-Nasri Sabine
PG & Research Department of Biotechnology, Mohamed Sathak College of Arts & Science, Shollinganallur, Chennai 600119, India.
Medical Research Core Facility and Platforms, King Abdullah International Medical Research Center (KAIMRC), King Saud bin Abdulaziz University for Health Sciences (KSAU-HS), Ministry of National Guard-Health Affairs (MNGHA), Riyadh 11481, Saudi Arabia.
Metabolites. 2022 Oct 25;12(11):1021. doi: 10.3390/metabo12111021.
The bark extract of (BERM) was recently reported for its prominent in vitro protective effects against liver cell line toxicity caused by various toxicants, including ethanol. Here, we aimed to verify the in vivo hepatoprotective effects of BERM against ethanol intoxication with the prediction of potential targets employing in silico studies. An oral administration of different concentrations (100, 200 and 400 mg/kg body weight) of BERM before high-dose ethanol via intraperitoneal injection was performed in mice. On day 7, liver sections were dissected for histopathological examination. The ethanol intoxication caused liver injury and large areas of necrosis. The pre-BERM administration decreased the ethanol-induced liver damage marker tumor necrosis factor-alpha () expression, reduced hepatotoxicity revealed by nuclear deoxyribonucleic acid (DNA) fragmentation and decreased oxidative stress indicated by malondialdehyde and glutathione contents. Our in silico studies have identified BERM-derived metabolites exhibiting the highest predicted antioxidant and free radical scavenger activities. Molecular docking studies showed that most of the metabolites were predicted to be enzyme inhibitors such as carbonic anhydrase inhibitors, which were reported to stimulate the antioxidant defense system. The metabolites predominantly presented acceptable pharmacokinetics and safety profiles, suggesting them as promising new antioxidant agents. Altogether, the BERM extract exerts antioxidative activities and shows promising hepatoprotective effects against ethanol intoxication. Identification of related bioactive compounds will be of interest for future use at physiological concentrations in ethanol-intoxicated individuals.
最近有报道称,[植物名称]树皮提取物(BERM)对包括乙醇在内的多种毒物引起的肝细胞系毒性具有显著的体外保护作用。在此,我们旨在通过计算机模拟研究预测潜在靶点,验证BERM对乙醇中毒的体内肝脏保护作用。在小鼠腹腔注射高剂量乙醇前,口服给予不同浓度(100、200和400 mg/kg体重)的BERM。在第7天,解剖肝脏切片进行组织病理学检查。乙醇中毒导致肝损伤和大面积坏死。预先给予BERM可降低乙醇诱导的肝损伤标志物肿瘤坏死因子-α(TNF-α)的表达,减少由核脱氧核糖核酸(DNA)片段化显示的肝毒性,并降低由丙二醛和谷胱甘肽含量表明的氧化应激。我们的计算机模拟研究确定了BERM衍生的代谢物具有最高预测的抗氧化和自由基清除活性。分子对接研究表明,大多数代谢物预计为酶抑制剂,如碳酸酐酶抑制剂,据报道可刺激抗氧化防御系统。这些代谢物主要呈现出可接受的药代动力学和安全性概况,表明它们是有前途的新型抗氧化剂。总之,BERM提取物具有抗氧化活性,对乙醇中毒显示出有前途的肝脏保护作用。鉴定相关生物活性化合物将有助于未来在乙醇中毒个体的生理浓度下使用。