Faculty of Food Science and Engineering, Kunming University of Science and Technology, Kunming, 650500, China; National and Local Joint Engineering Research Center for Green Preparation Technology of Biobased Materials, Yunnan Minzu University, Kunming, 650500, China.
Faculty of Food Science and Engineering, Kunming University of Science and Technology, Kunming, 650500, China.
Food Chem Toxicol. 2023 May;175:113752. doi: 10.1016/j.fct.2023.113752. Epub 2023 Mar 31.
Anneslea Fragrans Wall. (AF) is a medicinal and edible plant distributed in China. Its leaves and barks are generally used for the treatments of diarrhea, fever, and liver diseases. While its ethnopharmacological application against liver diseases has not been fully studied. This study was aimed to evaluate the hepatoprotective effect of ethanolic extract from A. fragrans (AFE) on CCl induced liver injury in mice. The results showed that AFE could effectively reduce plasma activities of ALT and AST, increase antioxidant enzymes activities (SOD and CAT) and GSH level, and decrease MDA content in CCl induced mice. AFE effectively decreased the expressions of inflammatory cytokines (IL-1β, IL-6, TNF-α, COX-2 and iNOS), cell apoptosis-related proteins (Bax, caspase-3 and caspase-9) and increased Bcl-2 protein expression via inhibiting MAPK/ERK pathway. Additionally, TUNEL staining, Masson and Sirius red staining, immunohistochemical analyses revealed that AFE could inhibit the CCl-induced hepatic fibrosis formation via reducing depositions of α-SMA, collagen I and collagen III proteins. Conclusively, the present study demonstrated that AFE had an hepatoprotective effect by suppressing MAPK/ERK pathway to inhibit oxidative stress, inflammatory response and apoptosis in CCl-induced liver injury mice, suggesting that AFE might be served as a hepatoprotective ingredient in the prevention and treatment of liver injury.
Anneslea fragrans Wall.(AF)是一种分布在中国的药用和食用植物。其叶和皮通常用于治疗腹泻、发热和肝脏疾病。然而,其在肝脏疾病方面的民族药理学应用尚未得到充分研究。本研究旨在评估来自 A. fragrans(AFE)的乙醇提取物对 CCl 诱导的小鼠肝损伤的保护作用。结果表明,AFE 能有效降低 CCl 诱导的小鼠血浆 ALT 和 AST 活性,增加抗氧化酶(SOD 和 CAT)活性和 GSH 水平,降低 MDA 含量。AFE 还通过抑制 MAPK/ERK 通路有效降低炎症细胞因子(IL-1β、IL-6、TNF-α、COX-2 和 iNOS)、细胞凋亡相关蛋白(Bax、caspase-3 和 caspase-9)的表达,增加 Bcl-2 蛋白表达。此外,TUNEL 染色、Masson 和 Sirius 红染色、免疫组化分析表明,AFE 通过减少α-SMA、胶原 I 和胶原 III 蛋白的沉积,抑制 CCl 诱导的肝纤维化形成。综上所述,本研究表明,AFE 通过抑制 MAPK/ERK 通路抑制 CCl 诱导的肝损伤小鼠的氧化应激、炎症反应和细胞凋亡,具有肝保护作用,提示 AFE 可能作为预防和治疗肝损伤的肝保护成分。