陈智伟, 杨建波, 陈子涵, 马双成, 孙华. 何首乌中顺式(反式)-大黄素-大黄素二蒽酮肝保护活性研究J. 药学学报, 2023, 58(3): 711-720. DOI: 10.16438/j.0513-4870.2022-1057
引用本文: 陈智伟, 杨建波, 陈子涵, 马双成, 孙华. 何首乌中顺式(反式)-大黄素-大黄素二蒽酮肝保护活性研究J. 药学学报, 2023, 58(3): 711-720. DOI: 10.16438/j.0513-4870.2022-1057
CHEN Zhi-wei, YANG Jian-bo, CHEN Zi-han, MA Shuang-cheng, SUN Hua. Hepatoprotective activity of cis-(trans)-emodin-emodin dianthrone from Polygonum multiflorum Thunb.J. Acta Pharmaceutica Sinica, 2023, 58(3): 711-720. DOI: 10.16438/j.0513-4870.2022-1057
Citation: CHEN Zhi-wei, YANG Jian-bo, CHEN Zi-han, MA Shuang-cheng, SUN Hua. Hepatoprotective activity of cis-(trans)-emodin-emodin dianthrone from Polygonum multiflorum Thunb.J. Acta Pharmaceutica Sinica, 2023, 58(3): 711-720. DOI: 10.16438/j.0513-4870.2022-1057

何首乌中顺式(反式)-大黄素-大黄素二蒽酮肝保护活性研究

Hepatoprotective activity of cis-(trans)-emodin-emodin dianthrone from Polygonum multiflorum Thunb.

  • 摘要: 顺式-大黄素-大黄素二蒽酮(化合物1) 和反式-大黄素-大黄素二蒽酮(化合物2) 均从何首乌的干燥块根中分离得到。在本研究中, 首先评价了化合物12的混合样品(大黄素-大黄素二蒽酮) 对刀豆蛋白A (concanavalin A, ConA) 诱导ICR小鼠急性肝损伤的保护作用及可能的作用机制。结果表明, 大黄素-大黄素二蒽酮在1 mg·kg-1可显著降低肝损伤小鼠血清谷丙转氨酶(alanine aminotransferase, ALT) 和谷草转氨酶(aspartate aminotransferase, AST) 水平(P < 0.05), 改善肝组织病理损伤。1 mg·kg-1大黄素-大黄素二蒽酮还能显著降低肝组织Bcl-2相关X蛋白(Bcl-2 assaciated X protein, Bax) mRNA水平, 同时升高B淋巴细胞瘤-2 (B-cell lymphoma-2, Bcl-2) mRNA表达水平(P < 0.05)。进一步利用过氧化氢(H2O2) 诱导的肝细胞损伤模型评价化合物12对肝细胞损伤的保护活性。结果表明, 化合物12可显著抑制H2O2诱导的肝细胞损伤, 降低细胞培养上清转氨酶ALT、AST及碱性磷酸酶(alkaline phosphatase, ALP)、乳酸脱氢酶(lactate dehydrogenase, LDH) 水平, 提高细胞存活率。化合物12显著改善H2O2诱导的肝细胞氧化应激状态, 0.5 µmol·L-1化合物1可显著提高肝细胞内超氧化物歧化酶(superoxide dismutase, SOD) 的酶活力(P < 0.01), 0.5 µmol·L-1化合物2可显著降低细胞内活性氧(reactive oxygen species, ROS) 含量、提高SOD酶活力和还原型谷胱甘肽(glutathione, GSH) 的含量(P < 0.01)。同时, 0.5 µmol·L-1化合物12可通过提高Bcl-2/Bax蛋白表达比例(P < 0.05)、降低剪切体半胱天冬酶3 (cleaved caspase-3) 和前体胱天蛋白酶3 (pro caspase-3) 的比例抑制肝细胞凋亡(P < 0.05)。本研究表明, 何首乌中大黄素-大黄素二蒽酮成分具有抗肝组织损伤活性, 其中化合物12可通过抑制细胞凋亡和氧化应激发挥肝保护作用。本研究为常用量何首乌肝补益功效提供了重要的物质基础。本研究中所有动物实验在开展前经过中国医学科学院药物研究所实验动物管理和使用委员会(IACUC) 的审查批准。

     

    Abstract: The cis-emodin-emodin dianthrone (compound 1) and trans-emodin-emodin dianthrone (compound 2) were extracted from Polygonum multiflorum Thunb. The protective effect and mechanism of compound 1 and compound 2 (emodin-emodin dianthrones) on acute liver injury induced by concanavalin A (ConA) in ICR mice was first investigated. The results indicated that emodin-emodin dianthrones at 1 mg·kg-1 significantly reduced serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) level (P < 0.05). Emodin-emodin dianthrones also improved liver histopathological damage in liver-injured mice. The level of Bcl-2-associated X protein (Bax) mRNA in liver was significantly reduced by 1 mg·kg-1 of emodin-emodin dianthrones, while the level of B-cell lymphoma-2 (Bcl-2) mRNA expression was significantly increased (P < 0.05). The protective activity of compounds 1 and 2 against hepatocyte injury was further evaluated by hydrogen peroxide (H2O2)-induced hepatocyte injury. Compounds 1 and 2 significantly inhibited H2O2-induced hepatocyte injury and reduced the levels of ALT, AST, alkaline phosphatase (ALP), and lactate dehydrogenase (LDH) in cell culture. Compounds 1 and 2 also significantly improved the cell survival rate and decreased H2O2-induced oxidative stress in hepatocytes. Compound 1 (0.5 µmol·L-1) significantly increased the enzymatic activity of superoxide dismutase (SOD) in hepatocytes (P < 0.01), and 0.5 µmol·L-1 of compound 2 significantly decreased the intracellular reactive oxygen species (ROS), increased SOD enzyme activity, and glutathione (GSH) content (P < 0.01). Compounds 1 and 2 at 0.5 µmol·L-1 also inhibited hepatocyte apoptosis by increasing the protein expression ratio of Bcl-2/Bax (P < 0.05) and decreasing the protein expression ratio of cleaved caspase-3 and pro caspase-3 (P < 0.05). This study indicates that the emodin-emodin dianthrones from Polygonum multiflorum Thunb. have liver-protective activity. Compounds 1 and 2 exerted hepatoprotective effects by inhibiting apoptosis and oxidative stress. The study provides an important material basis for the hepatoprotective effect of commonly used amounts of Polygonum multiflorum Thunb.

     

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