首页> 外文期刊>International Journal of Medicinal Mushrooms >Hepatoprotective Effects and Mechanisms of Action of Triterpenoids from Lingzhi or Reishi Medicinal Mushroom Ganoderma lucidum (Agaricomycetes) on alpha-Amanitin-Induced Liver Injury in Mice
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Hepatoprotective Effects and Mechanisms of Action of Triterpenoids from Lingzhi or Reishi Medicinal Mushroom Ganoderma lucidum (Agaricomycetes) on alpha-Amanitin-Induced Liver Injury in Mice

机译:灵芝或灵芝灵芝灵芝中三萜类化合物对小鼠肝损伤的保护作用及机制

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摘要

Most fatal mushroom poisonings are caused by species of the genus Amanita; the amatoxins arc responsible for acute liver failure and death in humans. Ganoderma lucidum is a well-known traditional medicinal mushroom that has been shown to have obvious hepatoprotective effects. This study evaluated the hepatoprotective effects of triterpenoids from G. lucidum on liver injury induced by a-amanitin (alpha-AMA) in mice and the mechanisms of action of these triterpenoids, including radical scavenging and antiapoptosis activities. Mice were treated with a-AMA, followed by G. lucidum total triterpenoids or individual triterpenoids, and their hepatoprotective effects were compared with those of the reference drug silibinin (SIL). Treatment with SIL, G. lucidum total triteipenoids, and each of the 5 individual triterpenoids significantly reduced serum alanine aminotransaminase and aspartate aminotransaminase concentrations and reduced mortality rates 20 L.10%. Moreover, triterpenoids and SIL significantly enhanced superoxide dismutase and catalase activity and reduced malondialdehyde content in livers. Treatment with ganoderic acid C2 significantly inhibited DNA fragmentation and decreased caspase-3, -8, and -9 activities. The results demonstrated that triterpenoids have hepatoprotective effects on alpha-AMA-induced liver injury and that their hepatoprotective mechanisms may be the result of their antioxidative and radical scavenging activities and their inhibition of apoptosis.
机译:大多数致命的蘑菇中毒是由鹅膏菌属引起的。 amatoxins是导致人类急性肝衰竭和死亡的原因。灵芝是一种众所周知的传统药用蘑菇,已被证明具有明显的保肝作用。这项研究评估了灵芝中的三萜类化合物对小鼠抗α-amanitin(alpha-AMA)诱导的肝损伤的肝保护作用,以及这些三萜类化合物的作用机理,包括自由基清除和抗凋亡活性。小鼠先用α-AMA治疗,然后再用灵芝总三萜或单个三萜治疗,并将它们的肝保护作用与参考药物水飞蓟宾(SIL)进行比较。 SIL,灵芝总三萜类化合物和5种单独的三萜类化合物分别治疗可显着降低血清丙氨酸氨基转氨酶和天冬氨酸氨基转氨酶的浓度,并将死亡率降低20 L.10%。此外,三萜类化合物和SIL可以显着增强肝脏中的超氧化物歧化酶和过氧化氢酶活性,并降低丙二醛含量。灵芝酸C2处理可显着抑制DNA片段化并降低caspase-3,-8和-9活性。结果表明三萜类化合物对α-AMA诱导的肝损伤具有保肝作用,其保肝机理可能是其抗氧化和自由基清除活性以及抑制细胞凋亡的结果。

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