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穿心莲内酯可保护大鼠肝细胞免受对乙酰氨基酚诱导的损伤。

Andrographolide protects rat hepatocytes against paracetamol-induced damage.

作者信息

Visen P K, Shukla B, Patnaik G K, Dhawan B N

机构信息

ICMR Centre for Advanced Pharmacological Research on Traditional Remedies, Central Drug Research Institute, Lucknow, India.

出版信息

J Ethnopharmacol. 1993 Oct;40(2):131-6. doi: 10.1016/0378-8741(93)90058-d.

Abstract

Andrographolide, the active constituent isolated from the plant Andrographis paniculata, showed a significant dose dependent (0.75-12 mg/kg p.o. x 7) protective activity against paracetamol-induced toxicity on ex vivo preparation of isolated rat hepatocytes. It significantly increased the percent viability of the hepatocytes as tested by trypan blue exclusion and oxygen uptake tests. It completely antagonized the toxic effects of paracetamol on certain enzymes (GOT, GPT and alkaline phosphatase) in serum as well as in isolated hepatic cells. Andrographolide was found to be more potent than silymarin, a standard hepatoprotective agent.

摘要

穿心莲内酯是从植物穿心莲中分离出的活性成分,在离体大鼠肝细胞制备实验中,对扑热息痛诱导的毒性表现出显著的剂量依赖性(口服0.75 - 12 mg/kg,连续7天)保护活性。通过台盼蓝排斥试验和氧摄取试验检测,它显著提高了肝细胞的存活百分比。它完全拮抗了扑热息痛对血清以及离体肝细胞中某些酶(谷草转氨酶、谷丙转氨酶和碱性磷酸酶)的毒性作用。发现穿心莲内酯比标准保肝剂水飞蓟素更有效。

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