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毛茛对黄曲霉毒素 B(1)诱导的大鼠肝损伤的保护作用。

Protective effect of Aquilegia vulgaris L. on aflatoxin B(1)-induced hepatic damage in rats.

机构信息

Department of Toxicology, Poznan University of Medical Sciences, Dojazd 30, 60-631 Poznań, Poland.

出版信息

Environ Toxicol Pharmacol. 2006 Jul;22(1):58-63. doi: 10.1016/j.etap.2005.12.005. Epub 2006 Jan 24.

Abstract

The aim of the study was to investigate the effect of ethanol and ethyl acetate extract obtained from Aquilegia vulgaris L. on microsomal lipid peroxidation, reduced glutathione level and antioxidant enzymes activity in the liver of rats intoxicated with aflatoxin B(1) (AFB(1)). Animals were pretreated with 12 daily p.o. doses of the extracts tested (100mg/kg body weight). Then AFB(1) was administered intraperitoneally at a single dose of 1.5mg/kg b.w. to evoke the liver damage. α-Tocopherol was used as a positive control. Reduced glutathione (GSH) was depleted in aflatoxin-treated rats by 80% in comparison with that in the controls. The extracts restored the GSH concentration up to the basal level. Microsomal lipid peroxidation stimulated by Fe(2+)/ascorbate (assessed by measuring TBARS) was enhanced in AFB(1)-treated rats by 28% as compared to that in the control group. The extracts caused a decrease in TBARS level by 40% and 27%. Only two antioxidant enzymes were affected by AFB(1) administration. The activity of catalase was reduced by 24% and the activity of glutathione-S-transferase (GST) was increased by 33%. The pretreatment with ethyl acetate and ethanol extract reduced the GST activity by 76% and 30%, respectively. No significant changes in the activity of other antioxidant enzymes were observed in rats treated with the extracts and AFB(1). It can be concluded that multiple pretreatment with the extracts obtained from A. vulgaris attenuated aflatoxin B(1)-induced hepatic damage as evidenced by inhibition of lipid peroxidation and preventing reduced glutathione depletion.

摘要

本研究旨在探讨从毛茛中提取得到的乙醇和乙酸乙酯提取物对黄曲霉毒素 B1(AFB1)诱导的大鼠肝微粒体脂质过氧化、还原型谷胱甘肽(GSH)水平和抗氧化酶活性的影响。动物经 12 天每天口服(100mg/kg 体重)给予测试提取物预处理,然后用 AFB1 腹腔内单次注射 1.5mg/kg 体重以诱发肝损伤。α-生育酚用作阳性对照。与对照组相比,AFB1 处理的大鼠 GSH 水平降低了 80%。提取物将 GSH 浓度恢复到基础水平。用 Fe(2+)/抗坏血酸(通过测量 TBARS 评估)刺激的微粒体脂质过氧化在 AFB1 处理的大鼠中增加了 28%,与对照组相比。提取物使 TBARS 水平降低了 40%和 27%。只有两种抗氧化酶受到 AFB1 给药的影响。过氧化氢酶的活性降低了 24%,谷胱甘肽-S-转移酶(GST)的活性增加了 33%。乙酸乙酯和乙醇提取物预处理分别使 GST 活性降低了 76%和 30%。用提取物和 AFB1 处理的大鼠中未观察到其他抗氧化酶活性的显著变化。可以得出结论,用毛茛中提取得到的提取物进行多次预处理可减轻 AFB1 诱导的肝损伤,其证据为抑制脂质过氧化和防止还原型谷胱甘肽耗竭。

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