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矮茎紫金牛叶提取物对苯菌灵诱导的培养大鼠肝细胞细胞毒性和遗传毒性的保护作用。

Protection of extract from leaves of Ardisia compressa against benomyl-induced cytotoxicity and genotoxicity in cultured rat hepatocytes.

作者信息

Ramírez-Mares M V, Fatell S, Villa-Treviño S, González de Mejía E

机构信息

Research and Graduate Studies in Food Science, School of Chemistry, University of Queretaro, Mexico.

出版信息

Toxicol In Vitro. 1999 Dec;13(6):889-96. doi: 10.1016/s0887-2333(99)00071-5.

Abstract

The potential of the Ardisia compressa extract (EA) was examined regarding its capacity to reduce the cytotoxic effect of benomyl on rat hepatocytes. The protective effect was evaluated by Janus Green dye exclusion method. An approximate 50% cytotoxic effect of benomyl on hepatocytes was observed at 35mug/ml after 2hr of incubation. (-)Epigallocatechin 3-gallato (EGCG) and EA decreased the viability of hepatocytes at concentrations above 3mug/ml and 2.52mug, equivalent to (+)catechin/ml, respectively. A protective effect against benomyl was observed when hepatocytes were previously exposed to EGCG (3mug/ml) or EA (2.52mug, equivalent to (+)catechin/ml) followed by incubation with benomyl (35mug/ml) alone. When EGCG or EA were in contact with cells, either simultaneously or after pretreatment with benomyl, did not protect hepatocytes. EGCG (1.3x10(-2)mug/ml) or EA (9.8x10(-2)mug, equivalent to (+)catechin/ml) inhibited 57% and 34%, respectively, the unscheduled DNA synthesis (UDS) induced by benomyl at a concentration of 23x10(-2)mum, when both were incubated with hepatocytes prior to benomyl. The simultaneous incubation of benomyl with EGCG or EA did not protect the cell against the genotoxic effect of benomyl. These results indicate that the dried leaves extract of Ardisia compressa protect rat hepatocytes from benomyl-induced cytotoxicity and genotoxicity.

摘要

研究了紫金牛提取物(EA)减轻苯菌灵对大鼠肝细胞细胞毒性作用的潜力。采用詹纳斯绿染料排除法评估其保护作用。孵育2小时后,在35μg/ml浓度下观察到苯菌灵对肝细胞约50%的细胞毒性作用。(-)表没食子儿茶素3-没食子酸酯(EGCG)和EA分别在浓度高于3μg/ml和2.52μg(相当于(+)儿茶素/ml)时降低了肝细胞的活力。当肝细胞预先暴露于EGCG(3μg/ml)或EA(2.52μg,相当于(+)儿茶素/ml),然后单独与苯菌灵(35μg/ml)孵育时,观察到对苯菌灵的保护作用。当EGCG或EA与细胞同时接触或在苯菌灵预处理后接触时,不能保护肝细胞。当EGCG(1.3×10⁻²μg/ml)或EA(9.8×10⁻²μg,相当于(+)儿茶素/ml)在苯菌灵之前与肝细胞孵育时,它们分别抑制了浓度为23×10⁻²μM的苯菌灵诱导的57%和34%的非程序性DNA合成(UDS)。苯菌灵与EGCG或EA同时孵育不能保护细胞免受苯菌灵的遗传毒性作用。这些结果表明,紫金牛干燥叶提取物可保护大鼠肝细胞免受苯菌灵诱导的细胞毒性和遗传毒性。

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