苦参树皮提取物对4-硝基喹啉-n -氧化物遗传毒性的体外保护作用。

R. Pasquini, G. Scassellati-Sforzolini, M. Villarini, M. Moretti, M. Marcarelli, C. Fatigoni, S. Kaur, Subodh Kumar, I. S. Grover
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引用次数: 19

摘要

采用沙门氏菌/微粒体、彗星和微核(MN)试验,测定了氯仿、丙酮、甲醇、甲醇+盐酸、乙醚和乙酸乙酯提取物对模型诱变剂4-硝基喹啉-n -氧化物(4-NQO)的抗诱变作用。鼠伤寒沙门菌TA100菌株与人外周血细胞用不同浓度(5 ~ 500 μ g)的6种提取物和4-NQO (0.05 ~ 2 μ g)共孵育。在沙门氏菌/微粒体试验中发现,乙酸乙酯(50 μ g/板)、氯仿(100 μ g/板)、丙酮(100 μ g/板)和甲醇(500 μ g/板)的最高无毒提取物剂量对4-NQO致突变性的抑制作用大于70%。酸性甲醇和乙醚提取物的抗诱变活性不太明显(抑制约40-45%)。彗星试验表明,丙酮提取物(100微克/毫升)对减少4-NQO引起的DNA损伤更有效(约90%),而氯仿、乙酸乙酯和乙醚提取物则具有细胞毒性。在MN试验中,用氯仿和乙酸乙酯提取物对4-NQO的致裂性有明显的降低(抑制作用约为40-45%)。丙酮和甲醇提取物的活性较低,分别为33%和37%。本研究结果表明,阿朱那树皮中含有对4-NQO具有抗诱变活性的非极性和极性化合物。可以提出几种解释,但需要进一步的研究来明确确定活性化合物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In vitro protective effects of Terminalia arjuna bark extracts against the 4-nitroquinoline-N-oxide genotoxicity.
We determined the antimutagenic potential of chloroform, acetone, methanol, methanol+HCl, diethyl ether, and ethyl acetate extracts of Terminalia arjuna bark against the model mutagen 4-nitroquinoline-N-oxide (4-NQO) using the Salmonella/microsome, comet, and micronucleus (MN) tests. Salmonella typhimurium TA100 strain and human peripheral white blood cells were coincubated with various concentrations (from 5 to 500 microg) of the six extracts and 4-NQO (from 0.05 to 2 microg). We found that the 4-NQO mutagenicity was inhibited by more than 70% in the Salmonella/microsome test at the highest nontoxic extract dose of ethyl acetate (50 microg/plate), chloroform (100 microg/plate), acetone, (100 microg/plate), and methanol (500 microg/plate). A less marked antimutagenicity activity (inhibition of about 40-45%) was observed for the acidic methanol and diethyl ether extracts. The comet assay showed that acetone extract (100 microg/mL) was more effective in reducing the DNA damage caused by 4-NQO (ca. 90%), whereas the chloroform, ethyl acetate, and diethyl ether extracts were cytotoxic. In the MN test, the decrease in 4-NQO clastogenicity was observed by testing the mutagen especially with chloroform and ethyl acetate extracts (inhibition about 40-45%). The acetone and methanol extracts showed a less marked activity (33% and 37%, respectively). The results of the present study suggest that T. arjuna bark contains some nonpolar as well as polar compounds with antimutagenic activity against 4-NQO. Several explanations can be suggested, but further investigations are necessary to definitely identify the active compounds.
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