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富勒醇纳米颗粒对啶虫脒诱导的人肺成纤维细胞毒性和遗传毒性的影响。

Effects of fullerenol nanoparticles on acetamiprid induced cytoxicity and genotoxicity in cultured human lung fibroblasts.

作者信息

Çavaş Tolga, Çinkılıç Nilüfer, Vatan Özgür, Yılmaz Dilek

机构信息

Cell Culture and Genetic Toxicology Laboratory, Department of Biology, Faculty of Sciences and Arts, Uludag University, 16059 Nilüfer, Bursa, Turkey.

Cell Culture and Genetic Toxicology Laboratory, Department of Biology, Faculty of Sciences and Arts, Uludag University, 16059 Nilüfer, Bursa, Turkey.

出版信息

Pestic Biochem Physiol. 2014 Sep;114:1-7. doi: 10.1016/j.pestbp.2014.07.008. Epub 2014 Jul 27.

Abstract

The aim of this study was to investigate the effects of water soluble fullerene (fullerenol) nanoparticles on the in vitro genotoxicity induced by the insecticide acetamiprid. Healthy human lung cells (IMR-90) were treated with fullerenol C60(OH)n (n: 18-22) alone and in combination with acetamiprid for 24h. The micronucleus test, comet assay and γ-H2AX foci formation assays were used as genotoxicity endpoints. Cytotoxicity was evaluated using the clonogenic assay. The maximum tested concentration of fullerenol (1.600 μg/ml) induced 77% survival where as the lowest concentration (25 μg/ml) was not cytotoxic where as acetamiprid was cytotoxic. Fullerenol did not induce genotoxicity at tested concentrations (50-1600 μg/L). On the other hand, acetamiprid (>50 μM) significantly induced formation of micronuclei, and double and single stranded DNA breaks in IMR-90 cells. For simultaneous exposure studies, two non-cytotoxic concentrations (50 and 200 μg/ml) of fullerenol and three cytotoxic concentrations of acetamiprid (100, 200 and 400 μM) were selected. As a result, we observed that co-exposure with fullerenol significantly reduced the cytotoxicity and genotoxicity of acetamiprid in IMR-90 cells. Our results indicated the protective effect of water soluble fullerene particles on herbicide induced genotoxicity.

摘要

本研究旨在探讨水溶性富勒烯(富勒醇)纳米颗粒对杀虫剂啶虫脒诱导的体外遗传毒性的影响。健康人肺细胞(IMR-90)分别单独用富勒醇C60(OH)n(n:18 - 22)处理以及与啶虫脒联合处理24小时。微核试验、彗星试验和γ-H2AX焦点形成试验被用作遗传毒性终点。使用克隆形成试验评估细胞毒性。富勒醇的最高测试浓度(1600μg/ml)诱导77%的细胞存活,而最低浓度(25μg/ml)无细胞毒性,啶虫脒则具有细胞毒性。在测试浓度(50 - 1600μg/L)下,富勒醇未诱导遗传毒性。另一方面,啶虫脒(>50μM)显著诱导IMR-90细胞中微核的形成以及双链和单链DNA断裂。对于同时暴露研究,选择了富勒醇的两个无细胞毒性浓度(50和200μg/ml)以及啶虫脒的三个细胞毒性浓度(100、200和400μM)。结果,我们观察到与富勒醇共同暴露显著降低了啶虫脒在IMR-90细胞中的细胞毒性和遗传毒性。我们的结果表明水溶性富勒烯颗粒对除草剂诱导的遗传毒性具有保护作用。

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