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啶虫脒对人外周血淋巴细胞遗传毒性的体外评价

In vitro evaluation of the genotoxicity of acetamiprid in human peripheral blood lymphocytes.

作者信息

Kocaman Ayşe Yavuz, Topaktaş Mehmet

机构信息

Department of Biology, Natural and Applied Sciences Institute, Cukurova University, Adana, Turkey.

出版信息

Environ Mol Mutagen. 2007 Jul;48(6):483-90. doi: 10.1002/em.20309.

Abstract

Acetamiprid, a neonicotinoid insecticide, is commonly used both in agriculture and domestic areas against a wide range of insects. The potential genotoxicity of a commercial formulation of acetamiprid (Mosetam 20 SP, containing 20% acetamiprid as the active ingredient) on human peripheral blood lymphocytes was examined in vitro by sister chromatid exchange (SCE), chromosomal aberrations (CAs), and micronucleus tests. Cells were treated with 25, 30, 35, and 40 mug/ml of acetamiprid for 24 and 48 hr. Acetamiprid induced SCEs and CAs significantly at all concentrations and treatment times and micronucleus formation was significantly induced at 30, 35, and 40 mug/ml of acetamiprid as compared with both the control and solvent control. Acetamiprid decreased the proliferation index (PI) at the two highest concentrations (35 and 40 mug/ml) for the 24-hr treatment period and only at the highest concentration (40 mug/ml) for the 48-hr treatment period when compared with the control and solvent control. Peripheral lymphocytes exposed to all concentrations of acetamiprid showed significant decreases in mitotic index (MI) and nuclear division index (NDI) for both treatment periods when compared with both the control and solvent control. Furthermore, acetamiprid decreased the MI in both treatment periods, and the NDI only in the 24-hr treatment period to the same extent as the positive control, mitomycin C (MMC). This study presents the first in vitro evidence for the genotoxicity of a commercial formulation of acetamiprid in human peripheral lymphocytes.

摘要

啶虫脒是一种新烟碱类杀虫剂,常用于农业和家庭领域,防治多种昆虫。本研究通过姐妹染色单体交换(SCE)、染色体畸变(CAs)和微核试验,在体外检测了啶虫脒商业制剂(莫赛特20 SP,含20%啶虫脒作为活性成分)对人外周血淋巴细胞的潜在遗传毒性。细胞分别用25、30、35和40μg/ml的啶虫脒处理24小时和48小时。啶虫脒在所有浓度和处理时间均显著诱导SCE和CAs,与对照组和溶剂对照组相比,30、35和40μg/ml的啶虫脒显著诱导微核形成。与对照组和溶剂对照组相比,在24小时处理期的两个最高浓度(35和40μg/ml)以及48小时处理期的最高浓度(40μg/ml)下,啶虫脒降低了增殖指数(PI)。在两个处理期,与对照组和溶剂对照组相比,暴露于所有浓度啶虫脒的外周淋巴细胞的有丝分裂指数(MI)和核分裂指数(NDI)均显著降低。此外,啶虫脒在两个处理期均降低了MI,仅在24小时处理期降低了NDI,且降低程度与阳性对照丝裂霉素C(MMC)相同。本研究首次提供了啶虫脒商业制剂对人外周淋巴细胞具有遗传毒性的体外证据。

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