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大量污染中氰戊菊酯的潜在危害影响细胞凋亡敏感性。

Potential hazards of fenvalerate in massive pollution influence the apoptosis sensitivity.

机构信息

Graduate School of Medicine, Henan Polytechnic University, Jiaozuo, 454000, China.

Department of Public Health, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, 2630 Sugitani, Toyama, 930-0194, Japan.

出版信息

J Appl Toxicol. 2018 Feb;38(2):240-247. doi: 10.1002/jat.3517. Epub 2017 Sep 26.

Abstract

Fenvalerate (Fen), a synthetic pyrethroid insecticide, is widely used in agricultural, domestic and veterinary applications. Fen induces abnormal cell proliferation and apoptosis, which are linked to its hazardous effects. However, this view is controversial and the underlying molecular mechanisms remain elusive. In the present study, the effects of Fen on cadmium (Cd)-induced apoptosis and the associated molecular mechanisms were investigated in human myeloid leukemia U937 cells. U937 cells were treated with 50 μm cadmium chloride (CdCl ) with or without Fen pretreatment at 1-50 μm. Apoptosis was evaluated by externalization of phosphatidylserine on the plasma membrane. The expression levels of apoptosis-related proteins, including Bcl-2 family members were determined by western blot analysis. The results revealed that pretreatment with Fen at 20 μm for 12 hours significantly inhibited Cd-induced apoptosis. Decreased expression of pro-apoptotic Bcl-2 family proteins (Noxa and Bid) and increased expression of anti-apoptotic proteins (Bcl-xL, Mcl-1 and XIAP) were observed after combined treatment with Fen and CdCl . Phosphorylation of ERK and AKT was increased, while phosphorylation of JNK was decreased by the combined treatment, compared with CdCl treatment alone. In conclusion, Fen decreased apoptotic sensitivity induced by Cd in U937 cells. This effect was associated with activation of ERK and AKT, suppression of JNK and changes in expression of Bcl-2 family proteins and XIAP. The present findings suggest a potential influence of Fen on Cd toxicity via suppression of apoptosis. Fen decreased apoptotic sensitivity induced by Cd, and thus it may contribute carcinogenic risk and influence on cancer therapy.

摘要

氰戊菊酯(Fen)是一种合成拟除虫菊酯杀虫剂,广泛应用于农业、家庭和兽医领域。Fen 可诱导异常细胞增殖和细胞凋亡,这与其有害作用有关。然而,这种观点存在争议,其潜在的分子机制尚不清楚。本研究旨在探讨 Fen 在人髓系白血病 U937 细胞中对镉(Cd)诱导凋亡的影响及其相关的分子机制。用 50μM 的氯化镉(CdCl )处理 U937 细胞,并用 1-50μM 的 Fen 进行预处理。用细胞膜磷酯酰丝氨酸外翻评估细胞凋亡。用 Western blot 分析测定凋亡相关蛋白(包括 Bcl-2 家族成员)的表达水平。结果显示,用 20μM 的 Fen 预处理 12 小时可显著抑制 Cd 诱导的凋亡。与单独用 CdCl 处理相比,联合处理后促凋亡 Bcl-2 家族蛋白(Noxa 和 Bid)表达降低,抗凋亡蛋白(Bcl-xL、Mcl-1 和 XIAP)表达增加。与单独用 CdCl 处理相比,联合处理后 ERK 和 AKT 磷酸化增加,JNK 磷酸化减少。总之,Fen 降低了 U937 细胞中 Cd 诱导的凋亡敏感性。这种作用与 ERK 和 AKT 的激活、JNK 的抑制以及 Bcl-2 家族蛋白和 XIAP 表达的变化有关。本研究结果表明,Fen 可能通过抑制细胞凋亡对 Cd 毒性产生潜在影响。Fen 降低了 Cd 诱导的凋亡敏感性,因此可能会增加致癌风险,并影响癌症治疗。

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