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首页> 外文期刊>Journal of pharmacological sciences. >N-nitrosocarbofuran induces apoptosis in mouse brain microvascular endothelial cells (bEnd.3).
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N-nitrosocarbofuran induces apoptosis in mouse brain microvascular endothelial cells (bEnd.3).

机译:N-亚硝基卡脲呋喃诱导小鼠脑微血管内皮细胞凋亡(bEnd.3)。

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摘要

In this study, we investigated whether carbofuran, a commonly used carbamate pesticide, and N-nitrosocarbofuran (NOCF), the N-nitroso metabolite of carbofuran, have cytotoxicity in mouse brain microvascular endothelial cells (bEnd.3). Results from the MTT assay in bEnd.3 cells showed that NOCF but not carbofuran caused a remarkable decrease in cell viability. The cell death induced by NOCF appeared to involve apoptosis, based on our results from annexin V staining and electron microscopy. To investigate the mechanism of the NOCF-induced cell death, we examined the effects of selective inhibitors for MAP kinase pathways, PD98059 (for MEK/ERK), SB202190 (for p38 MAP kinase), and SP600125 (for JNK), on the NOCF-induced cell death. The NOCF-induced cell death was significantly reduced by PD98059, but not by SB202190 or SP600125. NOCF increased ERK phosphorylation as early as 15 min after the treatment and this increase was maintained for 2 h. In summary, our results suggest that NOCF can induce apoptotic cell death, at least in part, through the ERK pathway in brain microvascular endothelial cells.
机译:在这项研究中,我们调查了常用的氨基甲酸酯农药呋喃丹和呋喃喃的N-亚硝基碳呋喃(NOCF)在小鼠脑微血管内皮细胞中是否具有细胞毒性(bEnd.3)。在bEnd.3细胞中进行的MTT分析结果表明,NOCF引起了细胞活力的显着下降,而卡百呋喃却没有。根据膜联蛋白V染色和电子显微镜的结果,NOCF诱导的细胞死亡似乎涉及凋亡。为了研究NOCF诱导的细胞死亡的机制,我们研究了选择性抑制剂对MAP激酶途径,PD98059(对于MEK / ERK),SB202190(对p38 MAP激酶)和SP600125(对JNK)的影响。诱导的细胞死亡。 PD98059显着降低了NOCF诱导的细胞死亡,但SB202190或SP600125却没有。早在治疗后15分钟,NOCF就会增加ERK磷酸化,并维持2小时。总而言之,我们的结果表明,NOCF可以至少部分通过脑微血管内皮细胞中的ERK途径诱导凋亡性细胞死亡。

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