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4'-碘-α-吡咯烷酮壬酮诱导人脑血管内皮细胞凋亡的机制:抗氧化特性下降的贡献。

Apoptotic mechanism in human brain microvascular endothelial cells triggered by 4'-iodo-α-pyrrolidinononanophenone: Contribution of decrease in antioxidant properties.

机构信息

Forensic Science Laboratory, Gifu Prefectural Police Headquarters, Gifu, 500-8501, Japan.

Laboratory of Biochemistry, Gifu Pharmaceutical University, Gifu, 501-1196, Japan.

出版信息

Toxicol Lett. 2022 Feb 1;355:127-140. doi: 10.1016/j.toxlet.2021.11.018. Epub 2021 Dec 2.

Abstract

In this study, we newly synthesized four α-pyrrolidinononanophenone (α-PNP) derivatives [4'-halogenated derivatives and α-pyrrolidinodecanophenone (α-PDP)], and then performed the structure-cytotoxicity relationship analyses. The results showed the rank order for the cytotoxic effects, α-PNP < α-PDP < 4'-fluoro-α-PNP < 4'-chrolo-α-PNP < 4'-bromo-α-PNP < 4'-iodo-α-PNP (I-α-PNP), and suggest that cytotoxicities of 4'-halogenated derivatives were more intensive than that of elongation of the hydrocarbon chain (α-PDP). We also surveyed the apoptotic mechanism of I-α-PNP in brain microvascular endothelial (HBME) cells that are utilized as the in vitro model of the blood-brain barrier. HBME cell treatment with I-α-PNP facilitated the apoptotic events (caspase-3 activation, externalization of phosphatidylserine, and DNA fragmentation), which were almost completely abolished by pretreating with antioxidants. In addition, the immunofluorescent staining revealed the enhanced production of hydroxyl radical in mitochondria by the I-α-PNP treatment, inferring that the I-α-PNP treatment triggers the apoptotic mechanism dependent on the enhanced ROS production in mitochondria. The treatment with I-α-PNP increased the production of cytotoxic aldehyde 4-hydroxy-2-nonenal and decreased the amount of reduced glutathione. Additionally, the treatment decreased the 26S proteasome-based proteolytic activities and aggresome formation. These results suggest that decrease in the antioxidant properties is also ascribable to HBME cell apoptosis elicited by I-α-PNP.

摘要

在这项研究中,我们新合成了四种α-吡咯烷酮壬基苯酮(α-PNP)衍生物[4'-卤代衍生物和α-吡咯烷基壬基苯酮(α-PDP)],然后进行了结构-细胞毒性关系分析。结果表明,细胞毒性的顺序为α-PNP < α-PDP < 4'-氟-α-PNP < 4'-氯-α-PNP < 4'-溴-α-PNP < 4'-碘-α-PNP(I-α-PNP),这表明4'-卤代衍生物的细胞毒性比烃链延长更强烈(α-PDP)。我们还调查了 I-α-PNP 在脑微血管内皮(HBME)细胞中的凋亡机制,HBME 细胞被用作血脑屏障的体外模型。I-α-PNP 处理 HBME 细胞促进了凋亡事件(半胱天冬酶-3 激活、磷脂酰丝氨酸外翻和 DNA 片段化),这些事件几乎完全被抗氧化剂预处理所抑制。此外,免疫荧光染色显示 I-α-PNP 处理增强了线粒体中羟自由基的产生,推断 I-α-PNP 处理触发了依赖于线粒体中 ROS 产生增强的凋亡机制。I-α-PNP 处理增加了细胞毒性醛 4-羟基-2-壬烯醛的产生,并减少了还原型谷胱甘肽的含量。此外,处理降低了 26S 蛋白酶体的蛋白水解活性和聚集体形成。这些结果表明,抗氧化特性的降低也是由 I-α-PNP 引起的 HBME 细胞凋亡所致。

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