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邻苯二甲酸二丁酯通过调节大鼠胰岛素瘤细胞的线粒体凋亡途径和氧化应激来影响胰岛素的合成和分泌。

Dibutyl phthalate affects insulin synthesis and secretion by regulating the mitochondrial apoptotic pathway and oxidative stress in rat insulinoma cells.

作者信息

Yang Ruoru, Zheng Jianheng, Qin Jin, Liu Shaojie, Liu Xinyuan, Gu Yiying, Yang Shuyu, Du Jun, Li Shuguang, Chen Bo, Dong Ruihua

机构信息

School of Public Health, Institute of Nutrition, Key Lab of Public Health Safety of the Ministry of Education, Fudan University, Shanghai 200032, China.

Nutrilite Health Institute, Shanghai 200023, China.

出版信息

Ecotoxicol Environ Saf. 2023 Jan 1;249:114396. doi: 10.1016/j.ecoenv.2022.114396. Epub 2022 Dec 9.

Abstract

Dibutyl phthalate (DBP) is a typical phthalate (PAEs). The environmental health risks of DBP have gradually attracted attention due to the common use in the production of plastics, cosmetics and skin care products. DBP was associated with diabetes, but its mechanism is not clear. In this study, an in vitro culture system of rat insulinoma (INS-1) cells was established to explore the effect of DBP on insulin synthesis and secretion and the potential mechanisms. INS-1 cells were cultured in RPMI-1640 medium containing 10% fetal bovine serum and treated with 15, 30, 60 and 120 μmol/L of DBP and dimethyl sulfoxide (vehicle, < 0.1%) for 24 h. The contents of insulin in the intracellular fluid and the extracellular fluid of the cells were measured. The results showed that insulin synthesis and secretion in INS-1 cells were significantly decreased in 120 μmol/L DBP group. The apoptosis rate and mitochondrial membrane potential of INS-1 cells were measured by flow cytometry with annexin V-FITC conjugate and PI, and JC-1, respectively. The results showed that DBP caused an increase in the apoptosis rate and a significant decrease in the mitochondrial membrane potential in INS-1 cells in 60 μmol/L and 120 μmol/L DBP group. The results of western blot showed that the expression of Bax/Bcl-2, caspase-3, caspase-9 and Cyt-C were significantly increased. Meanwhile, the level of oxidative stress in INS-1 cells was detected by fluorescent probes DCFH-DA and western blot. With the increase of DBP exposure, the oxidative stress levels (MDA, GSH/GSSG) were increased; and the antioxidant index (SOD) levels were decreased. Our experimental results provide reliable evidence that DBP induced apoptosis and functional impairment in INS-1 cells through the mitochondrial apoptotic pathway and oxidative stress. Therefore, we hypothesized that interference with these two pathways could be considered in the development of preventive protection measures.

摘要

邻苯二甲酸二丁酯(DBP)是一种典型的邻苯二甲酸酯(PAEs)。由于其在塑料、化妆品和护肤品生产中的广泛使用,DBP对环境健康的风险已逐渐引起关注。DBP与糖尿病有关,但其机制尚不清楚。在本研究中,建立了大鼠胰岛素瘤(INS-1)细胞的体外培养系统,以探讨DBP对胰岛素合成和分泌的影响及其潜在机制。将INS-1细胞培养于含10%胎牛血清的RPMI-1640培养基中,分别用15、30、60和120 μmol/L的DBP以及二甲基亚砜(溶剂,<0.1%)处理24小时。检测细胞内液和细胞外液中的胰岛素含量。结果显示,120 μmol/L DBP组INS-1细胞的胰岛素合成和分泌显著降低。分别用膜联蛋白V-FITC共轭物和PI以及JC-1通过流式细胞术检测INS-1细胞的凋亡率和线粒体膜电位。结果显示,60 μmol/L和120 μmol/L DBP组中,DBP导致INS-1细胞的凋亡率增加,线粒体膜电位显著降低。蛋白质印迹法结果显示,Bax/Bcl-2、半胱天冬酶-3、半胱天冬酶-9和细胞色素C的表达显著增加。同时,用荧光探针DCFH-DA和蛋白质印迹法检测INS-1细胞中的氧化应激水平。随着DBP暴露量的增加,氧化应激水平(丙二醛、谷胱甘肽/氧化型谷胱甘肽)升高;抗氧化指标(超氧化物歧化酶)水平降低。我们的实验结果提供了可靠的证据,表明DBP通过线粒体凋亡途径和氧化应激诱导INS-1细胞凋亡和功能损伤。因此,我们推测在制定预防保护措施时可以考虑干扰这两条途径。

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