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新型阻燃剂三(1,3-二氯-2-丙基)磷酸酯(TDCIPP)和磷酸三苯酯(TPhP)对人及大鼠胰岛β细胞系功能和稳态的影响。

Effects of novel flame retardants tris(1,3-dichloro-2-propyl) phosphate (TDCIPP) and triphenyl phosphate (TPhP) on function and homeostasis in human and rat pancreatic beta-cell lines.

机构信息

3LF UK, Departement of Biochemistry, Cell and Molecular Biology & Center for Research On Nutrition, Metabolism, and Diabetes, Third Faculty of Medicine, Charles University, Ruska 87, 100 00, Prague, Czech Republic.

Faculty of Science, RECETOX, Masaryk University, Kotlarska 2, 611 37, Brno, Czech Republic.

出版信息

Arch Toxicol. 2024 Nov;98(11):3859-3874. doi: 10.1007/s00204-024-03841-z. Epub 2024 Aug 27.

DOI:10.1007/s00204-024-03841-z
PMID:39192017
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11489283/
Abstract

Despite the fact that environmental pollution has been implicated in the global rise of diabetes, the research on the impact of emerging pollutants such as novel flame retardants remains limited. In line with the shift towards the use of non-animal approaches in toxicological testing, this study aimed to investigate the effects of two novel flame retardants tris(1,3-dichloro-2-propyl) phosphate (TDCIPP) and triphenyl phosphate (TPhP) in rat (INS1E) and human (NES2Y) pancreatic beta-cell lines. One-week exposure to 1 μM and 10 μM TDCIPP and TPhP altered intracellular insulin and proinsulin levels, but not the levels of secreted insulin (despite the presence of a statistically insignificant trend). The exposures also altered the protein expression of several factors involved in beta-cell metabolic pathways and signaling, including ATP citrate lyase, isocitrate dehydrogenase 1, perilipins, glucose transporters, ER stress-related factors, and antioxidant enzymes. This study has brought new and valuable insights into the toxicity of TDCIPP and TPhP on beta-cell function and revealed alterations that might impact insulin secretion after more extended exposure. It also adds to the scarce studies using in vitro pancreatic beta-cells models in toxicological testing, thereby promoting the development of non-animal testing strategy for identifying pro-diabetic effects of chemical pollutants.

摘要

尽管环境污染被认为是全球糖尿病发病率上升的一个因素,但新兴污染物(如新型阻燃剂)的影响研究仍然有限。本研究旨在采用非动物方法进行毒理学测试,因此,我们研究了两种新型阻燃剂三(1,3-二氯-2-丙基)磷酸酯(TDCIPP)和磷酸三苯酯(TPhP)对大鼠(INS1E)和人(NES2Y)胰岛β细胞系的影响。为期一周的 1 μM 和 10 μM TDCIPP 和 TPhP 暴露改变了细胞内胰岛素和胰岛素原的水平,但未改变分泌型胰岛素的水平(尽管存在统计学上无显著意义的趋势)。这些暴露还改变了参与β细胞代谢途径和信号转导的几种因子的蛋白表达,包括三磷酸腺苷柠檬酸裂解酶、异柠檬酸脱氢酶 1、脂联素、葡萄糖转运蛋白、内质网应激相关因子和抗氧化酶。本研究为 TDCIPP 和 TPhP 对β细胞功能的毒性提供了新的有价值的见解,并揭示了在更长时间暴露后可能影响胰岛素分泌的改变。它还增加了使用体外胰岛β细胞模型进行毒理学测试的稀缺研究,从而促进了非动物测试策略的发展,以识别化学污染物的致糖尿病作用。

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