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慢性砷暴露增加大鼠脑中 Aβ 的产生和晚期糖基化终产物受体的表达。

Chronic Arsenic Exposure Increases Aβ Production and Receptor for Advanced Glycation End Products Expression in Rat Brain.

机构信息

Laboratorio Nacional Forense Nuclear, Instituto Nacional de Investigaciones Nucleares , Carretera México-Toluca s/n, CP 52750 La Marquesa Ocoyoacac, México.

Centro de Biociencias, Universidad Autónoma de San Luis Potosí , Km. 14.5 carretera San Luis Potosí - Matehuala, Ejido "Palma de la Cruz", CP 78321 Soledad de Graciano Sánchez, San Luis Potosí, México.

出版信息

Chem Res Toxicol. 2018 Jan 16;31(1):13-21. doi: 10.1021/acs.chemrestox.7b00215. Epub 2017 Dec 4.

Abstract

Chronic arsenic exposure during development is associated with alterations of chemical transmission and demyelination, which result in cognitive deficits and peripheral neuropathies. At the cellular level, arsenic toxicity involves increased generation of reactive species that induce severe cellular alterations such as DNA fragmentation, apoptosis, and lipid peroxidation. It has been proposed that arsenic-associated neurodegeneration could evolve to Alzheimer disease in later life.1,2 In this study, the effects of chronic exposure to inorganic arsenic (3 ppm by drinking water) in Wistar rats on the production and elimination of Amyloid-β (Aβ) were evaluated. Male Wistar rats were exposed to 3 ppm of arsenic in drinking water from fetal development until 4 months of age. After behavioral deficits induced by arsenic exposure through contextual fear conditioning were verified, the brains were collected for the determination of total arsenic by inductively coupled plasma-mass spectrometry, the levels of amyloid precursor protein and receptor for advanced glycation end products (RAGE) by Western blot analysis as well as their transcript levels by RT-qPCR, Aβ estimation by ELISA assay and the enzymatic activity of β-secretase (BACE1). Our results demonstrate that chronic arsenic exposure induces behavioral deficits accompanied of higher levels of soluble and membranal RAGE and the increase of Aβ cleaved. In addition, BACE1 enzymatic activity was increased, while immunoblot assays showed no differences in the low-density lipoprotein receptor-related protein 1 (LRP1) receptor among groups. These results provide evidence of the effects of arsenic exposure on the production of Aβ and cerebral amyloid clearance through RAGE in an in vivo model that displays behavioral alterations. This work supports the hypothesis that early exposure to metals may contribute to neurodegeneration associated with amyloid accumulation.

摘要

慢性发育期砷暴露与化学传递和脱髓鞘改变有关,导致认知缺陷和周围神经病变。在细胞水平上,砷毒性涉及活性物质的产生增加,这些活性物质诱导严重的细胞改变,如 DNA 片段化、细胞凋亡和脂质过氧化。有人提出,砷相关性神经退行性变可能会在以后的生活中发展为阿尔茨海默病。1,2 在这项研究中,评估了慢性暴露于饮用水中的无机砷(3ppm)对淀粉样蛋白-β(Aβ)的产生和消除的影响。雄性 Wistar 大鼠从胎儿发育到 4 个月大时,通过饮用水摄入 3ppm 的砷。在通过情境恐惧条件反射验证砷暴露引起的行为缺陷后,收集大脑,通过电感耦合等离子体质谱法测定总砷含量,通过 Western blot 分析测定淀粉样前体蛋白和晚期糖基化终产物受体(RAGE)的水平,以及通过 RT-qPCR 测定其转录水平,通过 ELISA 测定 Aβ的含量,并测定β-分泌酶(BACE1)的酶活性。我们的结果表明,慢性砷暴露会引起行为缺陷,同时可溶性和膜结合型 RAGE 水平升高,Aβ 片段增加。此外,BACE1 酶活性增加,而免疫印迹分析显示各组之间低密度脂蛋白受体相关蛋白 1(LRP1)受体没有差异。这些结果提供了证据,证明砷暴露通过 RAGE 在体内模型中对 Aβ的产生和大脑淀粉样蛋白清除产生影响,该模型显示出行为改变。这项工作支持了早期暴露于金属可能导致与淀粉样蛋白积累相关的神经退行性变的假说。

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