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p53 基因敲除对壬基酚诱导的斑马鱼肾毒性的保护作用。

Protective effect of p53 knockout on 4-nonylphenol-induced nephrotoxicity in medaka (Oryzias latipes).

机构信息

Zoology Department, Faculty of Science, Assiut University, 71516, Assiut, Egypt.

Department of Anatomy and Histology, Faculty of Veterinary Medicine, Assiut University, 71516 Assiut, Egypt.

出版信息

Chemosphere. 2019 Dec;236:124314. doi: 10.1016/j.chemosphere.2019.07.045. Epub 2019 Jul 8.

DOI:10.1016/j.chemosphere.2019.07.045
PMID:31310970
Abstract

In the past few decades, environmental pollutants have become common because of misused nonionic surfactants and detergents. Nonylphenol ethoxylates (NPs) are one of the most important contaminants of water. Therefore, the present study aimed to investigate the protective blocking effect of apoptosis (deficient P53 gene) on 4-nonylphenol (4-NP)-induced nephrotoxicity of medaka (Oryzias latipes). We divided 36 fish into six groups: two different control groups of wild type (Wt; Hd-rR) control and p53 (-/-) control, and four different treated with 4-nonylphenol (50 μg/L and 100 μg/L) for 15 days. Histology, immunochemistry, and TUNEL assays confirmed that 4-NP causes nephrotoxicity. Our results showed that 4-NP administration significantly disturbed the kidney structure and function and 4-NP-treated fish showed dilated glomerular vessels, had less glomerular cellular content, decreased expression of glomerular proteins, and an increased level of apoptosis compared with a Wt control group (P < 0.05). As p53 is an apoptotic inducer, some protection in p53-deficient medaka was found as nephrotoxic effects of 4-NP were minimized significantly. Our study demonstrated for the first time to our knowledge that 4-NP induces apoptosis, causing nephrotoxicity in medaka. We found that blocking apoptosis blocking was able to protect the kidney from the toxic effects of 4-NP.

摘要

在过去的几十年中,由于非离子表面活性剂和清洁剂的滥用,环境污染物变得很常见。壬基酚聚氧乙烯醚(NPs)是最重要的水污染物质之一。因此,本研究旨在探讨凋亡(缺陷型 P53 基因)对 4-壬基酚(4-NP)诱导的泥鳅肾毒性的保护阻断作用。我们将 36 条鱼分为六组:两种不同的野生型(Wt;Hd-rR)对照组和 p53(-/-)对照组,以及四组不同浓度的 4-NP(50μg/L 和 100μg/L)处理组,处理时间为 15 天。组织学、免疫化学和 TUNEL 分析证实 4-NP 可引起肾毒性。我们的结果表明,4-NP 处理显著扰乱了肾脏结构和功能,与 Wt 对照组相比,4-NP 处理的鱼表现出肾小球血管扩张、肾小球细胞含量减少、肾小球蛋白表达减少以及凋亡增加(P<0.05)。由于 P53 是一种凋亡诱导剂,在 p53 缺陷型泥鳅中发现了一些保护作用,4-NP 的肾毒性作用显著降低。本研究首次证明,4-NP 诱导凋亡,导致泥鳅肾毒性。我们发现,阻断凋亡能够保护肾脏免受 4-NP 的毒性作用。

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