绿茶多酚可减轻邻苯二甲酸二(2-乙基己基)酯对小鼠的肾损伤。

IF 4.3 3区 医学 Q1 UROLOGY & NEPHROLOGY
American Journal of Nephrology Pub Date : 2024-01-01 Epub Date: 2023-09-21 DOI:10.1159/000534106
Heng Shi, Xinhai Zhao, Qin Peng, Xianling Zhou, Sisi Liu, Chuanchuan Sun, Qiuyu Cao, Shiping Zhu, Shengyun Sun
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引用次数: 0

摘要

背景:邻苯二甲酸二(2-乙基己基)酯(DEHP)是一种常见的增塑剂。研究表明,接触DEHP会导致肾脏损伤。绿茶是中国最受欢迎的饮料之一。绿茶多酚(GTPs)已被证明对重金属暴露引起的器官损伤具有治疗作用。然而,很少有研究报道GTP减轻DEHP诱导的肾损伤。方法:6~8周龄C57BL/6J雄性小鼠分别用蒸馏水(对照组)、1500mg/kg/dDEHP+玉米油(模型组)、1500mg/kg/dDEHP+玉米油+70mg/kg GTP(治疗组)、玉米油(油组)和70mg/kg GTP(GTP组)灌胃8周。评价各组小鼠的肾功能和肾组织病理学。使用高通量测序分析模型组、治疗组和对照组小鼠的肾组织。我们使用limma R软件包计算了差异表达的miRNA和mRNA,使用CIBERSORT算法预测免疫浸润,使用starBase数据库筛选miRNA mRNA调控轴,并进行免疫组织化学分析以验证蛋白质表达。结果:GTP减轻了DEHP引起的小鼠肾功能恶化、肾脏炎症和纤维化以及线粒体和内质网损伤。在模型组和治疗组之间观察到血浆、树突状细胞、T细胞和B细胞的不同免疫浸润。我们发现,当GTP减轻小鼠DEHP诱导的肾损伤时,三种差异表达的miRNA(mmu-miR-383-5p、mmu-miR-152-3p和mmu-miR-144-3p。结论:GTP可减轻DEHP引起的肾损伤,调节免疫细胞浸润。我们筛选了GTP减轻DEHP诱导的小鼠肾损伤的四个重要miRNA-mRNA蛋白调控轴。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Green Tea Polyphenols Alleviate Kidney Injury Induced by Di(2-Ethylhexyl) Phthalate in Mice.

Introduction: Di(2-ethylhexyl) phthalate (DEHP) is a common plasticizer. Studies have revealed that DEHP exposure can cause kidney damage. Green tea is among the most popular beverages in China. Green tea polyphenols (GTPs) have been proven to have therapeutic effects on organ damage induced by heavy metal exposure. However, few studies have reported on GTP-relieving DEHP-induced kidney damage.

Methods: C57BL/6J male mice aged 6-8 weeks were treated with distilled water (control group), 1,500 mg/kg/d DEHP + corn oil (model group), 1,500 mg/kg/d DEHP + corn oil + 70 mg/kg GTP (treatment group), corn oil (oil group), and 70 mg/kg GTP (GTP group) by gavage for 8 weeks, respectively. The renal function of mice and renal tissue histopathology of each group were evaluated. The renal tissues of mice in the model, treatment, and control groups were analyzed using high-throughput sequencing. We calculated the differentially expressed microRNAs (miRNAs) and messenger RNAs (mRNAs) using the limma R package, the CIBERSORT algorithm was used to predict immune infiltration, the starBase database was used to screen the miRNA-mRNA regulatory axis, and immunohistochemical analyses were performed to verify protein expression.

Results: GTP alleviated the deterioration of renal function, renal inflammation and fibrosis, and mitochondrial and endoplasmic reticulum lesions induced by DEHP in mice. Differential immune infiltrations of plasma, dendritic, T, and B cells were noted between the model and treatment groups. We found that three differentially expressed miRNAs (mmu-miR-383-5p, mmu-miR-152-3p, and mmu-miR-144-3p), three differentially expressed mRNAs (Ddit4, Dusp1, and Snx18), and three differentially expressed proteins (Ddit4, Dusp1, and Snx18) played crucial roles in the miRNA-mRNA-protein regulatory axes when GTPs mitigate DEHP-induced kidney damage in mice.

Conclusion: GTP can alleviate DEHP-induced kidney damage and regulate immune cell infiltration. We screened four important miRNA-mRNA-protein regulatory axes of GTP, mitigating DEHP-induced kidney damage in mice.

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来源期刊
American Journal of Nephrology
American Journal of Nephrology 医学-泌尿学与肾脏学
CiteScore
7.50
自引率
2.40%
发文量
74
审稿时长
4-8 weeks
期刊介绍: The ''American Journal of Nephrology'' is a peer-reviewed journal that focuses on timely topics in both basic science and clinical research. Papers are divided into several sections, including:
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