慢性乙醇摄入诱导大鼠肾小球滤过屏障蛋白基因表达改变,增加肾脏基质金属蛋白酶活性。

Q2 Medicine
Mahrokh Samadi, Alireza Shirpoor, Ali Taghizadeh Afshari, Fatemeh Kheradmand, Yousef Rasmi, Maryam Sadeghzadeh
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引用次数: 6

摘要

背景:慢性酒精摄入引起的肾脏结构和功能改变是众所周知的,但酒精引起肾脏异常的精确的潜在分子介质仍然是未知的。本研究旨在探讨慢性乙醇暴露对大鼠肾脏基质金属蛋白酶2,9 (MMP)、肾小球滤过屏障蛋白(nephrin和podocin)以及血管内皮生长因子受体1,2 (VEGFRs)亚型基因表达的影响。方法:选取初始体重为220±10 g的雄性Wistar大鼠16只,分为对照组和乙醇组(4.5 g/kg BW)。结果:治疗6周后,结果显示乙醇组与对照组相比,VEGFR基因的VEGFR1和VEGFR2亚型表达显著升高,MMP2和MMP9活性显著升高,nephrin和podocin基因表达显著降低。结论:这些研究结果表明,乙醇诱导的肾脏异常可能与VEGFRs、nephrin和podocin的表达改变以及MMP2和MMP9作为肾脏功能的关键分子介质的活性增加有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Chronic ethanol ingestion induces glomerular filtration barrier proteins genes expression alteration and increases matrix metalloproteinases activity in the kidney of rats.

Chronic ethanol ingestion induces glomerular filtration barrier proteins genes expression alteration and increases matrix metalloproteinases activity in the kidney of rats.

Chronic ethanol ingestion induces glomerular filtration barrier proteins genes expression alteration and increases matrix metalloproteinases activity in the kidney of rats.

Chronic ethanol ingestion induces glomerular filtration barrier proteins genes expression alteration and increases matrix metalloproteinases activity in the kidney of rats.

Background: Chronic alcohol ingestion-induced kidney structure and function alterations are very well known, but the precise underlying molecular mediators involved in ethanol-induced kidney abnormalities remain elusive. The aim of this study was to investigate the effect of chronic ethanol exposure on matrix metalloproteinase 2, 9 (MMP), glomerular filtration barrier proteins (nephrin and podocin), as well as vascular endothelial growth factor receptor 1, 2 (VEGFRs) isoforms gene expression in the kidney of rats.

Methods: Sixteen male Wistar rats with an initial body weight of 220 ± 10 g were divided into the following two groups: (1) control and (2) ethanol (4.5 g/kg BW).

Results: After 6 weeks of treatment, the results revealed a significant increase in isoforms VEGFR1 and VEGFR2 of VEGFR gene expression, significant increases of MMP2 and MMP9 activities, as well as significant decrease of nephrin and podocin gene expressions in the ethanol group, compared with that in the control group.

Conclusion: These findings indicate that ethanol-induced kidney abnormalities may be in part associated with alteration in expressions of VEGFRs, nephrin, and podocin and in increasing activities of MMP2 and MMP9 as key molecular mediators in the kidney function.

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来源期刊
Interventional Medicine and Applied Science
Interventional Medicine and Applied Science MEDICINE, GENERAL & INTERNAL-
CiteScore
1.60
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审稿时长
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