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大鼠亚慢性低氟暴露致近曲小管损伤。

Proximal renal tubular injury in rats sub-chronically exposed to low fluoride concentrations.

机构信息

Departmento de Toxicología, Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional (CINVESTAV-IPN), México, D. F., México.

出版信息

Toxicol Appl Pharmacol. 2013 Nov 1;272(3):888-94. doi: 10.1016/j.taap.2013.07.026. Epub 2013 Aug 7.

Abstract

Fluoride is usually found in groundwater at a very wide range of concentration between 0.5 and 25 ppm. At present, few studies have assessed the renal effects of fluoride at environmentally relevant concentrations. Furthermore, most of these studies have used insensitive and nonspecific biomarkers of kidney injury. The aim of this study was to use early and sensitive biomarkers to evaluate kidney injury after fluoride exposure to environmentally relevant concentrations. Recently weaned male Wistar rats were exposed to low (15 ppm) and high (50 ppm) fluoride concentrations in drinking water for a period of 40 days. At the end of the exposure period, kidney injury biomarkers were measured in urine and renal mRNA expression levels were assessed by real time RT-PCR. Our results showed that the urinary kidney injury molecule (Kim-1), clusterin (Clu), osteopontin (OPN) and heat shock protein 72 excretion rate significantly increased in the group exposed to the high fluoride concentration. Accordingly, fluoride exposure increased renal Kim-1, Clu and OPN mRNA expression levels. Moreover, there was a significant dose-dependent increase in urinary β-2-microglobulin and cystatin-C excretion rate. Additionally, a tendency towards a dose dependent increase of tubular damage in the histopathological light microscopy findings confirmed the preferential impact of fluoride on the tubular structure. All of these changes occurred at early stages in which, the renal function was not altered. In conclusion using early and sensitive biomarkers of kidney injury, we were able to found proximal tubular alterations in rats sub-chronically exposed to fluoride.

摘要

氟化物通常在地下水以非常广泛的浓度存在,介于 0.5 和 25ppm 之间。目前,很少有研究评估氟化物在环境相关浓度下对肾脏的影响。此外,这些研究大多使用不敏感和非特异性的肾脏损伤生物标志物。本研究旨在使用早期和敏感的生物标志物来评估环境相关浓度氟化物暴露后的肾脏损伤。最近断奶的雄性 Wistar 大鼠在饮用水中暴露于低(15ppm)和高(50ppm)氟化物浓度 40 天。在暴露期结束时,测量尿液中的肾脏损伤生物标志物,并通过实时 RT-PCR 评估肾脏 mRNA 表达水平。我们的结果表明,暴露于高氟浓度组的尿肾损伤分子(Kim-1)、簇蛋白(Clu)、骨桥蛋白(OPN)和热休克蛋白 72 的排泄率显著增加。相应地,氟化物暴露增加了肾脏 Kim-1、Clu 和 OPN mRNA 的表达水平。此外,尿β-2-微球蛋白和胱抑素 C 排泄率呈显著的剂量依赖性增加。此外,组织病理学光镜检查结果显示肾小管损伤呈剂量依赖性增加趋势,证实了氟化物对肾小管结构的优先影响。所有这些变化都发生在肾功能尚未改变的早期阶段。总之,我们使用肾脏损伤的早期和敏感生物标志物,发现亚慢性氟化物暴露的大鼠存在近端肾小管改变。

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