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环孢素A对大鼠肾脏中肾素和血管紧张素1型受体基因表达的影响。

Effect of CsA on the expression of renin and angiotensin type 1 receptor genes in the rat kidney.

作者信息

Tufro-McReddie A, Gomez R A, Norling L L, Omar A A, Moore L C, Kaskel F J

机构信息

Department of Pediatrics, University of Virginia School of Medicine, Charlottesville.

出版信息

Kidney Int. 1993 Mar;43(3):615-22. doi: 10.1038/ki.1993.90.

Abstract

To determine whether Cyclosporine A (CsA) alters the intrarenal expression of the renin and type 1 angiotensin II receptor genes, male adult Sprague-Dawley rats were given 25 mg/kg/day CsA s.c. for three weeks (CsA, N = 20) and were compared to pair-fed vehicle treated rats (Con, N = 20). The intrarenal distribution of renin and its mRNA was assessed by immunocytochemistry and in situ hybridization. In addition, kidney renin and type 1 angiotensin II (AT1) receptor mRNA levels were determined by Northern blot analysis. The percentage of juxtaglomerular apparatuses containing renin was higher in the CsA (84 +/- 5.5%) than in the Con (61 +/- 6.7%) group, (P < 0.05). The length of renin immunostaining along afferent arterioles was higher in the CsA (74 +/- 4.5 microns) than in the Con (37 +/- 5.1 microns) group, (P < 0.05). In contrast, neither renin mRNA levels nor its intrarenal distribution were altered by chronic CsA administration. Kidney AT1 receptor mRNA levels were lower in the CsA group than in the Con group. We conclude that chronic CsA: (1) induces recruitment of renin containing cells along the afferent arteriole, (2) causes no changes in intrarenal renin mRNA levels or distribution, suggesting that post-transcriptional events may be responsible for the persistence and/or uptake of renin by the preglomerular vasculature, (3) promotes a downregulation of AT1 receptor gene in the kidney, suggesting that local angiotensin II may control AT1 receptor gene expression by a negative feedback.

摘要

为了确定环孢素A(CsA)是否会改变肾内肾素和1型血管紧张素II受体基因的表达,对成年雄性Sprague-Dawley大鼠皮下注射25mg/kg/天的CsA,持续三周(CsA组,N = 20),并与配对喂养的给予赋形剂的大鼠(对照组,N = 20)进行比较。通过免疫细胞化学和原位杂交评估肾内肾素及其mRNA的分布。此外,通过Northern印迹分析测定肾脏肾素和1型血管紧张素II(AT1)受体mRNA水平。CsA组中含有肾素的球旁器百分比(84±5.5%)高于对照组(61±6.7%),(P < 0.05)。CsA组沿入球小动脉的肾素免疫染色长度(74±4.5微米)高于对照组(37±5.1微米),(P < 0.05)。相反,长期给予CsA并未改变肾素mRNA水平及其在肾内的分布。CsA组的肾脏AT1受体mRNA水平低于对照组。我们得出结论,长期给予CsA:(1)诱导沿入球小动脉的含肾素细胞募集,(2)不会引起肾内肾素mRNA水平或分布的变化,这表明转录后事件可能是导致肾素在肾小球前血管系统中持续存在和/或摄取的原因,(3)促进肾脏中AT1受体基因的下调,这表明局部血管紧张素II可能通过负反馈控制AT1受体基因表达。

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