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残余肾中肾内皮素基因表达增加,并与疾病进展相关。

Renal endothelin gene expression is increased in remnant kidney and correlates with disease progression.

作者信息

Orisio S, Benigni A, Bruzzi I, Corna D, Perico N, Zoja C, Benatti L, Remuzzi G

机构信息

Mario Negri Institute for Pharmacological Research, Bergamo, Italy.

出版信息

Kidney Int. 1993 Feb;43(2):354-8. doi: 10.1038/ki.1993.53.

DOI:10.1038/ki.1993.53
PMID:8441230
Abstract

We previously demonstrated that urinary endothelin excretion is increased in rats with extensive renal mass reduction, a model of progressive renal disease. Here we explored whether the increased urinary endothelin in this model were due to induction of renal pre-pro-endothelin-1 gene and whether changes in endothelin synthetic pathway correlated with the development of glomerulosclerosis. Four groups of rats with renal mass reduction and four groups of sham-operated control rats were studied 7, 30, 60 and 120 days after the surgical procedure. Urinary protein excretion in renal mass ablation animals did not differ from controls at seven days, but was already significantly elevated (P < 0.01) 30 days after surgery. Then proteinuria progressively increased in rats with remnant kidney at values above 400 mg/day at day 120. Serum creatinine concentration also progressively increased with time in renal mass ablation rats, unlike sham-operated animals, and values were significantly different (P < 0.01) at each of the points considered. Rats with renal mass reduction, unlike sham-operated animals, developed focal glomerulosclerosis that affected 8% of glomeruli at day 30, and 24% of glomeruli at day 120. Seven days after renal mass reduction renal pre-pro-endothelin-1 (pre-pro ET) mRNA was comparable to that of sham-operated rats, while a 2.5-, 5- and fourfold increase in 2.3 Kb pre-proET-1 transcript was observed at 30, 60 and 120 days, respectively. Urinary excretion of endothelin was significantly elevated (P < 0.01) in rats with renal mass reduction with respect to sham-operated rats, starting from 30 days after surgery and increased further thereafter.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们先前已证明,在广泛肾实质减少的大鼠(一种进行性肾病模型)中,尿内皮素排泄增加。在此,我们探究了该模型中尿内皮素增加是否归因于肾前内皮素原-1基因的诱导,以及内皮素合成途径的变化是否与肾小球硬化的发展相关。对四组肾实质减少的大鼠和四组假手术对照大鼠在手术操作后7、30、60和120天进行了研究。肾实质切除动物的尿蛋白排泄在7天时与对照组无差异,但在手术后30天已显著升高(P<0.01)。然后,残余肾大鼠的蛋白尿在第120天时逐渐增加,超过400mg/天。与假手术动物不同,肾实质切除大鼠的血清肌酐浓度也随时间逐渐增加,在每个观察点的值均有显著差异(P<0.01)。与假手术动物不同,肾实质减少的大鼠发生了局灶性肾小球硬化,在第30天时影响8%的肾小球,在第120天时影响24%的肾小球。肾实质减少7天后,肾前内皮素原-1(pre-pro ET)mRNA与假手术大鼠相当,而在30、60和120天时分别观察到2.3Kb pre-proET-1转录本增加了2.5倍、5倍和4倍。与假手术大鼠相比,肾实质减少的大鼠尿内皮素排泄从手术后30天开始显著升高(P<0.01),此后进一步增加。(摘要截短于250字)

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