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内皮素与肾神经的相互作用调节自发性高血压大鼠的肾功能。

Interaction of endothelin with renal nerves modulates kidney function in spontaneously hypertensive rats.

作者信息

Girchev Radoslav A, Bäcker Angela, Markova Petia P, Kramer Herbert J

机构信息

Renal Section, Medical Policlinic, University of Bonn, Bonn, Germany.

出版信息

Kidney Blood Press Res. 2006;29(2):126-34. doi: 10.1159/000094571. Epub 2006 Jul 21.

Abstract

BACKGROUND AND METHODS

We investigated kidney function, renal endothelin-1 concentration, prepro-endothelin-1 mRNA as well as endothelin receptor A and B mRNA expression and receptor properties in normotensive Wistar-Kyoto (WKY) rats and spontaneously hypertensive rats (SHR) with intact renal nerves and 7 days after renal denervation. In addition, responses of renal function to the non-selective ETA/ETB receptor blocker bosentan (10 mg/kg i.v. bolus injection) were studied.

RESULTS

In SHR, renal papillary prepro-endothelin-1 mRNA expression, endothelin-1 tissue concentrations and endothelin receptor density were significantly lower than in normotensive rats. Renal denervation was associated with a decrease in papillary tissue prepro-endothelin-1 mRNA and in WKY rats also with a significant reduction in papillary endothelin-1 content without affecting ET receptor density. Bosentan did not alter renal blood flow or glomerular filtration rate but decreased urine flow rate in both intact normotensive and hypertensive rats, whereas it decreased urine sodium and potassium excretion only in intact WKY. Bosentan had no effects on renal function in renal denervated rats.

CONCLUSION

Since renal papillary endothelin-1 appears to counteract the fluid and sodium retaining effects of renal nerve activity, an impaired renal endothelin-1 synthesis in SHR may contribute to excessive sodium retention and thus to the pathogenesis of hypertension in SHR.

摘要

背景与方法

我们研究了正常血压的Wistar-Kyoto(WKY)大鼠和自发性高血压大鼠(SHR)在肾神经完整及肾去神经支配7天后的肾功能、肾内皮素-1浓度、前内皮素原-1 mRNA以及内皮素A和B受体mRNA表达与受体特性。此外,还研究了肾功能对非选择性ETA/ETB受体阻滞剂波生坦(10 mg/kg静脉推注)的反应。

结果

在SHR中,肾乳头前内皮素原-1 mRNA表达、内皮素-1组织浓度和内皮素受体密度显著低于正常血压大鼠。肾去神经支配与乳头组织前内皮素原-1 mRNA减少有关,在WKY大鼠中还与乳头内皮素-1含量显著降低有关,而不影响ET受体密度。波生坦在完整的正常血压和高血压大鼠中均未改变肾血流量或肾小球滤过率,但降低了尿流率,而仅在完整的WKY大鼠中降低了尿钠和钾排泄。波生坦对肾去神经支配大鼠的肾功能无影响。

结论

由于肾乳头内皮素-1似乎可抵消肾神经活动的保液和保钠作用,SHR中肾内皮素-1合成受损可能导致钠潴留过多,从而促成SHR高血压的发病机制。

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