Impaired effect by NO synthase inhibition on tubuloglomerular feedback in rats after chronic renal denervation.

C Thorup, J Kurkus, P Morsing, A Ollerstam, A E Persson
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引用次数: 2

Abstract

Acute unilateral renal denervation (aDNX) is associated with reduced tubuloglomerular feedback (TGF) sensitivity. Six days after denervation (cDNX) TGF sensitivity is somewhat restored, but TGF reactivity increased. This study aimed to investigate if the increased TGF reactivity that was seen in cDNX kidneys was owing to reduced production of nitric oxide (NO). TGF characteristics were determined with micropuncture experiments in anaesthetized rats, using the stop-flow pressure (PSF) technique. Maximal drop in PSF (DeltaPSF) was used as an index of TGF reactivity and the loop of Henle perfusion rate that elicited half-maximal DeltaPSF, the turning point (TP) was used as a measure of TGF sensitivity. In cDNX kidneys, TP was higher than in control rats (25.4 +/- 1.5 nL min-1 vs. 19.1 +/- 1.1 nL min-1), but clearly lower than in aDNX rats (37. 3 +/- 3.1 nL min-1). TGF was more reactive in cDNX rats (DeltaPSF=14. 7 +/- 1.1 mmHg) than in aDNX (7.9 +/- 1.1 mmHg) and control rats (9. 6 +/- 0.9 mmHg). Intratubular inhibition of NO synthase N omega-nitro-L-arginine (L-NA) in sham-DNX animals, decreased TP to 13.9 +/- 2.2 nL min-1 and DeltaPSF was increased with 92%. In cDNX kidneys TP was not significantly reduced by L-NA, and TGF reactivity was only moderately increased by 31%. Intratubular infusion of L-arginine (L-Arg) reduced DeltaPSF from 10.2 +/- 0.7 to 6.5 +/- 0.6 mmHg in sham-DNX kidneys, but TP was unaffected. In cDNX kidneys, there was no effect on either DeltaPSF or TP by the addition of L-Arg. However, when NO was delivered via sodium nitroprusside in the tubular perfusate, a clear reduction of DeltaPSF was seen in both sham-DNX and cDNX kidneys (from 9.9 +/- 0.5 to 4.4 +/- 1.0 and from14.9 +/- 1.3 to 8.1 +/- 1.5 mmHg, respectively). This indicates that cDNX is a state of low renal NO production and that this low level of NO resets TGF to a higher sensitivity and more pronounced reactivity.

NO合酶抑制对大鼠慢性肾去神经后小管肾小球反馈的影响。
急性单侧肾去神经支配(aDNX)与小管肾小球反馈(TGF)敏感性降低有关。去神经支配6天后(cDNX) TGF敏感性有所恢复,但TGF反应性增高。本研究旨在探讨cDNX肾脏中TGF反应性的增加是否由于一氧化氮(NO)的产生减少。采用停止流压(PSF)技术,在麻醉大鼠的微穿刺实验中测定TGF的特征。以最大PSF下降(DeltaPSF)作为TGF反应性指标,以诱导半最大DeltaPSF的Henle灌注率环、转折点(TP)作为TGF敏感性指标。cDNX肾TP高于对照大鼠(25.4 +/- 1.5 nL min-1 vs. 19.1 +/- 1.1 nL min-1),但明显低于aDNX大鼠(37。3±3.1 nL min-1)。TGF在cDNX大鼠中的活性更高(DeltaPSF=14)。7 +/- 1.1 mmHg)高于aDNX组(7.9 +/- 1.1 mmHg)和对照组(9。6±0.9 mmHg)。假性dnx动物小管内NO合成酶N - omega-硝基- l -精氨酸(L-NA)抑制使TP降低至13.9 +/- 2.2 nL min-1, DeltaPSF增加92%。在cDNX肾脏中,TP未被L-NA显著降低,TGF反应性仅适度升高31%。在假dnx肾脏中,小管内输注l -精氨酸(L-Arg)可使DeltaPSF从10.2 +/- 0.7降至6.5 +/- 0.6 mmHg,但TP未受影响。在cDNX肾脏中,添加l -精氨酸对DeltaPSF和TP均无影响。然而,当NO通过硝普钠在小管灌注液中传递时,假性dnx和cDNX肾脏中DeltaPSF明显减少(分别从9.9 +/- 0.5降至4.4 +/- 1.0和从14.9 +/- 1.3降至8.1 +/- 1.5 mmHg)。这表明cDNX是一种低肾NO生成的状态,这种低水平的NO使TGF具有更高的敏感性和更明显的反应性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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