Roczniak A, Zimpelmann J, Burns K D
Department of Cellular and Molecular Medicine, University of Ottawa and Ottawa General Hospital, Ottawa, Ontario, Canada K1H 8L6.
Am J Physiol. 1998 Jul;275(1):F46-54. doi: 10.1152/ajprenal.1998.275.1.F46.
Nitric oxide (NO) derived from neuronal NO synthase (nNOS) in the kidney inner medulla has been implicated in the regulation of arterial blood pressure. The purpose of the present study was to determine the effect of high dietary NaCl on the expression of nNOS in the rat inner medullary collecting duct (IMCD). After 3 days or 3 wk of high (4.0%)-NaCl diet in rats, urinary NO-2/NO-3 excretion significantly increased. In freshly microdissected IMCD, nNOS was readily detected by immunofluorescence with polyclonal antibody, an effect that was completely blocked by neutralization of antibody with immunizing antigen. In rats fed a 4.0% NaCl diet for 3 days, IMCD nNOS mRNA, detected by RT-PCR, did not change from control values (0.3% NaCl, 19.84 +/- 1.57 x 10(3), vs. 4.0% NaCl, 20.44 +/- 3.14 x 10(3) cpm; P = not significant, n = 3). By Western blotting however, nNOS protein expression significantly increased (0.3% NaCl, 0.51 +/- 0.12, vs. 4.0% NaCl, 0.92 +/- 0.14 arbitrary units; P < 0. 05, n = 5). After 3 wk of 4.0% dietary NaCl, expression of nNOS mRNA and protein in IMCD did not differ significantly from control values. In contrast to these data, renal cortical expression of nNOS mRNA and protein was significantly decreased after 4.0% NaCl diet for 3 days. High dietary NaCl had no significant effect on expression of mRNA for inducible NO synthase (iNOS) in IMCD after either 3 days or 3 wk. In summary, our data indicate that nNOS mRNA and protein are expressed in IMCD and that high dietary NaCl differentially regulates nNOS expression in IMCD and cortex. The early increase in nNOS protein in IMCD may contribute to enhanced local production of NO and thereby represent an adaptive response to salt intake.
肾脏内髓质中由神经元型一氧化氮合酶(nNOS)产生的一氧化氮(NO)与动脉血压调节有关。本研究旨在确定高盐饮食对大鼠内髓集合管(IMCD)中nNOS表达的影响。给大鼠喂食高(4.0%)盐饮食3天或3周后,尿中NO-2/NO-3排泄显著增加。在新鲜显微解剖的IMCD中,用多克隆抗体通过免疫荧光很容易检测到nNOS,用免疫抗原中和抗体可完全阻断这种效应。给大鼠喂食4.0% NaCl饮食3天,通过RT-PCR检测到的IMCD nNOS mRNA与对照值无变化(0.3% NaCl,19.84±1.57×10(3), vs. 4.0% NaCl,20.44±3.14×10(3) cpm;P无显著性差异,n = 3)。然而,通过蛋白质免疫印迹法,nNOS蛋白表达显著增加(0.3% NaCl,0.51±0.12, vs. 4.0% NaCl,0.92±0.14任意单位;P < 0.05,n = 5)。喂食4.0%饮食NaCl 3周后,IMCD中nNOS mRNA和蛋白的表达与对照值无显著差异。与这些数据相反,喂食4.0% NaCl饮食3天后,肾皮质中nNOS mRNA和蛋白的表达显著降低。高盐饮食对IMCD中诱导型一氧化氮合酶(iNOS)mRNA的表达在3天或3周后均无显著影响。总之,我们的数据表明nNOS mRNA和蛋白在IMCD中表达,高盐饮食对IMCD和皮质中nNOS的表达有不同的调节作用。IMCD中nNOS蛋白的早期增加可能有助于增强局部NO的产生,从而代表对盐摄入的一种适应性反应。