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饮食盐分对肾脏中一氧化氮合酶、肾素和血管紧张素原mRNA表达的协同调节

Coordinate regulation of renal expression of nitric oxide synthase, renin, and angiotensinogen mRNA by dietary salt.

作者信息

Singh I, Grams M, Wang W H, Yang T, Killen P, Smart A, Schnermann J, Briggs J P

机构信息

Department of Physiology, University of Michigan, Ann Arbor 48104, USA.

出版信息

Am J Physiol. 1996 Jun;270(6 Pt 2):F1027-37. doi: 10.1152/ajprenal.1996.270.6.F1027.

Abstract

Experiments were performed to examine the effect of changes in dietary salt intake on the neuronal form of the constitutive nitric oxide synthase (ncNOS, type I NOS), renin, and angiotensinogen mRNA expression in the kidney. Three groups of Sprague-Dawley rats were studied as follows: rats maintained on a 3% Na diet plus 0.45% NaCl in the drinking fluid for 7 days (high salt), rats given a single injection of furosemide (2 mg/kg i.p.) and a 0.03% Na diet for 7 days (low salt), and rats on a diet containing 0.2% Na (control). mRNA expression was assessed with reverse transcription-polymerase chain reaction (RT-PCR) methods using cDNA prepared from samples of renal cortex and microdissected tubular segments. ncNOS PCR products were quantified by comparison with a dilution series of a mutant deletion template. Compared with their respective control, ncNOS mRNA levels in renal cortical tissue were elevated in rats on a low-salt diet and reduced in rats on a high-salt diet. Similar changes were seen in the expression of renin and angiotensinogen mRNA. Dietary salt intake did not alter the mRNA levels for ncNOS from the inner medulla or for endothelial constitutive NOS (ecNOS, type III NOS) and inducible NOS (iNOS, type II NOS) in the renal cortex. ncNOS mRNA was found in glomeruli dissected with the macula densa-containing segment (MDCS), but only at marginal levels in glomeruli without MDCS. Furthermore, a low-salt diet stimulated ncNOS mRNA in glomeruli with MDCS by 6.2-fold compared with a high-salt diet. There was no effect of salt diet on ncNOS mRNA in glomeruli without MDCS or in inner medullary collecting ducts. These results suggest that ncNOS expression in macula densa cells is inversely regulated by salt intake, thus following the known response of the renin-angiotensin system to changes in salt balance.

摘要

进行实验以研究饮食中盐摄入量的变化对肾脏中组成型一氧化氮合酶(ncNOS,I型一氧化氮合酶)、肾素和血管紧张素原mRNA表达的神经元形式的影响。研究了三组Sprague-Dawley大鼠,如下:大鼠在饮用液中维持3%的钠饮食加0.45%的氯化钠7天(高盐组),大鼠单次注射速尿(2mg/kg腹腔注射)并给予0.03%的钠饮食7天(低盐组),以及给予含0.2%钠饮食的大鼠(对照组)。使用从肾皮质和显微解剖的肾小管段样本制备的cDNA,通过逆转录聚合酶链反应(RT-PCR)方法评估mRNA表达。通过与突变缺失模板的稀释系列比较来定量ncNOS PCR产物。与各自的对照组相比,低盐饮食的大鼠肾皮质组织中的ncNOS mRNA水平升高,高盐饮食的大鼠中则降低。肾素和血管紧张素原mRNA的表达也有类似变化。饮食中的盐摄入量并未改变肾内髓质中ncNOS的mRNA水平,也未改变肾皮质中内皮型组成型一氧化氮合酶(ecNOS,III型一氧化氮合酶)和诱导型一氧化氮合酶(iNOS,II型一氧化氮合酶)的mRNA水平。在与含致密斑段(MDCS)一起解剖的肾小球中发现了ncNOS mRNA,但在没有MDCS的肾小球中仅处于边缘水平。此外,与高盐饮食相比,低盐饮食使含MDCS的肾小球中的ncNOS mRNA增加了6.2倍。盐饮食对没有MDCS的肾小球或肾内髓质集合管中的ncNOS mRNA没有影响。这些结果表明,致密斑细胞中的ncNOS表达受盐摄入量的反向调节,因此遵循肾素-血管紧张素系统对盐平衡变化的已知反应。

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