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原钒酸钠对体内肾素分泌的影响。

Effect of sodium orthovanadate on renal renin secretion in vivo.

作者信息

López Novoa J M, García J C, Cruz-Soto M A, Benabe J E, Martínez-Maldonado M

出版信息

J Pharmacol Exp Ther. 1982 Aug;222(2):447-51.

PMID:6284912
Abstract

The effect of vanadate (0.5 mumol/min) on renin secretory rate (RSR) of the kidney has been studied in nembutal-anesthetized, volume-expanded dogs. Intrarenal vanadate infusion caused a 69.3 +/- 8.8% decrease in RSR. This was accompanied by marked decreases in renal blood flow (RBF), glomerular filtration rate (GFR) and fractional excretion of sodium (FENa). Renal vascular resistance rose from 1.3 +/- 0.09 to 6.1 +/- 2.3 mm Hg/ml/min (P less than .0005). Papaverine infusion partially blunted the effect of vanadate on RSR (RSR only fell to 42. +/- 10% of basal values). The decreases in RBF and GFR were also less and FENa slightly higher than normal. Acetylcholine prevented the effects of vanadate more fully. There was no fall in RBF, GFR or FENa and it basically abolished the fall in RSR which fell only 19.4 +/- 25.3 of control (P = N.S.). Nifedipine (a slow Ca++ channels blocker) also prevented the fall in RBF, GFR and FENa induced by vanadate. RSR did not change significantly (7.8 +/- 10.9%). These results clearly demonstrate that vanadate is a potent inhibitor of renin secretion and suggest that inhibition of smooth muscle Na+, K+, adenasine triphosphatase and changes in the cystosolic concentration of Na and Ca are involved in its mechanism. Changes in perfusion pressure and sodium delivery to the macula densa appear to have little if any role in the inhibition.

摘要

在戊巴比妥麻醉、血容量扩张的犬中研究了钒酸盐(0.5微摩尔/分钟)对肾脏肾素分泌率(RSR)的影响。肾内输注钒酸盐导致RSR降低69.3±8.8%。这伴随着肾血流量(RBF)、肾小球滤过率(GFR)和钠分数排泄(FENa)的显著降低。肾血管阻力从1.3±0.09升高至6.1±2.3毫米汞柱/毫升/分钟(P<0.0005)。输注罂粟碱部分减弱了钒酸盐对RSR的影响(RSR仅降至基础值的42.±10%)。RBF和GFR的降低也较小,且FENa略高于正常水平。乙酰胆碱更充分地阻止了钒酸盐的作用。RBF、GFR或FENa没有下降,并且基本上消除了RSR的下降,RSR仅下降至对照值的19.4±25.3(P=无显著差异)。硝苯地平(一种慢钙通道阻滞剂)也阻止了钒酸盐诱导的RBF、GFR和FENa的下降。RSR没有显著变化(7.8±10.9%)。这些结果清楚地表明钒酸盐是肾素分泌的有效抑制剂,并提示平滑肌钠、钾、三磷酸腺苷酶的抑制以及钠和钙胞质浓度的变化参与了其作用机制。灌注压和致密斑钠输送的变化在这种抑制中似乎几乎没有作用。

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