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呋塞米对清醒大鼠肾血流动力学及近端肾小管钠重吸收的影响。

Effects of furosemide on renal haemodynamics and proximal tubular sodium reabsorption in conscious rats.

作者信息

Christensen S, Petersen J S

机构信息

Department of Pharmacology, University of Copenhagen, Denmark.

出版信息

Br J Pharmacol. 1988 Oct;95(2):353-60. doi: 10.1111/j.1476-5381.1988.tb11653.x.

Abstract
  1. The effects of furosemide given as constant i.v. infusion (7.5 mg kg-1 h-1) or bolus injections (0.5, 7.5 and 120 mg kg-1) on renal haemodynamics and proximal tubular Na reabsorption were studied in conscious water diuretic rats. The clearance of Li (CLi) was used as marker for Na delivery from the proximal tubules, and clearance of [14C]-tetraethylammonium (CTEA) and [3H]-inulin (CIn) as markers for renal plasma flow (RPF) and glomerular filtration rate (GFR), respectively. 2. Furosemide caused a transient increase of RPF and GFR followed by a secondary decrease below baseline levels; the latter could in part be counteracted by volume replacement. The filtration fraction (FF = GFR/RPF) was not significantly changed by furosemide. Fractional proximal Na excretion (CLi/CIn) was significantly increased by all doses of furosemide independent of changes in RPF, GFR and FF. 3. The peak diuretic/natriuretic effect of furosemide was markedly potentiated by volume replacement, probably due to prevention of antinatriuretic mechanisms triggered by volume depletion. 4. It is concluded that following i.v. furosemide administration there is a biphasic change in renal haemodynamics in conscious, restrained rats, and that the inhibition of proximal Na reabsorption, as manifested by changes in fractional Li excretion, is not likely to be due to changes in total renal haemodynamics.
摘要
  1. 在清醒的水利尿大鼠中,研究了持续静脉输注(7.5毫克/千克/小时)或推注(0.5、7.5和120毫克/千克)呋塞米对肾血流动力学和近端肾小管钠重吸收的影响。锂清除率(CLi)用作近端小管钠输送的标志物,[14C] - 四乙铵清除率(CTEA)和[3H] - 菊粉清除率(CIn)分别用作肾血浆流量(RPF)和肾小球滤过率(GFR)的标志物。2. 呋塞米导致RPF和GFR短暂增加,随后继发降低至基线水平以下;后者部分可通过补充容量来抵消。呋塞米对滤过分数(FF = GFR/RPF)无显著影响。所有剂量的呋塞米均显著增加近端钠排泄分数(CLi/CIn),而与RPF、GFR和FF的变化无关。3. 补充容量可显著增强呋塞米的利尿/利钠峰值效应,这可能是由于预防了容量减少引发的抗利钠机制。4. 得出结论,静脉注射呋塞米后,清醒、受限大鼠的肾血流动力学出现双相变化,并且以锂排泄分数变化表现出的近端钠重吸收抑制不太可能是由于总肾血流动力学的变化。

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