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肾锂重吸收的微穿刺研究:氨氯地平和呋塞米的作用

A micropuncture study of renal lithium reabsorption: effects of amiloride and furosemide.

作者信息

Shirley D G, Walter S J, Sampson B

机构信息

Department of Physiology, Charing Cross and Westminster Medical School, London, United Kingdom.

出版信息

Am J Physiol. 1992 Dec;263(6 Pt 2):F1128-33. doi: 10.1152/ajprenal.1992.263.6.F1128.

DOI:10.1152/ajprenal.1992.263.6.F1128
PMID:1481889
Abstract

The validity of the lithium clearance technique as a measure of end-proximal fluid delivery was assessed using micropuncture in sodium-replete, Inactin-anesthetized Sprague-Dawley rats. Three groups of animals were used: controls, amiloride treated, and furosemide treated. Diuretic-induced salt and water losses were replaced. Fractional lithium excretion (FELi) was 0.23 +/- 0.01, 0.24 +/- 0.02, and 0.40 +/- 0.03 in the control, amiloride, and furosemide groups, respectively. In each group, the tubular fluid-to-plasma lithium concentration ratio at the end of the proximal convoluted tubule (PCT) was significantly greater than unity (control, 1.16 +/- 0.03; amiloride, 1.16 +/- 0.02; furosemide, 1.17 +/- 0.02). In the control group, fractional lithium delivery (FDLi) at the late PCT was 0.50 +/- 0.02, while FDLi at the early distal tubule was 0.25 +/- 0.01; the latter did not differ significantly from FDLi at the late distal tubule or from FELi. Values in amiloride-treated rats were almost identical. Furosemide had no effect on FDLi at the late PCT, but raised that at the early distal tubule to 0.37 +/- 0.03. We conclude that 1) lithium reabsorption in the PCT lags slightly behind that of water, 2) substantial furosemide-sensitive lithium reabsorption occurs beyond the PCT, and 3) no significant lithium reabsorption occurs in nephron segments beyond the loop. These findings call into question the use of lithium clearance as a quantitative measure of end-proximal fluid delivery in sodium-replete animals.

摘要

在钠充足、用英纳酮麻醉的斯普拉格 - 道利大鼠中,采用微穿刺法评估锂清除技术作为近端终末液体输送量度的有效性。使用了三组动物:对照组、氨氯吡脒处理组和呋塞米处理组。利尿剂诱导的盐和水流失得到补充。对照组、氨氯吡脒组和呋塞米组的锂排泄分数(FELi)分别为0.23±0.01、0.24±0.02和0.40±0.03。在每组中,近端曲管(PCT)末端的肾小管液与血浆锂浓度比均显著大于1(对照组为1.16±0.03;氨氯吡脒组为1.16±0.02;呋塞米组为1.17±0.02)。在对照组中,PCT晚期的锂输送分数(FDLi)为0.50±0.02,而远端小管早期的FDLi为0.25±0.01;后者与远端小管晚期的FDLi或FELi无显著差异。氨氯吡脒处理的大鼠中的值几乎相同。呋塞米对PCT晚期的FDLi无影响,但将远端小管早期的FDLi提高到0.37±0.03。我们得出结论:1)PCT中锂的重吸收略落后于水的重吸收;2)在PCT之外发生了大量对呋塞米敏感的锂重吸收;3)在髓袢之外的肾单位节段中未发生显著的锂重吸收。这些发现对在钠充足的动物中使用锂清除作为近端终末液体输送的定量测量方法提出了质疑。

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