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锂清除率在评估糖尿病患者节段性肾小管对钠和水的重吸收中的应用

Lithium clearance in the evaluation of segmental renal tubular reabsorption of sodium and water in diabetes mellitus.

作者信息

Skøtt P

机构信息

Hvidøre Hospital, Copenhagen.

出版信息

Dan Med Bull. 1994 Feb;41(1):23-37.

PMID:8187564
Abstract

Lithium is the best available marker of proximal tubular reabsorption of fluid. The first part of the present thesis reviews the background for the use of the lithium clearance (CLi) method. Micropuncture studies on proximal reabsorption of lithium, showed that CLi is a reasonably correct measure of end-proximal fluid delivery rate, even during osmotic diuresis. During severe salt restriction, distal reabsorption of lithium renders the CLi method inappropriate in animals, but this problem does probably not occur in humans. The major current issue is whether a quantitatively significant reabsorption of lithium occurs in the loop of Henle. Available evidence is in accord with the interpretation that it does not occur. The interpretation of results form CLi studies depends to a surprising degree on the investigators beliefs about renal physiology. In the evaluation of proximal tubular function, the relevant parameter is the absolute proximal reabsorption rate of fluid and sodium. In the evaluation of integrated distal tubular reabsorption of sodium, the relevant parameter is the fractional distal reabsorption rate of sodium. The fractional CLi does not give meaningful information, and calculated absolute distal reabsorption rate of sodium is inherently not suited to detect modest changes in distal reabsorption leading to large changes in sodium excretion. Results from the use of the CLi method in relation to diabetes are reviewed in the second section. Even in IDDM patients with early diabetic nephropathy, the proximal reabsorption rate is elevated, resulting in a normal CLi despite glomerular hyperfiltration. Overnight euglycemia did not change GFR in IDDM patients, but during maintained euglycemia, GFR was normalized. A few hours of hyperglycemia prevented the decline in GFR, whereas CLi was unchanged. Thus hyperglycemia produced changes in renal function similar to those observed previously, but the time-course of the effect of euglycemia on kidney function is delayed. Plasma levels of atrial natriuretic peptide, renin and glucagon were not importantly affected by plasma glucose. In NIDDM patients CLi was normal, despite slight hyperfiltration, although this observation must be confirmed in a study with larger sample size. Prompted by the clinical observation of a marked decline in the GFR induced by carbonic anhydrase inhibitors, we studied the renal effects of acetazolamide in a controlled study.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

锂是近端肾小管对液体重吸收的最佳可用标志物。本论文的第一部分回顾了使用锂清除率(CLi)方法的背景。对锂近端重吸收的微穿刺研究表明,即使在渗透性利尿期间,CLi也是近端肾小管末端液体输送速率的合理准确测量指标。在严格限制盐分摄入期间,锂的远端重吸收使得CLi方法不适用于动物,但这个问题在人类中可能不会出现。当前的主要问题是在亨氏袢中是否发生了具有定量意义的锂重吸收。现有证据支持其未发生的解释。CLi研究结果的解释在很大程度上取决于研究者对肾脏生理学的看法。在评估近端肾小管功能时,相关参数是液体和钠的绝对近端重吸收率。在评估钠的远端肾小管综合重吸收时,相关参数是钠的远端重吸收分数率。CLi分数没有提供有意义的信息,并且计算得出的钠的绝对远端重吸收率本质上不适合检测导致钠排泄大幅变化的远端重吸收的适度变化。第二部分回顾了使用CLi方法与糖尿病相关的结果。即使在患有早期糖尿病肾病的胰岛素依赖型糖尿病(IDDM)患者中,近端重吸收率也会升高,尽管存在肾小球高滤过,但CLi仍正常。一夜的血糖正常化并未改变IDDM患者的肾小球滤过率(GFR),但在维持血糖正常期间,GFR恢复正常。数小时的高血糖可防止GFR下降,而CLi保持不变。因此,高血糖产生的肾功能变化与先前观察到的相似,但血糖正常化对肾功能影响的时间进程有所延迟。血浆心房利钠肽、肾素和胰高血糖素水平并未受到血浆葡萄糖的重要影响。在非胰岛素依赖型糖尿病(NIDDM)患者中,尽管存在轻微的高滤过,但CLi正常,不过这一观察结果必须在更大样本量的研究中得到证实。受碳酸酐酶抑制剂导致GFR显著下降这一临床观察结果的启发,我们在一项对照研究中研究了乙酰唑胺对肾脏的影响。(摘要截选至400字)

相似文献

1
Lithium clearance in the evaluation of segmental renal tubular reabsorption of sodium and water in diabetes mellitus.锂清除率在评估糖尿病患者节段性肾小管对钠和水的重吸收中的应用
Dan Med Bull. 1994 Feb;41(1):23-37.
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Eur J Clin Invest. 2005 May;35(5):330-6. doi: 10.1111/j.1365-2362.2005.01497.x.
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[Regulation of natriuresis in diabetic nephropathy].[糖尿病肾病中利钠作用的调节]
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Glomerular and tubular antinatriuretic actions of low-dose angiotensin II infusion in man.低剂量血管紧张素II输注对人体肾小球和肾小管的利钠作用。
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Effect of renal nerve activity on tubular sodium and water reabsorption in dog kidneys as determined by the lithium clearance method.用锂清除率法测定肾神经活动对犬肾肾小管钠和水重吸收的影响。
Acta Physiol Scand. 1986 Feb;126(2):251-7. doi: 10.1111/j.1748-1716.1986.tb07812.x.
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