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环孢素对大鼠肾脏稀释能力的影响。

Effect of cyclosporine on the diluting capacity of the rat kidney.

作者信息

Gnutzmann K H, Hering K, Gutsche H U

出版信息

Clin Nephrol. 1986;25 Suppl 1:S51-6.

PMID:3708937
Abstract

Micropuncture experiments were carried out on rat kidneys in order to analyze the diluting ability of the thick ascending limb of Henle's loop (TAL) after acute and chronic administration of cyclosporine. Male albino Wistar rats weighing 190 to 250 g were either given cyclosporine (CSA) orally for 10 days or received single i.v. infusions of the drug before the micropuncture experiments. Drug free vehicle was administered to animals of two respective control groups. The electrolyte concentration of fluid from individual TALs was measured by continuous conductivity monitoring of early distal tubular fluid during pulse perfusion procedures. The transport dependent decrease of the electrolyte concentrations within the diluting segment showed a semi-logarithmic time course in all groups of rats. Lowest conductivity values were reached within 60 seconds of flow equilibrium in controls as well as in CSA treated rats. Chronic CSA feeding (15 mg/24 h/kg b.w., dissolved in 0.3 ml olive oil) as well as a single i.v. infusion of 5 mg/kg b.w. resulted in a significantly higher electrolyte concentration of TAL fluid. Infusion of the solvent alone was without significant effect on the diluting segment. We conclude that the impairment of the diluting ability of the TAL and hence the delivery of tubular fluid with increased NaCl concentrations to the macula densa should lead to a stimulation of the tubulo-glomerular feedback mechanism. Feedback activation per se could be the cause of the consistent GFR decrease and thus contribute to the basic nephrotoxicity of CSA.

摘要

为了分析急性和慢性给予环孢素后亨利氏袢厚升支(TAL)的稀释能力,对大鼠肾脏进行了微穿刺实验。体重190至250克的雄性白化Wistar大鼠,要么口服环孢素(CSA)10天,要么在微穿刺实验前接受单次静脉注射该药物。给两个相应对照组的动物施用无药物载体。在脉冲灌注过程中,通过对早期远端肾小管液进行连续电导率监测,测量各个TAL的液体电解质浓度。在所有大鼠组中,稀释段内电解质浓度的运输依赖性降低呈现半对数时间进程。在对照组以及CSA处理的大鼠中,在流量平衡后60秒内达到最低电导率值。慢性给予CSA(15毫克/24小时/千克体重,溶于0.3毫升橄榄油)以及单次静脉注射5毫克/千克体重,均导致TAL液的电解质浓度显著升高。仅输注溶剂对稀释段无显著影响。我们得出结论,TAL稀释能力的损害以及因此向致密斑输送NaCl浓度升高的肾小管液应会导致肾小管-肾小球反馈机制的激活。反馈激活本身可能是GFR持续降低的原因,从而导致CSA的基本肾毒性。

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