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环孢素载体聚氧乙烯蓖麻油(Cremophor EL)对大鼠肾微血管血流的影响。

The influence of the cyclosporine vehicle, cremophor EL, on renal microvascular blood flow in the rat.

作者信息

Abraham J S, Bentley F R, Garrison R N, Cryer H M

机构信息

Department of Surgery, University of Louisville School of Medicine, Kentucky 40292.

出版信息

Transplantation. 1991 Jul;52(1):101-5. doi: 10.1097/00007890-199107000-00021.

Abstract

Cyclosporine nephrotoxicity may be due to glomerular hypoperfusion. Previous experimental and clinical studies have demonstrated a decrease in renal blood flow and an increase in renal vascular resistance. Cremophor EL, which is the vehicle in which CsA is dissolved, is thought to be a factor involved in intrarenal arteriolar vasoconstriction. To determine the relative contributions of the vehicle and CsA to intrarenal arteriolar vasoconstriction, we used in vivo videomicroscopy and Doppler velocimetry to measure changes in renal microvascular blood flow in the rat. A 5-min intravenous infusion of 20 mg/kg of CsA resulted in a 17% mean reduction (P less than 0.05) in the diameter of preglomerular interlobular arterioles and an associated 60% reduction (P less than 0.05) in microvascular blood flow by 15 min. Cremophor EL/ethanol equivalent caused less vasoconstriction (up to 10%) but resulted in a 42% mean decrease (P less than 0.05) in microvascular blood flow, probably secondary to a 38% mean decrease (P less than 0.05) in cardiac output and 13% decrease in arterial pressure. We conclude that cremophor EL does contribute to in vivo reduction of preglomerular microvascular blood flow in the rat. This may be particularly important when using this intravenous preparation in the study of CsA nephrotoxicity.

摘要

环孢素肾毒性可能归因于肾小球灌注不足。既往的实验和临床研究已证实肾血流量减少以及肾血管阻力增加。聚氧乙烯蓖麻油EL是溶解环孢素的溶媒,被认为是肾内小动脉血管收缩的一个相关因素。为了确定溶媒和环孢素对肾内小动脉血管收缩的相对作用,我们采用体内视频显微镜和多普勒测速法来测量大鼠肾微血管血流的变化。静脉输注20mg/kg环孢素5分钟导致入球小动脉直径平均减小17%(P<0.05),到15分钟时微血管血流相应减少60%(P<0.05)。聚氧乙烯蓖麻油EL/乙醇等效物引起的血管收缩较小(高达10%),但导致微血管血流平均减少42%(P<0.05),这可能继发于心输出量平均减少38%(P<0.05)和动脉压降低13%。我们得出结论,聚氧乙烯蓖麻油EL确实会导致大鼠体内入球微血管血流减少。在环孢素肾毒性研究中使用这种静脉制剂时,这可能尤为重要。

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