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钙通道阻滞可预防环孢素所致肾缺血性损伤加重的证据。

Evidence that calcium channel blockade prevents cyclosporine-induced exacerbation of renal ischemic injury.

作者信息

Bia M J, Tyler K

机构信息

Department of Medicine, Yale University School of Medicine, New Haven, Connecticut.

出版信息

Transplantation. 1991 Feb;51(2):293-5. doi: 10.1097/00007890-199102000-00002.

DOI:10.1097/00007890-199102000-00002
PMID:1847248
Abstract

The following study was performed to determine whether calcium channel blockers, delivered before or after an ischemic insult, were effective at reducing cyclosporine-induced exacerbation of renal ischemic injury. When cyclosporine (5 mg/kg) was administered intravenously to rats after 30 min of renal ischemia, GFR fell by 60% compared with values observed in rats subjected to ischemia alone (190 +/- 30 vs. 330 +/- 40 microliters/min/100 g; P less than 0.05). Pretreatment with verapamil (10 micrograms/kg/min delivered intravenously) prevented the fall in GFR (320 +/- 70 microliters/min 100 g), as did pretreatment with nitrendipine, 1 micrograms/kg/min (460 +/- 90 microliters/min/100 g). Verapamil was less effective if given after the ischemia-cyclosporine insult (GFR 260 +/- 90 microliters/min/100 g), and nitrendipine given at this time had no beneficial effect at all (GFR 180 +/- 10 microliters/min/100 g). The doses of calcium channel blockers used had no protective effect on renal ischemic injury alone. Blood pressure during study ranged between 105 and 119 mm Hg with minor differences between groups. Sodium and potassium excretion and urinary flow rates were similar in all groups, except for a slight increase in sodium excretion in verapamil-treated rats. These values demonstrate that calcium channel blockers ameliorate the exacerbation or renal ischemic injury induced by cyclosporine if given before but not after the ischemia-cyclosporine insult. The protective effect of these agents, used preischemia in cyclosporine-treated rats, is observed with intravenous use of the drugs at doses that have no protective effect on renal ischemic injury alone.

摘要

进行以下研究以确定钙通道阻滞剂在缺血性损伤之前或之后给药是否能有效减轻环孢素诱导的肾缺血损伤加重。在肾缺血30分钟后给大鼠静脉注射环孢素(5mg/kg),与仅接受缺血的大鼠相比,肾小球滤过率(GFR)下降了60%(190±30对330±40微升/分钟/100克;P<0.05)。维拉帕米预处理(静脉注射10微克/千克/分钟)可防止GFR下降(320±70微升/分钟/100克),尼群地平预处理(1微克/千克/分钟)也有同样效果(460±90微升/分钟/100克)。如果在缺血-环孢素损伤后给予维拉帕米,其效果较差(GFR为260±90微升/分钟/100克),此时给予尼群地平则完全没有有益作用(GFR为180±10微升/分钟/100克)。所用钙通道阻滞剂的剂量对单纯肾缺血损伤没有保护作用。研究期间血压在105至119mmHg之间,各组之间差异不大。除维拉帕米治疗的大鼠钠排泄略有增加外,所有组的钠和钾排泄以及尿流率相似。这些数值表明,如果在缺血-环孢素损伤之前而非之后给予钙通道阻滞剂,可改善环孢素诱导的肾缺血损伤加重。在环孢素治疗的大鼠缺血前使用这些药物,静脉注射这些药物时,在对单纯肾缺血损伤无保护作用的剂量下可观察到其保护作用。

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