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甲基强的松龙对肝素中和过程中补体激活的影响。

Effect of methylprednisolone on complement activation during heparin neutralization.

作者信息

Loubser P G

机构信息

Department of Anesthesiology, Baylor College of Medicine, Houston, Texas, USA.

出版信息

J Cardiovasc Pharmacol. 1997 Jan;29(1):23-7. doi: 10.1097/00005344-199701000-00004.

Abstract

During cardiac surgery, steroids are frequently administered before the initiation of cardiopulmonary bypass (CPB), termed "pre-treatment," to reduce "first phase" complement activation during cardiopulmonary bypass (CPB). "Second phase" complement activation also occurs during heparin neutralization with protamine, although the effects of steroid pretreatment on such activation are unknown. This study was performed in patients undergoing coronary artery bypass graft surgery to determine whether high-dose methylprednisolone pretreatment affected complement activation during heparin-protamine interaction after termination of CPB. In eight patients (group MP), methylprednisolone, 30 mg/kg, was administered before CPB commencement, whereas another eight patients received placebo (group C). By using 125I des Arg radioimmunoassay, C3a, C4a, and C5a were measured in the arterial blood samples drawn before and 10 min after administration of protamine. An increase in C3a and C4a was observed in both groups after protamine, suggesting classic pathway activation (delta C3a: group C, 4,484 +/- 3,320; group MP, 1,394 +/- 1,653; delta C4a: group C, 1,810 +/- 731; group MP, 717 +/- 580). C3a and C4a levels were significantly lower in group MP patients after protamine compared with controls [delta C3a, 3,499 +/- 1,826 (p < 0.05); delta C4a, 1,241 +/- 232 (p < 0.05)]. C5a was not detected in any samples. These results demonstrate that the effect of pretreatment persists beyond the period of CPB and that methylprednisolone inhibits second-phase complement activation during heparin-protamine interaction. These findings have implication for patients with severe anaphylactoid reactions to protamine.

摘要

在心脏手术期间,类固醇常在体外循环(CPB)开始前给药,即“预处理”,以减少体外循环期间的“第一阶段”补体激活。“第二阶段”补体激活也发生在鱼精蛋白中和肝素的过程中,尽管类固醇预处理对这种激活的影响尚不清楚。本研究对接受冠状动脉旁路移植手术的患者进行,以确定高剂量甲泼尼龙预处理是否会影响CPB结束后肝素-鱼精蛋白相互作用期间的补体激活。8名患者(MP组)在CPB开始前给予30mg/kg甲泼尼龙,而另外8名患者接受安慰剂(C组)。通过使用125I去精氨酸放射免疫测定法,在给予鱼精蛋白前和给药后10分钟采集的动脉血样本中测量C3a、C4a和C5a。两组患者在给予鱼精蛋白后均观察到C3a和C4a增加,提示经典途径激活(ΔC3a:C组,4484±3320;MP组,1394±1653;ΔC4a:C组,1810±731;MP组,717±580)。与对照组相比,MP组患者在给予鱼精蛋白后的C3a和C4a水平显著降低[ΔC3a,3499±1826(p<0.05);ΔC4a,1241±232(p<0.05)]。任何样本中均未检测到C5a。这些结果表明,预处理的效果在CPB期间之后仍然存在,并且甲泼尼龙在肝素-鱼精蛋白相互作用期间抑制第二阶段补体激活。这些发现对鱼精蛋白严重类过敏反应患者具有启示意义。

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