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超氧化物歧化酶和过氧化氢酶单独给药对心肌“顿抑”的影响。

Effect of superoxide dismutase and catalase, given separately, on myocardial "stunning".

作者信息

Jeroudi M O, Triana F J, Patel B S, Bolli R

机构信息

Department of Medicine, Baylor College of Medicine, Houston, Texas 77030.

出版信息

Am J Physiol. 1990 Sep;259(3 Pt 2):H889-901. doi: 10.1152/ajpheart.1990.259.3.H889.

Abstract

Controversy persists regarding which oxygen metabolites are cytotoxic. Although the combination of superoxide dismutase (SOD) and catalase has been shown to attenuate postischemic myocardial dysfunction ("stunning"), it is unknown whether this beneficial effect is due to scavenging of O2-., H2O2, or both. Accordingly, 85 open-chest dogs underwent a 15-min occlusion of the left anterior descending coronary artery followed by 4 h of reperfusion. In phase A, dogs received an intravenous infusion of saline (group I), SOD (5 mg/kg, group II), catalase (12,000 U/kg, group III), or the combination of SOD and catalase (same doses, group IV). Recovery of regional myocardial function (assessed as systolic wall thickening) after reperfusion was significantly improved by the combination of SOD and catalase but not by SOD alone or catalase alone. To determine whether higher doses of enzymes are more effective, in phase B dogs received an intracoronary infusion of normal saline (group V), SOD in low dose (1.5 mg/kg, group VI), SOD in high dose (6.3 mg/kg plus 1.5 mg/kg iv, group VII), catalase in low dose (18,000 U/kg, group VIII), or catalase in high dose (240,000 U/kg plus 40,000 U/kg iv, group IX). Despite the fact that the local plasma levels of enzymes were considerably higher than those achieved in phase A, none of the treatments in phase B significantly enhanced recovery of contractile function. This study demonstrates that the combination of SOD and catalase is more effective than either enzyme alone in attenuating postischemic myocardial dysfunction and that increasing the doses of SOD or catalase does not provide additional protection. The results suggest that both O2-. and H2O2 contribute significantly to the pathogenesis of myocardial stunning after regional ischemia in the intact animal. Furthermore, the data imply that if SOD and catalase are to be used clinically to prevent postischemic dysfunction, protection may be achieved most effectively by combining the two enzymes.

摘要

关于哪些氧代谢产物具有细胞毒性,目前仍存在争议。尽管超氧化物歧化酶(SOD)和过氧化氢酶的联合使用已被证明可减轻缺血后心肌功能障碍(“心肌顿抑”),但这种有益效果是由于清除了超氧阴离子(O2-.)、过氧化氢(H2O2),还是两者都有作用,尚不清楚。因此,85只开胸犬接受了15分钟的左前降支冠状动脉闭塞,随后再灌注4小时。在A阶段,犬分别接受静脉输注生理盐水(I组)、SOD(5mg/kg,II组)、过氧化氢酶(12,000U/kg,III组)或SOD与过氧化氢酶的联合使用(相同剂量,IV组)。再灌注后局部心肌功能的恢复(以收缩期室壁增厚来评估),SOD与过氧化氢酶联合使用组明显改善,而单独使用SOD或过氧化氢酶组则无明显改善。为了确定更高剂量的酶是否更有效,在B阶段,犬接受冠状动脉内输注生理盐水(V组)、低剂量SOD(1.5mg/kg,VI组)、高剂量SOD(6.3mg/kg加1.5mg/kg静脉注射,VII组)、低剂量过氧化氢酶(18,000U/kg,VIII组)或高剂量过氧化氢酶(240,000U/kg加40,000U/kg静脉注射,IX组)。尽管B阶段局部血浆中的酶水平明显高于A阶段,但B阶段的任何一种治疗均未显著增强收缩功能的恢复。本研究表明,SOD与过氧化氢酶联合使用在减轻缺血后心肌功能障碍方面比单独使用任何一种酶更有效,且增加SOD或过氧化氢酶的剂量并不能提供额外的保护。结果表明,超氧阴离子(O2-.)和过氧化氢(H2O2)在完整动物局部缺血后心肌顿抑的发病机制中均起重要作用。此外,数据表明,如果临床上要使用SOD和过氧化氢酶来预防缺血后功能障碍,将这两种酶联合使用可能最有效地实现保护作用。

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