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及时给予艾卡苷可减轻家兔的再灌注损伤。

Timely administration of AICA riboside reduces reperfusion injury in rabbits.

作者信息

Kingma J G, Simard D, Rouleau J R

机构信息

Department of Medicine, Faculty of Medicine, Laval University, Ste-Foy, Quebec, Canada.

出版信息

Cardiovasc Res. 1994 Jul;28(7):1003-7. doi: 10.1093/cvr/28.7.1003.

Abstract

OBJECTIVE

Agents which promote increased interstitial adenosine levels may be cardioprotective. The aim of this study was to evaluate the ability of 5-amino-1-beta-D- ribofuranosylimidazole-4-carboxamide (AICAr), an adenosine regulating agent, to limit infarct size when given before ischaemia, before coronary reperfusion, or postreperfusion in a rabbit preparation of ischaemia-reperfusion injury.

METHODS

The left coronary artery was occluded for 30 min and subsequently the ischaemic bed was reperfused for 180 min. Infarct size and risk zone size were delineated by tetrazolium staining and microsphere autoradiography, respectively. Four groups were studied: controls (n = 13), AICAr (2.5 mg.kg-1.min-1 intravenously for 5 min followed by 0.5 mg.kg-1.min-1 for 60 min) beginning either 5 min before coronary occlusion (n = 11), 5 min before coronary reperfusion (n = 11), or at 25 min coronary reperfusion (n = 10). Lignocaine was not given in these experiments.

RESULTS

Infarct size, normalised to risk zone, was significantly reduced with AICAr given 5 min before coronary reperfusion, at 35.0(SEM 4.4)% v 51.8(3.9)% in controls; p = 0.03. Cardioprotection was not observed when AICAr was given either 5 min before coronary occlusion [44.2(4.8)%] or 25 min postreperfusion [45.9(3.2)%].

CONCLUSIONS

These findings support the hypothesis that adenosine regulating agents, such as AICAr, can modulate infarct size in this rabbit preparation of ischaemia-reperfusion injury.

摘要

目的

促进间质腺苷水平升高的药物可能具有心脏保护作用。本研究的目的是评估腺苷调节剂5-氨基-1-β-D-呋喃核糖基咪唑-4-甲酰胺(AICAr)在兔缺血再灌注损伤模型中,于缺血前、冠状动脉再灌注前或再灌注后给药时限制梗死面积的能力。

方法

左冠状动脉闭塞30分钟,随后缺血心肌床再灌注180分钟。分别用四氮唑染色和微球放射自显影法确定梗死面积和危险区面积。研究分为四组:对照组(n = 13),AICAr组(静脉注射2.5mg·kg-1·min-1,持续5分钟,随后0.5mg·kg-1·min-1,持续60分钟),给药时间分别为冠状动脉闭塞前5分钟(n = 11)、冠状动脉再灌注前5分钟(n = 11)或冠状动脉再灌注25分钟时(n = 10)。本实验未给予利多卡因。

结果

以危险区面积标准化的梗死面积,在冠状动脉再灌注前5分钟给予AICAr时显著减小,为35.0(标准误4.4)%,而对照组为51.8(3.9)%;p = 0.03。在冠状动脉闭塞前5分钟[44.2(4.8)%]或再灌注后25分钟[45.9(3.2)%]给予AICAr时未观察到心脏保护作用。

结论

这些发现支持这样的假说,即腺苷调节剂如AICAr可在该兔缺血再灌注损伤模型中调节梗死面积。

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