Suppr超能文献

阿卡地新可延长清醒家兔缺血预处理所提供的保护时限。

Acadesine extends the window of protection afforded by ischaemic preconditioning in conscious rabbits.

作者信息

Burckhartt B, Yang X M, Tsuchida A, Mullane K M, Downey J M, Cohen M V

机构信息

Department of Medicine, University of South Alabama, College of Medicine, Mobile 36688, USA.

出版信息

Cardiovasc Res. 1995 May;29(5):653-7.

PMID:7606753
Abstract

OBJECTIVE

Ischaemic preconditioning protects myocardium from infarction if the reperfusion interval between the brief and prolonged ischaemic intervals is less than 1 h. In anaesthetised rabbits acadesine (5-amino-4-imidazolecarboxamide riboside, AICAR), an adenosine enhancer which increases tissue adenosine during ischaemia, prolongs the window of protection to 2 h. The aim of this study was to try to determine the maximum extension of this window of protection, using chronically instrumented, unsedated rabbits.

METHODS

Rabbits were instrumented with a balloon occluder around a major branch of the left coronary artery for reversible coronary occlusion. Five to seven days after surgery all animals underwent a 30 min coronary occlusion. Animals were randomised to one of seven groups: (1) No additional treatment (control); (2) Ischaemic preconditioning with 5 min regional ischaemia followed by 10 min reperfusion before the 30 min coronary occlusion; (3) and (4) Ischaemic preconditioning followed by 2 or 4 h of reperfusion before the 30 min occlusion, respectively; (5) Treatment with acadesine (2.5 mg.kg-1.min-1 intravenously for 5 min and then 0.5 mg.kg-1.min-1 beginning 45 min before and continuing until 30 min after release of the 30 min occlusion) without ischaemic preconditioning; (6) and (7) Treatment with the higher dose of acadesine for 5 min beginning 35 min before the 5 min ischaemic period, and then the lower dose continuing until 30 min after release of the 30 min coronary occlusion in rabbits with 4 or 6 h reperfusion intervals, respectively.

RESULTS

Rabbits with ischaemic preconditioning with 10 min reperfusion preceding the 30 min coronary occlusion (group 2) had only 5.6(SEM 1.1)% infarction of the ischaemic zone. Ischaemic preconditioning followed by 2 h reperfusion (group 3) offered continued protection [18.2(2.2)% infarction] as compared to control animals [37.7(2.6)% infarction]. However, protection waned if ischaemic preconditioning was followed by 4 h reperfusion (group 4) [36.7(3.0)% infarction]. Additionally, treatment with acadesine alone did not modify infarct size (group 7) [39.5(4.0)%], but acadesine largely restored the protection of ischaemic preconditioning despite a 4 h reperfusion interval (group 5) [20.4(3.0)% infarction, P < 0.01 v control]. However, when reperfusion was extended to 6 h (group 6) acadesine could no longer restore protection [36.2(0.9)% infarction].

CONCLUSIONS

The protection afforded by a 5 min ischaemic preconditioning period lasts from 2 to 4 h in the awake, unsedated rabbit, and acadesine can extend the duration of this window of protection to at least 4 h but not to 6 h.

摘要

目的

如果短暂缺血期和延长缺血期之间的再灌注间隔小于1小时,缺血预处理可保护心肌免于梗死。在麻醉兔中,阿卡地辛(5-氨基-4-咪唑甲酰胺核苷,AICAR)是一种腺苷增强剂,可在缺血期间增加组织腺苷,将保护窗口延长至2小时。本研究的目的是使用长期植入仪器、未使用镇静剂的兔子,试图确定该保护窗口的最大延长时间。

方法

在左冠状动脉一个主要分支周围用球囊阻塞器对兔子进行仪器植入,以实现可逆性冠状动脉阻塞。手术后5至7天,所有动物均接受30分钟的冠状动脉阻塞。动物被随机分为七组之一:(1)不进行额外治疗(对照组);(2)在30分钟冠状动脉阻塞前进行5分钟局部缺血,随后10分钟再灌注的缺血预处理;(3)和(4)分别在30分钟阻塞前进行缺血预处理,随后再灌注2或4小时;(5)在无缺血预处理的情况下,用阿卡地辛治疗(静脉注射2.5mg·kg-1·min-1,持续5分钟,然后从30分钟阻塞解除前45分钟开始,以0.5mg·kg-1·min-1持续至阻塞解除后30分钟);(6)和(7)分别在5分钟缺血期前35分钟开始用较高剂量的阿卡地辛治疗5分钟,然后用较低剂量持续至再灌注间隔为4或6小时的兔子30分钟冠状动脉阻塞解除后30分钟。

结果

在30分钟冠状动脉阻塞前进行10分钟再灌注的缺血预处理的兔子(第2组),缺血区梗死仅为5.6(标准误1.1)%。与对照动物[梗死37.7(2.6)%]相比,缺血预处理后再灌注2小时(第3组)提供了持续保护[梗死18.2(2.2)%]。然而,如果缺血预处理后再灌注4小时(第4组),保护作用减弱[梗死36.7(3.0)%]。此外,单独使用阿卡地辛治疗并未改变梗死面积(第7组)[梗死39.5(4.0)%],但尽管再灌注间隔为4小时,阿卡地辛在很大程度上恢复了缺血预处理的保护作用(第5组)[梗死20.4(3.0)%,与对照组相比P<0.01]。然而,当再灌注延长至6小时(第6组)时,阿卡地辛不再能恢复保护作用[梗死36.2(0.9)%]。

结论

在清醒、未使用镇静剂的兔子中,5分钟缺血预处理期提供的保护持续2至4小时,阿卡地辛可将该保护窗口的持续时间延长至至少4小时,但不能延长至6小时。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验