Adenosine, added to St Thomas' Hospital cardioplegic solution, improves functional recovery and reduces irreversible myocardial damage.

Cardioscience Pub Date : 1994-12-01
C van der Lee, T Huizer, M Janssen, M Tavenier, E J Stassen, M Arad, J W de Jong
{"title":"Adenosine, added to St Thomas' Hospital cardioplegic solution, improves functional recovery and reduces irreversible myocardial damage.","authors":"C van der Lee,&nbsp;T Huizer,&nbsp;M Janssen,&nbsp;M Tavenier,&nbsp;E J Stassen,&nbsp;M Arad,&nbsp;J W de Jong","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>St Thomas' Hospital cardioplegic solution is commonly used to arrest hearts during surgery. Pursuing the hypothesis that the cardioprotective properties of adenosine could be a beneficial adjunct to a solution containing high K+ and Mg2+, we tested a low and a high adenosine concentration added to this cardioplegic solution, aiming at improved recovery of function and energy status. We arrested 18 working rat hearts by a 3-minute infusion with the solution without or with 50 microM or 5 mM adenosine. We induced 30 minute stop-flow ischemia at 37 degrees C, followed by 10 minute washout (Langendorff mode) and 20 minute reperfusion (working heart). Control cardioplegia induced electrical arrest in 19.8 +/- 5.5 s. This took 9.1 +/- 0.9* and 12.7 +/- 1.8 s in the presence of 50 microM and 5 mM adenosine, respectively (*p < 0.05 vs no adenosine). During reperfusion a regular electrocardiogram appeared after 1.9 +/- 0.3 minutes in controls, after 1.0 +/- 0.0* and 1.7 +/- 0.2 minutes in hearts treated with low and high-dose adenosine, respectively (*p < 0.05 vs no adenosine). After 20 minute reperfusion, the pressure-rate product had recovered to 65 +/- 17% in controls, and to 107 +/- 11** and 72 +/- 11% of preischemic values in hearts treated with 50 microM and 5 mM adenosine, respectively (**p < 0.05 vs other groups). There was a good correlation between reperfusion function recovery and the postischemic release of creatine kinase, an index for irreversible cellular damage. This association was absent with ATP content, which increased with the adenosine concentration.(ABSTRACT TRUNCATED AT 250 WORDS)</p>","PeriodicalId":9629,"journal":{"name":"Cardioscience","volume":"5 4","pages":"269-75"},"PeriodicalIF":0.0000,"publicationDate":"1994-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cardioscience","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

St Thomas' Hospital cardioplegic solution is commonly used to arrest hearts during surgery. Pursuing the hypothesis that the cardioprotective properties of adenosine could be a beneficial adjunct to a solution containing high K+ and Mg2+, we tested a low and a high adenosine concentration added to this cardioplegic solution, aiming at improved recovery of function and energy status. We arrested 18 working rat hearts by a 3-minute infusion with the solution without or with 50 microM or 5 mM adenosine. We induced 30 minute stop-flow ischemia at 37 degrees C, followed by 10 minute washout (Langendorff mode) and 20 minute reperfusion (working heart). Control cardioplegia induced electrical arrest in 19.8 +/- 5.5 s. This took 9.1 +/- 0.9* and 12.7 +/- 1.8 s in the presence of 50 microM and 5 mM adenosine, respectively (*p < 0.05 vs no adenosine). During reperfusion a regular electrocardiogram appeared after 1.9 +/- 0.3 minutes in controls, after 1.0 +/- 0.0* and 1.7 +/- 0.2 minutes in hearts treated with low and high-dose adenosine, respectively (*p < 0.05 vs no adenosine). After 20 minute reperfusion, the pressure-rate product had recovered to 65 +/- 17% in controls, and to 107 +/- 11** and 72 +/- 11% of preischemic values in hearts treated with 50 microM and 5 mM adenosine, respectively (**p < 0.05 vs other groups). There was a good correlation between reperfusion function recovery and the postischemic release of creatine kinase, an index for irreversible cellular damage. This association was absent with ATP content, which increased with the adenosine concentration.(ABSTRACT TRUNCATED AT 250 WORDS)

分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
在圣托马斯医院的心脏麻痹治疗方案中加入腺苷,可以改善功能恢复,减少不可逆的心肌损伤。
圣托马斯医院的心脏停搏液通常用于手术期间的心脏停搏。假设腺苷的心脏保护特性可能是含有高K+和Mg2+的溶液的有益辅助物,我们测试了低浓度和高浓度的腺苷添加到这种心脏麻痹溶液中,旨在改善功能和能量状态的恢复。我们将不含或含50微米或5毫米腺苷的溶液灌注3分钟,使18只工作大鼠心脏停止跳动。我们在37℃下诱导30分钟的缺血停流,然后是10分钟的冲洗(Langendorff模式)和20分钟的再灌注(工作心脏)。控制心脏骤停引起的电骤停在19.8±5.5 s。在50 μ m和5 μ m腺苷存在时,分别需要9.1 +/- 0.9*和12.7 +/- 1.8 s(与不含腺苷相比,*p < 0.05)。再灌注时,对照组分别在1.9 +/- 0.3分钟、低剂量和高剂量腺苷组分别在1.0 +/- 0.0和1.7 +/- 0.2分钟出现正常心电图(与无腺苷组比较,*p < 0.05)。再灌注20分钟后,对照组的压率积恢复到65 +/- 17%,50 μ m和5 μ m腺苷组的压率积恢复到缺血前值的107 +/- 11%和72 +/- 11%(与其他组比较,**p < 0.05)。再灌注功能恢复与缺血后肌酸激酶的释放有良好的相关性,肌酸激酶是不可逆细胞损伤的指标。而ATP含量则随着腺苷浓度的增加而增加。(摘要删节250字)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Cellular basis of ventricular remodeling after myocardial infarction in rats. Incorporation of cholesterol oxidation products into cell lipids and their influence on the proliferation of cultured cardiomyocytes. Assessment of subrenal banding of the abdominal aorta as a method of inducing cardiac hypertrophy in the guinea pig. The effects of distension of the stomach and the descending colon on phasic coronary blood flow in the anesthetized pig. The functional and metabolic responses of the heart to catecholamines are attenuated in diabetic rats.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1