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[普萘洛尔对腺苷合成心脏腺嘌呤核苷酸的加速作用]

[Acceleration of the synthesis of cardiac adenine nucleotides from adenosine as affected by propranolol].

作者信息

Giacomelli M, Aussedat J, Lavanchy N, Rossi A

出版信息

C R Acad Sci III. 1984;299(19):779-84.

PMID:6442183
Abstract

DL-propranolol, at a dose of 2 mg . l-1, induced in the isolated rat heart an increase in adenine nucleotide synthesis from exogenous 5 microM adenosine (+20%). If supplied during reperfusion following low-flow ischaemia (0.5 ml . min-1, 30 min.), propranolol annulled the decrease in adenosine incorporation (-23%) provoked by ischaemia. When propranolol was given during ischaemia and reperfusion, ATP degradation during the ischaemic period was reduced and adenosine uptake was strongly stimulated on reperfusion (+60%).

摘要

剂量为2毫克·升-1的DL-普萘洛尔在离体大鼠心脏中可使外源性5微摩尔腺苷的腺嘌呤核苷酸合成增加(增加20%)。如果在低流量缺血(0.5毫升·分钟-1,30分钟)后的再灌注期间给予普萘洛尔,它可消除缺血引起的腺苷掺入减少(-23%)。当在缺血和再灌注期间给予普萘洛尔时,缺血期的ATP降解减少,再灌注时腺苷摄取受到强烈刺激(增加60%)。

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