Acadesine and myocardial protection. Studies of time of administration and dose-response relations in the rat.
Author(s) -
Manuel Galiñanes,
Kevin Mullane,
David A. Bullough,
David J. Hearse
Publication year - 1992
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/01.cir.86.2.598
Subject(s) - medicine , adenosine , ischemia , reperfusion injury , adenine nucleotide , anesthesia , in vivo , pharmacology , nucleotide , biochemistry , chemistry , biology , microbiology and biotechnology , gene
Although there are many factors that might contribute to tissue injury during ischemia and reperfusion, the loss of adenine nucleotides has long been considered to be of importance. This has led to the study of interventions designed to limit the loss of nucleotides or to enhance the rate of nucleotide resynthesis during reperfusion. Alternatively, the breakdown of adenosine triphosphate to adenosine might represent a protective response of the ischemic heart because adenosine is considered an anti-injury autocoid. Augmentation of endogenous adenosine levels might be beneficial. For these reasons, the protective properties of acadesine (AICAr: 5-amino-4-imidazole carboxamide riboside) were assessed in a rat model of myocardial ischemia and reperfusion.
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