Literature DB >> 3783724

Superoxide dismutase and catalase reduce infarct size in a porcine myocardial occlusion-reperfusion model.

U Näslund, S Häggmark, G Johansson, S L Marklund, S Reiz, A Oberg.   

Abstract

We investigated if superoxide dismutase and catalase could reduce myocardial infarct size in an open chest occlusion-reperfusion model. Thirty pigs were used for the experiment. The left anterior descending artery was ligated for 60 min followed by a 5 h reperfusion period. After randomisation and blinding the two enzymes or placebo were injected into the left atrium as a bolus immediately before and at the end of the occlusion and as a continuous infusion over the first hour of the reperfusion period. The total dose for each enzyme was 8 mg/kg bw. Tetrazolium staining was used to determine infarct size. The study code was not broken until all calculations and exclusions had been made. Nine animals died from intractable ventricular fibrillation, most commonly during the occlusion. Another three were excluded for technical reasons. We found that superoxide dismutase and catalase reduced infarct size in relation to myocardium at risk from a mean of 89% to 63% (P less than 0.01). Initial plasma half life for the two enzymes after the bolus infusions were calculated to be 30 min.

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Year:  1986        PMID: 3783724     DOI: 10.1016/s0022-2828(86)80294-2

Source DB:  PubMed          Journal:  J Mol Cell Cardiol        ISSN: 0022-2828            Impact factor:   5.000


  13 in total

1.  A possible involvement of oxygen free radicals in the development of myocardial acidosis during coronary occlusion in dogs.

Authors:  K Sakai; K Ichihara; H Ohmi; Y Abiko
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1989-08       Impact factor: 3.000

2.  Protective action of hydroxyethyl rutosides on singlet oxygen challenged cardiomyocytes.

Authors:  H G Olbrich; P Grabisch; A Grossmann; T Rinne; H Klepzig; E Mutschler
Journal:  Br J Pharmacol       Date:  1996-10       Impact factor: 8.739

Review 3.  The structural biochemistry of the superoxide dismutases.

Authors:  J J P Perry; D S Shin; E D Getzoff; J A Tainer
Journal:  Biochim Biophys Acta       Date:  2009-11-13

Review 4.  Tetracyclines: a pleitropic family of compounds with promising therapeutic properties. Review of the literature.

Authors:  Michael O Griffin; Eduardo Fricovsky; Guillermo Ceballos; Francisco Villarreal
Journal:  Am J Physiol Cell Physiol       Date:  2010-06-30       Impact factor: 4.249

Review 5.  Biochemical events associated with rapid cellular damage during the oxygen- and calcium-paradoxes of the mammalian heart.

Authors:  C J Duncan
Journal:  Experientia       Date:  1990-01-15

Review 6.  Alterations in fatty acid oxidation in ischemic and reperfused myocardium.

Authors:  X Q Huang; A J Liedtke
Journal:  Mol Cell Biochem       Date:  1989 Jun 27-Jul 24       Impact factor: 3.396

7.  The Protective Effect of Epigallocatechin-3 Gallate on Ischemia/Reperfusion Injury in Isolated Rat Hearts: An ex vivo Approach.

Authors:  Cheng Shi Piao; Do-Sung Kim; Ki-Chan Ha; Hyung-Ryong Kim; Han-Jung Chae; Soo-Wan Chae
Journal:  Korean J Physiol Pharmacol       Date:  2011-10-31       Impact factor: 2.016

8.  Targeted intracellular catalase delivery protects neonatal rat myocytes from hypoxia-reoxygenation and ischemia-reperfusion injury.

Authors:  Vishnu Undyala; Stanley R Terlecky; Richard S Vander Heide
Journal:  Cardiovasc Pathol       Date:  2010-08-12       Impact factor: 2.185

Review 9.  Oxygen-derived free radicals and myocardial reperfusion injury: an overview.

Authors:  R Bolli
Journal:  Cardiovasc Drugs Ther       Date:  1991-03       Impact factor: 3.727

10.  Effect of vitamins A and E on ischemia-reperfusion damage in rabbit heart.

Authors:  S Llesuy; J Milei; V Picone; B González Flecha; R Beigelman; A Boveris
Journal:  Mol Cell Biochem       Date:  1995-04-12       Impact factor: 3.396

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