Literature DB >> 3682858

Protection of the pediatric myocardium. Differential susceptibility to ischemic injury of the neonatal rat heart.

Y Yano1, M V Braimbridge, D J Hearse.   

Abstract

Myocardial protection during pediatric cardiac operations has been suggested to be less successful than in adult hearts. In the present study we have compared the resistance of adult, infant, and neonatal rat hearts to various periods of ischemic arrest with normothermic (37 degrees C) crystalloid cardioplegia. Isolated hearts with intraventricular balloons, from adult (50 to 60 days of age, heart weight 865 +/- 13 mg), infant (20 to 25 days of age, heart weight 251 +/- 3 mg), and neonatal rats (3 to 5 days of age, heart weight 40 +/- 1 mg) were subjected to 10, 20, 30, 40, 50, 60, 80, and 100 minutes of ischemia (n = 6 hearts for each time point and for each age group). St. Thomas' Hospital cardioplegic solution was infused at the onset of the period of arrest. With increasing durations of ischemia there was a declining postischemic recovery of function. Up to 40 minutes of ischemia there was no significant difference between the three age groups in postischemic recovery of left ventricular developed pressure: 40.3% +/- 4.4%, 45.4% +/- 6.5%, and 44.4% +/- 2.2% of preischemic control for adult, infant, and neonatal hearts, respectively. Beyond 40 minutes adult and infant hearts showed an identical deterioration with effectively no recovery beyond 60 minutes of ischemia. By contrast, neonatal hearts were much more resistant to ischemia. After 100 minutes of ischemia the mean recovery of left ventricular developed pressure was 20.9% +/- 1.1%, whereas in infant and adult hearts the values were 0.6% +/- 0.3% after 80 minutes of ischemia and 0% after 100 minutes, respectively. Analysis of creatine kinase leakage also indicated that with ischemic durations in excess of 40 minutes, the neonatal heart was far more resistant to ischemia, and creatine kinase leakage per gram dry weight was much less than in infant or adult rats. Analysis of the rates of recovery during reperfusion again revealed differences between neonatal hearts and hearts from the other two age groups. We conclude that in the normal rat the neonatal heart has a greater inherent tolerance to ischemia than that of the infant or adult rat.

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Year:  1987        PMID: 3682858

Source DB:  PubMed          Journal:  J Thorac Cardiovasc Surg        ISSN: 0022-5223            Impact factor:   5.209


  5 in total

1.  Na/H exchange inhibition protects newborn heart from ischemia/reperfusion injury by limiting Na+-dependent Ca2+ overload.

Authors:  Hong Liu; Peter M Cala; Steve E Anderson
Journal:  J Cardiovasc Pharmacol       Date:  2010-03       Impact factor: 3.105

2.  Three-dimensional paper-based model for cardiac ischemia.

Authors:  Bobak Mosadegh; Borna E Dabiri; Matthew R Lockett; Ratmir Derda; Patrick Campbell; Kevin Kit Parker; George M Whitesides
Journal:  Adv Healthc Mater       Date:  2014-02-12       Impact factor: 9.933

3.  Deferoxamine reduces the reperfusion injury in isolated neonatal rabbit hearts after hypothermic preservation.

Authors:  S Katoh; J Toyama; I Kodama; K Kamiya; T Akita; T Abe
Journal:  Surg Today       Date:  1993       Impact factor: 2.549

4.  Sex differences in the tolerance of immature rat myocardium to global ischemia.

Authors:  M Avkiran; D J Hearse
Journal:  Basic Res Cardiol       Date:  1988 Nov-Dec       Impact factor: 17.165

5.  Newborn hearts are at greater 'metabolic risk' during global ischemia--advantages of continuous coronary washout.

Authors:  Carin Wittnich; Michael P Belanger; Karim S Bandali
Journal:  Can J Cardiol       Date:  2007-03-01       Impact factor: 5.223

  5 in total

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