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Tolerance of the developing cyanotic heart to ischemia-reperfusion injury in the rat.

AbstractOBJECTIVE:
Whether chronic hypoxia attenuates myocardial ischemia-reperfusion injury remains controversial because conflicting data have been reported probably due to the existence of many factors influencing the functional recovery of hearts. These factors include the differences of species, the time at which hypoxia begins, the degree of hypoxia, and so on. Regarding chronic hypoxia from birth, so far the only available data are based on findings in rabbit hearts. The purpose of this study was to describe the effect of chronic hypoxia from birth on myocardial reperfusion injury in the rat heart.
METHODS:
Normoxic hearts were obtained from rats housed in ambient air for 6 weeks (normoxic group); hypoxic hearts were obtained from rats housed in a hypoxic chamber (13%-14% oxygen) from birth for 6 weeks (hypoxic group). Isolated, crystalloid perfused working hearts were subjected to 30 min of global normothermic ischemia followed by 15 min of reperfusion; functional recovery was then measured in the two groups. The excretion of cyclic guanosine monophosphate (cGMP) in the coronary drainage was measured at the end of the preischemia and reperfusion periods.
RESULTS:
The percent recovery of the left ventricular developed pressure and the first derivative of left ventricular pressure were significantly better in the hypoxic group than in the normoxic group. cGMP excretion in the coronary drainage was significantly increased during both the preischemia and reperfusion periods.
CONCLUSION:
Chronic hypoxia from birth increased myocardial tolerance to ischemia-reperfusion injury with increased cGMP synthesis in the isolated heart model in rats.
AuthorsYasuhiro Fujii, Kozo Ishino, Tomoko Tomii, Hitoshi Kanamitsu, Hideya Mitsui, Shunji Sano
JournalGeneral thoracic and cardiovascular surgery (Gen Thorac Cardiovasc Surg) Vol. 58 Issue 4 Pg. 174-81 (Apr 2010) ISSN: 1863-6713 [Electronic] Japan
PMID20401710 (Publication Type: Journal Article)
Chemical References
  • KATP Channels
  • Cyclic GMP
Topics
  • Animals
  • Chronic Disease
  • Cyanosis (metabolism, physiopathology)
  • Cyclic GMP (metabolism)
  • Disease Models, Animal
  • Heart (growth & development, physiopathology)
  • Hypoxia (metabolism, physiopathology)
  • KATP Channels (metabolism)
  • Male
  • Myocardial Contraction
  • Myocardial Reperfusion Injury (metabolism, physiopathology, prevention & control)
  • Myocardium (metabolism)
  • Rats
  • Rats, Sprague-Dawley
  • Recovery of Function
  • Up-Regulation
  • Ventricular Function, Left
  • Ventricular Pressure

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