Xanthine oxidase activity and lipid peroxide content following different types of ischemia in the isolated rat heart
- PMID: 7942321
- DOI: 10.1007/BF02001908
Xanthine oxidase activity and lipid peroxide content following different types of ischemia in the isolated rat heart
Abstract
It is currently believed that reactive oxygen species are produced in the heart post-ischemia reperfusion, causing pathophysiological disorders. Studies reported in the literature dealing with this subject have generated contradictory findings. The aim of this study was to assess the catalytic activity of the superoxide anion-producing enzyme xanthine oxidase, and the level of lipid peroxides in isolated rat heart muscle undergoing ischemia of varying duration and severity followed by reperfusion. Three levels of ischemia were investigated: total, and partial at either 0.10 or 0.35 ml/min (residual flow rate). Three different periods of ischemia were examined in each case. After each period of ischemia, followed by 10 min of reperfusion, the heart was frozen in liquid nitrogen. Xanthine oxidase activity and lipid peroxide levels were assayed in the cardiac homogenate and in the centrifuged supernatant, respectively. In the different experimental protocols studied here, both cardiac xanthine oxidase and lipid peroxide levels remained statistically unchanged compared to the continuously perfused control hearts. Moreover, in a recent study (Boucher et al., FEBS Lett. 203, 261-264, 1992), we were unable to detect reactive oxygen species in perfusate upon reperfusion of ischemic rat hearts. These results suggest that changes in xanthine oxidase activity during myocardial ischemia-reperfusion, and lipid peroxidation, as assessed by measuring thiobarbituric acid reactants and lipid hydroperoxides, are not predominant phenomena in ischemia-reperfusion-induced injury, at least in the experimental model used in this study.(ABSTRACT TRUNCATED AT 250 WORDS)
Similar articles
-
Ischemia and reperfusion injury in isolated rat heart: effect of reperfusion duration on xanthine oxidase, lipid peroxidation, and enzyme antioxidant systems in myocardium.Basic Res Cardiol. 1992 Sep-Oct;87(5):478-88. doi: 10.1007/BF00795060. Basic Res Cardiol. 1992. PMID: 1463431
-
Allopurinol improves cardiac dysfunction after ischemia-reperfusion via reduction of oxidative stress in isolated perfused rat hearts.Circ J. 2003 Sep;67(9):781-7. doi: 10.1253/circj.67.781. Circ J. 2003. PMID: 12939555
-
Lipid peroxidation and alterations to oxidative metabolism in mitochondria isolated from rat heart subjected to ischemia and reperfusion.Free Radic Biol Med. 1999 Jul;27(1-2):42-50. doi: 10.1016/s0891-5849(99)00032-5. Free Radic Biol Med. 1999. PMID: 10443918
-
[Formation and removal of reactive oxygen species, lipid peroxides and free radicals, and their biological effects].Yakugaku Zasshi. 2002 Mar;122(3):203-18. doi: 10.1248/yakushi.122.203. Yakugaku Zasshi. 2002. PMID: 11905046 Review. Japanese.
-
[Detection and characterization of free radicals, radical scavenging activity, and lipid peroxides in cerebral ischemia-reperfusion injury by electron spin resonance and chemiluminescence high-performance liquid chromatography].Nihon Shinkei Seishin Yakurigaku Zasshi. 1997 Aug;17(4):153-8. Nihon Shinkei Seishin Yakurigaku Zasshi. 1997. PMID: 9365963 Review. Japanese.
Cited by
-
Tolerance of isolated rat hearts to low-flow ischemia and hypoxia of increasing duration: protective role of down-regulation and ATP during ischemia.Mol Cell Biochem. 2001 Oct;226(1-2):141-51. doi: 10.1023/a:1012708324876. Mol Cell Biochem. 2001. PMID: 11768234