cardiovascular system
• significantly higher than in controls after ischemia
(J:60470)
• extent of myocardial necrosis following ischemia and reperfusion is similar to that observed in wild-type
(J:89952)
|
• following ischemia and 30 minutes reperfusion, creatine kinase release is significantly higher from mutant hearts, and release progressively increases with reperfusion duration
|
• after 30 minutes of global ischemia, developed force (dF) in mutant hearts does not recover beyond 90% of baseline after 30 minutes of reperfusion
• significantly slower recovery of dF and dF/dTmax is observed in mutant hearts after 15 minutes of reperfusion
|
• infarct size is significantly greater relative to wild-type and heterozygous animals after 30 minutes of global ischemia
|
muscle
• significantly higher than in controls after ischemia
(J:60470)
• extent of myocardial necrosis following ischemia and reperfusion is similar to that observed in wild-type
(J:89952)
|
• after 30 minutes of global ischemia, developed force (dF) in mutant hearts does not recover beyond 90% of baseline after 30 minutes of reperfusion
• significantly slower recovery of dF and dF/dTmax is observed in mutant hearts after 15 minutes of reperfusion
|
homeostasis/metabolism
• infarct size is significantly greater relative to wild-type and heterozygous animals after 30 minutes of global ischemia
|
cellular
• mutant hearts produce increased amounts of hydroxyl radicals following ischemia/reperfusion
• hearts produce significantly higher amounts of malonaldehyde during the postischemic period compared to controls
|