<p>Using two different compounds they developed, scientists from the Florida campus of The Scripps Research Institute (TSRI) have been able to show in animal models that inhibiting a specific enzyme protects heart cells and surrounding tissue against serious damage from heart attacks. The compounds also protect against additional injury from restored blood flow after an attack, a process known as reperfusion. <br /><br />The study was led by Philip LoGrasso, a professor and senior scientific director of discovery biology at Scripps Florida. <br /><br />A heart attack severely restricts blood supply, starving heart cells and surrounding tissue of oxygen, which can cause enormous damage in relatively little time—sometimes in just a few minutes. Known as an ischemic cascade, this drop-off of oxygen results in a sudden crush of metabolic waste that damages cell membranes as well as the mitochondria, a part of the cell that generates chemical energy and is involved in cell growth and death.<br /><br />Unfortunately, restoring blood flow adds significantly to the damage, a serious medical issue when it comes to treating major ischemic events such as heart attack and stroke. Reperfusion re-invigorates production of free radicals and reactive oxygen species that attack and damage cells, exacerbating inflammation, turning loose white blood cells to attack otherwise salvageable cells and maybe even inducing potentially fatal cardiac arrhythmias. <br /><br />The new study found that inhibiting the enzyme, c-jun-N-terminal kinase (JNK), pronounced “junk,” protected against ischemic/reperfusion injury in rats, reducing the total volume of tissue death by as much as 34 per cent. It also significantly reduced levels of reactive oxygen species and mitochondrial dysfunction.<br /></p>
<p>Using two different compounds they developed, scientists from the Florida campus of The Scripps Research Institute (TSRI) have been able to show in animal models that inhibiting a specific enzyme protects heart cells and surrounding tissue against serious damage from heart attacks. The compounds also protect against additional injury from restored blood flow after an attack, a process known as reperfusion. <br /><br />The study was led by Philip LoGrasso, a professor and senior scientific director of discovery biology at Scripps Florida. <br /><br />A heart attack severely restricts blood supply, starving heart cells and surrounding tissue of oxygen, which can cause enormous damage in relatively little time—sometimes in just a few minutes. Known as an ischemic cascade, this drop-off of oxygen results in a sudden crush of metabolic waste that damages cell membranes as well as the mitochondria, a part of the cell that generates chemical energy and is involved in cell growth and death.<br /><br />Unfortunately, restoring blood flow adds significantly to the damage, a serious medical issue when it comes to treating major ischemic events such as heart attack and stroke. Reperfusion re-invigorates production of free radicals and reactive oxygen species that attack and damage cells, exacerbating inflammation, turning loose white blood cells to attack otherwise salvageable cells and maybe even inducing potentially fatal cardiac arrhythmias. <br /><br />The new study found that inhibiting the enzyme, c-jun-N-terminal kinase (JNK), pronounced “junk,” protected against ischemic/reperfusion injury in rats, reducing the total volume of tissue death by as much as 34 per cent. It also significantly reduced levels of reactive oxygen species and mitochondrial dysfunction.<br /></p>