potassium-ascorbyl-tocopheryl-phosphate and Ischemia

EPC-K1, a phosphate diester of alpha-tocopherol and ascorbic acid, is a new hydroxyl radical scavenger. We examined the effects of EPC-K1 according to differences in the timing of its administration. Warm ischemia, produced by vascular pedicle clamping, was sustained for 4 hours. After 24 hours of reperfusion, muscle injury was evaluated in 4 groups: the first group received a sham operation, the second group was treated with an intravenous injection of EPC-K1 prior to ischemia, the third group was treated with EPC-K1 prior to reperfusion, and the fourth group was controls. Compared with the control group, both the preischemic and pre-reperfusion EPC-K1-treated groups showed a statistically significant amelioration in the reduction of isometric muscle contraction. There were also significant reductions in the muscle and serum levels of thiobarbituric acid reactive substances (TBA-RS) and muscle damage, indicated by the biochemical and histological study. A comparison of the timing of EPC-K1 administration revealed that only the muscle TBA-RS level in the pre-reperfusion EPC-K1-treated group was significantly higher than that in the preischemic EPC-K1-treated group. These observations indicate that EPC-K1 not only by preischemic but also by pre-reperfusion administration acted effectively on reperfusion injury in muscle, thereby improving muscle function.

Topics: Animals; Antioxidants; Ascorbic Acid; Biopsy; Disease Models, Animal; Drug Administration Schedule; Drug Evaluation, Preclinical; Free Radical Scavengers; Injections, Intravenous; Ischemia; Isometric Contraction; Male; Muscle, Skeletal; Random Allocation; Rats; Rats, Inbred Lew; Reperfusion Injury; Thiobarbituric Acid Reactive Substances; Time Factors; Vitamin E