Tullson P C, Arabadjis P G, Rundell K W, Terjung R L
Department of Physiology, State University of New York, Syracuse 13210, USA.
Am J Physiol. 1996 Apr;270(4 Pt 1):C1067-74. doi: 10.1152/ajpcell.1996.270.4.C1067.
Inosine 5'-monophosphate (IMP) reamination in skeletal muscle fiber sections of the rat hindlimb was studied. High IMP concentrations were established during ischemic contractions in each fiber section: 3.1, 2.8, or 0.6 mumol/g in the fast-twitch white (FTW), fast-twitch red (FTR), and slow-twitch red (STR) muscle sections, respectively. Thereafter blood flow was restored and stimulation was discontinued to allow reamination of IMP. After 0, 2, 5, 10, 15, or 20 min of recovery, muscle sections were freeze-clamped and analyzed for metabolite contents. IMP was nearly fully reaminated after 10 and 20 min of recovery in STR and FTR muscles, respectively. Reamination in TW fibers was delayed and slower, with only 50% of the IMP reaminated after 20 min of recovery. Significant recovery (approximately 75%) of phosphocreatine occurs in each fiber section before the onset of reamination. Reamination was also evaluated after high-speed treadmill running with or without inhibition of reamination by hadacidin. Running resulted in large accumulations of IMP in FTW and FTR fibers (3.5 and 1.4 mumul/g, respectively); IMP in FTR fibers was higher with hadacidin treatment. Reamination after running was much greater in FTR than in FTW fibers and was associated with recovery of phosphocreatine. After running, the purine degradation products inosine and hypoxanthine were increased in FTW and FTR fibers in normal and hadacidin-treated animals. Plasma inosine, hypoxanthine, and urate increased after exercise; concentrations continued to increase if reamination was inhibited by hadacidin. These results demonstrate that when muscle IMP is increased, subsequent degradation and loss of purines occur. Rapid reamination should minimize the quantity of purine lost from muscle and limit the metabolic cost of replenishing purines by the de novo synthesis or salvage pathways.
研究了大鼠后肢骨骼肌纤维切片中的肌苷5'-单磷酸(IMP)再氨基化过程。在每个纤维切片的缺血收缩过程中建立了高IMP浓度:在快肌白肌(FTW)、快肌红肌(FTR)和慢肌红肌(STR)肌肉切片中分别为3.1、2.8或0.6 μmol/g。此后恢复血流并停止刺激以使IMP再氨基化。在恢复0、2、5、10、15或20分钟后,将肌肉切片冷冻钳夹并分析代谢物含量。在STR和FTR肌肉中分别恢复10和20分钟后,IMP几乎完全再氨基化。FTW纤维中的再氨基化延迟且较慢,恢复20分钟后只有50%的IMP再氨基化。在再氨基化开始前,每个纤维切片中的磷酸肌酸都有显著恢复(约75%)。在高速跑步机跑步后,还评估了再氨基化情况,跑步过程中使用或不使用哈西丁抑制再氨基化。跑步导致FTW和FTR纤维中IMP大量积累(分别为3.5和1.4 μmol/g);使用哈西丁处理后,FTR纤维中的IMP更高。跑步后FTR纤维中的再氨基化比FTW纤维大得多,并且与磷酸肌酸的恢复有关。跑步后,正常和使用哈西丁处理的动物的FTW和FTR纤维中的嘌呤降解产物肌苷和次黄嘌呤增加。运动后血浆肌苷、次黄嘌呤和尿酸增加;如果用哈西丁抑制再氨基化,浓度会持续增加。这些结果表明,当肌肉IMP增加时,随后会发生嘌呤的降解和损失。快速再氨基化应使肌肉中损失的嘌呤量最小化,并限制通过从头合成或补救途径补充嘌呤的代谢成本。