Sesodia S, Choksi R M, Nemeth P M
Department of Neurology, Washington University School of Medicine, St Louis, MO 63110.
J Muscle Res Cell Motil. 1994 Oct;15(5):573-81. doi: 10.1007/BF00121163.
The metabolic recovery potential of muscle was studied in regenerating soleus muscles of young adult rats. Degeneration was induced by subfascial injection of a myotoxic snake venom. After regeneration for selected periods up to 2 weeks, samples of whole muscle were analysed for hexokinase (EC 2.7.1.1), phosphofructokinase (EC 2.7.1.11), lactate dehydrogenase (EC 1.1.11.27), adenylokinase (EC 2.7.4.3), creatine kinase (EC 2.7.3.2), malate dehydrogenase (EC 1.1.11.37), citrate synthase (EC 4.1.3.7) and beta-hydroxyacyl CoA dehydrogenase (EC 1.1.1.35). Lactate dehydrogenase, adenylokinase, malate dehydrogenase and beta-hydroxyacyl CoA dehydrogenase were also measured in individual fibres of muscle regenerating up to 4 weeks. We found that in the presence of nerve there was complete recovery of muscle metabolic capacity. However, there were differences in the rate of recovery of the activity of enzymes belonging to different energy-generating pathways. Lactate dehydrogenase, an enzyme representing glycolytic metabolism, reached normal activity immediately upon myofibre formation, only 3 days after venom injection, while oxidative enzymes required a week or more to reach normal activity levels. The delay in oxidative enzyme recovery coincided with physiological parameters of reinnervation. Therefore, to further test the role of nerve on the metabolic recovery process, muscle regeneration was studied following venom-induced degeneration coupled with denervation. In the absence of innervation, most enzymes failed to recover to normal activity levels. Lactate dehydrogenase was the only enzyme to achieve normal levels, and it did so as rapidly as in innervated-regenerating soleus muscles. The remainder of the glycolytic enzymes and the high energy phosphate enzymes recovered only partially. Oxidative enzymes showed no recovery and were severely reduced in the absence of reinnervation.(ABSTRACT TRUNCATED AT 250 WORDS)
在年轻成年大鼠再生的比目鱼肌中研究了肌肉的代谢恢复潜力。通过筋膜下注射肌毒性蛇毒诱导肌肉退化。在长达2周的选定再生期后,对整块肌肉样本进行分析,检测己糖激酶(EC 2.7.1.1)、磷酸果糖激酶(EC 2.7.1.11)、乳酸脱氢酶(EC 1.1.1.27)、腺苷酸激酶(EC 2.7.4.3)、肌酸激酶(EC 2.7.3.2)、苹果酸脱氢酶(EC 1.1.1.37)、柠檬酸合酶(EC 4.1.3.7)和β-羟酰基辅酶A脱氢酶(EC 1.1.1.35)。还在长达4周再生的肌肉的单个肌纤维中检测了乳酸脱氢酶、腺苷酸激酶、苹果酸脱氢酶和β-羟酰基辅酶A脱氢酶。我们发现,在有神经存在的情况下,肌肉代谢能力完全恢复。然而,属于不同能量产生途径的酶的恢复速率存在差异。乳酸脱氢酶是代表糖酵解代谢的酶,在肌纤维形成时,即毒液注射后仅3天就达到正常活性,而氧化酶需要一周或更长时间才能达到正常活性水平。氧化酶恢复的延迟与神经再支配的生理参数一致。因此,为了进一步测试神经在代谢恢复过程中的作用,研究了毒液诱导退化并伴有去神经支配后的肌肉再生。在没有神经支配的情况下,大多数酶未能恢复到正常活性水平。乳酸脱氢酶是唯一达到正常水平的酶,并且其达到正常水平的速度与有神经支配的再生比目鱼肌一样快。其余的糖酵解酶和高能磷酸酶仅部分恢复。氧化酶没有恢复,并且在没有神经再支配的情况下严重减少。(摘要截短至250字)