缺氧、衰老和药物治疗对肌肉代谢产物和酶活性的影响。

Il Farmaco; edizione scientifica Pub Date : 1988-07-01
O Pastoris, L Vercesi, F Allorio, M Dossena
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引用次数: 0

摘要

研究了幼犬和成年犬腓肠肌缺氧及缺氧后恢复的影响。此外,在这些条件下,评估了尼麦角林药物治疗的可能干扰。评估肌肉糖酵解燃料、中间产物和最终产物(糖原、葡萄糖、葡萄糖- 6-磷酸、丙酮酸、乳酸)、克雷伯循环中间产物(柠檬酸、α -酮戊二酸、琥珀酸、苹果酸)和相关的游离氨基酸(谷氨酸、丙氨酸)、铵离子、能量储存和介质(ATP、ADP、AMP和磷酸肌酸)以及能量电荷势。此外,在同一腓肠肌另一部分的粗提物和/或线粒体部分中,与厌氧糖酵解途径(己糖激酶、乳酸脱氢酶)、克雷布斯循环(柠檬酸合成酶、苹果酸脱氢酶)、克雷布斯循环相关的氨基酸库(谷氨酸脱氢酶和天冬氨酸转氨酶)、克雷布斯循环相关的一些肌肉酶的最大速率(Vmax)评估电子传递链(细胞色素氧化酶)和NAD+/NADH交换(总NADH细胞色素c还原酶)。一些糖酵解代谢物和克雷布斯循环中间体被急性缺氧修饰,而游离氨基酸和能量介质几乎保持不变。药物治疗维持葡萄糖和琥珀酸肌浓度在正常范围内,在缺氧期间。在缺氧和/或缺氧后恢复过程中,肌肉代谢产物的行为与年龄有关。事实上,只有年轻的成年动物在缺氧恢复后,这些改变的值才恢复正常。在目前的实验条件下,就肌肉酶活性而言,只观察到微小的变化。在任何情况下,一些酶活性测试显示,与成年狗相比,年轻成年狗的Vmax不同。
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Effect of hypoxia, aging and pharmacological treatment on muscular metabolites and enzyme activities.

The effect of hypoxia and post-hypoxic recovery were studied in gastrocnemius muscle of young-adult and mature beagle dogs. Furthermore, the possible interference of pharmacological treatment with nicergoline was evaluated in these conditions. Muscular glycolytic fuels, intermediates and end-products (glycogen, glucose, glucose 6-phosphate, pyruvate, lactate), Kreb's cycle intermediates (citrate, alpha-ketoglutarate, succinate, malate) and related free amino acids (glutamate, alanine), ammonium ion, energy store and mediators (ATP, ADP, AMP and creatine phosphate), and the energy charge potential were evaluated. Furthermore, in the crude extract and/or mitochondrial fraction of another portion of the same gastrocnemius muscle the maximum rate (Vmax) of some muscular enzymes related to the anaerobic glycolytic pathway (hexokinase, lactate dehydrogenase), the Kreb's cycle (citrate synthase, malate dehydrogenase), the aminoacid pool related to the Krebs' cycle (glutamate dehydrogenase and aspartate aminotransferase), the electron transfer chain (cytochrome oxidase) and NAD+/NADH exchanges (total NADH cytochrome c reductase) was evaluated. Some glycolytic metabolites and Krebs' cycle intermediates were modified by acute hypoxia, while free amino acids and energy mediators remained practically unchanged. The pharmacological treatment maintained the glucose and succinate muscular concentrations within the normal range, during hypoxia. The behaviour of muscular metabolites during hypoxia and/or post-hypoxic recovery is an age-related event. In fact, only in young-adult animals did the altered values return to normal in post-hypoxic recovery. In the present experimental conditions, only minor changes were observed as far as muscular enzyme activities are concerned. In any case, some enzyme activities tested showed different Vmax in young-adult dogs in comparison with mature ones.

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