Pastoris O, Vercesi L, Allorio F, Dossena M
Institute of Pharmacology, University of Pavia, Italy.
Farmaco Sci. 1988 Jul-Aug;43(7-8):627-42.
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.
研究了低氧及低氧后恢复对成年和成熟比格犬腓肠肌的影响。此外,还评估了在这些条件下尼麦角林药物治疗可能产生的干扰。对肌肉糖酵解燃料、中间产物和终产物(糖原、葡萄糖、6-磷酸葡萄糖、丙酮酸、乳酸)、三羧酸循环中间产物(柠檬酸、α-酮戊二酸、琥珀酸、苹果酸)及相关游离氨基酸(谷氨酸、丙氨酸)、铵离子、能量储备和介质(三磷酸腺苷、二磷酸腺苷、一磷酸腺苷和磷酸肌酸)以及能量电荷电位进行了评估。此外,在同一块腓肠肌另一部分的粗提物和/或线粒体部分中,评估了与无氧糖酵解途径(己糖激酶、乳酸脱氢酶)、三羧酸循环(柠檬酸合酶、苹果酸脱氢酶)、与三羧酸循环相关的氨基酸池(谷氨酸脱氢酶和天冬氨酸转氨酶)、电子传递链(细胞色素氧化酶)以及烟酰胺腺嘌呤二核苷酸/还原型烟酰胺腺嘌呤二核苷酸交换(总还原型烟酰胺腺嘌呤二核苷酸细胞色素c还原酶)相关的一些肌肉酶的最大反应速度(Vmax)。急性低氧使一些糖酵解代谢产物和三羧酸循环中间产物发生了改变,而游离氨基酸和能量介质基本保持不变。药物治疗在低氧期间使肌肉中的葡萄糖和琥珀酸浓度维持在正常范围内。低氧和/或低氧后恢复期间肌肉代谢产物的变化是一个与年龄相关的现象。事实上,只有成年动物在低氧后恢复时,改变的值才会恢复正常。在本实验条件下,就肌肉酶活性而言,仅观察到轻微变化。无论如何,与成熟犬相比,成年犬中一些检测的酶活性显示出不同的Vmax。