Pastoris O, Foppa P, Catapano M, Dossena M
Institute of Pharmacology, University of Pavia, Italy.
Pharmacol Res. 1995 Dec;32(6):375-81. doi: 10.1016/s1043-6618(05)80043-x.
The activities of enzymes related to energy metabolism in the gastrocnemius and soleus muscles in young-adult (4 months), mature (12 months) and senescent (24 months) rats were compared after 72 h of continuous exposure to normobaric hypoxia or normoxia after alpha-adrenergic antagonist nicergoline or saline solution had been given intraperitoneally for 30 consecutive days. The maximum rates (Vmax) of the following enzyme activities in the crude extract and/or the mitochondrial fraction of each muscle specimen were evaluated: (1) for the anaerobic glycolytic pathway: hexokinase, phosphofructokinase, pyruvate kinase and lactate dehydrogenase; (2) for the tricarboxylic acid cycle; citrate synthase and malate dehydrogenase; (3) for the electron transfer chain; cytochrome oxidase; and (4) for the NAD+/NADH redox state: total NADH cytochrome c reductase. The significant differences between the enzyme activities at different ages or under different experimental conditions in the two tissue preparations of the two muscles were determined by ANOVA. MCA and ETA were used to evaluate the net effects of the experimental conditions. Ageing did not seem to affect the soleus and gastrocnemius muscles in the same way. Changes were seen only in the glycolytic pathway enzymes in the crude extract from the gastrocnemius muscle. In the soleus muscle changes in enzyme activities as a function of ageing were also found in the mitochondrial fraction. We also found that hypoxia caused greater changes in 12-month-old rats than in those of other ages (especially in the enzyme activities of the gastrocnemius muscle). Finally out data show that only in certain cases was the pharmacological treatment able to modify the influence of hypoxic conditions on the levels of enzyme activities, regardless of the age of animals.
在连续30天腹腔注射α-肾上腺素能拮抗剂尼麦角林或生理盐水后,将年轻成年(4个月)、成熟(12个月)和衰老(24个月)大鼠持续暴露于常压缺氧或常氧环境72小时后,比较其腓肠肌和比目鱼肌中与能量代谢相关的酶的活性。评估每个肌肉标本的粗提物和/或线粒体部分中以下酶活性的最大速率(Vmax):(1)无氧糖酵解途径:己糖激酶、磷酸果糖激酶、丙酮酸激酶和乳酸脱氢酶;(2)三羧酸循环:柠檬酸合酶和苹果酸脱氢酶;(3)电子传递链:细胞色素氧化酶;(4)NAD⁺/NADH氧化还原状态:总NADH细胞色素c还原酶。通过方差分析确定两种肌肉的两种组织制剂在不同年龄或不同实验条件下酶活性之间的显著差异。使用主成分分析(MCA)和效应大小分析(ETA)来评估实验条件的净效应。衰老似乎并未以相同方式影响比目鱼肌和腓肠肌。仅在腓肠肌粗提物中的糖酵解途径酶中观察到变化。在比目鱼肌中,线粒体部分也发现酶活性随衰老而变化。我们还发现,缺氧在12个月大的大鼠中引起的变化比其他年龄的大鼠更大(尤其是在腓肠肌的酶活性方面)。最后,我们的数据表明,仅在某些情况下,药物治疗能够改变缺氧条件对酶活性水平的影响,而与动物年龄无关。