Gross M, Gresser U
Medizinische Poliklinik, Ludwig-Maximilians-Universität München.
Clin Investig. 1993 Jun;71(6):461-5. doi: 10.1007/BF00180060.
Three patients with primary myoadenylate deaminase deficiency were subjected to exercise on a bicycle ergometer at 125 W for 30 minutes. Blood samples prior to, during, and at the end of exercise were analyzed for lactate, ammonia, and hypoxanthine. In addition, urinary hypoxanthine excretion was measured. In these patients the serum lactate level increased to concentrations between 7.9 and 9.0 mmol/l at the end of exercise whereas the mean lactate level in nine control subjects at the end of exercise was 3.3 mmol/l (range 1.1-8.1 mmol/l). There was no difference to control subjects in the exercise-induced increase in plasma levels of ammonia and hypoxanthine or in the increase in urinary hypoxanthine excretion. The findings support the hypothesis of a reduced substrate supply to the citric acid cycle in myoadenylate deaminase deficiency. The normal formation of ammonia and hypoxanthine excludes a marked loss of adenine nucleotides in working muscles in these patients.
三名原发性肌腺苷酸脱氨酶缺乏症患者在功率为125瓦的自行车测力计上进行了30分钟的运动。在运动前、运动期间和运动结束时采集血样,分析其中的乳酸、氨和次黄嘌呤含量。此外,还测量了尿次黄嘌呤排泄量。这些患者运动结束时血清乳酸水平升至7.9至9.0毫摩尔/升,而九名对照受试者运动结束时的平均乳酸水平为3.3毫摩尔/升(范围为1.1至8.1毫摩尔/升)。在运动引起的血浆氨和次黄嘌呤水平升高或尿次黄嘌呤排泄增加方面,这些患者与对照受试者没有差异。这些发现支持了肌腺苷酸脱氨酶缺乏症中柠檬酸循环底物供应减少的假说。氨和次黄嘌呤的正常生成排除了这些患者工作肌肉中腺嘌呤核苷酸的显著损失。