Palmer W K, Doukas S
Can J Physiol Pharmacol. 1983 Sep;61(9):1017-24. doi: 10.1139/y83-152.
Running exercise trained rats at either 60 or 76% of their VO2max caused myocardial cyclic AMP phosphodiesterase (PDE) activity to be increased above control levels for at least 24 h following work. Neither training nor the exercise had any effect on the total concentration of calmodulin in heart tissues. The affinity of PDE for cyclic AMP was not changed by the exercise or training. The chelating agent, EGTA, had the same influence on PDE activity regardless of whether it was present in assays of control or exercised heart extract. Km and EGTA results suggest that calcium-bound calmodulin does not account for the higher PDE activity in the hearts of exercised rats. Supernatants from hearts homogenized in the presence of charcoal, to remove nucleotides from the extract, did not eliminate the exercise-associated increase in PDE activity. These results suggest that the elevated activity was not caused by an in vitro nucleotide activation. Preincubation of the enzyme from exercised and control rat hearts with snake venom activated PDE when assays were performed with the low concentration of cyclic AMP (1 microM). Moreover, the activity reached in the extract of exercisers (23.3 pmol X 100 microL-1 X min-1) was significantly greater than the activity found in control hearts (17.59 pmol X 100 microL-1 X min-1). Exercise increases PDE activity in the myocardium of trained rats.(ABSTRACT TRUNCATED AT 250 WORDS)
让大鼠以其最大摄氧量(VO2max)的60%或76%进行跑步训练,会使心肌环磷酸腺苷磷酸二酯酶(PDE)活性在运动后至少24小时内升高至对照水平以上。训练和运动对心脏组织中钙调蛋白的总浓度均无影响。运动或训练不会改变PDE对环磷酸腺苷的亲和力。螯合剂乙二醇双四乙酸(EGTA)对PDE活性的影响相同,无论其存在于对照心脏提取物还是运动心脏提取物的检测中。米氏常数(Km)和EGTA的结果表明,与钙结合的钙调蛋白并非运动大鼠心脏中PDE活性较高的原因。在存在活性炭的情况下对心脏进行匀浆以从提取物中去除核苷酸,所得上清液并未消除与运动相关的PDE活性增加。这些结果表明,活性升高并非由体外核苷酸激活所致。当使用低浓度环磷酸腺苷(1微摩尔)进行检测时,将运动大鼠和对照大鼠心脏中的酶与蛇毒激活的PDE一起预孵育。此外,运动大鼠提取物中的活性(23.3皮摩尔×100微升-1×分钟-1)显著高于对照心脏中的活性(17.59皮摩尔×100微升-1×分钟-1)。运动可增加训练大鼠心肌中的PDE活性。(摘要截短于250字)