MacNeil B, Hoffman-Goetz L
Department of Kinesiology, Faculty of Applied Health Sciences, University of Waterloo, Ontario, Canada.
J Appl Physiol (1985). 1993 Jan;74(1):388-95. doi: 10.1152/jappl.1993.74.1.388.
This study investigated the influence of 9 wk of chronic exercise on natural cytotoxicity in male C3H mice. Both in vivo cytotoxicity (pulmonary vasculature) and in vitro cytotoxicity (spleen) were determined for voluntary (wheel running; n = 30) and forced (treadmill running, 15 m/min, 30 min/day; n = 30) exercise protocols. A sedentary control group (n = 30) and a treadmill control group (5 m/min, 5 min/day; n = 30) were also included. After 9 wk of chronic exercise, submaximal exercise O2 uptake was reduced in the wheel-running group relative to that in sedentary or treadmill-trained mice. Maximal citrate synthase activity of soleus muscle was higher in treadmill-trained group compared with that in sedentary or wheel-running mice. Chronic exercise consistently reduced percent retention of CIRAS 3 tumor cells in the lungs of treadmill- (15.3 +/- 1.4) and wheel- (17.9 +/- 1.4) trained mice below that of sedentary (29.5 +/- 2.7) and treadmill control (25.8 +/- 1.8) groups (P < 0.001). Injection of anti-asialo GM1 (ASGM1) antibody increased tumor cell retention in the lungs for all groups but did not alter the differences between activity conditions. In vitro cytotoxicity was enhanced in treadmill- and wheel-trained mice relative to that in sedentary controls but was not elevated in the treadmill control group. Anti-ASGM1 injection eliminated in vitro cytotoxicity for all groups. Chronic exercise slightly increased the frequency of ASGM1-positive splenocytes in treadmill-trained mice only. These results indicate that chronic exercise enhances natural cytotoxic mechanisms in vivo and in vitro and that this enhancement is present for both forced and voluntary exercise.(ABSTRACT TRUNCATED AT 250 WORDS)
本研究调查了9周慢性运动对雄性C3H小鼠自然细胞毒性的影响。针对自主运动(跑轮运动;n = 30)和强迫运动(跑步机跑步,15米/分钟,每天30分钟;n = 30)方案,测定了体内细胞毒性(肺血管系统)和体外细胞毒性(脾脏)。还纳入了久坐对照组(n = 30)和跑步机对照组(5米/分钟,每天5分钟;n = 30)。经过9周的慢性运动后,跑轮运动组的次最大运动摄氧量相对于久坐或跑步机训练的小鼠有所降低。与久坐或跑轮运动的小鼠相比,跑步机训练组比目鱼肌的最大柠檬酸合酶活性更高。慢性运动持续降低了跑步机训练组(15.3±1.4)和跑轮运动组(17.9±1.4)小鼠肺部CIRAS 3肿瘤细胞的保留率,低于久坐组(29.5±2.7)和跑步机对照组(25.8±1.8)(P < 0.001)。注射抗去唾液酸GM1(ASGM1)抗体增加了所有组肺部的肿瘤细胞保留率,但未改变运动条件之间的差异。相对于久坐对照组,跑步机训练和跑轮运动训练的小鼠体外细胞毒性增强,但跑步机对照组未升高。注射抗ASGM1消除了所有组的体外细胞毒性。慢性运动仅略微增加了跑步机训练小鼠中ASGM1阳性脾细胞的频率。这些结果表明,慢性运动在体内和体外均增强了自然细胞毒性机制,并且这种增强在强迫运动和自主运动中均存在。(摘要截断于250字)