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运动对小鼠流感和兔热病心肌临床病程及生化反应的调节作用。

Modifying effects of exercise on clinical course and biochemical response of the myocardium in influenza and tularemia in mice.

作者信息

Ilbäck N G, Friman G, Beisel W R, Johnson A J, Berendt R F

出版信息

Infect Immun. 1984 Aug;45(2):498-504. doi: 10.1128/iai.45.2.498-504.1984.

Abstract

For a study of the interactions of strenuous physical exercise (daily swimming to exhaustion) and a viral as compared with a bacterial infection with regard to the clinical course and the biochemical response of the myocardium, influenza and tularemia of similar lethality were used in mice. In both infections, expected infection-induced catabolic alterations in the ventricular myocardium were evident 2 days before median lethality was achieved, with a more pronounced wasting in influenza than in tularemia. Exercise before inoculation (preconditioning) was beneficial in that the catabolic effects of both infections were limited and lethality in influenza was reduced. Thus, the myocardial protein-degrading effect of influenza did not occur with preconditioning, and oxidative tissue enzyme activities decreased less. In tularemia, cytochrome c oxidase activity was fully preserved with preconditioning, and activation of catalase was less pronounced. Exercise during ongoing infection counteracted the infection-induced decrease in the activities of glycolytic and oxidative enzymes in tularemia, but lethality and bacterial counts in the spleen were uninfluenced. Conversely, exhaustive exercise in influenza increased lethality and had no significant effect on cardiac enzymes. These exercise models caused no major alterations in activation of lysosomal enzymes (beta-glucuronidase and cathepsin D).

摘要

为了研究剧烈体育锻炼(每日游泳至精疲力竭)与病毒感染及细菌感染相互作用对心肌临床病程和生化反应的影响,在小鼠中使用了致死率相似的流感和土拉菌病。在两种感染中,在达到半数致死率前2天,心室心肌中预期的感染诱导的分解代谢改变明显,流感比土拉菌病的消瘦更明显。接种前运动(预处理)有益,因为两种感染的分解代谢作用均受到限制,且流感的致死率降低。因此,预处理后流感的心肌蛋白降解作用未发生,氧化组织酶活性降低较少。在土拉菌病中,预处理后细胞色素c氧化酶活性完全保留,过氧化氢酶的激活不太明显。正在感染期间运动可抵消土拉菌病中感染诱导的糖酵解和氧化酶活性降低,但致死率和脾脏细菌计数不受影响。相反,流感中的力竭运动增加了致死率,对心脏酶无显著影响。这些运动模型未引起溶酶体酶(β-葡萄糖醛酸酶和组织蛋白酶D)激活的重大改变。

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