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体育活动作为饮食限制对衰老作用的一个因素:对费希尔344大鼠的影响

Physical activity as a factor in the action of dietary restriction on aging: effects in Fischer 344 rats.

作者信息

McCarter R J, Shimokawa I, Ikeno Y, Higami Y, Hubbard G B, Yu B P, McMahan C A

机构信息

Department of Physiology, University of Texas Health Science Center, San Antonio 78284-7756, USA.

出版信息

Aging (Milano). 1997 Feb-Apr;9(1-2):73-9. doi: 10.1007/BF03340130.

Abstract

Dietary restriction (DR) slows the rate of aging in laboratory rodents but the mechanism of action is unknown. DR is known to induce beneficial effects in a variety of tissues and organ systems. DR also maintains high levels of physical activity over the life span. We tested the hypothesis that lifelong physical activity is an important component of the anti-aging action of DR. Male specific pathogen-free Fischer 344 rats were divided into 4 groups at 6 weeks of age: A: fed old libitum; AE: fed ad libitum and in cages with running wheels; B: fed 60% ad libitum; BE: fed 60% ad libitum and in cages with running wheels. Running activity and spontaneous cage activity were measured over 24 hours and over the life span. Metabolic rate was measured indirectly by analysis of air entering and leaving cages. AE rats exhibited low levels of running activity and ran very little beyond 6 months of age. In contrast, BE rats sustained high running levels even after all A and AE rats had died. High levels of wheel running did not decrease spontaneous cage activity. Median life span (50% survival) was in the order A = AE < B < BE. Ten percent survival was in the order A = AE < B = BE. BE rats had greatest median life span and also highest specific metabolic rate. Exercise and DR altered pathology: At death BE rats had a high incidence of cardiomyopathy, whereas A and AE rats had high incidence of chronic nephropathy and pituitary tumors. The data indicate that increased physical activity is probably not an important factor in the action of DR on aging.

摘要

饮食限制(DR)可减缓实验啮齿动物的衰老速度,但其作用机制尚不清楚。已知DR能在多种组织和器官系统中产生有益影响。DR还能在整个生命周期内维持较高水平的身体活动。我们检验了这样一个假设,即终身身体活动是DR抗衰老作用的一个重要组成部分。6周龄的雄性无特定病原体Fischer 344大鼠被分为4组:A组:随意进食;AE组:随意进食并饲养在带有跑轮的笼子里;B组:按随意摄入量的60%进食;BE组:按随意摄入量的60%进食并饲养在带有跑轮的笼子里。在24小时内及整个生命周期内测量跑步活动和自发笼内活动。通过分析进出笼子的空气间接测量代谢率。AE组大鼠的跑步活动水平较低,6个月龄后跑步量很少。相比之下,即使所有A组和AE组大鼠都死亡后,BE组大鼠仍保持较高的跑步水平。高水平的跑轮运动并未降低自发笼内活动。中位寿命(50%存活)顺序为A = AE < B < BE。10%存活顺序为A = AE < B = BE。BE组大鼠的中位寿命最长,其特定代谢率也最高。运动和DR改变了病理状况:死亡时,BE组大鼠心肌病发病率高,而A组和AE组大鼠慢性肾病和垂体肿瘤发病率高。数据表明,增加身体活动可能不是DR对衰老作用的重要因素。

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