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热量限制会限制衰老骨骼肌中线粒体异常的产生,但不会限制其进展。

Calorie restriction limits the generation but not the progression of mitochondrial abnormalities in aging skeletal muscle.

作者信息

Bua Entela, McKiernan Susan H, Aiken Judd M

机构信息

Department of Animal Health and Biomedical Sciences, University of Wisconsin, Madison, Wisconsin 53706, USA.

出版信息

FASEB J. 2004 Mar;18(3):582-4. doi: 10.1096/fj.03-0668fje. Epub 2004 Jan 20.

Abstract

The effect of early-onset calorie restriction and aging on the accumulation of electron transport system (ETS) abnormalities was studied in rat skeletal muscle. Rectus femoris and vastus lateralis muscle fibers were analyzed for cytochrome c oxidase (COX) and succinate dehydrogenase (SDH) enzyme activities. Fibers displaying COX negative and SDH hyper reactive (COX-/SDH++) phenotype were followed through 1000-2000 micrometers to determine the frequency and length of these abnormalities as well as the physiological impact on fiber structure. Calorie restricted rats had fewer ETS abnormal muscle fibers. The mean length of ETS abnormal regions in ad libitum rat muscle fibers was similar to calorie restricted rat muscles. ETS abnormal fibers from both diet groups exhibited intra-fiber atrophy. A negative correlation between ETS abnormality length and fiber cross-sectional area (CSA) ratio was observed in both ad libitum and calorie- restricted rats. Although calorie restriction reduced the number of ETS abnormalities, it did not affect the length or associated fiber atrophy of ETS abnormal regions once the abnormality was established. Thus, calorie restriction affects the onset but not the progression of electron transport system abnormalities, thereby, limiting a process that ultimately results in fiber breakage and fiber loss.

摘要

在大鼠骨骼肌中研究了早发性热量限制和衰老对电子传递系统(ETS)异常积累的影响。分析了股直肌和股外侧肌纤维的细胞色素c氧化酶(COX)和琥珀酸脱氢酶(SDH)酶活性。对显示COX阴性和SDH高反应性(COX-/SDH++)表型的纤维进行长达1000 - 2000微米的追踪,以确定这些异常的频率和长度以及对纤维结构的生理影响。热量限制的大鼠中ETS异常的肌纤维较少。自由摄食大鼠肌纤维中ETS异常区域的平均长度与热量限制大鼠的肌肉相似。来自两个饮食组的ETS异常纤维均表现出纤维内萎缩。在自由摄食和热量限制的大鼠中均观察到ETS异常长度与纤维横截面积(CSA)比值之间呈负相关。尽管热量限制减少了ETS异常的数量,但一旦异常形成,它并不影响ETS异常区域的长度或相关的纤维萎缩。因此,热量限制影响电子传递系统异常的发生,但不影响其进展,从而限制了最终导致纤维断裂和纤维丢失的过程。

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