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骨骼肌肌球蛋白同工酶随肥大和运动的变化。

Changes in skeletal-muscle myosin isoenzymes with hypertrophy and exercise.

作者信息

Gregory P, Low R B, Stirewalt W S

出版信息

Biochem J. 1986 Aug 15;238(1):55-63. doi: 10.1042/bj2380055.

Abstract

The patterns of myosin isoenzymes in fast- and slow-twitch muscles of the rat hindlimb were studied, by pyrophosphate/polyacrylamide-gel electrophoresis, with hypertrophy (induced by synergist removal) and with spontaneous running exercise of 4 and 11 weeks duration. At 11 weeks, changes with hypertrophy in the slow-twitch soleus, composed of greater than 95% SM2 (slow myosin 2) in normal muscles, were minor, and consisted of an increase in the SM1 and SM1', and a loss of intermediate myosin (IM), an isoenzyme characteristic of Type IIa fibres [Fitzsimons & Hoh (1983) J. Physiol. (London) 343, 539-550]. The changes were dramatic, however, in the fast-twitch plantaris muscle. There was a 3-fold increase in the proportion of SM. In addition, IM became the predominant isoenzyme in the profile of hypertrophied plantaris by 4 weeks. These increases were balanced by decreases in the proportion of FM2 (fast myosin 2), with FM1 completely absent from the profile at 11 weeks. The changes in the plantaris with exercise were similar in direction but not as extensive as those with hypertrophy, and FM1 remained present at control levels throughout the study. When hypertrophy and exercise were combined, the increase in slow myosin was equal to the sum of the increases with each treatment alone. Changes at 4 weeks were intermediate between those of control and 11-week muscles. Peptide mapping of individual myosin isoenzymes showed that the heavy chains of IM were different from either fast or slow heavy chains. Furthermore, IM was found to be composed of a mixture of fast and slow light chains. These changes suggest that a transformation of myosin from fast to slow isoforms was in progress in the plantaris in response to hypertrophy, via a Type-IIa-myosin (IM) intermediate stage, a phenomenon similar to that occurring in chronically stimulated fast muscles during fast-to-slow transformation [Brown, Salmons & Whalen (1983) J. Biol. Chem. 258, 14686-14692].

摘要

通过焦磷酸/聚丙烯酰胺凝胶电泳,研究了大鼠后肢快肌和慢肌中肌球蛋白同工酶的模式,包括协同肌切除诱导的肥大以及持续4周和11周的自发跑步运动。在11周时,正常肌肉中超过95%为SM2(慢肌球蛋白2)的慢肌比目鱼肌,肥大引起的变化较小,包括SM1和SM1'增加,以及中间肌球蛋白(IM)减少,IM是IIa型纤维的一种同工酶特征[菲茨西蒙斯和霍(1983年)《生理学杂志》(伦敦)343, 539 - 550]。然而,在快肌跖肌中变化显著。SM的比例增加了3倍。此外,到4周时,IM成为肥大跖肌中的主要同工酶。这些增加被FM2(快肌球蛋白2)比例的下降所平衡,到11周时FM1在图谱中完全消失。运动引起的跖肌变化方向相似,但不如肥大引起的变化广泛,并且在整个研究过程中FM1保持在对照水平。当肥大和运动相结合时,慢肌球蛋白的增加等于每种单独处理增加量的总和。4周时的变化介于对照和11周肌肉之间。对单个肌球蛋白同工酶的肽图分析表明,IM的重链与快链或慢链均不同。此外,发现IM由快链和慢链混合组成。这些变化表明,跖肌中肌球蛋白正通过IIa型肌球蛋白(IM)中间阶段从快型向慢型同工型转变,这一现象类似于在快 - 慢转变过程中慢性刺激的快肌中发生的情况[布朗、萨尔蒙斯和惠伦(1983年)《生物化学杂志》258, 14686 - 14692]。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0212/1147097/78ac4f0e7952/biochemj00273-0063-a.jpg

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