Effect of eccentric and concentric contraction mode on myogenic regulatory factors expression in human vastus lateralis muscle.

IF 1.7 3区 生物学 Q4 CELL BIOLOGY
Mostafa Sabouri, Pejman Taghibeikzadehbadr, Fatemeh Shabkhiz, Zahra Izanloo, Farahnaz Amir Shaghaghi
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引用次数: 2

Abstract

Skeletal muscle contractions are caused to release myokines by muscle fiber. This study investigated the myogenic regulatory factors, as MHC I, IIA, IIX, Myo-D, MRF4, Murf, Atrogin-1, Decorin, Myonection, and IL-15 mRNA expression in the response of eccentric vs concentric contraction. Eighteen healthy men were randomly divided into two eccentric and concentric groups, each of 9 persons. Isokinetic contraction protocols included maximal single-leg eccentric or concentric knee extension tasks at 60°/s with the dominant leg. Contractions consisted of a maximum of 12 sets of 10 reps, and the rest time between each set was 30 s. The baseline biopsy was performed 4 weeks before the study, and post-test biopsies were taken immediately after exercise protocols from the vastus lateralis muscle. The gene expression levels were evaluated using Real-Time PCR methods. The eccentric group showed a significantly lower RPE score than the concentric group (P ≤ 0.05). A significant difference in MyoD, MRF4, Myonection, and Decorin mRNA, were observed following eccentric or concentric contractions (P ≤ 0.05). The MHC I, MHC IIA, IL-15 mRNA has been changed significantly compared to the pre-exercise in the concentric group (P ≤ 0.05). While only MHC IIX and Atrogin-1 mRNA changed significantly in the eccentric group (P ≤ 0.05). Additionally, the results showed a significant difference in MyoD, MRF4, IL-15, and Decorin at the follow-up values between eccentric or concentric groups (P ≤ 0.05). Our findings highlight the growing importance of elucidating the different responses of muscle growth factors associated with a myogenic activity such as MHC IIA, Decorin, IL-15, Myonectin, Decorin, MuRF1, and MHC IIX mRNA in following various types of exercise.

偏心和同心收缩方式对股外侧肌生肌调节因子表达的影响。
骨骼肌收缩是由肌纤维引起的肌因子释放。本研究探讨了MHC I、IIA、IIX、Myo-D、MRF4、Murf、Atrogin-1、Decorin、Myonection和IL-15 mRNA在偏心收缩和同心收缩反应中的表达。18名健康男性随机分为偏心组和同心组,每组9人。等速收缩方案包括最大单腿偏心或同心膝关节伸展任务,以60°/s的速度伸展主腿。收缩最多12组,每组10次,每组之间的休息时间为30秒。基线活检在研究前4周进行,测试后活检在运动方案后立即从股外侧肌进行。采用Real-Time PCR方法检测基因表达水平。偏心组RPE评分明显低于同心组(P≤0.05)。心肌偏心收缩与同心收缩后MyoD、MRF4、Myonection、Decorin mRNA表达差异有统计学意义(P≤0.05)。与运动前相比,同心组MHC I、MHC IIA、IL-15 mRNA有显著变化(P≤0.05)。偏心组只有MHC IIX和Atrogin-1 mRNA有显著变化(P≤0.05)。偏心组与同心组随访值MyoD、MRF4、IL-15、Decorin差异有统计学意义(P≤0.05)。我们的研究结果强调了阐明与肌肉生成活动相关的肌肉生长因子(如MHC IIA、Decorin、IL-15、Myonectin、Decorin、MuRF1和MHC IIX mRNA)在以下各种类型运动中的不同反应的重要性。
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来源期刊
CiteScore
6.20
自引率
0.00%
发文量
21
审稿时长
>12 weeks
期刊介绍: The Journal of Muscle Research and Cell Motility has as its main aim the publication of original research which bears on either the excitation and contraction of muscle, the analysis of any one of the processes involved therein, the processes underlying contractility and motility of animal and plant cells, the toxicology and pharmacology related to contractility, or the formation, dynamics and turnover of contractile structures in muscle and non-muscle cells. Studies describing the impact of pathogenic mutations in genes encoding components of contractile structures in humans or animals are welcome, provided they offer mechanistic insight into the disease process or the underlying gene function. The policy of the Journal is to encourage any form of novel practical study whatever its specialist interest, as long as it falls within this broad field. Theoretical essays are welcome provided that they are concise and suggest practical ways in which they may be tested. Manuscripts reporting new mutations in known disease genes without validation and mechanistic insight will not be considered. It is the policy of the journal that cells lines, hybridomas and DNA clones should be made available by the developers to any qualified investigator. Submission of a manuscript for publication constitutes an agreement of the authors to abide by this principle.
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