Diffee G M, Caiozzo V J, Herrick R E, Baldwin K M
Department of Physiology and Biophysics, University of California, Irvine 92717.
Am J Physiol. 1991 Mar;260(3 Pt 1):C528-34. doi: 10.1152/ajpcell.1991.260.3.C528.
This study examined the relationship between contractile and isomyosin changes occurring in rat soleus (SOL) and plantaris (PLAN) muscles after 28 days of hindlimb suspension. SOL muscles from suspended animals exhibited a 45% decline in muscle weight compared with controls (P less than 0.05) accompanied by a 49% decrease in peak twitch tension (Pt) and a 59% reduction in peak tetanic tension (Po). Smaller reductions were observed in muscle weight, Pt, and Po (12, 43, and 24%, respectively) for the suspended PLAN. Maximal shortening velocity (Vmax) of the suspended SOL and the velocity of unloaded shortening were increased by 36 and 35%, respectively, but there was no suspension-induced change in PLAN Vmax. Suspension induced a 22% increase in SOL myosin adenosinetriphosphatase (ATPase) activity that was accompanied by a shift in the native myosin isoform distribution characterized by an increase in the relative amounts of intermediate and fast myosin. The more modest changes in the contractile function of suspended PLAN were accompanied by a small (7%) increase in myosin ATPase activity but no significant changes in myosin isoform distribution. The results of this study confirm that hindlimb suspension results in significant speeding of SOL contractile properties and suggest that the shift toward faster myosin isoforms with a higher myosin ATPase activity likely accounts for these mechanical changes.
本研究检测了后肢悬吊28天后大鼠比目鱼肌(SOL)和跖肌(PLAN)发生的收缩变化与同工型肌球蛋白变化之间的关系。与对照组相比,悬吊动物的SOL肌重量下降了45%(P<0.05),同时单收缩峰值张力(Pt)下降了49%,强直收缩峰值张力(Po)下降了59%。悬吊的PLAN肌在肌肉重量、Pt和Po方面的下降幅度较小(分别为12%、43%和24%)。悬吊的SOL肌的最大缩短速度(Vmax)和无负荷缩短速度分别增加了36%和35%,但悬吊并未引起PLAN肌Vmax的变化。悬吊使SOL肌肌球蛋白三磷酸腺苷酶(ATPase)活性增加了22%,同时天然肌球蛋白同工型分布发生改变,其特征是中间型和快肌球蛋白的相对含量增加。悬吊的PLAN肌收缩功能变化较小,同时肌球蛋白ATPase活性小幅增加(7%),但肌球蛋白同工型分布无显著变化。本研究结果证实,后肢悬吊导致SOL肌收缩特性显著加快,并表明向具有较高肌球蛋白ATPase活性的更快肌球蛋白同工型转变可能是这些力学变化的原因。