DeVol D L, Rotwein P, Sadow J L, Novakofski J, Bechtel P J
Department of Animal Sciences, University of Illinois, Urbana 61801.
Am J Physiol. 1990 Jul;259(1 Pt 1):E89-95. doi: 10.1152/ajpendo.1990.259.1.E89.
We have investigated the hypothesis that there is local regulation of insulin-like growth factor (IGF) gene expression during skeletal muscle growth. Compensatory hypertrophy was induced in the soleus, a predominantly slow-twitch muscle, and plantaris, a fast-twitch muscle, in 11- to 12-wk-old female Wistar rats by unilateral cutting of the distal gastrocnemius tendon. Animals were killed 2, 4, or 8 days later, and muscles of the nonoperated leg served as controls. Muscle weight increased throughout the experimental period, reaching 127% (soleus) or 122% (plantaris) of control values by day 8. In both growing muscles, IGF-I mRNA, quantitated by a solution-hybridization nuclease-protection assay, rose by nearly threefold on day 2 and remained elevated throughout the experimental period. IGF-II mRNA levels also increased over controls. A more dramatic response was seen in hypophysectomized rats, where IGF-I mRNA levels rose by 8- to 13-fold, IGF-II values by 3- to 7-fold, and muscle mass increased on day 8 to 149% (soleus) or 133% (plantaris) of the control contralateral limb. These results indicate that signals propagated during muscle hypertrophy enhance the expression of both IGF genes, that modulation of IGF-I mRNA levels can occur in the absence of growth hormone, and that locally produced IGF-I and IGF-II may play a role in skeletal muscle growth.
我们研究了关于骨骼肌生长过程中存在胰岛素样生长因子(IGF)基因表达局部调控的假说。通过单侧切断11至12周龄雌性Wistar大鼠的腓肠肌远端肌腱,诱导比目鱼肌(一种主要为慢肌纤维的肌肉)和跖肌(一种快肌纤维的肌肉)发生代偿性肥大。在2、4或8天后处死动物,未手术侧腿的肌肉作为对照。在整个实验期间,肌肉重量均增加,到第8天时,比目鱼肌重量达到对照值的127%,跖肌达到122%。在两块生长的肌肉中,通过溶液杂交核酸酶保护试验定量检测发现,IGF-I mRNA在第2天增加了近三倍,并在整个实验期间保持升高。IGF-II mRNA水平也高于对照。在垂体切除的大鼠中观察到更显著的反应,其中IGF-I mRNA水平增加了8至13倍,IGF-II值增加了3至7倍,并且在第8天时肌肉质量增加到对侧对照肢体的149%(比目鱼肌)或133%(跖肌)。这些结果表明,在肌肉肥大过程中传播的信号增强了两种IGF基因的表达,在没有生长激素的情况下也可以发生IGF-I mRNA水平的调节,并且局部产生的IGF-I和IGF-II可能在骨骼肌生长中起作用。