Stevens L, Firinga C, Gohlsch B, Bastide B, Mounier Y, Pette D
Laboratoire de Plasticité Neuromusculaire, Université des Sciences et Technologies de Lille, F-59655 Villeneuve d'Ascq, France.
Am J Physiol Cell Physiol. 2000 Nov;279(5):C1558-63. doi: 10.1152/ajpcell.2000.279.5.C1558.
To investigate the plasticity of slow and fast muscles undergoing slow-to-fast transition, rat soleus (SOL), gastrocnemius (GAS), and extensor digitorum longus (EDL) muscles were exposed for 14 days to 1) unweighting by hindlimb suspension (HU), or 2) treatment with the beta(2)-adrenergic agonist clenbuterol (CB), or 3) a combination of both (HU-CB). In general, HU elicited atrophy, CB induced hypertrophy, and HU-CB partially counteracted the HU-induced atrophy. Analyses of myosin heavy (MHC) and light chain (MLC) isoforms revealed HU- and CB-induced slow-to-fast transitions in SOL (increases of MHCIIa with small amounts of MHCIId and MHCIIb) and the upregulation of the slow MHCIa isoform. The HU- and CB-induced changes in GAS consisted of increases in MHCIId and MHCIIb ("fast-to-faster transitions"). Changes in the MLC composition of SOL and GAS consisted of slow-to-fast transitions and mainly encompassed an exchange of MLC1s with MLC1f. In addition, MLC3f was elevated whenever MHCIId and MHCIIb isoforms were increased. Because the EDL is predominantly composed of type IID and IIB fibers, HU, CB, and HU-CB had no significant effect on the MHC and MLC patterns.
为了研究经历慢到快转变的慢肌和快肌的可塑性,将大鼠的比目鱼肌(SOL)、腓肠肌(GAS)和趾长伸肌(EDL)暴露于以下环境14天:1)通过后肢悬吊(HU)使其失重;2)用β2 -肾上腺素能激动剂克伦特罗(CB)处理;3)两者结合(HU - CB)。一般来说,HU引起萎缩,CB诱导肥大,HU - CB部分抵消了HU诱导的萎缩。对肌球蛋白重链(MHC)和轻链(MLC)同工型的分析显示,HU和CB诱导了SOL从慢到快的转变(MHCIIa增加,伴有少量的MHCIId和MHCIIb)以及慢肌MHCIa同工型的上调。HU和CB诱导的GAS变化包括MHCIId和MHCIIb增加(“从快到更快的转变”)。SOL和GAS的MLC组成变化包括从慢到快的转变,主要涉及MLC1s与MLC1f的交换。此外,每当MHCIId和MHCIIb同工型增加时,MLC3f也会升高。由于EDL主要由IID型和IIB型纤维组成,HU、CB和HU - CB对MHC和MLC模式没有显著影响。