Picquet F, De-Doncker L, Falempin M
Laboratoire de Plasticité Neuromusculaire, UPRES EA 1032, IFR 118, Université des Sciences et Technologies de Lille, Villeneuve d'Ascq, France.
Can J Physiol Pharmacol. 2004 May;82(5):311-8. doi: 10.1139/y04-034.
Our objective was to determine the effects of a clenbuterol (CB) treatment orally administered (2 mg per kg) to rats submitted to 14 days of hindlimb unloading (HU). The morphological and the contractile properties as well as the myosin heavy chain isoforms contained in each fiber type were determined in whole soleus muscles. As classically described after HU, a decrease in muscle wet weight and in body mass associated with a loss of muscular force, an evolution of the contractile parameters towards those of a fast muscle type, and the emergence of fast myosin heavy chain isoforms were observed. The CB treatment in the HU rats helped reduce the decrease in 1) muscle and body weights, 2) force and 3) the proportion of slow fibers, without preventing the emergence of fast myosin isoforms. Clenbuterol induced a complex remodelling of the muscle typing promoting the combination of both slow and fast myosin isoforms within one fiber. To conclude, our data demonstrate that CB administration partially counteracts the effects produced by HU, and they allow us to anticipate advances in the treatment of muscular atrophy.
我们的目的是确定对后肢卸载(HU)14天的大鼠口服给予克伦特罗(CB,2毫克/千克)的效果。在整个比目鱼肌中测定了形态学和收缩特性以及每种纤维类型中所含的肌球蛋白重链同工型。如经典描述的那样,在HU后观察到肌肉湿重和体重下降,伴随着肌肉力量丧失,收缩参数向快肌类型演变,以及快肌球蛋白重链同工型出现。对HU大鼠进行CB治疗有助于减少1)肌肉和体重、2)力量以及3)慢肌纤维比例的下降,同时并不阻止快肌球蛋白同工型的出现。克伦特罗诱导了肌肉类型的复杂重塑,促进了快慢肌球蛋白同工型在同一纤维内的组合。总之,我们的数据表明,给予CB可部分抵消HU产生的影响,并且使我们能够预期在肌肉萎缩治疗方面取得进展。