Tardif-de Géry S, Vilquin J, Carlier P, Raynaud J S, Wary C, Schwartz K, Leroy-Willig A
Unité RMN, Institut de Myologie, Hôpital de la Pitié-Salpêtrière, 47 Boulevard de l'Hôpital, 75651 Cedex 13, Paris, France.
Neuromuscul Disord. 2000 Oct;10(7):507-13. doi: 10.1016/s0960-8966(00)00122-x.
Muscular transverse relaxation times values were measured in vivo in normal mice (strain C57BL6/J, n=14) and in murine models of human congenital muscular dystrophy (dy/dy, n=9; dy(2j)/dy(2j), n=8). A single-slice multi-echo sequence was used. Gastrocnemius/soleus complex, thigh and buttock muscles were studied. Muscular transverse relaxation times values were compared between different muscle groups in each type of animal and between animal groups. Differences were observed between normal and dy(2j)/dy(2j) mice from 3 to 12 weeks of age, and between normal and dy/dy mice at 6 weeks. In specific age ranges, the values of muscular transverse relaxation times in two dystrophic models are different from those in normal mice, and could thus be used as an index of modifications in dystrophic muscle to evaluate therapies.
在正常小鼠(C57BL6/J品系,n = 14)以及人类先天性肌营养不良的小鼠模型(dy/dy,n = 9;dy(2j)/dy(2j),n = 8)体内测量肌肉横向弛豫时间值。使用单切片多回波序列。研究了腓肠肌/比目鱼肌复合体、大腿和臀部肌肉。比较了每种动物不同肌肉群之间以及动物组之间的肌肉横向弛豫时间值。在3至12周龄的正常小鼠和dy(2j)/dy(2j)小鼠之间,以及6周龄的正常小鼠和dy/dy小鼠之间观察到差异。在特定年龄范围内,两种营养不良模型中肌肉横向弛豫时间值与正常小鼠不同,因此可作为营养不良性肌肉变化的指标来评估治疗效果。