Rehunen S, Karli P, Härkönen M
J Neurol Sci. 1985 Mar;67(3):299-306. doi: 10.1016/0022-510x(85)90154-6.
Concentrations of the high-energy phosphates, ATP and creatine phosphate, were investigated in slow-twitch (ST) and fast-twitch (FT) muscle fibres of patients with myotonia congenita (n = 6), dystrophia myotonica (n = 5), myopathia ocularis (n = 2) and hyperornithinemia with gyrate atrophy (HOGA) (n = 3) and compared with those of normal subjects (n = 4). At rest, the patients with HOGA had lower values of ATP in ST muscle fibres than the controls (P less than 0.05). They also had lower values of creatine phosphate in these fibres than the patients with dystrophia myotonica (P less than 0.03) and myotonia congenita (P less than 0.05). After 30 s bicycle ergometer exercises there was an increase in ATP in the ST muscle fibres of the patients with myotonia congenita, but in all other patient groups there was a decrease.
对先天性肌强直患者(n = 6)、强直性肌营养不良患者(n = 5)、眼肌病患者(n = 2)和伴有回旋状萎缩的高鸟氨酸血症(HOGA)患者(n = 3)的慢肌纤维(ST)和快肌纤维(FT)中的高能磷酸盐三磷酸腺苷(ATP)和磷酸肌酸的浓度进行了研究,并与正常受试者(n = 4)的浓度进行了比较。静息时,HOGA患者ST肌纤维中的ATP值低于对照组(P < 0.05)。这些纤维中的磷酸肌酸值也低于强直性肌营养不良患者(P < 0.03)和先天性肌强直患者(P < 0.05)。在进行30秒自行车测力计运动后,先天性肌强直患者的ST肌纤维中的ATP增加,但在所有其他患者组中均减少。