Cederholm T, Sylvén C, Esbjörnsson-Liljedahl M, Jansson E
Department of Geriatric Medicine, Huddinge University Hospital, Huddinge, Sweden.
Clin Physiol. 2000 Sep;20(5):354-9. doi: 10.1046/j.1365-2281.2000.00269.x.
The effects of insulin treatment on skeletal muscle characteristics were studied in 18 patients (62 +/- 11 years) with poorly controlled diabetes mellitus type 2 (mean duration 7.5 +/- 6 years). Skeletal muscle biopsy samples were taken from the lateral portion of the quadriceps muscle before and after a period of insulin treatment of 40 +/- 14 days. Enzyme activities (phosphofructokinase, 3-hydroxyacyl-CoA dehydrogenase, citrate synthase, lactate dehydrogenase and creatine kinase) and myoglobin content were assessed. In a subgroup of 11 patients (60 +/- 11 years), skeletal muscle fibre type composition (type I, IIA, IIB and IIC) and fibre type cross-sectional area were also analysed. Following insulin treatment there were 32 and 38% increases, respectively, in the cross-sectional areas of type IIA and IIB fast-twitch fibres (P<0. 02). The fibre type distribution did not change. The myoglobin content in muscle decreased by 20% (P<0.01). Of the enzymes tested, the 3-hydroxyacyl-CoA dehydrogenase activity decreased by 10% (P<0. 04). Serum glucose, HbA1C and serum triglyceride levels decreased (P<0.001) and body weight and arm muscle circumference increased (P<0.02). In conclusion, insulin treatment of patients with poorly controlled non-insulin-dependent diabetes mellitus increased the fast-twitch fibre area, reduced myoglobin levels and decreased muscle enzyme activity related to fatty acid oxidation.
对18例2型糖尿病控制不佳(平均病程7.5±6年)的患者(62±11岁)研究了胰岛素治疗对骨骼肌特征的影响。在40±14天的胰岛素治疗前后,从股四头肌外侧取骨骼肌活检样本。评估酶活性(磷酸果糖激酶、3-羟酰基辅酶A脱氢酶、柠檬酸合酶、乳酸脱氢酶和肌酸激酶)和肌红蛋白含量。在11例患者(60±11岁)的亚组中,还分析了骨骼肌纤维类型组成(I型、IIA型、IIB型和IIC型)和纤维类型横截面积。胰岛素治疗后,IIA型和IIB型快肌纤维的横截面积分别增加了32%和38%(P<0.02)。纤维类型分布未改变。肌肉中的肌红蛋白含量下降了20%(P<0.01)。在所测试的酶中,3-羟酰基辅酶A脱氢酶活性下降了10%(P<0.04)。血糖、糖化血红蛋白和血清甘油三酯水平下降(P<0.001),体重和上臂肌肉周长增加(P<0.02)。总之,对非胰岛素依赖型糖尿病控制不佳的患者进行胰岛素治疗可增加快肌纤维面积,降低肌红蛋白水平,并降低与脂肪酸氧化相关的肌肉酶活性。