Kruszynska Y T, Petranyi G, Home P D, Taylor R, Alberti K G
Diabetologia. 1986 Oct;29(10):699-75. doi: 10.1007/BF00870279.
The mechanisms of insulin insensitivity in diabetes are poorly understood. We have therefore assessed the relationship between glucose disposal during a euglycaemic clamp, muscle glycogen formation, and the activities of insulin regulated enzymes within skeletal muscle in five Type 1 (insulin-dependent) diabetic patients, both on conventional injection therapy (HbA1 11.0 +/- 1.0 (SD) %) and after 6 weeks continuous subcutaneous insulin infusion (HbA1 7.6 +/- 1.4%, p less than 0.01). On both regimens, overnight euglycaemia before the clamp was maintained with an intravenous insulin infusion. The increase in clamp glucose requirements (insulin 0.1 U X kg-1 X h-1) between injection therapy and continuous subcutaneous insulin infusion was significant (6.2 +/- 0.9 (SE) to 7.0 +/- 0.9 mg X kg-1 X min-1, p less than 0.05), but small compared to differences between subjects. Glucose requirement remained lower than in control subjects (10.4 +/- 0.7 mg X kg-1 X min-1, p less than 0.05). The increase in muscle glycogen with the clamp was slightly higher on continuous subcutaneous insulin infusion (9.5 +/- 2.5 mg/g protein) than on injection therapy (8.5 +/- 2.4 mg/g, p less than 0.05), but less than in control subjects (17.9 +/- 2.1 mg/g, p less than 0.05). The expressed activity of glycogen synthase and pyruvate dehydrogenase increased significantly between fasting and the end of the clamps in the patients (p less than 0.001 and less than 0.005), but was not significantly different between the two treatment regimens. Expressed glycogen synthase activity at the end of the clamp was lower on both treatments than in control subjects (p less than 0.05). Both enzyme activities were, however, highly correlated with glucose requirement between patients, (r = 0.89-0.94, p less than 0.05-0.02), and glycogen synthase was similarly correlated in the control subjects (r = 0.84, p less than 0.05).(ABSTRACT TRUNCATED AT 250 WORDS)
糖尿病中胰岛素不敏感的机制目前还知之甚少。因此,我们评估了五名1型(胰岛素依赖型)糖尿病患者在正常血糖钳夹试验期间的葡萄糖处置、肌肉糖原形成与骨骼肌中胰岛素调节酶活性之间的关系。这五名患者分别接受传统注射治疗(糖化血红蛋白HbA1为11.0±1.0(标准差)%)和持续皮下胰岛素输注6周后(糖化血红蛋白HbA1为7.6±1.4%,p<0.01)。在两种治疗方案中,钳夹试验前均通过静脉输注胰岛素维持夜间正常血糖水平。从注射治疗到持续皮下胰岛素输注,钳夹试验中葡萄糖需求量(胰岛素0.1U·kg⁻¹·h⁻¹)的增加具有显著意义(从6.2±0.9(标准误)增至7.0±0.9mg·kg⁻¹·min⁻¹,p<0.05),但与受试者之间的差异相比仍较小。葡萄糖需求量仍低于对照组受试者(10.4±0.7mg·kg⁻¹·min⁻¹,p<0.05)。持续皮下胰岛素输注时,钳夹试验导致的肌肉糖原增加量(9.5±2.5mg/g蛋白质)略高于注射治疗时(8.5±2.4mg/g,p<0.05),但低于对照组受试者(17.9±2.1mg/g,p<0.05)。患者在禁食至钳夹试验结束期间,糖原合酶和丙酮酸脱氢酶的活性显著增加(p<0.001和<0.005),但两种治疗方案之间无显著差异。钳夹试验结束时,两种治疗方案下的糖原合酶活性均低于对照组受试者(p<0.05)。然而,患者中两种酶的活性均与葡萄糖需求量高度相关(r = 0.89 - 0.94,p<0.05 - 0.02),对照组受试者中糖原合酶也有类似的相关性(r = 0.84,p<0.05)。(摘要截断于250字)