García-Estévez D A, Araújo-Vilar D, Cabezas-Cerrato J
Departamento de Medicina, Complejo Hospitalario Universitario de Santiago de Compostela (Hospital Xeral de Galicia), Facultad de Medicina, Spain.
Diabetes Res Clin Pract. 1998 Feb;39(2):107-13. doi: 10.1016/s0168-8227(97)00124-1.
The aim of our work was to study non-insulin-mediated glucose uptake (NIMGU), in the postabsorptive state, in several pathologies characterized by peripheral insulin resistance, namely, obesity (n = 10), NIDDM (n = 7), acromegaly (n = 7) and Cushing's disease (n = 6). These groups were compared with a group of 16 healthy subjects. To estimate peripheral insulin sensitivity (SI) and glucose effectiveness (SG), we used the minimal model of glucose metabolism. Although all of these pathologies showed severe insulin resistance (control: 6.44 +/- 2.63, obesity: 2.84 +/- 1.57, NIDDM: 1.71 +/- 0.77, acromegaly: 1.88 +/- 1.23, Cushing's disease: 1.87 +/- 0.66 x 10(-4) min-1 (microU/ml)-1, P < 0.01), fasting insulin-mediated glucose uptake (IMGU) did not differ significantly among the five groups, because reactive hyperinsulinaemia was present in all of these states. The contribution of NIMGU to whole-body glucose uptake did not differ significantly among the five groups (control: 77 +/- 8%; obesity: 77 +/- 9%; acromegaly: 82 +/- 8%; Cushing's disease: 83 +/- 8%; NIDDM: 84 +/- 7%). In conclusion, our data show that, in the postabsorptive period, non-insulin mediated glucose uptake is a major determinant of glucose disposal and is similar in the different pathologies studied; on the other hand, although absolute rates of basal insulin-mediated glucose uptake are reduced in insulin-resistant states, they did not achieve statistical value compared with control subjects because of compensatory hyperinsulinaemia.
我们研究的目的是在吸收后状态下,对几种以外周胰岛素抵抗为特征的病症,即肥胖症(n = 10)、非胰岛素依赖型糖尿病(NIDDM,n = 7)、肢端肥大症(n = 7)和库欣病(n = 6),研究非胰岛素介导的葡萄糖摄取(NIMGU)。将这些组与一组16名健康受试者进行比较。为了评估外周胰岛素敏感性(SI)和葡萄糖效能(SG),我们采用了葡萄糖代谢的最小模型。尽管所有这些病症均表现出严重的胰岛素抵抗(对照组:6.44±2.63,肥胖症:2.84±1.57,NIDDM:1.71±0.77,肢端肥大症:1.88±1.23,库欣病:1.87±0.66×10⁻⁴ min⁻¹(微单位/毫升)⁻¹,P < 0.01),但五组之间空腹胰岛素介导的葡萄糖摄取(IMGU)并无显著差异,因为所有这些状态均存在反应性高胰岛素血症。五组之间NIMGU对全身葡萄糖摄取的贡献并无显著差异(对照组:77±8%;肥胖症:77±9%;肢端肥大症:82±8%;库欣病:83±8%;NIDDM:84±7%)。总之,我们的数据表明,在吸收后期,非胰岛素介导的葡萄糖摄取是葡萄糖处置的主要决定因素,并且在所研究的不同病症中相似;另一方面,尽管在胰岛素抵抗状态下基础胰岛素介导的葡萄糖摄取的绝对速率降低,但由于代偿性高胰岛素血症,与对照组相比未达到统计学意义。