Fonteles M C, Huang L C, Larner J
Clinical Research Unit, Federal University of Ceara/UECe, Fortaleza, Ceara, Brazil.
Diabetologia. 1996 Jun;39(6):731-4. doi: 10.1007/BF00418546.
We compared the effects of infusing a chemically defined chiro-inositol glycan putative insulin mediator with an equivalent dose of insulin in low-dose (45 mg/kg) streptozotocin diabetic rats. Insulin decreased plasma glucose levels from 17.32 +/- 0.17 to 3.96 +/- 0.064 mmol/l (p < 0.0002) in 120 min, a decrease of 77.13%, while the putative mediator promoted a decrease in plasma glucose from 14.85 +/- 0.084 to 7.22 +/- 0.13 mmol/l (p < 0.007) in 60 min. The putative mediator maintained euglycaemia over the ensuing 60 min with a plasma glucose level of 7.01 +/- 0.10 mmol/l at 120 min. Thus, insulin further reduced the plasma glucose from euglycaemia at 60 min to produce hypoglycaemia at 120 min. The lack of production of hypoglycaemia by the putative mediator can be explained by its inhibition of glucose-stimulated insulin secretion by the islet beta cells, thus providing a potential negative feedback regulatory mechanism; or by its selective action on muscle to increase glycogen synthesis. The significance of these results in terms of future directions in drug design is herein considered.
我们比较了在低剂量(45毫克/千克)链脲佐菌素诱导的糖尿病大鼠中,输注化学定义的手性肌醇聚糖假定胰岛素介质与等量胰岛素的效果。胰岛素在120分钟内将血糖水平从17.32±0.17降至3.96±0.064毫摩尔/升(p<0.0002),降幅为77.13%,而假定介质在60分钟内使血糖从14.85±0.084降至7.22±0.13毫摩尔/升(p<0.007)。假定介质在随后的60分钟内维持血糖正常,120分钟时血糖水平为7.01±0.10毫摩尔/升。因此,胰岛素在60分钟时将血糖从正常血糖水平进一步降低,在120分钟时导致低血糖。假定介质未产生低血糖的原因可能是它抑制了胰岛β细胞的葡萄糖刺激胰岛素分泌,从而提供了一种潜在的负反馈调节机制;或者是它对肌肉有选择性作用以增加糖原合成。本文考虑了这些结果在药物设计未来方向方面的意义。