Hartmann H, Korf J, Ottmers U, Creutzfeldt W
Department of Medicine, Georg August University, Göttingen, Germany.
Acta Diabetol. 1993;30(2):108-14. doi: 10.1007/BF00578224.
Metabolic potencies of the destetrapeptide insulin analogues des-(B27-B30)-insulin, des-(B27-B30)-insulin-B26-amide, [ThrB26] des-(B27-B30)-insulin-B26-amide and [GluB26] des-(B27-B30)-insulin-B26-amide were studied in anaesthetized adult rats and in primary cultures of rat hepatocytes and compared with that of the native hormone. Hypoglycaemic effects following intravenous bolus injection of insulin or analogues were similar, as were the stimulatory actions on total body glucose disposal during euglycaemic clamping. In these latter studies a maximal stimulation in the range 16-20 mg glucose/kg per hour was observed and identical half-maximally effective serum concentrations for all peptides of about 1 pmol/ml were obtained. Analogue actions on individual peripheral tissues estimated by the uptake of 2-deoxyglucose were not different from those of insulin. In hepatocyte cultures the stimulatory action of destetrapeptide analogues on glycogenesis and on aminoisobutyric acid transport was indistinguishable from that of native insulin, with identical half-maximally effective concentrations. These data demonstrate that des-(B27-B30)-insulin and related destetrapeptide analogues have high biological activity. Since the truncated non-amidated analogue appeared to be monomeric in solution, this peptide could be a candidate for an insulin preparation potentially showing rapid absorption from subcutaneous tissue.
在麻醉的成年大鼠和大鼠肝细胞原代培养物中研究了去四肽胰岛素类似物des-(B27 - B30)-胰岛素、des-(B27 - B30)-胰岛素-B26-酰胺、[ThrB26] des-(B27 - B30)-胰岛素-B26-酰胺和[GluB26] des-(B27 - B30)-胰岛素-B26-酰胺的代谢活性,并与天然激素进行了比较。静脉推注胰岛素或类似物后的降血糖作用相似,在正常血糖钳夹期间对全身葡萄糖处置的刺激作用也相似。在这些后期研究中,观察到最大刺激范围为每小时16 - 20毫克葡萄糖/千克,所有肽的半数最大有效血清浓度约为1皮摩尔/毫升。通过2-脱氧葡萄糖摄取估计的类似物对各个外周组织的作用与胰岛素的作用没有差异。在肝细胞培养物中,去四肽类似物对糖原合成和氨基异丁酸转运的刺激作用与天然胰岛素的作用无法区分,半数最大有效浓度相同。这些数据表明des-(B27 - B30)-胰岛素和相关的去四肽类似物具有高生物活性。由于截短的非酰胺化类似物在溶液中似乎是单体,这种肽可能是一种潜在的胰岛素制剂候选物,可能显示出从皮下组织快速吸收的特性。