Osei K, O'Dorisio T M, Malarkey W B, Cataland S
Division of Endocrinology and Metabolism, Ohio State University Hospitals, Columbus.
J Lab Clin Med. 1991 Jul;118(1):56-64.
Octreotide (Sandostatin), a potent and long-acting octapeptide analogue of somatostatin, exhibits variable metabolic effects in type 1 diabetes. We have postulated that interindividual variability in octreotide metabolism could be responsible in part for the differences in metabolic responses reported in previous clinical studies. To this end, we determined plasma levels and MCR of octreotide during 24-hour continuous SC infusion (low dose, 200 micrograms; high dose, 400 micrograms) in nine female, C peptide-negative patients with type 1 diabetes. The metabolic effects of the analogue were assessed by measuring serum glucose, free insulin, glucagon, GH, and PP levels before and at 1- to 2-hour intervals during each dose of the analogue or control (0.9% saline solution) infusion in a single-blind randomized manner. Mean daytime (0800-0000 hours) and bedtime (0000-0800 hours) serum glucose levels decreased significantly (p less than 0.05 to 0.02) during analogue therapy compared with control. Mean serum free insulin levels were significantly (p less than 0.02) greater during octreotide infusion compared with control, despite the similar daily insulin requirements. Both doses of the analogue effectively suppressed 24-hour GH by 50%, glucagon by 50%, and PP by 80%. Steady-state octreotide levels varied considerably among patients (low, mean +/- SEM), 1000 +/- 101, range 638 to 1375 pg/ml; high, mean 1940 +/- 147, range 1032 to 2462 pg/ml). Although mean MCR values were similar with both doses, we observed greater interindividual variability (low, mean 2.45 +/- 0.30, range 1.31 to 3.78 ml/kg/min; high, mean 2.36 +/- 0.19, range 1.68 to 3.48 ml/kg/min).(ABSTRACT TRUNCATED AT 250 WORDS)
奥曲肽(善得定)是一种强效长效的生长抑素八肽类似物,在1型糖尿病中表现出不同的代谢效应。我们推测,奥曲肽代谢的个体差异可能部分导致了先前临床研究中报道的代谢反应差异。为此,我们测定了9名1型糖尿病C肽阴性女性患者在24小时持续皮下输注(低剂量,200微克;高剂量,400微克)期间奥曲肽的血浆水平和代谢清除率(MCR)。以单盲随机方式,在每次输注类似物或对照(0.9%盐水溶液)期间,于给药前及给药后1至2小时间隔测量血清葡萄糖、游离胰岛素、胰高血糖素、生长激素(GH)和胰多肽(PP)水平,评估该类似物的代谢效应。与对照相比,类似物治疗期间白天(08:00 - 00:00时)和睡前(00:00 - 08:00时)的平均血清葡萄糖水平显著降低(p < 0.05至0.02)。尽管每日胰岛素需求量相似,但与对照相比,奥曲肽输注期间平均血清游离胰岛素水平显著更高(p < 0.02)。两种剂量的类似物均有效抑制24小时GH达50%、胰高血糖素达50%、PP达80%。患者间的奥曲肽稳态水平差异很大(低剂量,平均±标准误),1000±101,范围638至1375 pg/ml;高剂量,平均1940±147,范围1032至2462 pg/ml)。尽管两种剂量的平均MCR值相似,但我们观察到个体间差异更大(低剂量,平均2.45±0.30,范围1.31至3.78 ml/kg/min;高剂量,平均2.36±0.19,范围1.68至3.48 ml/kg/min)。(摘要截断于250字)