Fløgstad A K, Halse J, Grass P, Abisch E, Djøseland O, Kutz K, Bodd E, Jervell J
Medical Department B, Rikshospitalet, National Hospital, Oslo, Norway.
J Clin Endocrinol Metab. 1994 Aug;79(2):461-5. doi: 10.1210/jcem.79.2.8045964.
We investigated the pharmacokinetics of bromocriptine and octreotide, both individually and in combination, in 12 patients with active acromegaly. The pharmacodynamics of the drugs were assessed by 12-h profiles of GH secretion and insulin-like growth factor-I (IGF-I) measurements. During the 42-day study period, bromocriptine was administered for 28 days (from day 8; 5 mg, orally, twice daily) and octreotide (200 micrograms, sc, twice daily) from days 15-42. IGF-I levels, 12-h GH, and plasma bromocriptine and octreotide profiles were obtained on days 0, 14, 28, and 42. During bromocriptine treatment, both the area under the GH day curves (AUC) and mean IGF-I decreased to 64% (95% confidence limits, 43-72% and 48-82%, respectively) of initial values. During octreotide treatment, the respective values were 23% (18-30%) and 32% (21-36%), which were greater decreases than those during bromocriptine treatment [36% (95% confidence limits, 32-54%) for AUC for GH and 50% (95% confidence limits, 34-58%) for IGF-I]. With combined treatment, the AUC for GH was reduced to 16% (12-21%) and that of IGF-I to 25% (16-27%) of initial values. This combination was more effective than bromocriptine [25% (95% confidence limits, 22-37%) for AUC for GH and 39% (95% confidence limits, 25-43%) for IGF-I] and octreotide alone [78% (95% confidence limits, 53-89%) for AUC for GH and 78% (95% confidence limits, 57-98%) for IGF-I]. The pharmacokinetic parameters of octreotide were unchanged by the coadministration of bromocriptine. The bioavailability of bromocriptine increased by approximately 40% when bromocriptine was administered together with octreotide compared with administration alone (P < 0.01). Bromocriptine disposition parameters were unaltered. In conclusion, treatment of acromegalics with a combination of octreotide and bromocriptine increases the bioavailability of bromocriptine and reduces both GH and IGF-I levels more effectively than treatment with either drug alone. This presents the possibility of less frequent drug administrations, lower doses of octreotide, and, consequently, lower treatment costs.
我们对12例活动性肢端肥大症患者单独及联合使用溴隐亭和奥曲肽的药代动力学进行了研究。通过生长激素(GH)分泌的12小时曲线及胰岛素样生长因子-I(IGF-I)测定来评估药物的药效学。在为期42天的研究期间,溴隐亭从第8天开始服用28天(5毫克,口服,每日两次),奥曲肽从第15天至42天使用(200微克,皮下注射,每日两次)。在第0、14、28和42天获取IGF-I水平、12小时GH以及血浆溴隐亭和奥曲肽曲线。在溴隐亭治疗期间,GH日曲线下面积(AUC)和平均IGF-I分别降至初始值的64%(95%置信限,分别为43 - 72%和48 - 82%)。在奥曲肽治疗期间,相应的值分别为23%(18 - 30%)和32%(21 - 36%),下降幅度大于溴隐亭治疗期间[GH的AUC为36%(95%置信限,32 - 54%),IGF-I为50%(95%置信限,34 - 58%)]。联合治疗时,GH的AUC降至初始值的16%(12 - 21%),IGF-I降至25%(16 - 27%)。这种联合治疗比单独使用溴隐亭[GH的AUC为25%(95%置信限,22 - 37%),IGF-I为39%(95%置信限,25 - 43%)]和单独使用奥曲肽[GH的AUC为78%(95%置信限,53 - 89%),IGF-I为78%(95%置信限,57 - 98%)]更有效。奥曲肽的药代动力学参数不受溴隐亭合用的影响。与单独给药相比,溴隐亭与奥曲肽合用时其生物利用度提高了约40%(P < 0.01)。溴隐亭的处置参数未改变。总之,奥曲肽和溴隐亭联合治疗肢端肥大症患者可提高溴隐亭的生物利用度,比单独使用任何一种药物更有效地降低GH和IGF-I水平。这使得减少给药频率、降低奥曲肽剂量成为可能,从而降低治疗成本。