Molitch M E, Raiti S, Baumann G, Belknap S, Reichlin S
J Clin Endocrinol Metab. 1987 Aug;65(2):299-304. doi: 10.1210/jcem-65-2-299.
Previous estimates of PRL pharmacokinetics have been made using radioiodinated human PRL (hPRL) infusions or by measuring serum PRL disappearance following prolactinoma resection. The recent purification of hPRL in significant quantities made it possible to measure the clearance and volume of distribution directly. Studies were also carried out to determine absorption and clearance after im injection. In five normal men whose endogenous PRL secretion was suppressed by dopamine, a loading dose of hPRL (70-90 micrograms) followed by a constant infusion (1.39-2.9 ng/min) produced steady state serum PRL levels of 15.2-25.4 ng/mL by 30-60 min. The calculated mean volume of distribution was 7.3 +/- 2.9 (+/- SD) L. The calculated MCR was 71 +/- 19 mL/min X m2, and the calculated production rate was 802 +/- 377 micrograms/24 h X m2. The plasma disappearance half-life following discontinuation of the infusion was 37 +/- 10 min. The PRL infusate consisted primarily (75.6%) of a 22.5 K dalton species, probably PRL monomer, a component eluting at 45K daltons (16.1% of the total radioimmunoreactivity), probably dimer, and a small amount of a larger mol wt species. Serum obtained during dopamine infusion but before hPRL infusion contained 68.1% of the 22.5K, 7.2% of the 45K, and 24.7% of the larger mol wt moieties. During hPRL infusion in two men there was a relative decrease in the proportion of PRL monomer to 55% and 69% and a relative increase in the PRL dimer to 33% and 18%, respectively. hPRL was injected im in doses of 1, 2, 4, and 8 micrograms/kg without prior dopamine infusion. No significant changes in serum PRL levels occurred after the 1 and 2 micrograms/kg doses (n = 5). After the 4 micrograms/kg dose (n = 8), mean serum PRL levels rose from 10.0 +/- 1.8 (+/- SEM) ng/mL to peak levels of 13.1 +/- 1.8 ng/mL (P less than 0.01). After the 8 micrograms/kg dose (n = 7), PRL levels rose from 9.3 +/- 1.6 to 16.5 +/- 1.8 ng/mL (P less than 0.01). The PRL rise began between 60 and 80 min after injection; peak levels occurred at 160-180 min. In two men given 8 micrograms/kg who were sampled for an additional 3 h, PRL levels peaked at 200-220 min and began to fall by 220-240 min, but had not returned to baseline by 6 h. There were no side-effects of PRL administration, although the 8 micrograms/kg dose caused transient local discomfort.(ABSTRACT TRUNCATED AT 400 WORDS)
以往对催乳素(PRL)药代动力学的估计是通过放射性碘化人PRL(hPRL)输注或在催乳素瘤切除后测量血清PRL清除率来进行的。近期大量纯化hPRL使得直接测量清除率和分布容积成为可能。还开展了研究以确定肌肉注射后的吸收和清除情况。在5名内源性PRL分泌被多巴胺抑制的正常男性中,给予hPRL负荷剂量(70 - 90微克),随后持续输注(1.39 - 2.9纳克/分钟),30 - 60分钟时血清PRL稳态水平达到15.2 - 25.4纳克/毫升。计算得出的平均分布容积为7.3±2.9(±标准差)升。计算得出的代谢清除率(MCR)为71±19毫升/分钟×平方米,计算得出的生成率为802±377微克/24小时×平方米。输注停止后血浆清除半衰期为37±10分钟。PRL输注液主要由一种22.5千道尔顿的成分(75.6%)组成,可能是PRL单体,一种在45千道尔顿处洗脱的成分(占总放射免疫活性的16.1%),可能是二聚体,以及少量更大分子量的成分。在多巴胺输注期间但在hPRL输注前获得的血清中,22.5K成分占68.1%,45K成分占7.2%,更大分子量成分占24.7%。在两名男性hPRL输注期间,PRL单体比例相对下降至55%和69%,PRL二聚体比例相对增加至33%和18%。在未预先进行多巴胺输注的情况下,以1、2、4和8微克/千克的剂量肌肉注射hPRL。1和2微克/千克剂量后血清PRL水平无显著变化(n = 5)。4微克/千克剂量后(n = 8),平均血清PRL水平从10.0±1.8(±标准误)纳克/毫升升至峰值水平13.1±1.8纳克/毫升(P<0.01)。8微克/千克剂量后(n = 7),PRL水平从9.3±1.6升至16.5±1.8纳克/毫升(P<0.01)。PRL升高在注射后60至80分钟开始;峰值水平出现在160 - 180分钟。在两名接受8微克/千克剂量并额外采样3小时的男性中,PRL水平在200 - 220分钟达到峰值,220 - 240分钟开始下降,但6小时时未恢复至基线水平。PRL给药没有副作用,尽管8微克/千克剂量引起短暂局部不适。(摘要截断于400字)