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苯海索与左旋多巴联合给药对年轻志愿者口服左旋多巴外周药代动力学的影响。

The effects of co-administration of benzhexol on the peripheral pharmacokinetics of oral levodopa in young volunteers.

作者信息

Roberts J, Waller D G, von Renwick A G, O'Shea N, Macklin B S, Bulling M

机构信息

Clinical Pharmacology Group, University of Southampton, UK.

出版信息

Br J Clin Pharmacol. 1996 Apr;41(4):331-7. doi: 10.1046/j.1365-2125.1996.32311.x.

DOI:10.1046/j.1365-2125.1996.32311.x
PMID:8730980
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2042585/
Abstract
  1. The effects of benzhexol on the absorption and pharmacokinetics of an oral dose of levodopa have been studied in 10 young healthy volunteers. Subjects were given a suspension of levodopa (250 mg) 90 min after either benzhexol (5 mg) or placebo in a randomized cross over design with doses separated by at least 1 week; on each occasion carbidopa was given 1 h before and 5 h after the dose of levodopa. Soluble paracetamol and radiolabelled DTPA were given with the levodopa as markers of gastric emptying. 2. Most subjects showed two peaks in the levodopa plasma concentration-time curve on the placebo day, with the second minor peak occurring 1-2 h after the dose. After benzhexol administration all subjects showed two or more peak levodopa concentrations in plasma. Benzhexol administration caused a significant decrease in the maximum concentration (43%; P < 0.05) of the initial peak and an increase (22%; P < 0.1) in the maximum concentration of the second peak. This change in absorption profile caused by benzhexol significantly altered the ratios of the second peak compared with the initial peak for both the maximum concentrations (P < 0.02) and for the AUC values (P < 0.05). Benzhexol administration did not affect the total AUC of levodopa (7.30 +/- 1.09 vs 7.19 +/- 1.26 micrograms ml-1 h; means +/- s.d.). 3. The plasma concentration-time curves for paracetamol showed similar profiles to those for levodopa and the ratios of the peak concentrations and AUC values for the second peak compared with the initial peak were increased significantly by benzhexol administration (P < 0.05). The total AUC of paracetamol was not affected by benzhexol administration (39.4 +/- 8.2 vs 40.0 +/- 8.9 micrograms ml-1 h; mean +/- s.d.) 4. Benzhexol altered the gastric emptying profile, shown by gamma-scintigraphy, with a reduced extent of initial emptying prior to the establishment of the plateau which is characteristic of levodopa administration in the fasting state. In consequence the ratio of the second to the initial phase of emptying was significantly higher (P < 0.01) following benzhexol treatment. 5. Benzhexol reduces the initial phase of gastric emptying after a dose of levodopa so that there is a decrease in the initial peak and a greater proportion of the dose is absorbed subsequently following the second phase of gastric emptying which occurs approximately 1 h later. Theoretically, this altered concentration-time profile could be an advantage for some patients with Parkinson's disease.
摘要
  1. 已在10名年轻健康志愿者中研究了苯海索对口服左旋多巴吸收及药代动力学的影响。采用随机交叉设计,在服用苯海索(5毫克)或安慰剂90分钟后,给予受试者左旋多巴混悬液(250毫克),两次给药间隔至少1周;每次在左旋多巴给药前1小时和给药后5小时给予卡比多巴。将可溶性对乙酰氨基酚和放射性标记的二乙三胺五乙酸与左旋多巴一起给予,作为胃排空的标志物。2. 在服用安慰剂当天,大多数受试者的左旋多巴血浆浓度 - 时间曲线出现两个峰值,第二个较小的峰值在给药后1 - 2小时出现。服用苯海索后,所有受试者血浆中出现两个或更多个左旋多巴浓度峰值。服用苯海索导致初始峰值的最大浓度显著降低(43%;P < 0.05),第二个峰值的最大浓度增加(22%;P < 0.1)。苯海索引起的这种吸收曲线变化,使第二个峰值与初始峰值相比,最大浓度(P < 0.02)和AUC值(P < 0.05)的比值均发生显著改变。服用苯海索不影响左旋多巴的总AUC(7.30±1.09对7.19±1.26微克·毫升⁻¹·小时;均值±标准差)。3. 对乙酰氨基酚的血浆浓度 - 时间曲线与左旋多巴相似,服用苯海索后,第二个峰值与初始峰值相比,峰值浓度和AUC值的比值显著增加(P < 0.05)。服用苯海索不影响对乙酰氨基酚的总AUC(39.4±8.2对40.0±8.9微克·毫升⁻¹·小时;均值±标准差)。4. 苯海索改变了γ闪烁扫描显示的胃排空曲线,在禁食状态下左旋多巴给药后出现的平台期之前,初始排空程度降低。因此,苯海索治疗后,排空第二阶段与初始阶段的比值显著更高(P < 0.01)。5. 苯海索降低了服用左旋多巴后的胃排空初始阶段,使得初始峰值降低,且在大约1小时后出现的胃排空第二阶段后,有更大比例的剂量被吸收。从理论上讲,这种改变的浓度 - 时间曲线对一些帕金森病患者可能是有利的。

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