Abstract | OBJECTIVES: METHODS: In a randomized crossover design, 18 hospitalized patients with PD received a single dose of levodopa/ benserazide, 100/25 mg, with or without domperidone, 10 mg, under fasting conditions. Plasma levodopa concentrations were determined up to 3 hours after dose administration. RESULTS: Mean ± SEM levodopa maximum plasma concentration (Cmax) (14.1 ± 2.9 vs 9.7 ± 1.6 μmol/L; P < 0.01), plasma concentration at 30 min (C30 min) (13.7 ± 3.0 vs 8.1 ± 2.0 μmol/L; P < 0.01), and area under the plasma concentration-time curve from 0 to 3 hours (AUC0-3 hr) (15.9 ± 3.1 vs 12.1 ± 2.4 μmol/L · hour; P < 0.05) were significantly higher after coadministration of levodopa with domperidone compared to levodopa alone. Thus, domperidone increased levodopa Cmax and AUC0-3 hr by 1.5- and 1.3-fold, respectively. There were no exacerbations of PD by concomitant domperidone administration. CONCLUSIONS: The results demonstrate that coadministration of domperidone increased the bioavailability of levodopa. This may be the reason for no exacerbation of PD in concomitant administration of domperidone, a dopamine D2-receptor blocker.
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Authors | Noriko Nishikawa, Masahiro Nagai, Tomoaki Tsujii, Hirotaka Iwaki, Hayato Yabe, Masahiro Nomoto |
Journal | Clinical neuropharmacology
(Clin Neuropharmacol)
2012 Jul-Aug
Vol. 35
Issue 4
Pg. 182-4
ISSN: 1537-162X [Electronic] United States |
PMID | 22751085
(Publication Type: Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Chemical References |
- Dopamine D2 Receptor Antagonists
- Levodopa
- Domperidone
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Topics |
- Aged
- Biological Availability
- Cross-Over Studies
- Domperidone
(administration & dosage, blood)
- Dopamine D2 Receptor Antagonists
- Drug Synergism
- Drug Therapy, Combination
- Female
- Humans
- Levodopa
(administration & dosage, blood)
- Male
- Middle Aged
- Parkinson Disease
(blood, drug therapy)
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