Abstract
We studied the effectiveness of OR-611 and OR-462, two novel inhibitors of the enzyme catechol-O-methyltransferase (COMT), on 3-O-methyldopa (OMD) formation in cynomolgus monkeys following intravenous levodopa administration. OR-611 dose-dependently reduced the area under the OMD concentration-vs-time curve, reduced maximum plasma OMD concentrations, delayed the time to peak OMD levels, reduced systemic levodopa clearance, and prolonged the elimination half-life of levodopa. Similar effects on peripheral levodopa metabolism were seen with doses of 15 mg/kg of OR-611 and OR-462, its sister compound, which lacks the ability to penetrate the central nervous system (CNS).
| Original language | English |
|---|---|
| Pages (from-to) | 330-342 |
| Number of pages | 13 |
| Journal | Clinical Neuropharmacology |
| Volume | 14 |
| Issue number | 4 |
| DOIs | |
| State | Published - 1991 |
Keywords
- 3-O-Methyldopa
- Catechol-O-methyltransferase
- Levodopa
- Pharmacokinetics Parkinson's disease
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