TY - JOUR
T1 - Reduction of circulating 3-O-methyldopa by inhibition of catechol-O-methyltransferase with OR-611 and OR-462 in cynomolgus monkeys
T2 - Implications for the treatment of Parkinson's disease
AU - Cedarbaum, J. M.
AU - Leger, G.
AU - Guttman, M.
PY - 1991
Y1 - 1991
N2 - 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).
AB - 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).
KW - 3-O-Methyldopa
KW - Catechol-O-methyltransferase
KW - Levodopa
KW - Pharmacokinetics Parkinson's disease
UR - http://www.scopus.com/inward/record.url?scp=0025911879&partnerID=8YFLogxK
U2 - 10.1097/00002826-199108000-00005
DO - 10.1097/00002826-199108000-00005
M3 - Article
C2 - 1913700
AN - SCOPUS:0025911879
SN - 0362-5664
VL - 14
SP - 330
EP - 342
JO - Clinical Neuropharmacology
JF - Clinical Neuropharmacology
IS - 4
ER -