Modifications of plasma and platelet levels of L-DOPA and its direct metabolites during treatment with tolcapone or entacapone in patients with Parkinson's disease

被引:12
作者
Blandini, F
Nappi, G
Fancellu, R
Mangiagalli, A
Samuele, A
Riboldazzi, G
Calandrella, D
Pacchetti, C
Bono, G
Martignoni, E
机构
[1] Univ Pavia, Neurol Inst C Mondino, Lab Funct Neurochem, I-27100 Pavia, Italy
[2] Univ Pavia, Neurol Inst C Mondino, Ctr Parkinsons Dis & Movement Disorders, I-27100 Pavia, Italy
[3] Univ Roma La Sapienza, Dept Neurol & Otorhinolaryngol, Rome, Italy
[4] Univ Insubria, Varese, Italy
[5] Univ Piemonte Orientale, Novara, Italy
关键词
Catechol-O-methyltransferase; 3-O-methyldopa; dopamine; intracellular; extracellular;
D O I
10.1007/s00702-003-0004-z
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We compared-retrospectively-the effects of a 3-month therapy with catechol-O-methyltransferase (COMT) inhibitors tolcapone (100 mg, t.i.d.) and entacapone (200 mg, t.i.d.), on L-DOPA metabolism in two groups of parkinsonian patients with motor fluctuations. Plasma and platelets concentrations of L-DOPA and its direct metabolites, dopamine and 3-O-methyldopa (3-OMD), were measured before starting treatment, after two weeks and at the end of treatment. Patients treated with tolcapone showed significant increases in plasma and platelet L-DOPA levels and marked reduction of plasma and platelet 3-OMD levels, both at short- and long-term. Entacapone did not modify L-DOPA levels, while inducing a less marked reduction of plasma and platelet 3-OMD concentrations, with respect to tolcapone, at both time points. Both drugs were similarly effective in increasing plasma and platelet levels of dopamine. These results confirm the different profiles of activity of the two drugs, with tolcapone proving more effective on both the intra- and extra-cellular levels of L-DOPA and 3-OMD.
引用
收藏
页码:911 / 922
页数:12
相关论文
共 47 条
  • [1] AXELROD J, 1958, J BIOL CHEM, V233, P697
  • [2] Simultaneous determination of L-dopa and 3-O-methyldopa in human platelets and plasma using high-performance liquid chromatography with electrochemical detection
    Blandini, F
    Martignoni, E
    Pacchetti, C
    Desideri, S
    Rivellini, D
    Nappi, G
    [J]. JOURNAL OF CHROMATOGRAPHY B, 1997, 700 (1-2): : 278 - 282
  • [3] New, selective catechol-O-methyltransferase inhibitors as therapeutic agents in Parkinson's disease
    Bonifati, V
    Meco, G
    [J]. PHARMACOLOGY & THERAPEUTICS, 1999, 81 (01) : 1 - 36
  • [4] 18F-dopa PET evidence that tolcapone acts as a central COMT inhibitor in Parkinson's disease
    Ceravolo, R
    Piccini, P
    Bailey, DL
    Jorga, KM
    Bryson, H
    Brooks, DJ
    [J]. SYNAPSE, 2002, 43 (03) : 201 - 207
  • [5] DAPRADA M, 1994, CLIN NEUROPHARMACOL, V17, pS26
  • [6] DOPAMINE UPTAKE BY PLATELETS IS SELECTIVE, TEMPERATURE-DEPENDENT AND NOT INFLUENCED BY THE DOPAMINE-D1 OR DOPAMINE-D2 RECEPTOR
    DEAN, B
    COPOLOV, DL
    [J]. LIFE SCIENCES, 1989, 45 (05) : 401 - 411
  • [7] INTEGRATED PHARMACOKINETICS AND PHARMACODYNAMICS OF THE NOVEL CATECHOL-O-METHYLTRANSFERASE INHIBITOR TOLCAPONE DURING FIRST ADMINISTRATION TO HUMANS
    DINGEMANSE, J
    JORGA, KM
    SCHMITT, M
    GIESCHKE, R
    FOTTELER, B
    ZURCHER, G
    DAPRADA, M
    VANBRUMMELEN, P
    [J]. CLINICAL PHARMACOLOGY & THERAPEUTICS, 1995, 57 (05) : 508 - 517
  • [8] Dingemanse J, 1997, DRUG DEVELOP RES, V42, P1, DOI 10.1002/(SICI)1098-2299(199709)42:1<1::AID-DDR1>3.0.CO
  • [9] 2-I
  • [10] Dingemanse J, 2000, NEUROLOGY, V55, pS24