Tolcapone increases plasma catecholamine levels in patients with Parkinson's disease

被引:13
作者
Rojo, A
Fontán, A
Mena, MA
Herranz, A
Casado, S
de Yébenes, JG
机构
[1] Hosp Ramon & Cajal, Monoamine Res Lab, Fdn Jimenez Diaz, Dept Neurol, Madrid 28040, Spain
[2] Hosp Ramon & Cajal, Monoamine Res Lab, Fdn Jimenez Diaz, Dept Nephrol, Madrid 28040, Spain
关键词
Parkinson's disease; catechol-o-methyl tranferase; tolcapone; plasma catecholamines;
D O I
10.1016/S1353-8020(00)00027-4
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Tolcapone is a catechol-ortho-methyl-tranferase (COMT) inhibitor that increases the L-DOPA half-life and the duration of effect in Parkinson's disease. We investigated the effect of tolcapone on the plasma catecholamine levels. We measured plasma catecholamines 2 h after the first daily dose of L-DOPA or L-DOPA + tolcapone while resting and 2 and 10 min after standing. We also measured the pharmacokinetics of L-DOPA and 3-OM-DOPA and the clinical response to the medication for 6 h after the early morning dose. The levels of dopamine, norepinephrine, adrenaline and total catecholamines significantly increased and 3-OM-DOPA decreased with tolcapone. We did not observe significant changes in the plasma L-DOPA levels at the doses of tolcapone used in this study. Tolcapone side effects included worsening of dyskinesia and psychosis, diarrhea and elevation of liver enzymes. Twenty-four-hour ambulatory recording of arterial blood pressure and heart rate did not reveal cardiovascular side effects in patients treated with tolcapone for less than I year. Since adrenergic stimulation may increase the hepatotoxic potential of commonly used drugs, usually thought of as safe for the liver, we postulate that some of the already reported life threatening complications of tolcapone could be related to excessive adrenergic stimulation by high catecholamine levels caused by inhibition of COMT activity. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:93 / 96
页数:4
相关论文
共 13 条
[1]   Tolcapone and fulminant hepatitis [J].
Assal, F ;
Spahr, L ;
Hadengue, A ;
Rubbici-Brandt, L ;
Burkhard, PR .
LANCET, 1998, 352 (9132) :958-958
[2]   SIDE-EFFECTS OF THE CATECHOL-O-METHYL-TRANSFERASE INHIBITOR RO-40-7592 IN RABBITS [J].
GARRIDO, JM ;
MENA, MA ;
CORREA, C ;
HERRARAS, O ;
JORGE, P ;
LEENDERS, K ;
ANTONINI, A ;
GUNTHER, I ;
PSYLLA, M ;
DEYEBENES, JG .
CLINICAL NEUROPHARMACOLOGY, 1994, 17 (03) :270-276
[3]   ACCURACY OF CLINICAL-DIAGNOSIS OF IDIOPATHIC PARKINSONS-DISEASE - A CLINICOPATHOLOGICAL STUDY OF 100 CASES [J].
HUGHES, AJ ;
DANIEL, SE ;
KILFORD, L ;
LEES, AJ .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1992, 55 (03) :181-184
[4]  
ILLI A, 1994, INT J CLIN PHARM TH, V32, P582
[5]  
JORGA K, 1993, CLIN NEUROPHARMAC S2, V53, P4
[6]   ACUTE EFFECTS OF ETHANOL ON BRAIN, PLASMA AND ADRENAL MONOAMINE CONCENTRATIONS IN VIRGIN AND PREGNANT RATS AND THEIR FETUSES [J].
MENA, MA ;
ZORZANO, A ;
HERRERA, E .
NEUROCHEMISTRY INTERNATIONAL, 1986, 9 (03) :371-378
[7]  
MENA MA, 1998, UNDERSTANDING GLIAL, P213
[8]  
MENA MA, 1986, ADV NEUROL, V45, P481
[9]   Tolcapone improves motor function in parkinsonian patients with the ''wearing-off'' phenomenon: A double-blind, placebo-controlled, multicenter trial [J].
Rajput, AH ;
Martin, W ;
SaintHilaire, MH ;
Dorflinger, E ;
Pedder, S .
NEUROLOGY, 1997, 49 (04) :1066-1071
[10]   Adrenergic modulation of hepatotoxicity [J].
Roberts, SM ;
DeMott, RP ;
James, RC .
DRUG METABOLISM REVIEWS, 1997, 29 (1-2) :329-353