T. Muller et al., Decrease of methionine and S-adenosylmethionine and increase of homocysteine in treated patients with Parkinson's disease, NEUROSCI L, 308(1), 2001, pp. 54-56
Levodopa is administered with dopa decarboxylase inhibitors (DDI) to preven
t its peripheral degradation. This increases conversion of levodopa to 3-O-
methyldopa (3-OMD) by catechol-O-methyltransferase (COMT). S-adenosyl methi
onine (SAM), which is synthesized from adenosintriphosphate and methionine
(MET), serves as methyl donor for this O-metabolisation of levodopa with re
sulting conversion of SAM to total homocysteine (tHcy) via S-adenosylhomocy
steine (SAH). Previous studies showed augmented plasma levels of tHcy in lo
ng-term levodopa/DDI-treated patients with Parkinson's disease (PP). Object
ive of this study was to compare MET, SAM, levodopa, 3-OMD, tHcy and SAH in
plasma of 20 levodopa/DDI treated PP and corresponding controls. A signifi
cant decrease of MET respectively SAM and an increase of tHcy appeared in P
P. SAH with its short half-life did not differ. Levodopa/DDI long-term trea
tment contributes to altered levels of substrates of the O-methylation cycl
e in PP. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.