TY - JOUR
T1 - L-DOPA treatment from the viewpoint of neuroprotection
T2 - Possible mechanism of specific and progressive dopaminergic neuronal death in Parkinson's disease
AU - Ogawa, Norio
AU - Asanuma, Masato
AU - Miyazaki, Ikuko
AU - Diaz-Corrales, Francisco J.
AU - Miyoshi, Ko
PY - 2005/10
Y1 - 2005/10
N2 - With regard to the mechanism of selective dopaminergic neuronal death, experimental results of studies on the neurotoxicity of MPTP and rotenone indicate that degeneration of dopamine neurons is closely related to mitochondrial dysfunction, inflammatory process and oxidative stress, particularly with regard to the generation of quinones as dopamine neuron-specific oxidative stress. Thus, it is now clear that the presence of high levels of discompart-mentalized free dopamine in dopaminergic neurons may explain the specific vulnerability of dopaminergic neurons through the generation of highly toxic quinones.
AB - With regard to the mechanism of selective dopaminergic neuronal death, experimental results of studies on the neurotoxicity of MPTP and rotenone indicate that degeneration of dopamine neurons is closely related to mitochondrial dysfunction, inflammatory process and oxidative stress, particularly with regard to the generation of quinones as dopamine neuron-specific oxidative stress. Thus, it is now clear that the presence of high levels of discompart-mentalized free dopamine in dopaminergic neurons may explain the specific vulnerability of dopaminergic neurons through the generation of highly toxic quinones.
KW - Dopamine quinone
KW - Inflammation
KW - L-DOPA
KW - Mitochondrial dysfunction
KW - Oxidative stress
KW - Remodelling
KW - Rotenone
UR - http://www.scopus.com/inward/record.url?scp=26444465185&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=26444465185&partnerID=8YFLogxK
U2 - 10.1007/s00415-005-4006-7
DO - 10.1007/s00415-005-4006-7
M3 - Article
C2 - 16222434
AN - SCOPUS:26444465185
SN - 0340-5354
VL - 252
SP - iv23-iv31
JO - Journal of Neurology
JF - Journal of Neurology
IS - SUPPL. 4
ER -