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From: Linda Carlton <[log in to unmask]>
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Subject:
 http://207.155.63.2/medscape/cgi-bin/taos_doc.pl?msw+0+med93-95+490843+query+(reduced-glutathione)
Date: Tue, 25 Mar 1997 02:40:20 -0800

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 Title: Alterations in glutathione levels in Parkinson's disease and other
 neurodegenerative disorders affecting basal ganglia [see comments]
 Title Abreviation: Ann Neurol         Date of Pub: 1994 Sep
 Author: Sian J; Dexter DT; Lees AJ; Daniel S; Agid Y; Javoy-Agid F; Jenner
 P; Marsden CD;

 Issue/Part/Supplement: 3  Volume      Pagination: 348-55
                           Issue: 36
 MESH Headings: Aged; Aged, 80 and over; Atrophy (ME); Basal Ganglia
 Diseases (ME); Brain (*ME); Brain Diseases (ME); Female; Glutathione
 (AA/*ME); Human; Huntington's Disease (ME); Male; Middle Age; Nervous
 System Diseases (*ME); Parkinson Disease (*ME); Support, Non-U.S. Gov't;
 Supranuclear Palsy, Progressive (ME); -RN-;
 Journal Title Code: 6AE   Publication Type: JOURNAL ARTICLE
 Date of Entry: 941004N    Entry Month: 9412
 Country: UNITED STATES    Index Priority: 1
 Language: Eng             Unique Identifier: 94361464
 Unique Identifier:
 94361464                  ISSN: 0364-5134
 Abstract: Reduced glutathione (GSH) and oxidized glutathione (GSSG) levels
 were measured in various brain areas (substantia nigra, putamen, caudate
 nucleus, globus pallidus, and cerebral cortex) from patients dying with
 Parkinson's disease, progressive supranuclear palsy, multiple-system
 atrophy, and Huntington's disease and from control subjects with no
 neuropathological changes in substantia nigra. GSH levels were reduced in
 substantia nigra in Parkinson's disease patients (40% compared to control
 subjects) and GSSG levels were marginally (29%) but insignificantly
 elevated; there were no changes in other brain areas. The only significant
 change in multiple-system atrophy was an increase of GSH (196%) coupled
 with a reduction of GSSG (60%) in the globus pallidus. The only change in
 progressive supranuclear palsy was a reduced level of GSH in the caudate
 nucleus (51%). The only change in Huntington's disease was a reduction of
 GSSG in the caudate nucleus (50%). Despite profound nigral cell loss in
 the substantia nigra in Parkinson's disease, multiple-system atrophy, and
 progressive supranuclear palsy, the level of GSH in the substantia nigra
 was significantly reduced only in Parkinson's disease. This suggests that
 the change in GSH in Parkinson's disease is not solely due to nigral cell
 death, or entirely explained by drug therapy, for multiple-system atrophy
 patients were also treated with levodopa. The altered GSH/GSSG ratio in
 the substantia nigra in Parkinson's disease is consistent with the concept
 of oxidative stress as a major component in the pathogenesis of nigral
 cell death in Parkinson's disease.
 Abstract By: Author
 Address: Parkinson's Disease Society Experimental Research Laboratories,
 Pharmacology Group, Biomedical Sciences Division, King's College London,
 UK.