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DOI 10.1016/j.nbd.2003.10.003

Медицинская библиотека · Neurobiology of disease · 2004

Plasma and CSF markers of oxidative stress are increased in Parkinson's disease and influenced by antiparkinsonian medication.

Buhmann Carsten, Arlt Sönke, Kontush Anatol, Möller-Bertram Tobias, Sperber Sinje, Oechsner Matthias, Stuerenburg Hans Joerg, Beisiegel Ulrike

Сравнительное исследованиеСтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

We determined systemic oxidative stress in Parkinson's disease (PD) patients, patients with other neurological diseases (OND) and healthy controls by measurement of in vitro lipoprotein oxidation and levels of hydro- and lipophilic antioxidants in plasma and cerebrospinal fluid (CSF). Additionally, we investigated the influence of levodopa (LD) and dopamine agonist therapy (DA) on the oxidative status in PD patients. We found increased oxidative stress, seen as higher levels of lipoprotein oxidation in plasma and CSF, decrease of plasma levels of protein sulfhydryl (SH) groups and lower CSF levels of alpha-tocopherol in PD patients compared to OND patients and controls. Levodopa treatment did not significantly change the plasma lipoprotein oxidation but LD monotherapy tended to result in an increase of autooxidation and in a decrease of plasma antioxidants with significance for ubiquinol-10. DA monotherapy was significantly associated with higher alpha-tocopherol levels. Patients with DA monotherapy or co-medication with DA showed a trend to lower lipoprotein oxidation. These data support the concept of oxidative stress as a factor in the pathogenesis of PD and might be an indicator of a potential prooxidative role of LD and a possible antioxidative effect of DA in PD treatment.

Для цитирования: Buhmann Carsten, Arlt Sönke, Kontush Anatol, Möller-Bertram Tobias, Sperber Sinje, Oechsner Matthias, Stuerenburg Hans Joerg, Beisiegel Ulrike. Plasma and CSF markers of oxidative stress are increased in Parkinson's disease and influenced by antiparkinsonian medication.. Neurobiology of disease. 2004. DOI: 10.1016/j.nbd.2003.10.003.

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