6-hydroxydopamine increases hydroxyl free radical production and DNA damage in rat striatum

被引:37
|
作者
Ferger, B
Rose, S
Jenner, A
Halliwell, B
Jenner, P
机构
[1] Kings Coll London, Guys Kings & St Thomas Sch Biomed Sci, Wolfson Ctr Age Related Dis, London SE1 1UL, England
[2] Kings Coll London, Dept Pharm, Biochem Toxicol Grp, London SE1 8WA, England
[3] Natl Univ Singapore, Dept Biochem, Singapore 119260, Singapore
关键词
DNA base damage; 6-hydroxydopamine; microdialysis; Parkinson's disease; reactive oxygen species; salicylate assay;
D O I
10.1097/00001756-200105080-00021
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Oxidative damage is considered to be an important factor of 6-hydroxydopamine (6-OHDA) toxicity. To address this issue, microdialysis probes were implanted into the striatum of Wistar rats and perfused with 6-OHDA. Salicylate was included in the perfusion fluid to measure 2,3-dihydroxybenzoic acid (2,3-DHBA) as a marker of hydroxyl radical formation using HPLC with electrochemical detection. Additionally, striatal tissue was analysed for DNA base alterations using gas chromatography-mass spectrometry. 6-OHDA administration resulted in a rapid and substantial 6.6-fold increase in 2,3-DHBA formation and also increased levels of the modified DNA bases 5-hydroxycytosine, hypoxanthine and 2,6-diamino-4-hydroxy-5-formamidopyrimidine. Hydroxyl radical formation and DNA base alterations are early phenomena of 6-OHDA toxicity and provide clues to the processes that may be involved in the initiation of cell death in Parkinson's disease. NeuroReport 12:1155-1159 (C) 2001 Lippincott Williams & Wilkins.
引用
收藏
页码:1155 / 1159
页数:5
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