Oxidative DNA Damage in Relation to Neurotoxicity in the Brain of Mice Exposed to Arsenic at Environmentally Relevant Levels

• Published in: Journal of Occupational Health 2005-09, Vol.47 (5), p.445-449
• Main Authors: Piao, Fengyuan, Ma, Ning, Hiraku, Yusuke, Murata, Mariko, Oikawa, Shinji, Cheng, Fanyin, Zhong, Laifu, Yamauchi, Toru, Kawanishi, Shosuke, Yokoyama, Kazuhito
• Format: Article
• Language: English
• Subjects: 8‐Hydroxy‐2′‐deoxyguanosine (8‐OHdG); Animals; Arsenic; Arsenic Trioxide; Arsenicals; Brain - drug effects; Brain - metabolism; Brain - pathology; Cerebellar cortex; Cerebral cortex; Deoxyguanosine - analogs & derivatives; Deoxyguanosine - biosynthesis; Deoxyguanosine - metabolism; Deoxyribonucleic acid; DNA; DNA Damage; Drinking water; Electrochemistry; Liquid chromatography; Mice; Neurotoxicity; Neurotoxicity Syndromes - metabolism; Occupational health; Oxidative DNA damage; Oxides - toxicity; Purkinje cell; Tissue Distribution
• ISSN: 1341-9145; 1348-9585; 1348-9585
• DOI: 10.1539/joh.47.445

To clarify the association between oxidative DNA damage and the neurotoxicity of arsenic, the formation of 8-hydroxy-2'deoxyguanosine (8-OHdG) as an index of oxidative DNA damage in the brain was examined in mice fed with drinking water containing 1 or 2 ppm arsenic, using an HPLC-electrochemical detector and immunohistochemical method. 8-OHdG levels were significantly increased in the brain of mice given arsenic and its immunoreactivity was distributed in the cerebral and cerebellar cortexes. Cerebral cortex neurons and Purkinje cells in the cerebellar cortex showed degenerative changes in accordance with the distribution of 8-OHdG immunoreactivity. The levels of arsenic in this study were lower than those reported in epidemiological studies. Thus, we conclude that environmentally relevant levels of arsenic induce pathological changes through oxidative DNA damage in the brain tissues in vivo and that cerebral and cerebellar cortex neurons seem to be the major targets of arsenic neurotoxicity.