Kaempferol Derivatives Prevent Oxidative Stress–Induced Cell Death in a DJ-1–Dependent Manner

• Published in: Journal of Pharmacological Sciences Vol. 110; no. 2; pp. 191 - 200
• Main Authors: Qu, Wei, Fan, Li, Kim, Yun-chul, Ishikawa, Shizuma, Iguchi-Ariga, Sanae M.M., Pu, Xiao-Ping, Ariga, Hiroyoshi
• Format: Journal Article
• Language: English
• Published: Japan Elsevier B.V 2009; The Japanese Pharmacological Society; Elsevier
• Subjects: Animals; Antioxidants - isolation & purification; Antioxidants - pharmacology; Carthamus - chemistry; cell death; Cell Death - drug effects; DJ-1; Hydrogen Peroxide - administration & dosage; Kaempferols - isolation & purification; Kaempferols - pharmacology; Medicine, Chinese Traditional; Microtubule-Associated Proteins - drug effects; Microtubule-Associated Proteins - metabolism; oxidative stress; Oxidative Stress - drug effects; Parkinson’s disease; PC12 Cells; Protein Deglycase DJ-1; Rats; Reactive Oxygen Species - metabolism; RNA, Small Interfering - metabolism; traditional Chinese medicine; Tyrosine 3-Monooxygenase - drug effects; Tyrosine 3-Monooxygenase - metabolism; traditional Chinese medicine; DJ-1; cell death; oxidative stress; Parkinson’s disease
• ISSN: 1347-8613; 1347-8648
• DOI: 10.1254/jphs.09045FP

DJ-1, a causative gene product of a familial form of Parkinson’s disease (PD), PARK7, plays a role in anti-oxidative stress, and loss of its function is thought to result in the onset of PD. Superfluous oxidation of cysteine at amino acid 106 (C106) of DJ-1 renders DJ-1 inactive, and such oxidized DJ-1 was observed in patients with the sporadic form of PD. In this study, we examined the relationship between DJ-1 and compounds extracted from traditional Chinese medicines possessing anti-oxidant activity. Of the 12 compounds tested, 5 were found to specifically bind to the C106 region by using a quartz crystal microbalance. Although 4 compounds prevented rat PC12 and primary neuronal cells from undergoing H2O2-induced cell death, the protective activity of 2 compounds, kaempferol 3-O-β-rutinoside and 6-hydroxykaempferol 3,6-di-O-β-D-glucoside, was diminished in cells transfected with siRNA targeting DJ-1, indicating DJ-1–dependent reaction of these compounds. Furthermore, these compounds reduced the level of reactive oxygen species and restored tyrosine hydroxylase activity that had been induced and compromised, respectively, by treatment of cells with H2O2. The results suggest that these compounds are useful lead compounds for PD therapy.