Reactive oxygen species generation through NADH oxidation by 6-formylpterin derivatives in the dark

被引:8
|
作者
Nonogawa, Mitsuru
Pack, Seung Pil
Arai, Toshiyuki
Endo, Nobuyuki
Sommani, Piyanart
Kodaki, Tsutomu
Makino, Keisuke [1 ]
机构
[1] Kyoto Univ, Inst Adv Energy, Uji 6110011, Japan
[2] Kyoto Univ, Japan Sci & Technol Agcy, JST, CREST, Uji 6110011, Japan
[3] Kyoto Univ Hosp, Dept Anesthesia, Sakyo Ku, Kyoto 6068507, Japan
[4] Wakasa Wan Energy Res Ctr, Tsuruga 9140129, Japan
基金
日本学术振兴会;
关键词
6-formylpterin; 6-formylpterin derivatives; oxidation of NADH to NAD(+); generation of reactive oxygen species in the dark; H2O2 formation from O-2;
D O I
10.1016/j.bbrc.2006.12.171
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
6-Formylpterin (6FP) has been reported to produce reactive oxygen species (ROS) such as O-center dot(2)- and H2O2 from O-2 in the presence of NADH under light condition. In the present study, we prepared a variety of 6FP derivatives and found that 2-(N,N-dimethylaminomethyleneamino)-6-formyl-3-pivaloylpteridin-4-one and 2-(N,N-dimethylaminomethyleneamino)-6-formyl-3-methylpteridin-4-one, in which the 2-amino groups are modified by a dimethylaminomethylene group and the 3-positions by pivaloyl and methyl groups and 2-amino-6-formyl-3-methylpteridin-4-one in which the amino group at the 2-position is free and the 3-position is modified by a methyl group generated H2O2 from O-2 on oxidation of NADH to NAD(+) in the dark. However, 6FP and 2-(N,N-dimethylaminomethyleneamino)-6-formylpteridin-4-one, in which the 3-position is free did not yield H2O2. These results indicate that modification of the 3-position is essential to make the activities of 6FP available in the dark and would be suggestive for designing pharmaceutical compounds that generate appropriate and controllable amounts of ROS in vivo. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:1105 / 1110
页数:6
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