N1-acetyl-N2-formyl-5-methoxykynuramine, a biogenic amine and melatonin metabolite, functions as a potent antioxidant

被引:220
作者
Tan, DX
Manchester, LC
Burkhardt, S
Sainz, RM
Mayo, JC
Kohen, R
Shohami, E
Huo, YS
Hardeland, R
Reiter, RJ
机构
[1] Univ Texas, Hlth Sci Ctr, Dept Cellular & Struct Biol, San Antonio, TX 78229 USA
[2] Univ Gottingen, D-37073 Gottingen, Germany
[3] Antropol Inst Zool, D-37073 Gottingen, Germany
[4] Hebrew Univ Jerusalem, David R Bloom Ctr Pharm, Jerusalem, Israel
关键词
cyclic voltammetry; glutamate; amyloid beta-peptide; hydrogen peroxide; 8-hydroxydeoxyguanosine; lipid peroxidation; free radical; neuron;
D O I
10.1096/fj.01-0309fje
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
The biogenic amine N-1-acetyl-N-2-formyl-5-methoxykynuramine (AFMK) was investigated for its potential antioxidative capacity. AFMK is a metabolite generated through either an enzymatic or a chemical reaction pathway from melatonin. The physiological function of AFMK remains unknown. To our knowledge, this report is the first to document the potent antioxidant action of this biogenic amine. Cyclic voltammetry (CV) shows that AFMK donates two electrons at potentials of 456 mV and 668 mV, and therefore it functions as a reductive force. This function contrasts with all other physiological antioxidants that donate a single electron only when they neutralize free radicals. AFMK reduced 8-hydroxydeoxyguanosine formation induced by the incubation of DNA with oxidants significantly. Lipid peroxidation resulting from free radical damage to rat liver homogenates was also prevented by the addition of AFMK. The inhibitory effects of AFMK on both DNA and lipid damage appear to be dose-response related. In cell culture, AFMK efficiently reduced hippocampal neuronal death induced by either hydrogen peroxide, glutamate, or amyloid beta (25-35) peptide. AFMK is a naturally occurring molecule with potent free radical scavenging capacity (donating two electrons/molecule) and thus may be a valuable new antioxidant for preventing and treating free radical-related disorders.
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页码:2294 / +
页数:16
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