Low intensity light stimulates nitrite-dependent nitric oxide synthesis but not oxygen consumption by cytochrome c oxidase: Implications for phototherapy

被引:85
|
作者
Ball, Kerri A. [1 ]
Castello, Pablo R. [1 ]
Poyton, Robert O. [1 ]
机构
[1] Univ Colorado, Dept Mol Cellular & Dev Biol, Boulder, CO 80309 USA
基金
美国国家卫生研究院;
关键词
Nitrite; Nitric oxide; Mitochondria; Cytochrome c oxidase; Phototherapy; Photobiomodulation; ENERGY LASER IRRADIATION; NEAR-INFRARED LIGHT; HELIUM-NEON LASER; REDUCTASE-ACTIVITY; IN-VIVO; GENE-EXPRESSION; PHOTODYNAMIC THERAPY; CELL-PROLIFERATION; IR RADIATION; MITOCHONDRIA;
D O I
10.1016/j.jphotobiol.2010.12.002
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
Cytochrome c oxidase (Cco) has been reported to be a receptor for some of the beneficial effects of low intensity visible and near-infrared light on cells and tissues. Here, we have explored the role of low intensity light in affecting a newly described function of Cco, its ability to catalyze nitrite-dependent nitric oxide (NO) synthesis (Cco/NO). Using a new assay for Cco/NO we have found that both yeast and mouse brain mitochondria! Cco produce NO over a wide range of oxygen concentrations and that the rate of NO synthesis increases as the oxygen concentration decreases, becoming optimal under hypoxic conditions. Low intensity broad-spectrum light increases Cco/NO activity in an intensity-dependent fashion but has no effect on oxygen consumption by Cco. By using a series of bandpass filters and light emitting devices (LEDs) we have determined that maximal stimulation of Cco/NO activity is achieved by exposure to light whose central wavelength is 590 +/- 14 nm. This wavelength of light stimulates Cco/NO synthesis at physiological nitrite concentrations. These findings raise the interesting possibility that low intensity light exerts a beneficial effect on cells and tissues by increasing NO synthesis catalyzed by Cco and offer a new explanation for the increase in NO bioavailability experienced by tissue exposed to light. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:182 / 191
页数:10
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