Nitrite reduction by the red cell membrane: a mechanism with a biological role?

A. G. Pinder, S. C. Rogers, K. Morris, P. E. James
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Abstract

The possible role of nitric oxide (NO) metabolites in vivo has gained much interest in recent years, in particular, the interaction of these species with red blood cells. We investigated the potential for the membrane of red blood cells to act as a nitrite reductase site. Using both EPR (electromagnetic resonance spectroscopy) and ozone based chemiluminescence we were able to demonstrate NO generation from nitrite by the red cell membrane. The exact components responsible for this action are yet to be elucidated, but the response was unchanged by L-NMMA suggesting that eNOS is not involved. Reduction at the membrane could provide an entry route for NO into the red cell where it could produce potentially bioactive species e.g. nitrosylated proteins (RSNOs). If the nitrite reduction occurred on the outer surface of the red cell membrane it is also feasible that some NO may escape auto capture by that red cell, however in whole blood it is likely to be rapidly metabolised. In conclusion, this mechanism could provide a route by which nitrite, acting as a substrate, could be reduced to NO and form other, more biologically accessible species.

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红细胞亚硝酸盐还原:一种具有生物学作用的机制?
近年来,一氧化氮(NO)代谢物在体内的可能作用引起了人们的极大兴趣,特别是这些物质与红细胞的相互作用。我们研究了红细胞膜作为亚硝酸盐还原酶位点的潜力。使用EPR(电磁共振光谱)和基于臭氧的化学发光,我们能够证明亚硝酸盐通过红细胞膜生成NO。导致这一作用的确切成分尚未阐明,但L-NMMA的反应没有改变,这表明eNOS与此无关。膜上的还原可以为NO进入红细胞提供进入途径,在那里它可以产生潜在的生物活性物质,例如亚硝基化蛋白(RSNOs)。如果亚硝酸盐还原发生在红细胞的外表面,也有可能一些NO可能会逃脱红细胞的自动捕获,然而在全血中,它可能会被迅速代谢。综上所述,这一机制可能为亚硝酸盐作为底物还原为NO并形成其他更容易获得的物种提供了一条途径。
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Issue Information Autonomic and Autacoid Pharmacology: Goodbye and thank you Attenuation of the anti-contractile effect of cooling in the rat aorta by perivascular adipose tissue Retraction: Dopamine receptor immunohistochemistry in the rat choroid plexus. Issue Information
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