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自由基的生物学起源及抗氧化保护机制。

Biological origin of free radicals, and mechanisms of antioxidant protection.

作者信息

Gutteridge J M

机构信息

Oxygen Chemistry Laboratory, Royal Brompton Hospital, London, UK.

出版信息

Chem Biol Interact. 1994 Jun;91(2-3):133-40. doi: 10.1016/0009-2797(94)90033-7.

Abstract

Reduced intermediates of molecular oxygen, such as superoxide and hydrogen peroxide, are ubiquitous inorganic products of normal aerobic metabolism. Certain cells, such as phagocytes, have evolved to use superoxide and hydrogen peroxide for purposeful chemistry beneficial to the host, but most cells require antioxidant protection against excessive production of these intermediates. Superoxide and hydrogen peroxide are themselves poorly reactive in aqueous solution, and unable to directly damage DNA, lipids and proteins. Excessive generation, however, of superoxide and hydrogen peroxide invariably accompanies molecular damage. Substantial evidence suggests that conversion of these poorly reactive intermediates of oxygen to highly reactive forms requires the participation of transition metal ions, particularly iron. Iron ions react with hydrogen peroxide (Fenton chemistry) to generate hydroxyl radicals that can damage all organic molecules.

摘要

分子氧的还原中间体,如超氧化物和过氧化氢,是正常有氧代谢普遍存在的无机产物。某些细胞,如吞噬细胞,已经进化到利用超氧化物和过氧化氢进行对宿主有益的有目的化学反应,但大多数细胞需要抗氧化保护,以防止这些中间体的过量产生。超氧化物和过氧化氢本身在水溶液中的反应性较差,无法直接损伤DNA、脂质和蛋白质。然而,超氧化物和过氧化氢的过量生成总是伴随着分子损伤。大量证据表明,将这些反应性较差的氧中间体转化为高反应性形式需要过渡金属离子,特别是铁的参与。铁离子与过氧化氢反应(芬顿化学反应)生成能损伤所有有机分子的羟基自由基。

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