Aust S D, Morehouse L A, Thomas C E
J Free Radic Biol Med. 1985;1(1):3-25. doi: 10.1016/0748-5514(85)90025-x.
Partially-reduced forms of dioxygen or "oxy-radicals" (superoxide, O2-/HO2; hydrogen peroxide, H2O2; hydroxyl radical X OH) and oxidants of comparable reactivity are implicated in an increasing number of physiological, toxicological, and pathological states. Transition metal catalysis is recognized as being integral to the generation and the reactions of these activated oxygen species. Factors such as pH and chelation govern the reactivity of the transition metals with dioxygen and "oxy-radicals" and therefore influence the apparent mechanisms by which oxidative damage to phospholipids, DNA, and other biomolecules is initiated. In biological systems the concentrations of redox-active transition metals capable of catalyzing these reactions appears to be relatively low. However, under certain conditions metal storage and transport proteins (ferritin, transferrin, ceruloplasmin, etc.) may furnish additional redox active metals.
部分还原形式的二氧或“氧自由基”(超氧化物,O2-/HO2;过氧化氢,H2O2;羟基自由基·OH)以及具有类似反应活性的氧化剂与越来越多的生理、毒理和病理状态有关。过渡金属催化被认为是这些活性氧物种生成和反应所不可或缺的。诸如pH值和螯合作用等因素决定了过渡金属与二氧和“氧自由基”的反应活性,因此影响了引发对磷脂、DNA和其他生物分子氧化损伤的表观机制。在生物系统中,能够催化这些反应的具有氧化还原活性的过渡金属浓度似乎相对较低。然而,在某些条件下,金属储存和转运蛋白(铁蛋白、转铁蛋白、铜蓝蛋白等)可能会提供额外的氧化还原活性金属。