Nohl H, Gille L, Staniek K
Institute of Pharmacology and Toxicology, Veterinary University of Vienna, Austria.
Ann N Y Acad Sci. 1998 Nov 20;854:394-409. doi: 10.1111/j.1749-6632.1998.tb09919.x.
Ubiquinone (Q) shares its biological implication in membrane-associated redox reactions with a variety of other redox carriers, such as dehydrogenases, non-heme-iron proteins, and cytochromes. Peculiarities arise from the lack of transition metals, which in contrast to the other electron carriers do not participate in redox-shuttle activities of Q. Another peculiarity is the lipophilicity of Q, which allows free movement between reductants and oxidants of a membrane. The chemistry of Q reduction and ubiquinol oxidation requires the stepwise acceptance and transfer of two single electrons associated with the addition or release of two single H+. These special qualities are widely used in biological membranes for linear electron transfer and transmembranous H+ translocation. In mitochondria it was long reported that under certain conditions linear e- transfer from the semireduced form (SQ.) to native oxidants of the respiratory chain may run out of control, thereby establishing a permanent source of oxygen radical release. It should be mentioned that in mitochondria e- transfer to dioxygen out of sequence requires a particular treatment with inhibitors and uncouplers of the respiratory chain. Nevertheless, it is generally assumed that Q is mainly involved in mitochondrial O2.- generation and that mitochondria represent the major source of O2.- radicals under physiological and various pathophysiological conditions. The ever-increasing application of coenzyme Q as an antioxidant for the prophylaxis and treatment of a great variety of functional disorders, including senescence, has considerably stimulated our interest in the potential prooxidative potency of this natural electron carrier. Experimental evidence will be presented that under physiological conditions Q implicated in mitochondrial e- transfer of the respiratory chain is not involved in cellular oxygen activation. It will also be shown that alterations of Q from an e- carrier to an active radical promotor is possible under various conditions. In addition, reaction products emerging from the antioxidant activity of ubiquinol were found to stimulate the formation of inorganic as well as organic oxygen radicals.
泛醌(Q)与多种其他氧化还原载体(如脱氢酶、非血红素铁蛋白和细胞色素)在膜相关氧化还原反应中具有共同的生物学意义。其独特之处在于缺乏过渡金属,与其他电子载体不同,过渡金属不参与泛醌的氧化还原穿梭活动。另一个独特之处是泛醌的亲脂性,这使其能够在膜的还原剂和氧化剂之间自由移动。泛醌还原和泛醇氧化的化学过程需要逐步接受和转移与两个单个H⁺的添加或释放相关的两个单个电子。这些特殊性质在生物膜中广泛用于线性电子转移和跨膜H⁺转运。长期以来,线粒体中已有报道称,在某些条件下,从半还原形式(SQ·)到呼吸链天然氧化剂的线性电子转移可能失控,从而建立一个永久性的氧自由基释放源。应该提到的是,在呼吸链的抑制剂和解偶联剂进行特殊处理的情况下,线粒体中电子向二氧的不按顺序转移才会发生。然而,一般认为泛醌主要参与线粒体O₂⁻的生成,并且在生理和各种病理生理条件下,线粒体是O₂⁻自由基的主要来源。辅酶Q作为抗氧化剂在预防和治疗包括衰老在内的多种功能障碍中的应用日益增加,这极大地激发了我们对这种天然电子载体潜在促氧化能力的兴趣。将展示实验证据,即在生理条件下,参与呼吸链线粒体电子转移的泛醌不参与细胞氧激活。还将表明,在各种条件下,泛醌从电子载体转变为活性自由基促进剂是可能的。此外,发现泛醇抗氧化活性产生的反应产物会刺激无机和有机氧自由基的形成。