Instituto de Química, Universidade de São Paulo, São Paulo, Brazil.
Département de Médecine Nucléaire et de Radiobiologie, Université de Sherbrooke, Sherbrooke, QC, Canada.
Photochem Photobiol. 2021 Nov;97(6):1456-1483. doi: 10.1111/php.13470. Epub 2021 Jul 8.
Photosensitization reactions have been demonstrated to be largely responsible for the deleterious biological effects of UV and visible radiation, as well as for the curative actions of photomedicine. A large number of endogenous and exogenous photosensitizers, biological targets and mechanisms have been reported in the past few decades. Evolving from the original definitions of the type I and type II photosensitized oxidations, we now provide physicochemical frameworks, classifications and key examples of these mechanisms in order to organize, interpret and understand the vast information available in the literature and the new reports, which are in vigorous growth. This review surveys in an extended manner all identified photosensitization mechanisms of the major biomolecule groups such as nucleic acids, proteins, lipids bridging the gap with the subsequent biological processes. Also described are the effects of photosensitization in cells in which UVA and UVB irradiation triggers enzyme activation with the subsequent delayed generation of superoxide anion radical and nitric oxide. Definitions of photosensitized reactions are identified in biomolecules with key insights into cells and tissues.
光致敏反应已被证明是紫外线和可见光辐射产生有害生物学效应的主要原因,也是光医学治疗作用的基础。在过去几十年中,已经报道了大量内源性和外源性的光敏剂、生物靶标和机制。从最初的 I 型和 II 型光氧化敏化反应的定义出发,我们现在提供了物理化学框架、分类和这些机制的关键示例,以便对文献和新报告中大量可用的信息进行组织、解释和理解,这些信息正在迅速增长。本综述以扩展的方式调查了主要生物分子组如核酸、蛋白质、脂质的所有已确定的光致敏机制,与随后的生物学过程相衔接。还描述了 UVA 和 UVB 辐射触发细胞中酶激活的光致敏作用,随后会延迟产生超氧阴离子自由基和一氧化氮。在生物分子中确定了光致敏反应的定义,为细胞和组织提供了关键的见解。
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