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吩噻嗪衍生物对生物分子的光敏化作用。

Photosensitization of biomolecules by phenothiazine derivatives.

作者信息

Viola Giampietro, Dall'Acqua Francesco

机构信息

Department of Pharmaceutical Sciences, University of Padova, via Marzolo 5, Padova, Italy.

出版信息

Curr Drug Targets. 2006 Sep;7(9):1135-54. doi: 10.2174/138945006778226561.

Abstract

It is well known that many drugs act as photosensitizers towards cells by interacting with various cellular components such as lipids, proteins and nucleic acids. The structural modifications of the cellular components may occur by direct interactions of the excited states (singlets or triplets) of the drugs with the biological substrate or indirectly, through reactive species of oxygen sensitised by the drug themselves. In particular, the phototoxic activity of various drugs correlated with their potential photomutagenic and photocarcinogenic effects, takes place through DNA modification. Phenothiazines, a class of antihistaminic (anti-H1) or neuroleptic drugs used in the therapy of mental illness, such as schizophrenia, organic psychoses and other mental disorders, are known to induce photosensitization of the skin by systemic use or by topical applications as antiallergic drugs. In this review we have focused our attention on the photosensitizing property of phenothiazines and related compounds both in vitro and in vivo systems. Particular attention has been given to the mechanism of photo reaction with biomolecules such as lipids, proteins and DNA. Moreover there is a growing interest in drugs having photobiological effects because of their possible application as phototherapeutics. It has been interesting in this context to mention briefly the possible application of phenothiazine derivatives as new photosensitizers for their therapeutic application in photodynamic therapy (PDT) or in the light inactivation of viruses and bacteria.

摘要

众所周知,许多药物通过与各种细胞成分(如脂质、蛋白质和核酸)相互作用而对细胞起到光敏剂的作用。细胞成分的结构修饰可能通过药物的激发态(单线态或三线态)与生物底物的直接相互作用而发生,也可能通过药物自身敏化产生的活性氧物种间接发生。特别是,各种药物的光毒性活性与其潜在的光致突变和光致癌作用相关,是通过DNA修饰发生的。吩噻嗪类药物是一类用于治疗精神疾病(如精神分裂症、器质性精神病和其他精神障碍)的抗组胺药(抗H1)或抗精神病药物,已知通过全身用药或作为抗过敏药物局部应用会引起皮肤光敏化。在本综述中,我们将注意力集中在吩噻嗪类及其相关化合物在体外和体内系统中的光敏特性上。我们特别关注了它们与脂质、蛋白质和DNA等生物分子的光反应机制。此外,由于具有光生物学效应的药物可能作为光治疗剂应用,人们对它们的兴趣日益增加。在这种背景下,简要提及吩噻嗪衍生物作为新型光敏剂在光动力疗法(PDT)或病毒和细菌的光灭活中的治疗应用可能会很有意思。

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