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阿托伐他汀光毒性的机制研究:一种菲类光产物产生单线态氧

A mechanistic study on the phototoxicity of atorvastatin: singlet oxygen generation by a phenanthrene-like photoproduct.

作者信息

Montanaro Sara, Lhiaubet-Vallet Virginie, Iesce MariaRosaria Iesce, Previtera Lucio, Miranda Miguel Angel

机构信息

Instituto de Tecnologia Quimica, UPV-CSIC, UniVersidad Polité cnica de Valencia, AVenida de Los Naranjos, s/n, 46022, Valencia, Spain.

出版信息

Chem Res Toxicol. 2009 Jan;22(1):173-78. doi: 10.1021/tx800294z.

Abstract

Atorvastatin calcium (ATV) is one of the most frequently prescribed drugs worldwide. Among the adverse effects observed for this lipid-lowering agent, clinical cases of cutaneous adverse reactions have been reported and associated with photosensitivity disorders. Previous work dealing with ATV photochemistry has shown that exposure to natural sunlight in aqueous solution leads to photoproducts resulting from oxidation of the pyrrole ring and from cyclization to a phenanthrene derivative. Laser flash photolysis of ATV, at both 266 and 308 nm, led to a transient spectrum with two maxima at lambda= 360 and lambda= 580 nm (tau= 41 micro), which was assigned to the primary intermediate of the stilbene-like photocyclization. On the basis of the absence of a triplet-triplet absorption, the role of the parent drug as singlet oxygen photosensitizer can be discarded. By contrast, a stable phenanthrene-like photoproduct would be a good candidate to play this role. Laser flash photolysis of this compound showed a triplet-triplet transient absorption at lambdamax = 460 nm with a lifetime of 26 micro, which was efficiently quenched by oxygen (kq = 3 (+/-0.2) x 10(9) M(-1) s(-1)). Its potential to photosensitize formation of singlet oxygen was confirmed by spin trapping experiments, through conversion of TEMP to the stable free radical TEMPO. The photoreactivity of the phenanthrene-like photoproduct was investigated using Trp as a marker. The disappearance of the amino acid fluorescence (lambdamax = 340 nm) after increasing irradiation times at 355 nm was taken as a measurement of photodynamic oxidation. To confirm the involvement of a type II mechanism, the same experiment was also performed in D2O; this resulted in a significant enhancement of the reaction rate. On the basis of the obtained photophysical and photochemical results, the phototoxicity of atorvastatin can be attributed to singlet oxygen formation with the phenanthrene-like photoproduct as a photosensitizer.

摘要

阿托伐他汀钙(ATV)是全球处方量最高的药物之一。在这种降脂药物观察到的不良反应中,已报告了皮肤不良反应的临床病例,并与光敏性疾病有关。之前关于ATV光化学的研究表明,在水溶液中暴露于自然阳光下会导致光产物的产生,这些光产物是由吡咯环氧化和环化形成菲衍生物所致。在266和308nm波长下对ATV进行激光闪光光解,得到一个瞬态光谱,在λ = 360和λ = 580nm处有两个最大值(τ = 41微秒),该光谱被归因于类芪光环化的初级中间体。基于不存在三重态-三重态吸收,母体药物作为单线态氧光敏剂的作用可以被排除。相比之下,一种稳定的类菲光产物可能是发挥这一作用的良好候选物。对该化合物进行激光闪光光解,在λmax = 460nm处显示出三重态-三重态瞬态吸收,寿命为26微秒,可被氧有效猝灭(kq = 3(±0.2)×109 M-1 s-1)。通过自旋捕集实验,通过将TEMP转化为稳定的自由基TEMPO,证实了其光敏化单线态氧形成的潜力。使用色氨酸作为标记物研究了类菲光产物的光反应性。在355nm波长下增加照射时间后氨基酸荧光(λmax = 340nm)的消失被用作光动力氧化的测量指标。为了证实II型机制的参与,同样的实验也在重水中进行;这导致反应速率显著提高。基于所获得的光物理和光化学结果,阿托伐他汀的光毒性可归因于以类菲光产物作为光敏剂形成单线态氧。

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