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首页> 外文期刊>Chemical research in toxicology >Karlsson, I.a , Persson, E.a , Ekebergh, A.b , M?rtensson, J.b , B?rje, A.a Ketoprofen-induced formation of amino acid photoadducts: Possible explanation for photocontact allergy to ketoprofen
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Karlsson, I.a , Persson, E.a , Ekebergh, A.b , M?rtensson, J.b , B?rje, A.a Ketoprofen-induced formation of amino acid photoadducts: Possible explanation for photocontact allergy to ketoprofen

机译:卡尔森(I.a),佩尔森(Persson),埃克贝格(Ekebergh),阿布(A.b),墨尔森(M?rtensson),杰布(B.rje),阿贝(A.a)

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摘要

Photocontact allergy is a well-known side effect of topical preparations of the nonsteroidal anti-inflammatory drug ketoprofen. Photocontact allergy to ketoprofen appears to induce a large number of photocross allergies to both structurally similar and structurally unrelated compounds. Contact and photocontact allergies are explained by structural modification of skin proteins by the allergen. This complex is recognized by the immune system, which initiates an immune response. We have studied ketoprofen's interaction with amino acids to better understand ketoprofen's photoallergenic ability. Irradiation of ketoprofen and amino acid analogues resulted in four different ketoprofen photodecarboxylation products (6-9) together with a fifth photoproduct (5). Dihydroquinazoline 5 was shown to be a reaction product between the indole moiety of 3-methylindole (Trp analogue) and the primary amine benzylamine (Lys analogue). In presence of air, dihydroquinazoline 5 quickly degrades into stable quinazolinone 12. The corresponding quinazolinone (17) was formed upon irradiation of ketoprofen and the amino acids N-acetyl-l-Trp ethyl ester and l-Lys ethyl ester. The formation of these models of an immunogenic complex starts with the ketoprofen-sensitized formation of singlet oxygen, which reacts with the indole moiety of Trp. The formed intermediate subsequently reacts with the primary amino functionality of Lys, or its analogue, to form a Trp-Lys adduct or a mimic thereof. The formation of a specific immunogenic complex that does not contain the allergen but that can still induce photocontact allergy would explain the large number of photocross allergies with ketoprofen. These allergens do not have to be structurally similar as long as they can generate singlet oxygen. To the best of our knowledge, there is no other suggested explanation for ketoprofen's photoallergenic properties that can account for the observed photocross allergies. The formation of a specific immunogenic complex that does not contain the allergen is a novel hypothesis in the field of contact and photocontact allergy.
机译:光接触过敏是非甾体抗炎药酮洛芬局部用药的众所周知的副作用。对酮洛芬的光接触过敏似乎对结构相似和结构无关的化合物引起大量的光敏交叉过敏。接触和光接触过敏是通过过敏原对皮肤蛋白的结构修饰来解释的。该复合物被免疫系统识别,并引发免疫反应。我们已经研究了酮洛芬与氨基酸的相互作用,以更好地了解酮洛芬的光变应原能力。辐照酮洛芬和氨基酸类似物会产生四种不同的酮洛芬光脱羧产物(6-9)和第五种光产物(5)。已表明二氢喹唑啉5是3-甲基吲哚的吲哚部分(Trp类似物)与伯胺苄基胺(Lys类似物)之间的反应产物。在空气存在下,二氢喹唑啉5迅速降解成稳定的喹唑啉酮12。在酮洛芬和氨基酸N-乙酰基-1-Trp乙酯和1-Lys乙酯照射下形成相应的喹唑啉酮(17)。这些免疫原性复合物模型的形成始于对酮洛芬敏感的单线态氧的形成,单线态氧与Trp的吲哚部分反应。形成的中间体随后与Lys或其类似物的伯氨基官能团反应,形成Trp-Lys加合物或其模拟物。不含过敏原但仍可引起光接触过敏的特定免疫原性复合物的形成将说明酮洛芬对大量光敏交叉过敏的原因。这些变应原只要能够产生单线态氧就不必在结构上相似。据我们所知,对于酮洛芬的光致敏特性,没有其他建议的解释可以解释所观察到的光交叉过敏。不包含变应原的特异性免疫原性复合物的形成是接触和光接触变态反应领域的新假设。

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