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Chlortetracycline and melanin biopolymer - The risk of accumulation and implications for phototoxicity: An in vitro study on normal human melanocytes

机译:Chlortetracycline和黑色素生物聚合物 - 光毒性积累和影响的风险:对正常人黑素细胞的体外研究

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Tetracyclines belong to antimicrobial classes with the highest consumption in veterinary medicine and agriculture, which leads to the contamination of the environment and food products, as well as to antibiotic resistance and adverse drug reactions. Chloro-derivatives of tetracyclines are thought to be relatively more phototoxic than others and belong to the most frequently cited drugs as photosensitizers. Melanins are heterogenous biopolymers determining skin, hair and eye colour. They are biosynthesized in a multistep process in melanocytes. Melanins, besides photoprotective and antioxidant properties, may also contribute to adverse skin drug reactions, which involve e.g. hyperpigmentation disorders and phototoxic reactions. Furthermore, they have the ability to form a drug-melanin complex, which leads to deposition of the drug or its metabolites in pigmented tissues. The aim of the study was to examine the ability of chlortetracycline to form a complex with melanin, as well as the effect of the drug on viability, antioxidant defence system and melanogenesis in normal human epidermal melanocytes exposed to the UVA radiation. The obtained results show for the first time that chlortetracycline forms a complex with melanin polymers, which creates a possibility of the drug accumulation in pigmented tissues. A simultaneous exposition of normal melanocytes to chlortetracycline and to the UVA radiation decreases cell viability, proportionally to the drug concentration and the irradiation time. The phototoxic effect appears to be related to the induction of oxidative stress in melanocytes, mainly through an increase of SOD and a decrease of the CAT activity. Chlortetracycline itself does not influence the melanin content or the activity of tyrosinase. The UVA radiation appeared to be a conditioning factor stimulating melanogenesis, whereas the presence of the drug augmented this effect.
机译:四环素属于兽医药物和农业消费量最高的抗菌类,这导致环境和食品的污染,以及抗生素抗性和不良药物反应。四环素的氯衍生物被认为比其他环毒性相对更光毒性,属于最常被引用的药物作为光敏剂。黑色素是确定皮肤,头发和眼睛颜色的异质生物聚合物。它们在Melanocytes的多步骤过程中是生物合成的。黑色素除了光保护和抗氧化特性外,也可能有助于不良的皮肤药物反应,这涉及例如v。高度沉着障碍和光毒性反应。此外,它们具有形成药物 - 黑色素复合物的能力,这导致药物或其代谢物在着色组织中沉积。该研究的目的是检查氯化碳苷嘧啶与黑色素形成复合物的能力,以及药物在暴露于UVA辐射的正常人体表皮黑色细胞中的活力,抗氧化剂防御系统和糖胺的作用。所得结果首次显示碳氯素素与黑色素聚合物形成复合物,这产生了色素组织中的药物积累的可能性。将正常黑色素细胞同时阐述对氯化萘曲线和UVA辐射降低细胞活力,与药物浓度和照射时间成比例。光毒性效果似乎与黑素细胞中氧化应激的诱导有关,主要是通过SOD的增加和猫活性的降低。 Chlortetracycline本身不会影响黑色素含量或酪氨酸酶的活性。 UVA辐射似乎是调节因子刺激素化,而药物的存在增强了这种效果。

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