Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Medical University of Silesia, Jagiellońska 4, PL 41-200, Sosnowiec, Poland.
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Medical University of Silesia, Jagiellońska 4, PL 41-200, Sosnowiec, Poland.
Chem Biol Interact. 2019 Apr 25;303:27-34. doi: 10.1016/j.cbi.2019.02.005. Epub 2019 Feb 12.
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.
四环素类属于在兽医和农业中消耗最高的抗菌药物类别,这导致了环境和食品产品的污染,以及抗生素耐药性和药物不良反应。与其他四环素类药物相比,氯代衍生物被认为具有相对更高的光毒性,并且属于最常被引用的光敏药物。黑色素是决定皮肤、头发和眼睛颜色的异质生物聚合物。它们在黑色素细胞中通过多步生物合成过程合成。黑色素除了具有光保护和抗氧化特性外,还可能导致不良的皮肤药物反应,例如色素沉着紊乱和光毒性反应。此外,它们还有能力形成药物-黑色素复合物,导致药物或其代谢物在色素沉着组织中沉积。本研究的目的是研究金霉素与黑色素形成复合物的能力,以及该药物对暴露于 UVA 辐射下的正常人表皮黑色素细胞活力、抗氧化防御系统和黑色素生成的影响。研究结果首次表明,金霉素与黑色素聚合物形成复合物,从而有可能使药物在色素沉着组织中蓄积。正常人黑色素细胞同时暴露于金霉素和 UVA 辐射下会降低细胞活力,与药物浓度和辐照时间成正比。光毒性作用似乎与黑色素细胞中氧化应激的诱导有关,主要是通过增加 SOD 和降低 CAT 活性。金霉素本身不会影响黑色素含量或酪氨酸酶的活性。UVA 辐射似乎是刺激黑色素生成的条件因素,而药物的存在增强了这种作用。