Department of Toxicology, Faculty of Pharmacy, Yeditepe University, Istanbul, Turkey.
Department of Toxicology, Faculty of Pharmacy, Acibadem Mehmet Ali Aydinlar University, Istanbul, Turkey.
Hum Exp Toxicol. 2021 Sep;40(9):1445-1462. doi: 10.1177/0960327121997986. Epub 2021 Mar 9.
Smoking is one of the most important leading death cause worldwide. From a toxicological perspective, cigarette smoke serves hazards especially for the human being exposed to passive smoke. Over the last decades, the effects of natural compounds on smoking-mediated respiratory diseases such as COPD, asthma, and lung cancer have been under investigation, as well as the mechanistic aspects of disease progression. In the present study, the protective mechanism of eucalyptol (EUC), curcumin (CUR), and their combination on BEAS-2B cells were investigated to understand their impact on cell death, oxidative cell injury, and inflammatory response induced by 3R4F reference cigarette extract (CSE). According to the present findings, EUC, CUR, and their combination improved cell viability, attenuated CSE-induced apoptosis, and LC3B expression. Further, CSE-induced oxidative damage and inflammatory response in human bronchial epithelial cells were remarkably reduced by the combination treatment through modification of enzymatic antioxidant activity, GSH, MDA, and intracellular ROS levels as well as nitrite and IL-6 levels. In addition, nuclear translocation of Nrf2, a regulatory protein involved in the indirect antioxidant response, was remarkably up-regulated with the combination pre-treatment. In conclusion, EUC and CUR in combination might be a potential therapeutic against smoking-induced lung diseases through antioxidant and inflammatory pathways and results represent valuable background for future pulmonary toxicity studies.
吸烟是全球最重要的导致死亡的原因之一。从毒理学的角度来看,香烟烟雾对暴露于被动吸烟的人类尤其危险。在过去的几十年中,人们一直在研究天然化合物对 COPD、哮喘和肺癌等与吸烟有关的呼吸道疾病的影响,以及疾病进展的机制方面。在本研究中,研究了桉油精(EUC)、姜黄素(CUR)及其组合对 BEAS-2B 细胞的保护机制,以了解它们对 3R4F 参考香烟提取物(CSE)诱导的细胞死亡、氧化细胞损伤和炎症反应的影响。根据目前的研究结果,EUC、CUR 及其组合可提高细胞活力,减轻 CSE 诱导的细胞凋亡和 LC3B 表达。此外,通过调节抗氧化酶活性、GSH、MDA 和细胞内 ROS 水平以及亚硝酸盐和 IL-6 水平,联合治疗可显著减轻 CSE 诱导的人支气管上皮细胞的氧化损伤和炎症反应。此外,与单独处理相比,联合预处理可显著上调参与间接抗氧化反应的调节蛋白 Nrf2 的核易位。总之,EUC 和 CUR 的联合应用可能是一种通过抗氧化和炎症途径治疗吸烟引起的肺部疾病的潜在疗法,研究结果为未来的肺部毒性研究提供了有价值的背景。