Raza Haider, John Annie, Nemmar Abderrahim
Department of Biochemistry College of Medicine and Health Sciences, UAE University, Al Ain, United Arab Emirates.
Cell Physiol Biochem. 2013;31(4-5):683-92. doi: 10.1159/000350087. Epub 2013 May 16.
BACKGROUND/AIMS: The components of cigarette smoke (CS) have been implicated in the development of cancer as well as in cardiopulmonary diseases. We have previously reported increased oxidative stress in rat tissues induced by tobacco-specific toxins nicotine and 4-(N-methyl-N-nitrosamino)-1-(3-pyridyl)-1-butanone (NNK). Recently, we have also shown increased oxidative stress and associated inflammatory responses in various tissues after exposure to cigarette smoke.
In this study, we have further investigated the effects of nose-only cigarette smoke exposure on mitochondrial functions and glutathione-dependent redox metabolism in tissues of BALB/C mice. Liver, kidney, heart and lung tissues were analyzed for oxidative stress, glutathione (GSH) and cytochrome P450 dependent enzyme activities and mitochondrial functions after exposure to smoke generated by 9 cigarettes/day for 4 days. Control mice were exposed to air only.
An increase in oxidative stress as observed by increased production of reactive oxygen species (ROS) and altered GSH metabolism was apparent in all the tissues, but lung and heart appeared to be the main targets. Increased expression and activity of CYP450 1A1 and 1A2 were also observed in the tissues after exposure to cigarette smoke. Mitochondrial respiratory dysfunction in the tissues, as observed by alterations in the activities of Complex I and IV enzymes, was also observed after exposure to cigarette smoke. SDS-PAGE and Western blot results also indicate that alterations in the expression of enzyme proteins were in accordance with the changes in their catalytic functions.
These results suggest that even short term exposure of cigarette smoke have adverse effects on mitochondrial functions and redox homeostasis in tissues which may progress to further complications associated with chronic smoking.
背景/目的:香烟烟雾(CS)的成分与癌症以及心肺疾病的发生有关。我们之前报道过烟草特异性毒素尼古丁和4-(N-甲基-N-亚硝基氨基)-1-(3-吡啶基)-1-丁酮(NNK)可诱导大鼠组织氧化应激增加。最近,我们还发现暴露于香烟烟雾后,各种组织中的氧化应激和相关炎症反应增加。
在本研究中,我们进一步研究了仅经鼻暴露于香烟烟雾对BALB/C小鼠组织中线粒体功能和谷胱甘肽依赖性氧化还原代谢的影响。在每天暴露于9支香烟产生的烟雾中4天后,分析肝脏、肾脏、心脏和肺组织的氧化应激、谷胱甘肽(GSH)、细胞色素P450依赖性酶活性和线粒体功能。对照小鼠仅暴露于空气中。
所有组织中活性氧(ROS)生成增加和GSH代谢改变所观察到的氧化应激增加都很明显,但肺和心脏似乎是主要靶点。暴露于香烟烟雾后,组织中CYP450 1A1和1A2的表达和活性也增加。暴露于香烟烟雾后,还观察到组织中线粒体呼吸功能障碍,表现为复合体I和IV酶活性改变。SDS-PAGE和蛋白质印迹结果还表明,酶蛋白表达的改变与其催化功能的变化一致。
这些结果表明,即使短期暴露于香烟烟雾也会对组织中的线粒体功能和氧化还原稳态产生不利影响,这可能会进一步发展为与慢性吸烟相关的并发症。