Polli Joseph R, Dobbins Dorothy L, Kobet Robert A, Farwell Mary A, Zhang Baohong, Lee Myon-Hee, Pan Xiaoping
Department of Biology, East Carolina University, Greenville, NC 27858, USA.
Department of Medicine, East Carolina University, Greenville, NC 27858, USA.
Neurotoxicology. 2015 Mar;47:27-36. doi: 10.1016/j.neuro.2014.12.005. Epub 2014 Dec 19.
Nicotine, the major psychoactive compound in tobacco, targets nicotinic acetylcholine receptors (nAChRs) and results in drug dependence. The nematode Caenorhabditis elegans' (C. elegans) genome encodes conserved and extensive nicotinic receptor subunits, representing a useful system to investigate nicotine-induced nAChR expressions in the context of drug dependence. However, the in vivo expression pattern of nAChR genes under chronic nicotine exposure has not been fully investigated. To define the role of nAChR genes involved in nicotine-induced locomotion changes and the development of tolerance to these effects, we characterized the locomotion behavior combining the use of two systems: the Worm Tracker hardware and the WormLab software. Our results indicate that the combined system is an advantageous alternative to define drug-dependent locomotion behavior in C. elegans. Chronic (24-h dosing) nicotine exposure at 6.17 and 61.7μM induced nicotine-dependent behaviors, including drug stimulation, tolerance/adaption, and withdrawal responses. Specifically, the movement speed of naïve worms on nicotine-containing environments was significantly higher than on nicotine-free environments, suggesting locomotion stimulation by nicotine. In contrast, the 24-h 6.17μM nicotine-treated worms exhibited significantly higher speeds on nicotine-free plates than on nicotine-containing plates. Furthermore significantly increased locomotion behavior during nicotine cessation was observed in worms treated with a higher nicotine concentration of 61.7μM. The relatively low locomotion speed of nicotine-treated worms on nicotine-containing environments also indicates adaption/tolerance of worms to nicotine following chronic nicotine exposure. In addition, this study provides useful information regarding the comprehensive in vivo expression profile of the 28 "core" nAChRs following different dosages of chronic nicotine treatments. Eleven genes (lev-1, acr-6, acr-7, acr-11, lev-8, acr-14, acr-16, acr-20, acr-21, ric-3, and unc-29) were significantly up-regulated following 61.7μM nicotine treatment, in which worms showed significantly increased locomotion behavior. This study provides insights into the linkage between nicotine-induced locomotion behavior and the regulation of nicotinic acetylcholine receptors.
尼古丁是烟草中的主要精神活性化合物,作用于烟碱型乙酰胆碱受体(nAChRs)并导致药物依赖。秀丽隐杆线虫(C. elegans)的基因组编码保守且广泛的烟碱型受体亚基,是研究药物依赖背景下尼古丁诱导的nAChR表达的有用系统。然而,慢性尼古丁暴露下nAChR基因的体内表达模式尚未得到充分研究。为了确定参与尼古丁诱导的运动变化和对这些作用耐受性发展的nAChR基因的作用,我们结合使用两种系统:蠕虫追踪器硬件和蠕虫实验室软件来表征运动行为。我们的结果表明,该组合系统是定义秀丽隐杆线虫药物依赖性运动行为的有利替代方法。6.17和61.7μM的慢性(24小时给药)尼古丁暴露诱导了尼古丁依赖性行为,包括药物刺激、耐受性/适应性和戒断反应。具体而言,未接触过尼古丁的蠕虫在含尼古丁环境中的移动速度明显高于在无尼古丁环境中的速度,表明尼古丁对运动有刺激作用。相比之下,经24小时6.17μM尼古丁处理的蠕虫在无尼古丁平板上的速度明显高于在含尼古丁平板上的速度。此外,在用较高尼古丁浓度61.7μM处理的蠕虫中,观察到尼古丁戒断期间运动行为显著增加。尼古丁处理的蠕虫在含尼古丁环境中的相对较低移动速度也表明,慢性尼古丁暴露后蠕虫对尼古丁有适应性/耐受性。此外,本研究提供了关于28个“核心”nAChRs在不同剂量慢性尼古丁处理后的全面体内表达谱的有用信息。在61.7μM尼古丁处理后,11个基因(lev-1、acr-6、acr-7、acr-11、lev-8、acr-14、acr-16、acr-20、acr-21、ric-3和unc-29)显著上调,其中蠕虫的运动行为显著增加。本研究为尼古丁诱导的运动行为与烟碱型乙酰胆碱受体调节之间的联系提供了见解。