Hoegberg Bethany G, Lomazzo Ermelinda, Lee Norman H, Perry David C
Department of Pharmacology and Physiology, The George Washington University, 2300 Eye Street NW, Washington, DC, 20037, USA.
Institute of Physiological Chemistry, University Medical Center of the Johannes Gutenberg University, 55099, Mainz, Germany.
Neuropharmacology. 2015 Dec;99:347-55. doi: 10.1016/j.neuropharm.2015.08.015. Epub 2015 Aug 10.
Chronic nicotine administration in animals, and smoking in humans, causes up-regulation of α4β2* neuronal nicotinic receptors (nAChRs), which has been hypothesized to contribute to the addictive actions of nicotine. We used a rat model to test whether such up-regulatory effects differ in adolescents versus adults, and in males versus females. Following chronic treatment with nicotine or saline via subcutaneous osmotic minipumps, we measured α4β2 and α4β2α5 nAChRs in cerebral cortex using [3H]epibatidine to label assembled nAChRs, and selective antibodies to measure the individual subunits via immunoprecipitation. For the first time, we provide a detailed characterization of the response of both α4β2 and α4β2α5 nAChRs in female adolescent rat cerebral cortex. We found differences in nicotine-induced up-regulation between males and females in early adolescence that are absent in both late adolescence and adulthood. Males showed significant up-regulation at PN28 which was absent in age-matched females. These results demonstrate sex differences in the susceptibility of α4β2* nAChRs to the effects of chronic nicotine exposure in the cerebral cortex based on age.
在动物中进行慢性尼古丁给药以及人类吸烟会导致α4β2神经元烟碱型乙酰胆碱受体(nAChRs)上调,据推测这与尼古丁的成瘾作用有关。我们使用大鼠模型来测试这种上调效应在青少年与成年人之间以及雄性与雌性之间是否存在差异。通过皮下渗透微型泵用尼古丁或生理盐水进行慢性治疗后,我们使用[3H]厄瓜多尔箭毒蛙毒素标记组装好的nAChRs,并通过免疫沉淀用选择性抗体测量各个亚基,从而测定大脑皮层中的α4β2和α4β2α5 nAChRs。我们首次详细描述了雌性青春期大鼠大脑皮层中α4β2和α4β2α5 nAChRs的反应。我们发现,在青春期早期,雄性和雌性在尼古丁诱导的上调方面存在差异,而在青春期晚期和成年期均不存在这种差异。雄性在出生后第28天表现出显著上调,而年龄匹配的雌性则没有。这些结果表明,基于年龄,大脑皮层中α4β2 nAChRs对慢性尼古丁暴露影响的易感性存在性别差异。