Doura Menahem B, Gold Allison B, Keller Ashleigh B, Perry David C
Department of Pharmacology and Physiology, George Washington University Medical Center, Washington, DC 20037, USA.
Brain Res. 2008 Jun 18;1215:40-52. doi: 10.1016/j.brainres.2008.03.056. Epub 2008 Apr 4.
Adolescence is a time of significant brain development, and exposure to nicotine during this period is associated with higher subsequent rates of dependence. Chronic nicotine exposure alters expression of nicotinic acetylcholine receptors (nAChRs), changing the pattern of nicotine responsiveness. We used quantitative autoradiography to measure three major subtypes of nAChRs after chronic nicotine exposure by osmotic minipump in adult and periadolescent rats. Comparison of control animals at the two different ages revealed that periadolescents express consistently greater numbers of alpha4beta2* nAChRs compared to the same brain regions of adults. Similar but less pronounced increases in alpha7 nAChRs were found in control periadolescent rats compared to adults. Binding of [(125)I]alpha-conotoxin MII (largely to alpha6* nAChRs) did not systematically differ between adults and periadolescents. The response to chronic nicotine exposure also differed by age. Up-regulation of alpha4beta2* nAChRs was prominent and widespread in adult animals; in periadolescents, alpha4beta2* up-regulation also occurred, but in fewer regions and to a lesser extent. A similar pattern of response was seen with alpha7 receptors: adults were more responsive than periadolescents to nicotine-induced up-regulation. In adult animals, chronic nicotine exposure did not cause up-regulation of alpha6* nAChRs; binding was down-regulated in three regions. Unlike the other subtypes, the response of alpha6* nAChRs to chronic nicotine was greater in periadolescents, with more regions showing greater down-regulation compared to adults. These differences in receptor expression and regulation between age groups are likely to be important given the unique vulnerability of adolescents to nicotine-induced behavioral changes and susceptibility to drug abuse.
青春期是大脑发育的重要时期,在此期间接触尼古丁会导致日后更高的成瘾率。长期接触尼古丁会改变烟碱型乙酰胆碱受体(nAChRs)的表达,从而改变对尼古丁的反应模式。我们使用定量放射自显影技术,通过渗透微型泵对成年和青春期大鼠进行长期尼古丁暴露后,测量三种主要亚型的nAChRs。对两个不同年龄段的对照动物进行比较发现,与成年动物相同脑区相比,青春期大鼠始终表达更多数量的α4β2* nAChRs。与成年动物相比,对照青春期大鼠中α7 nAChRs也有类似但不太明显的增加。[(125)I]α-芋螺毒素MII(主要与α6* nAChRs结合)在成年和青春期大鼠之间的结合没有系统性差异。对长期尼古丁暴露的反应也因年龄而异。α4β2* nAChRs的上调在成年动物中显著且广泛;在青春期大鼠中,α4β2上调也有发生,但区域较少且程度较轻。α7受体也呈现出类似的反应模式:成年动物对尼古丁诱导的上调比青春期大鼠更敏感。在成年动物中,长期尼古丁暴露并未导致α6 nAChRs上调;三个区域的结合下调。与其他亚型不同,青春期大鼠中α6* nAChRs对长期尼古丁的反应更大,与成年动物相比,更多区域显示出更大程度的下调。考虑到青少年对尼古丁诱导的行为变化具有独特的易感性以及对药物滥用的易感性,不同年龄组之间受体表达和调节的这些差异可能很重要。