Chronic Nicotine Effects on Receptor Subtypes

尼古丁对受体亚型的慢性影响

• 批准号: 8489264
• 负责人: Norman H Lee
• 金额: $ 32.46万
• 依托单位: GEORGE WASHINGTON UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2004
• 资助国家: 美国
• 起止时间: 2004-07-01 至 2015-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8489264
• 关键词: Acute; Address; Adolescence; Adolescent; Adult; Age; Animals; Antibodies; Autoradiography; Behavior; Biological Assay; Birth; Brain; Brain region; Candidate Disease Gene; Cholinergic Receptors; Chronic; Cigarette; Dependence; Development; Drug Addiction; Exposure to; Gene Expression; Goals; Health; Immunoprecipitation; Individual; Knowledge; Length; Measures; Mediating; Methods; Microarray Analysis; Modeling; Morphology; Mothers; Neurons; Neurotransmitters; Nicotine; Nicotine Dependence; Pattern; Pharmacology; Phenotype; Pregnancy; Preparation; Quantitative Autoradiography; Rattus; Receptor Gene; Regimen; Regulation; Research Design; Rubidium; Saline; Smoke; Smoker; Staging; Structure; Testing; Tobacco; Vertebral column; Work; cholinergic; critical period; density; desensitization; drug of abuse; fetal tobacco exposure; functional status; in utero; mature animal; neurochemistry; neurodevelopment; neurophysiology; neurotransmitter release; offspring; postnatal; pregnant; prenatal; prenatal exposure; receptor; receptor expression; receptor function; research study; response

DESCRIPTION (provided by applicant): The CNS effects of nicotine are mediated by multiple subtypes of neuronal nicotinic cholinergic receptors (nAChRs). The effects of nicotine after chronic administration differ from those after acute administration, and nicotine effects also vary at different stages of development. Our previous work characterized the effects of chronic nicotine on expression and function of different subtypes of nAChRs. Knowledge of the shifting expression pattern of these receptors during nicotine use is critical for understanding cholinergic neurophysiology as well as nicotine pharmacology. Chronic nicotine is associated with dependence, changes in gene expression and behavior, and altered neural development. This latter effect is of critical importance given the widespread exposure to nicotine that occurs during periods of critical neural development, particularly due to prenatal exposure from mothers who smoke or use NRT products, and adolescents who are beginning to experiment with tobacco. Prenatal nicotine exposure can have profound effects upon subsequent development and behavior of offspring. Adolescent exposure to nicotine is associated with higher rates of adult dependence, both to nicotine and to other drugs of abuse. Thus these represent uniquely vulnerable periods for nicotine exposure. The overarching goal of the present proposal is to compare the effects of chronic nicotine exposure at three critical ages: prenatal, adolescence and adult. We will employ rat models to study the overlapping effects of chronic nicotine exposure on nAChR expression and function, neuronal morphology and gene expression; we will focus on receptors, genes and brain regions associated with nicotine dependence. In particular, we will examine for persistent effects of nicotine exposure on these parameters. These studies will test the general hypothesis that nicotine's effects on these parameters differ at different developmental stages of exposure. In particular, Aim 4 will test the hypothesis that prenatal nicotine exposure inhibits the response of adolescents to subsequent nicotine challenge, increasing the number of cigarettes smoked and thus the likelihood of subsequent dependence. For each of the following Specific Aims, we will test for both the short-term and persistent effects of chronic nicotine exposure on expression (using autoradiography and immunoprecipitation) and function (using rubidium efflux and neurotransmitter release) of nAChR subtypes, alteration of neuronal morphology (measuring dendritic length and spine density), and changes in global gene expression (using microarrays and rtPCR) in brain regions associated with nicotine dependence. Differential developmental effects will be determined by comparison across aims. SPECIFIC AIMS 1. Determine the immediate and the persistent direct effects of prenatal chronic nicotine exposure. 2. Determine the immediate and the persistent direct effects of adolescent chronic nicotine exposure. 3. Determine the immediate and the persistent direct effects of adult nicotine exposure. 4. Determine the persistent indirect effects of prenatal nicotine exposure by determining how prenatal nicotine exposure alters the ability of the adolescent to respond to a new nicotine exposure

描述（由申请方提供）：尼古丁的CNS效应由多种亚型的神经元烟碱胆碱能受体（nAChR）介导。尼古丁在长期给药后的作用与急性给药后的作用不同，尼古丁的作用在不同的发育阶段也不同。我们以前的工作特点慢性尼古丁对不同亚型的nAChR的表达和功能的影响。了解尼古丁使用过程中这些受体表达模式的变化对于理解胆碱能神经生理学和尼古丁药理学至关重要。慢性尼古丁与依赖、基因表达和行为的变化以及神经发育的改变有关。后一种效应至关重要，因为在关键的神经发育时期，人们广泛接触尼古丁，特别是由于吸烟或使用NRT产品的母亲和开始尝试烟草的青少年的产前暴露。产前尼古丁暴露可对后代的后续发育和行为产生深远影响。青少年接触尼古丁与成人对尼古丁和其他滥用药物的依赖率较高有关。因此，这是尼古丁暴露的独特脆弱时期。本提案的总体目标是比较三个关键年龄（产前、青春期和成人）的慢性尼古丁暴露的影响。我们将采用大鼠模型来研究慢性尼古丁暴露对nAChR表达和功能，神经元形态和基因表达的重叠影响;我们将专注于与尼古丁依赖相关的受体，基因和大脑区域。特别是，我们将检查尼古丁暴露对这些参数的持续影响。这些研究将检验尼古丁对这些参数的影响在不同发育阶段暴露不同的一般假设。特别是，目标4将检验以下假设：产前尼古丁暴露会抑制青少年对随后尼古丁挑战的反应，增加吸烟数量，从而增加随后依赖的可能性。对于以下每个特定目标，我们将测试慢性尼古丁暴露对表达的短期和持续影响。（使用放射自显影和免疫沉淀）和功能（使用铷流出和神经递质释放）nAChR亚型，神经元形态学的改变（测量树突长度和棘密度），以及与尼古丁依赖相关的大脑区域中整体基因表达的变化（使用微阵列和rtPCR）。不同的发展效果将通过比较不同的目标来确定。具体目标1.确定产前慢性尼古丁暴露的立即和持续直接影响。2.确定青少年慢性尼古丁暴露的直接和持久影响。3.确定成人尼古丁暴露的即时和持续直接影响。4.通过确定产前尼古丁暴露如何改变青少年对新尼古丁暴露的反应能力，确定产前尼古丁暴露的持续间接影响

项目成果

Prenatal exposure of rats to nicotine causes persistent alterations of nicotinic cholinergic receptors.

• DOI: 10.1016/j.brainres.2008.10.076
• 发表时间: 2009-01-23
• 期刊: Brain research
• 影响因子: 2.9
• 作者: Gold AB;Keller AB;Perry DC
• 通讯作者: Perry DC

Regulation of α4β2α5 nicotinic acetylcholinergic receptors in rat cerebral cortex in early and late adolescence: Sex differences in response to chronic nicotine.

• DOI: 10.1016/j.neuropharm.2015.08.015
• 发表时间: 2015-12
• 期刊: Neuropharmacology
• 影响因子: 4.7
• 作者: Hoegberg BG;Lomazzo E;Lee NH;Perry DC
• 通讯作者: Perry DC

An autoradiographic analysis of [125I]alpha-bungarotoxin binding in rat brain after chronic nicotine exposure.

慢性尼古丁暴露后大鼠脑中[125I]α-银环蛇毒素结合的放射自显影分析。

• DOI: 10.1016/j.neulet.2006.05.010
• 发表时间: 2006
• 期刊: Neuroscience letters
• 影响因子: 2.5
• 作者: Rasmussen,BruceA;Perry,DavidC
• 通讯作者: Perry,DavidC