Amygdalar neuropeptides and anxiety

杏仁核神经肽和焦虑

• 批准号: 6794104
• 负责人: Marlene A. Wilson
• 金额: $ 29.1万
• 依托单位: UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA
• 依托单位国家: 美国
• 财政年份: 2002
• 资助国家: 美国
• 起止时间: 2002-09-15 至 2007-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6794104
• 关键词: Alphaherpesvirinae; amygdala; anxiety; anxiety disorders; behavior test; benzodiazepines; biological models; biotechnology; buspirone; enkephalins; ethanol; fear; gene expression; genetically modified animals; immunocytochemistry; laboratory rat; neuropeptides; neuropharmacology; opioid receptor; psychopharmacology; radioimmunoassay; tranquilizer; transfection; transfection /expression vector

DESCRIPTION (provided by applicant): The amygdala is a brain structure that plays a crucial role in fear and anxiety, and the actions of anxiety-reducing compounds. The opioid peptide has also been shown to modulate anxiety-related responses within the amygdala. Using herpes virus-mediated gene transfer, we have demonstrated that overexpression of enkephalin in the amygdala enhances the anxiety-reducing influences of the benzodiazepine diazepam (Valium) in rats. These initial results demonstrate that herpes virus-mediated gene transfer can transiently alter expression of neuropeptides in confined brain sites of adult rats, and that these changes can modify behavioral responses. The present studies continue to utilize this powerful technique to examine the role of amygdalar enkephalin in regulating anxiety-related behaviors and the actions of anxiolytic drugs. Both decreases and cell-targeted increases in peptide expression will be examined in several animal models of anxiety. Aim 1 will verify the ability of virus-mediated gene transfer to decrease and cell-specifically increase expression of enkephalin in select areas of amygdala. Anatomical and quantitative methods will assess changes in mRNA expression, while peptide changes will be assessed with immunohistochemistry and radioimmunoassay. AIM 2 examines if altered enkephalin expression in central amygdala modifies anxiety-related behaviors in additional animal tests of anxiety behaviors and/or the effectiveness of other anxiolytics in these tests. These studies 1) compare decreases with cell-specific increases in enkephalin expression, 2) test the activity of other anxiolytics (alcohol, the serotonergic compound buspirone), and 3) tests effects in several models of anxiety. AIM 3 assesses the effects of pharmacological modulation of enkephalin activity in amygdala. Using more traditional techniques selective opioid receptor (mu, delta) agonists and antagonists will be locally applied in amygdala, and the effect of these compounds on responses to anxiolytic drugs will be tested. These studies will lead to a better understanding of the role of amygdala and enkephalin in anxiety and anxiolytic responses, as well as elucidate the differences between animal models of anxiety. This understanding may also suggest novel, avenues for development of treatments for anxiety or affective disorders.

描述（由申请人提供）：杏仁核是一种大脑结构，在恐惧和焦虑以及减轻焦虑化合物的作用中起着至关重要的作用。阿片肽也被证明可以调节杏仁核内与焦虑相关的反应。使用疱疹病毒介导的基因转移，我们已经证明，脑啡肽在杏仁核中的过度表达增强了苯二氮卓类安定（安定）在大鼠中的焦虑减轻影响。这些初步的结果表明，疱疹病毒介导的基因转移可以短暂改变成年大鼠脑内神经肽的表达，这些变化可以改变行为反应。目前的研究继续利用这一强大的技术来检查杏仁脑啡肽在调节焦虑相关行为和抗焦虑药物的作用。将在几种焦虑动物模型中检查肽表达的减少和细胞靶向增加。目的1验证病毒介导的基因转移是否能够降低和细胞特异性增加杏仁核特定区域脑啡肽的表达。解剖学和定量方法将评估mRNA表达的变化，而肽的变化将用免疫组织化学和放射免疫分析法评估。目的2检查是否改变脑啡肽在中央杏仁核的表达修改焦虑相关的行为，在额外的动物试验的焦虑行为和/或其他抗焦虑药物在这些测试的有效性。这些研究1）比较脑啡肽表达的减少与细胞特异性增加，2）测试其他抗焦虑药（酒精，肾上腺素能化合物丁螺环酮）的活性，3）测试几种焦虑模型的效果。目的3评价杏仁核脑啡肽活性的药理学调节作用。使用更传统的技术，选择性阿片受体（μ，δ）激动剂和拮抗剂将局部应用于杏仁核，这些化合物对抗焦虑药物的反应的影响将被测试。这些研究将导致更好地了解杏仁核和脑啡肽在焦虑和抗焦虑反应中的作用，以及阐明焦虑动物模型之间的差异。这种理解也可能为开发焦虑或情感障碍的治疗提供新的途径。