INTEGRITY OF THE DORSAL RAPHE SEROTONIN SYSTEM IN ALCOHOL DEPENDENCE AND SUICIDE

这个子项目是利用由NIH/NCRR资助的中心拨款提供的资源的许多研究子项目之一。子项目和调查员(PI)可能从另一个NIH来源获得了主要资金，因此可能会出现在其他CRISE条目中。列出的机构是针对中心的，而不一定是针对调查员的机构。一些证据表明，5-羟色胺神经传递功能障碍使人容易产生酒精依赖，并有助于维持过度饮酒。各种研究提供的证据表明，酒精依赖受试者和喜欢酒精的动物的大脑中的5-羟色胺神经传递减少。酒精依赖人群的终生自杀率很高，酒精中毒是自杀案例中最常见的两种精神障碍之一。此外，重度抑郁是酒精依赖患者的常见共病，自杀行为和抑郁也与5-羟色胺变化有关。目前尚不清楚是什么神经化学底物或机制导致了酒精依赖中5-羟色胺神经传递的缺陷，也不清楚在表现出自杀行为的酒精依赖患者中，5-羟色胺能调节是否进一步减弱。这项研究将检验一种假设，即与非自杀、非抑郁的酒精依赖和正常对照组相比，被诊断为酒精依赖和严重抑郁症的自杀患者中脑5-羟色胺神经元的5-羟色胺神经传递存在缺陷，这是由于5-羟色胺生物合成的一个或多个关键神经元调节因子的改变造成的。我们将进一步检测几种5-羟色胺分子，包括色氨酸羟化酶、5-羟色胺(1A)受体和特定的5-羟色胺转录因子在两个酒精使用受试组、抑郁症组和正常对照组的人死后标本的中缝背核和中缝正中核中的基因和蛋白表达。这项建议的目的是了解5-羟色胺神经传递缺陷的生化机制，特别是在酒精依赖自杀和严重抑郁症共病的受试者中。鉴于酒精依赖人群自杀行为的严重性、致命性和破坏性后果，了解导致酒精依赖个体这种有害行为的神经生物学机制可能为开发新的治疗策略和预防酒精中毒自杀行为的可能途径提供线索。

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. Several lines of evidence suggest that dysfunction of serotonin neurotransmission predisposes individuals to alcohol dependence and contributes to the maintenance of excessive alcohol consumption. A variety of studies have provided evidence that serotonin neurotransmission is reduced in the brain of alcohol-dependent subjects and alcohol-preferring animals. Alcohol-dependent populations have a high lifetime suicide rate, and alcoholism is one of two psychiatric disorders most frequently found in suicidal cases. Furthermore, major depression is a frequent co-morbid condition among individuals with alcohol dependence, and suicidal behavior and depression have also been linked to alterations in serotonin. It remains unclear what neurochemical substrate or mechanism is responsible for the deficit in serotonin neurotransmission in alcohol dependence or if serotonergic regulation is further diminished in alcohol-dependent subjects with major depression that exhibit suicidal behavior. This research will test the hypothesis that there is a deficit in serotonin neurotransmission in midbrain serotonin neurons in suicide subjects diagnosed with alcohol-dependence and major depression relative to non-suicide, non-depressed alcohol-dependent and normal control subjects which is caused by an alteration in one or more key neuronal regulators of serotonin biosynthesis. We will further examine gene and protein expression of several serotonin molecules including tryptophan hydroxylase, 5-HT(1A) receptors and specific serotonin transcription factors in the dorsal and median raphe nucleus of human postmortem specimens of two alcohol-use subject groups, a major depression group and a normal control subject group. The goals of this proposal are to understand the biochemical mechanisms underlying the deficiency in serotonin neurotransmission specifically in subjects committing suicide with alcohol dependence and co-morbid major depression. Given the seriousness, lethality and devastating consequences associated with suicidal behavior in alcohol-dependent populations, understanding the neurobiological mechanisms contributing to such harmful behavior in alcohol-dependent individuals may offer clues for developing new treatment strategies and possible avenues to prevent suicidal behavior in alcoholism.