Clinical Studies Investigating Aggressive Behaviors And

调查攻击行为和

基本信息

项目摘要

Alcoholism is frequently associated with aggressive behaviors, smoking and dietary changes/deficiencies. To explore facets of each of these common co-morbidities, we have initiated several clinical research studies designed to explore their association with the pathophysiology of alcoholism. The aspect of our research related to smoking cessation in recently detoxified alcoholics revealed that smoking alcoholics had significantly lower concentrations of CSF Homovanillic Acid (HVA) compared with non-smoking alcoholics. We also found that there was no significant difference for various measures of alcohol consumption between smoking and non-smoking alcoholics. Unfortunately, plasma cotinine levels revealed that protocol participants were unable to totally refrain from smoking during the course of our study, therefore, we were unable to determine the effects of smoking cessation of CSF HVA concentrations. It has been shown that there is a strong association between alcohol consumption and violent behavior, however, the actual mechanism(s) by which alcohol induces aggressive behavior is poorly understood. Our research initiative to determine if treatment with a serotonin reuptake inhibitor can produce a significant improvement on standardized measures used to quantify aggression in individuals characterized by frequent episodes of domestic violence is currently in progress. To date five subjects have been enrolled in the study. In our 2DG study, sober alcoholics frequently report that they binge on sweets to decrease their desire to drink alcohol. This exaggerated desire for sweets has contributed to the postulate that alcohol consumption is regulated by the same mechanisms that regulate the intake of carbohydrates. To explore this postulate we examined the effects of glucoprivation on carbohydrate consumption in long-term sober alcoholics. Our finding showing that there were no differences in food consumption between alcoholics and healthy volunteers following 2DG stimulus will be published in Alcohol & Alcoholism in 2002. In this study we also found that the alcoholic group had a significantly blunted response in blood glucose. We concluded that the atypical blood glucose response may antedate the onset of alcoholism or it may be secondary to alcohol-related damage that persists beyond six months. Previous accounts of increased sweet consumption in alcoholics were not substantiated, although they may be present during the peri-withdrawal period. In a new area of research that we are about to begin, the literature suggests that alcoholics frequently have disturbances in nutritional intake that may contribute to changes in mood (i.e., depression and hostility) as well as cognition. One possible nutrient that has been implicated in both of these clinical states is docosahexaenoic acid (DHA). Since chronic alcohol intake depletes DHA from the brain, we designed a study that would allow us to quantify and image the uptake of DHA in the brains of recently detoxified alcoholics and healthy controls. This study is important because there is no methodology currently available that will allow us to assess DHA metabolism in the human brain.
酒精中毒通常与攻击性行为、吸烟和饮食变化/缺乏有关。为了探索这些常见合并症的各个方面,我们已经启动了几项临床研究,旨在探索它们与酒精中毒的病理生理学之间的关系。我们的研究与最近戒毒的酗酒者戒烟有关,结果显示,吸烟的酗酒者与不吸烟的酗酒者相比,CSF高香草酸(HVA)浓度显著降低。我们还发现,吸烟和不吸烟的酗酒者之间的各种饮酒量没有显着差异。不幸的是,血浆可替宁水平显示,方案参与者在我们的研究过程中无法完全戒烟,因此,我们无法确定戒烟对CSF HVA浓度的影响。研究表明,饮酒与暴力行为之间存在很强的关联,然而,酒精诱导攻击行为的实际机制却知之甚少。我们的研究计划,以确定是否与5-羟色胺再摄取抑制剂的治疗可以产生一个显着的改善标准化的措施,用于量化侵略的特点是频繁发作的家庭暴力的个人目前正在进行中。迄今为止,已有5名受试者入组本研究。在我们的2DG研究中,清醒的酗酒者经常报告说,他们狂饮甜食,以减少他们喝酒的欲望。这种对甜食的过度渴望促成了这样一种假设,即酒精的消耗受到调节碳水化合物摄入的相同机制的调节。为了探索这一假设,我们研究了葡萄糖缺乏对长期清醒酗酒者碳水化合物消耗的影响。我们的研究结果表明,在2DG刺激后,酗酒者和健康志愿者之间的食物消费量没有差异,这一发现将发表在2002年的《酒精与酒精中毒》杂志上。在这项研究中,我们还发现酒精组对血糖的反应明显迟钝。我们的结论是,非典型血糖反应可能早于酒精中毒的发作,也可能是继发于酒精相关的损害,持续超过6个月。先前关于酗酒者甜食消费量增加的说法没有得到证实,尽管它们可能存在于戒断期。在我们即将开始的一个新的研究领域,文献表明,酗酒者经常在营养摄入方面受到干扰,这可能会导致情绪的变化(即,抑郁和敌意)以及认知。与这两种临床状态有关的一种可能的营养素是二十二碳六烯酸(DHA)。由于长期酒精摄入会消耗大脑中的DHA,我们设计了一项研究,使我们能够量化和成像最近解毒的酗酒者和健康对照者大脑中DHA的摄取。这项研究很重要,因为目前还没有方法可以让我们评估DHA在人脑中的代谢。

项目成果

期刊论文数量(0)
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会议论文数量(0)
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David T George其他文献

The CRF1 Antagonist Verucerfont in Anxious Alcohol-Dependent Women: Translation of Neuroendocrine, But not of Anti-Craving Effects
焦虑型酒精依赖女性中的 CRF1 拮抗剂 Verucerfont:神经内分泌的翻译,但不是抗渴望效应的翻译
  • DOI:
    10.1038/npp.2016.61
  • 发表时间:
    2016-04-25
  • 期刊:
  • 影响因子:
    7.100
  • 作者:
    Melanie L Schwandt;Carlos R Cortes;Laura E Kwako;David T George;Reza Momenan;Rajita Sinha;Dimitri E Grigoriadis;Emilio Merlo Pich;Lorenzo Leggio;Markus Heilig
  • 通讯作者:
    Markus Heilig

David T George的其他文献

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{{ truncateString('David T George', 18)}}的其他基金

Assessment,Treatment, and Pharmacological Interventions in Alcoholic Patients
酗酒患者的评估、治疗和药理学干预
  • 批准号:
    8156730
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
Characterization Of Perpetrators Of Domestic Violence
家庭暴力施暴者的特征
  • 批准号:
    7146174
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
Clinical trial of SR141716, Rimonabant, to reduce volunt
SR141716、利莫那班的临床试验,以减少自愿
  • 批准号:
    6983095
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
Characterization Of Perpetrators Of Domestic Violence
家庭暴力施暴者的特征
  • 批准号:
    6983065
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
Clinical Studies Investigating Aggressive Behaviors And
调查攻击行为和
  • 批准号:
    6983107
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
Clinical Studies Investigating Aggressive Behaviors And
调查攻击行为和
  • 批准号:
    7317742
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
Characterization of Perpetrators of Domestic Violence
家庭暴力施暴者的特征
  • 批准号:
    6431370
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
YOHIMBINE CHALLENGE TO STUDY NORADRENERGIC FUNCTION IN INDIVIDUALS
育亨宾挑战研究个体去甲肾上腺素能功能
  • 批准号:
    6097574
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
NK1 receptor antagonism for treatment of alcohol-dependent patients
NK1受体拮抗剂治疗酒精依赖患者
  • 批准号:
    7732104
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
Clinical Assessment and Treatment Evaluation of Alcohol Dependent Patients
酒精依赖患者的临床评估和治疗评价
  • 批准号:
    7963833
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
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