2013 Cannabinoid Function in the CNS Gordon Research Conference & Gordon Research

2013 CNS Gordon 研究会议上的大麻素功能

基本信息

  • 批准号:
    8597593
  • 负责人:
  • 金额:
    $ 4.04万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2013
  • 资助国家:
    美国
  • 起止时间:
    2013-06-01 至 2014-05-31
  • 项目状态:
    已结题

项目摘要

DESCRIPTION (provided by applicant): The present R13 grant requests support for a joint Gordon Research Conference and Gordon Research Seminars (GRC/GRS) on Cannabinoid Function in the CNS to be held in 2013. We will exploit the innovative GRC/GRS format to accomplish three Specific Aims: 1. To promote and sustain a scientific forum that allows for in depth presentation and adequate discussion of cutting edge unpublished data in the area of Cannabinoid Function in the CNS. 2. To foster opportunities for cutting edge collaborative science that propels the next generation of scientific advances and unites basic researchers studying cannabinoid-related neuroplasticity with clinical researchers studying long term impact of altered neuoroplasticity in disease states. 3. To promote and mentor the next generation of cannabinoid scientists while encouraging diversity and inclusiveness in the cannabinoid field through the Gordon Research Seminar. The joint meeting format is warranted based upon the critical role of the endocannabinoid system in controlling neuronal excitability, the contribution f endocannabinoid dysregulation to disease states, the therapeutic potential of endocannabinoid modulators and the increasingly widespread use of both recreational (e.g. spice) and medicinal (e.g. Sativex, medical marijuana) cannabinoids in humans. The recent advent of cannabinoid- based medicines requires that continued research emphasis be placed on understanding cannabinoid effects in humans, especially long-term consequences (i.e. abuse liability, adverse side-effects, safety considerations). Clinical studies of cannabinoids have not been represented at any prior Gordon Research Conference on cannabinoids, mandating that program organizers specifically reach out to clinical researchers that would not typically attend a Gordon Research Conference focused on basic as opposed to clinical science. The format of the GRC thus provides an important opportunity to build bridges in interdisciplinary science between preclinical researchers studying neuroplasticity and clinical researchers studying human disease states marked by altered neuroplasticity (e.g. pathological pain, addiction, neurodegenerative diseases). The Gordon Research Seminar (GRS 2013: "Endocannabinoids in Neurophysiology and Neuropathology") is organized by and for graduate students and post-doctoral fellows and has been highly ranked by trainees as a venue for providing mentoring and networking opportunities at a critical stage of trainee development. The GRS directly precedes the GRC (GRC 2013: "Synapses, Circuits and the Human Brain"). R13 support of the 2013 joint GRC-GRS is expected to promote mutually beneficial increases in diversity in the cannabinoid field. The present R13 grant is expected to foster opportunities for cutting edge collaborative science while ensuring the continued success and sustainability of a highly rated GRC devoted to cannabinoid research.
描述(由申请人提供):本R13拨款要求支持将于2013年举行的关于大麻素在中枢神经系统中的功能的联合戈登研究会议和戈登研究研讨会(GRC/GRS)。我们将利用创新的GRC/GRS格式,实现三个具体目标:促进和维持一个科学论坛,允许深入介绍和充分讨论大麻素在中枢神经系统功能领域未发表的前沿数据。2. 促进前沿合作科学的机会,推动下一代科学进步,并将研究大麻素相关神经可塑性的基础研究人员与研究疾病状态下神经可塑性改变的长期影响的临床研究人员联合起来。3. 通过戈登研究研讨会促进和指导下一代大麻素科学家,同时鼓励大麻素领域的多样性和包容性。鉴于内源性大麻素系统在控制神经元兴奋性方面的关键作用,内源性大麻素失调对疾病状态的贡献,内源性大麻素调节剂的治疗潜力以及娱乐性(如香料)和药用(如Sativex,医用大麻)大麻素在人类中的日益广泛使用,联合会议形式是有必要的。最近以大麻素为基础的药物的出现要求继续研究重点放在了解大麻素对人类的影响,特别是长期后果(即滥用责任、不良副作用、安全考虑)。大麻素的临床研究在之前的任何戈登大麻素研究会议上都没有代表,这就要求项目组织者专门联系那些通常不会参加戈登研究会议的临床研究人员,这些会议的重点是基础科学,而不是临床科学。因此,GRC的形式为研究神经可塑性的临床前研究人员和研究以神经可塑性改变为标志的人类疾病状态(如病理性疼痛、成瘾、神经退行性疾病)的临床研究人员之间建立跨学科科学的桥梁提供了重要机会。戈登研究研讨会(GRS 2013:“神经生理学和神经病理学中的内源性大麻素”)由研究生和博士后研究员组织,并为学员提供了在学员发展的关键阶段提供指导和交流机会的场所,受到学员的高度评价。GRS直接先于GRC (GRC 2013:“突触、电路和人脑”)。R13对2013年联合GRC-GRS的支持有望促进大麻素领域多样性的互利增加。目前的R13拨款预计将促进前沿合作科学的机会,同时确保致力于大麻素研究的高评价GRC的持续成功和可持续性。

项目成果

期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)

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Andrea Grace Hohmann其他文献

Andrea Grace Hohmann的其他文献

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{{ truncateString('Andrea Grace Hohmann', 18)}}的其他基金

Therapeutic antibodies for treating chemotherapy induced peripheral neuropathic pain
用于治疗化疗引起的周围神经性疼痛的治疗性抗体
  • 批准号:
    9910117
  • 财政年份:
    2019
  • 资助金额:
    $ 4.04万
  • 项目类别:
CB2 Cannabinoid Mechanisms for Suppressing Opioid Tolerance and Dependence
CB2 大麻素抑制阿片类药物耐受性和依赖性的机制
  • 批准号:
    9914099
  • 财政年份:
    2019
  • 资助金额:
    $ 4.04万
  • 项目类别:
CB2 Cannabinoid Mechanisms for Suppressing Opioid Tolerance and Dependence
CB2 大麻素抑制阿片类药物耐受性和依赖性的机制
  • 批准号:
    10579196
  • 财政年份:
    2019
  • 资助金额:
    $ 4.04万
  • 项目类别:
Therapeutic antibodies for treating chemotherapy induced peripheral neuropathic pain
用于治疗化疗引起的周围神经性疼痛的治疗性抗体
  • 批准号:
    10259561
  • 财政年份:
    2019
  • 资助金额:
    $ 4.04万
  • 项目类别:
Therapeutic antibodies for treating chemotherapy induced peripheral neuropathic pain
用于治疗化疗引起的周围神经性疼痛的治疗性抗体
  • 批准号:
    10401479
  • 财政年份:
    2019
  • 资助金额:
    $ 4.04万
  • 项目类别:
CB2 Cannabinoid Mechanisms for Suppressing Opioid Tolerance and Dependence
CB2 大麻素抑制阿片类药物耐受性和依赖性的机制
  • 批准号:
    10343812
  • 财政年份:
    2019
  • 资助金额:
    $ 4.04万
  • 项目类别:
CB2 Cannabinoid Mechanisms for Suppressing Opioid Tolerance and Dependence
CB2 大麻素抑制阿片类药物耐受性和依赖性的机制
  • 批准号:
    10117221
  • 财政年份:
    2019
  • 资助金额:
    $ 4.04万
  • 项目类别:
Role of CB2 in Analgesic Mechanisms
CB2 在镇痛机制中的作用
  • 批准号:
    9127680
  • 财政年份:
    2016
  • 资助金额:
    $ 4.04万
  • 项目类别:
A Novel Mechanism for Decreasing Opioid Reward
减少阿片类药物奖励的新机制
  • 批准号:
    9197559
  • 财政年份:
    2016
  • 资助金额:
    $ 4.04万
  • 项目类别:
Protein-protein interaction inhibitors as novel analgesics
蛋白质-蛋白质相互作用抑制剂作为新型镇痛药
  • 批准号:
    8731190
  • 财政年份:
    2013
  • 资助金额:
    $ 4.04万
  • 项目类别:

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