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中文摘要
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项目摘要 基于价值的决策是对环境中的选项进行评估以提供最佳方案的过程 行动的一部分。大量的行为证据表明,基于价值的决策在 上瘾。更好地理解基于价值的决策是如何由Defined计算和执行的 细胞类型对于识别和最终治疗导致适应不良的电路干扰至关重要 上瘾时的决策。到目前为止,绝大多数检验价值的神经关联的研究- 在行为灵长类动物中,已经进行了基于决策的研究。而灵长类动物能够 复杂的认知任务,我们目前缺乏与灵长类兼容的工具来记录和操纵活动 精确定义的神经元群体。这限制了灵长类研究能得出多少结论。 关于解剖学和基因定义的细胞类型在基于价值的决策中的作用。这 Proposal通过开发一个新的任务来研究老鼠的基于价值的决策,从而克服了这一障碍。老鼠 能够执行复杂的认知任务,但他们也服从于现代技术 记录和操作已定义的单元类型的活动。初步数据显示,老鼠是 能够做出适当的基于价值的决策,并证明基于价值的决策是 严重依赖于眼眶额叶皮质的活动。这项提案的目标是描述如何 眶前叶皮质中的神经元与下游神经回路相互作用,介导基于价值的 决策。在K99指导阶段,候选人将通过光遗传抑制眶前额轴突 动物不同大脑区域的终末,做出基于价值的决定,以确定关键的输出途径 通过它来实现在眼眶额叶皮质中计算的选择。初步工作显示, 从眶前叶皮质到背侧纹状体的投射可能是关键的输出通路,通过它 以价值为基础的决策是经过调解的。然后,应聘者将询问信息是如何按原样转换的 联合轴突的光遗传抑制从眶前叶皮质传递到背侧纹状体 终末与在体细胞外电生理记录执行基于价值的决策的大鼠 制造任务。拟议的K99研究不仅将确定眼眶前额叶皮质中的神经元 与下游神经回路相互作用,以调节选择,但也将为候选人提供关键的 为分析世界大数据而进行的体内电生理学和降维技术培训- 斯坦福大学的课堂实验室。在R00独立阶段,申请者将应用此培训来询问 不同的决策相关参数如何映射到背侧纹状体的不同细胞类型。总体而言, 拟议的研究将提供一些关于基于价值的决策是如何通过 解剖学和遗传学定义的细胞类型。这有望为临床提供新的治疗策略。 上瘾,同时也为申请人作为独立调查员产生了许多新的调查线索。
英文摘要
Project Summary Value-based decision-making is the process of evaluating options in the environment to inform the best course of action. Abundant behavioral evidence demonstrates that value-based decision-making is impaired in addiction. An improved understanding of how value-based decisions are computed and executed by defined cell types is critical to identifying and ultimately treating the circuit disturbances that underlie maladaptive decision-making in addiction. To date, the vast majority of studies examining the neural correlates of value- based decision-making have been conducted in behaving primates. While primates are capable of performing complex cognitive tasks, we currently lack primate-compatible tools for recording and manipulating the activity of precisely defined populations of neurons. This has placed limitations on how much primate studies can tell us about the role of anatomically and genetically defined cell types in value-based decision-making. This proposal overcomes this obstacle by developing a new task to study value-based decision-making in rats. Rats are capable of performing complex cognitive tasks, but they are also amenable to modern techniques for recording and manipulating the activity of defined cell types. Preliminary data demonstrate that rats are capable of making appropriate value-based decisions, and demonstrate that value-based decision-making is critically dependent on activity in the orbitofrontal cortex. The goal of this proposal is to characterize how neurons in the orbitofrontal cortex interact with downstream neural circuits to mediate value-based decision-making. In the K99 mentored phase, the candidate will optogenetically inhibit orbitofrontal axon terminals in distinct brain areas in animals making value-based decisions to identify the critical output pathway through which choices computed in the orbitofrontal cortex are implemented. Preliminary efforts reveal that the projection from the orbitofrontal cortex to the dorsal striatum is likely the key output pathway through which value-based decisions are mediated. The candidate will then ask how information is transformed as it is transmitted from the orbitofrontal cortex to the dorsal striatum by combining optogenetic inhibition of axon terminals with in vivo extracellular electrophysiological recordings in rats performing the value-based decision- making task. The proposed K99 research will not only determine how neurons in the orbitofrontal cortex interact with downstream neural circuits to mediate choice, but will also provide the candidate with critical training in in vivo electrophysiology and dimensionality reduction techniques for analysing big data in world- class labs at Stanford University. In the R00 independent phase, the applicant will apply this training to ask how different decision-related parameters map onto distinct cell types in the dorsal striatum. Collectively, the proposed research will provide some of the first insights into how value-based decisions are mediated by anatomically and genetically defined cell types. This promises to illuminate new therapeutic strategies for addiction, while also generating many new lines of enquiry for the applicant as an independent investigator.
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