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BDNF-TrkB signalling in fear learning: from genetics to neural networks.

机译:恐惧学习中的BDNF-TrkB信号传导:从遗传学到神经网络。

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摘要

Abstract Discovering the basic mechanisms in fear encoding and expression is important in many fields, including psychology, sociology, medicine, and neuroscience. Effective treatment for fear-based pathology depends on understanding how fear is learned and regulated. Among the molecular systems required for fear learning and amygdalar synaptic plasticity, brain derived neurtrophic factor (BDNF) and its high affinity receptor Ntrk2/TrkB have been shown to play essential roles. Therefore, we will focus this review on three main aspects; first of all, the impact of Bdnf polymorphism on fear related characteristics in humans and animal models. Secondly, we will discuss BDNF-TrkB activity regulation by epigenetic, transcriptional and post-translational events, and finally we will discuss TrkB-BDNF signalling in fear learning. BDNF-TrkB and the signalling activated in this particular form of plasticity are becoming crucial players in fear learning and memory thus highlighting these molecules as potential therapeutic targets in fear-related pathologies.
机译:摘要发现恐惧编码和表达的基本机制在心理学,社会学,医学和神经科学等许多领域都很重要。对基于恐惧的病理学的有效治疗取决于了解如何学习和调节恐惧。在恐惧学习和杏仁核突触可塑性所需的分子系统中,脑源性神经营养因子(BDNF)及其高亲和力受体Ntrk2 / TrkB已显示出必不可少的作用。因此,我们将把重点放在三个方面。首先,Bdnf多态性对人类和动物模型中与恐惧相关的特征的影响。其次,我们将讨论表观遗传,转录和翻译后事件对BDNF-TrkB活性的调节,最后,我们将讨论恐惧学习中的TrkB-BDNF信号传导。 BDNF-TrkB和以这种特殊形式的可塑性激活的信号正在成为恐惧学习和记忆中的关键角色,从而突显了这些分子作为与恐惧相关的病理学中潜在的治疗靶标。

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