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首页> 外文期刊>Annual Review of Neuroscience >Long-Term Plasticity of Neurotransmitter Release: Emerging Mechanisms and Contributions to Brain Function and Disease
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Long-Term Plasticity of Neurotransmitter Release: Emerging Mechanisms and Contributions to Brain Function and Disease

机译:神经递质的长期可塑性:新兴机制和脑功能和疾病的贡献

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摘要

Long-lasting changes of brain function in response to experience rely on diverse forms of activity-dependent synaptic plasticity. Chief among them are long-term potentiation and long-term depression of neurotransmitter release, which are widely expressed by excitatory and inhibitory synapses throughout the central nervous system and can dynamically regulate information flow in neural circuits. This review article explores recent advances in presynaptic long-term plasticity mechanisms and contributions to circuit function. Growing evidence indicates that presynaptic plasticity may involve structural changes, presynaptic protein synthesis, and transsynaptic signaling. Presynaptic long-term plasticity can alter the short-term dynamics of neurotransmitter release, thereby contributing to circuit computations such as novelty detection, modifications of the excitatory/ inhibitory balance, and sensory adaptation. In addition, presynaptic long-term plasticity underlies forms of learning and its dysregulation participates in several neuropsychiatric conditions, including schizophrenia, autism, intellectual disabilities, neurodegenerative diseases, and drug abuse.
机译:脑功能的长期变化,以响应经验依赖于多种活动依赖性突触可塑性的经验。它们中间的主要职业是长期的增强性和神经递质释放的长期抑制,这些释放是广泛的兴奋性和抑制突触的兴奋和抑制突触,并且可以动态调节神经电路中的信息流。该综述文章探讨了突触前长期可塑性机制的最近进步和对电路功能的贡献。日益增长的证据表明突触前可塑性可能涉及结构性变化,突触蛋白合成和突触突触信号。突触前的长期可塑性可以改变神经递质释放的短期动态,从而有助于电路计算,例如新奇检测,兴奋/抑制平衡的修改,以及感官适应。此外,突触前的长期可塑性是学习的形式,其失呼量参与了几种神经精神病症,包括精神分裂症,自闭症,智力疾病,神经退行性疾病和药物滥用。

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