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Long-Term Plasticity of Neurotransmitter Release: Emerging Mechanisms and Contributions to Brain Function and Disease

机译:神经递质释放的长期可塑性:新兴机制和对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:响应经验,大脑功能的持久变化依赖于多种形式的活动依赖性突触可塑性。其中主要的是神经递质释放的长期增强和长期抑制,它们在整个中枢神经系统中由兴奋性和抑制性突触广泛表达,并且可以动态调节神经回路中的信息流。这篇综述文章探讨了突触前长期可塑性机制和电路功能的贡献的最新进展。越来越多的证据表明,突触前可塑性可能涉及结构变化,突触前蛋白合成和突触信号传导。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,例如新颖性检测,兴奋性/抑制性平衡的改变和感觉适应。另外,突触前的长期可塑性是学习形式的基础,并且其失调参与多种神经精神疾病,包括精神分裂症,自闭症,智力障碍,神经退行性疾病和药物滥用。

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