嘌呤能受体
神经科学
神经传递
突触可塑性
突触后电位
兴奋性突触后电位
生物
变质塑性
嘌呤能信号
突触药理学
突触疲劳
抑制性突触后电位
受体
腺苷受体
生物化学
兴奋剂
作者
Ulyana Lalo,Yuriy Pankratov
标识
DOI:10.1016/j.neuropharm.2023.109477
摘要
ATP released from the synaptic terminals and astrocytes can activate neuronal P2 receptors at a variety of locations across the CNS. Although the postsynaptic ATP-mediated signalling does not bring a major contribution into the excitatory transmission, it is instrumental for slow and diffuse modulation of synaptic dynamics and neuronal firing in many CNS areas. Neuronal P2X and P2Y receptors can be activated by ATP released from the synaptic terminals, astrocytes and microglia and thereby can participate in the regulation of synaptic homeostasis and plasticity. There is growing evidence of importance of purinergic regulation of synaptic transmission in different physiological and pathological contexts. Here, we review the main mechanisms underlying the complexity and diversity of purinergic signalling and purinergic modulation in central neurons.
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