4.7 Article

ATP-mediated signalling in the central synapses

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NEUROPHARMACOLOGY
卷 229, 期 -, 页码 -

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PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neuropharm.2023.109477

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ATP released from synaptic terminals and astrocytes can activate neuronal P2 receptors, contributing to slow and diffuse modulation of synaptic dynamics and neuronal firing in the CNS. Neuronal P2X and P2Y receptors can be activated by ATP released from synaptic terminals, astrocytes, and microglia, participating in the regulation of synaptic homeostasis and plasticity. Purinergic regulation of synaptic transmission plays an important role in various physiological and pathological contexts.
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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