Presynaptic glutamate receptors in nociception

IF 12 1区 医学 Q1 PHARMACOLOGY & PHARMACY Pharmacology & Therapeutics Pub Date : 2023-11-01 DOI:10.1016/j.pharmthera.2023.108539
Rou-Gang Xie , Guang-Yin Xu , Sheng-Xi Wu , Ceng Luo
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Abstract

Chronic pain is a frequent, distressing and poorly understood health problem. Plasticity of synaptic transmission in the nociceptive pathways after inflammation or injury is assumed to be an important cellular basis for chronic, pathological pain. Glutamate serves as the main excitatory neurotransmitter at key synapses in the somatosensory nociceptive pathways, in which it acts on both ionotropic and metabotropic glutamate receptors. Although conventionally postsynaptic, compelling anatomical and physiological evidence demonstrates the presence of presynaptic glutamate receptors in the nociceptive pathways. Presynaptic glutamate receptors play crucial roles in nociceptive synaptic transmission and plasticity. They modulate presynaptic neurotransmitter release and synaptic plasticity, which in turn regulates pain sensitization. In this review, we summarize the latest understanding of the expression of presynaptic glutamate receptors in the nociceptive pathways, and how they contribute to nociceptive information processing and pain hypersensitivity associated with inflammation / injury. We uncover the cellular and molecular mechanisms of presynaptic glutamate receptors in shaping synaptic transmission and plasticity to mediate pain chronicity, which may provide therapeutic approaches for treatment of chronic pain.

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伤害感受中的突触前谷氨酸受体。
慢性疼痛是一个常见的、令人痛苦的、鲜为人知的健康问题。炎症或损伤后伤害性通路中突触传递的可塑性被认为是慢性病理性疼痛的重要细胞基础。谷氨酸是体感伤害性通路中关键突触的主要兴奋性神经递质,在该通路中,谷氨酸同时作用于离子型和代谢型谷氨酸受体。尽管传统上是突触后的,但令人信服的解剖学和生理学证据表明,伤害性通路中存在突触前谷氨酸受体。突触前谷氨酸受体在伤害性突触传递和可塑性中起着至关重要的作用。它们调节突触前神经递质的释放和突触可塑性,进而调节疼痛致敏。在这篇综述中,我们总结了对突触前谷氨酸受体在伤害性通路中表达的最新理解,以及它们如何促进与炎症/损伤相关的伤害性信息处理和疼痛超敏反应。我们揭示了突触前谷氨酸受体在形成突触传递和可塑性以介导疼痛慢性性方面的细胞和分子机制,这可能为治疗慢性疼痛提供治疗方法。
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来源期刊
CiteScore
23.00
自引率
0.70%
发文量
222
审稿时长
90 days
期刊介绍: Pharmacology & Therapeutics, in its 20th year, delivers lucid, critical, and authoritative reviews on current pharmacological topics.Articles, commissioned by the editor, follow specific author instructions.This journal maintains its scientific excellence and ranks among the top 10 most cited journals in pharmacology.
期刊最新文献
Lipoprotection in cardiovascular diseases. Nutraceuticals target androgen receptor-splice variants (AR-SV) to manage castration resistant prostate cancer (CRPC). Editorial Board The voltage sensitivity of G-protein coupled receptors: Unraveling molecular mechanisms and physiological implications. Oxytocin in neurodevelopmental disorders: Autism spectrum disorder and Prader-Willi syndrome.
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