Pleiotropic neurotransmitters: neurotransmitter-receptor crosstalk regulates excitation-inhibition balance in social brain functions and pathologies.

IF 3.2 3区 医学 Q2 NEUROSCIENCES
Frontiers in Neuroscience Pub Date : 2025-03-14 eCollection Date: 2025-01-01 DOI:10.3389/fnins.2025.1552145
Anping Chai
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Abstract

Neuronal excitation-inhibition (E/I) balance is essential for maintaining neuronal stability and proper brain functioning. Disruptions in this balance are implicated in various neurological disorders, including autism spectrum disorder, schizophrenia and epilepsy. The E/I balance is thought to be primarily mediated by intrinsic excitability, governed by an array of voltage-gated ion channels, and extrinsic excitability, maintained through a counterbalance between excitatory synaptic transmission primarily mediated by excitatory transmitter glutamate acting on excitatory ion-tropic glutamate receptors and inhibitory synaptic transmissions chiefly mediated by GABA or glycine acting on their respective inhibitory ion-tropic receptors. However, recent studies reveal that neurotransmitters can exhibit interactions that extend beyond their traditional targets, leading to a phenomenon called neurotransmitter-receptor crosstalk. Examples of such crosstalks include earlier discovery of inhibitory glycine functioning as co-transmitter gating on the NMDA subtype of excitatory glutamate receptor, and the most recent demonstration that shows the excitatory glutamate transmitter binds to the inhibitory GABAA receptor, thereby allosterically potentiating its inhibitory function. These studies demonstrate structurally and physiologically important crosstalk between excitatory and inhibitory synaptic transmission, blurring the distinction between the concepts of classic excitatory and inhibitory synaptic transmission. In this article, evidence supporting the forms of excitatory and inhibitory crosstalks will be briefly summarized and their underlying mechanisms will be discussed. Furthermore, this review will discuss the implications of these crosstalks in maintaining the E/I balance, as well as their potential involvement in synaptic plasticity and cognition in the context of social conditions.

多效性神经递质:神经递质-受体串扰调节社会脑功能和病理中的兴奋-抑制平衡。
神经元兴奋-抑制(E/I)平衡是维持神经元稳定和正常脑功能的必要条件。这种平衡的破坏与各种神经系统疾病有关,包括自闭症谱系障碍、精神分裂症和癫痫。E/I平衡被认为主要由内生性兴奋性介导,由一系列电压门控离子通道控制;外源性兴奋性,通过主要由兴奋性递质谷氨酸作用于兴奋性嗜离子受体介导的兴奋性突触传递和主要由GABA或甘氨酸作用于各自的抑制性嗜离子受体介导的抑制性突触传递之间的平衡来维持。然而,最近的研究表明,神经递质可以表现出超越其传统目标的相互作用,导致一种称为神经递质-受体串扰的现象。这种串扰的例子包括早期发现的抑制性甘氨酸在兴奋性谷氨酸受体NMDA亚型上作为共递质门控的功能,以及最近的证明表明,兴奋性谷氨酸递质与抑制性GABAA受体结合,从而变构增强其抑制功能。这些研究证明了兴奋性突触传递和抑制性突触传递之间在结构和生理上的重要串扰,模糊了经典兴奋性突触传递和抑制性突触传递概念之间的区别。本文将简要总结支持兴奋性和抑制性串音形式的证据,并讨论其潜在机制。此外,本文将讨论这些串音在维持E/I平衡方面的意义,以及它们在社会条件下对突触可塑性和认知的潜在参与。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Frontiers in Neuroscience
Frontiers in Neuroscience NEUROSCIENCES-
CiteScore
6.20
自引率
4.70%
发文量
2070
审稿时长
14 weeks
期刊介绍: Neural Technology is devoted to the convergence between neurobiology and quantum-, nano- and micro-sciences. In our vision, this interdisciplinary approach should go beyond the technological development of sophisticated methods and should contribute in generating a genuine change in our discipline.
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