Time and space profiling ofNMDAreceptor co‐agonist functions

兴奋剂 NMDA受体 神经科学 受体 化学 细胞生物学 计算生物学 计算机科学 生物 生物化学
作者
Jean‐Pierre Mothet,Matildé Le Bail,Jean‐Marie Billard
出处
期刊:Journal of Neurochemistry [Wiley]
卷期号:135 (2): 210-225 被引量:89
标识
DOI:10.1111/jnc.13204
摘要

Abstract The N ‐Methyl D‐Aspartic acid ( NMDA ) receptors ( NMDAR ) are key tetrameric ionotropic glutamate receptors that transduce glutamatergic signals throughout the central nervous system ( CNS ) and spinal cord. Although NMDAR s are diverse in their subunit composition, subcellular localization, and biophysical and pharmacological properties, their activation always requires the binding of a co‐agonist that has long been thought to be glycine. However, intense research over the last decade has challenged this classical model by showing that another amino acid, d ‐serine, is the preferential co‐agonist for a subset of synaptic NMDAR s in many areas of the adult brain. Nowadays, a totally new picture of glutamatergic synapses at work is emerging where both glycine and d ‐serine are involved in a complex interplay to regulate NMDAR functions in the CNS following time and space constraints. The purpose of this review was to highlight the particular role of each co‐agonist in modulating NMDAR ‐dependent activities in healthy and diseased brains. We have herein integrated our most advanced knowledge of how glycine and d ‐serine may orchestrate synapse dynamics and drive neuronal network activity in a time‐ and synapse‐specific manner and how changes in synaptic availability of these amino acids may contribute to cognitive impairments such as those associated with healthy aging, epilepsy, and schizophrenia. image The N ‐Methyl D‐Aspartic acid (NMDA) subtype of glutamate receptors are central to many physiological functions and are linked to brain disorders. Their functions require glutamate and a co‐agonist d ‐serine or glycine. After years of intense research and controversy on the identity of the amino acid that serves as the right co‐agonist, we are just entering a new era of consensus where glycine and d ‐serine are teaming up to regulate the function of different subsets of NMDA receptors and at different synapses during different time windows of brain development.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
斯文败类应助Anqiang采纳,获得10
1秒前
ANK完成签到,获得积分10
1秒前
白马爱毛驴完成签到,获得积分10
1秒前
2秒前
琉光完成签到,获得积分10
2秒前
2秒前
量子星尘发布了新的文献求助10
2秒前
仁爱誉完成签到,获得积分10
3秒前
怡然的雪柳完成签到,获得积分10
3秒前
XF完成签到,获得积分10
4秒前
hsss完成签到,获得积分10
4秒前
wakkkkk完成签到,获得积分10
4秒前
智慧金刚完成签到 ,获得积分10
4秒前
矮小的飞松完成签到,获得积分10
4秒前
Love完成签到,获得积分10
5秒前
5秒前
5秒前
goldNAN完成签到,获得积分10
6秒前
大成子完成签到,获得积分10
6秒前
科隆龙完成签到,获得积分10
6秒前
NERV发布了新的文献求助10
6秒前
Fryanto完成签到,获得积分10
7秒前
优美甜瓜完成签到,获得积分10
7秒前
雪白炎彬完成签到,获得积分10
7秒前
周星星完成签到,获得积分10
8秒前
simbol发布了新的文献求助10
8秒前
失眠的香菇完成签到 ,获得积分10
8秒前
Yolo完成签到,获得积分10
8秒前
kehan完成签到,获得积分10
8秒前
饿了么滴完成签到,获得积分10
8秒前
木悠完成签到,获得积分10
8秒前
包包包包完成签到,获得积分10
8秒前
8秒前
王大锤完成签到,获得积分10
8秒前
继往开来完成签到,获得积分10
9秒前
Love发布了新的文献求助10
9秒前
一只生物狗完成签到,获得积分10
10秒前
稳重的蜜蜂完成签到,获得积分10
11秒前
碧蓝的母鸡完成签到,获得积分10
11秒前
U2完成签到,获得积分10
11秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
List of 1,091 Public Pension Profiles by Region 1001
Active-site design in Cu-SSZ-13 curbs toxic hydrogen cyanide emissions 500
On the application of advanced modeling tools to the SLB analysis in NuScale. Part I: TRACE/PARCS, TRACE/PANTHER and ATHLET/DYN3D 500
L-Arginine Encapsulated Mesoporous MCM-41 Nanoparticles: A Study on In Vitro Release as Well as Kinetics 500
Elements of Evolutionary Genetics 400
Unraveling the Causalities of Genetic Variations - Recent Advances in Cytogenetics 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 生物化学 物理 纳米技术 计算机科学 内科学 化学工程 复合材料 物理化学 基因 遗传学 催化作用 冶金 量子力学 光电子学
热门帖子
关注 科研通微信公众号,转发送积分 5464219
求助须知:如何正确求助?哪些是违规求助? 4568734
关于积分的说明 14314327
捐赠科研通 4495044
什么是DOI,文献DOI怎么找? 2462574
邀请新用户注册赠送积分活动 1451459
关于科研通互助平台的介绍 1427057