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Glycine binding sites of presynaptic NMDA receptors may tonically regulate glutamate release in the rat visual cortex.
J Neurophysiol. 2007 Jan; 97(1):817-23.JN

Abstract

In the CNS, activation of N-methyl-D-aspartate receptor (NMDA-R) glycine binding sites is a prerequisite for activation of postsynaptic NMDA-Rs by the excitatory neurotransmitter glutamate. Here we provide electrophysiological evidence that the glycine binding sites of presynaptic NMDA-Rs regulate glutamate release in layer II/III pyramidal neurons of the rat visual cortex. Specifically, our results reveal that the frequency of miniature excitatory postsynaptic currents is significantly reduced by 7-chloro-kynurenic acid (7-Cl KYNA), a NMDA-R glycine binding site antagonist, and glycine or D-serine reverses this effect. Similar results are obtained when the open-channel NMDA receptor blocker, MK-801, is included in the recording pipette. Our data indicate that the glycine binding site of postsynaptic NMDA-Rs is not saturated. Moreover, they suggest that presynaptic NMDA-Rs are located in layer II/III pyramidal neurons of the rat visual cortex and that the glycine binding site of presynaptic NMDA-Rs tonically regulates glutamate release.

Authors+Show Affiliations

Dept. of Physiology, School of Medicine, Xi'an Jiaotong University, Zhuque Dajie 205, Xi'an, Shaanxi 710061, PR China.No affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

17093111

Citation

Li, Yan-Hai, and Tai-Zhen Han. "Glycine Binding Sites of Presynaptic NMDA Receptors May Tonically Regulate Glutamate Release in the Rat Visual Cortex." Journal of Neurophysiology, vol. 97, no. 1, 2007, pp. 817-23.
Li YH, Han TZ. Glycine binding sites of presynaptic NMDA receptors may tonically regulate glutamate release in the rat visual cortex. J Neurophysiol. 2007;97(1):817-23.
Li, Y. H., & Han, T. Z. (2007). Glycine binding sites of presynaptic NMDA receptors may tonically regulate glutamate release in the rat visual cortex. Journal of Neurophysiology, 97(1), 817-23.
Li YH, Han TZ. Glycine Binding Sites of Presynaptic NMDA Receptors May Tonically Regulate Glutamate Release in the Rat Visual Cortex. J Neurophysiol. 2007;97(1):817-23. PubMed PMID: 17093111.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Glycine binding sites of presynaptic NMDA receptors may tonically regulate glutamate release in the rat visual cortex. AU - Li,Yan-Hai, AU - Han,Tai-Zhen, Y1 - 2006/11/08/ PY - 2006/11/10/pubmed PY - 2007/3/10/medline PY - 2006/11/10/entrez SP - 817 EP - 23 JF - Journal of neurophysiology JO - J Neurophysiol VL - 97 IS - 1 N2 - In the CNS, activation of N-methyl-D-aspartate receptor (NMDA-R) glycine binding sites is a prerequisite for activation of postsynaptic NMDA-Rs by the excitatory neurotransmitter glutamate. Here we provide electrophysiological evidence that the glycine binding sites of presynaptic NMDA-Rs regulate glutamate release in layer II/III pyramidal neurons of the rat visual cortex. Specifically, our results reveal that the frequency of miniature excitatory postsynaptic currents is significantly reduced by 7-chloro-kynurenic acid (7-Cl KYNA), a NMDA-R glycine binding site antagonist, and glycine or D-serine reverses this effect. Similar results are obtained when the open-channel NMDA receptor blocker, MK-801, is included in the recording pipette. Our data indicate that the glycine binding site of postsynaptic NMDA-Rs is not saturated. Moreover, they suggest that presynaptic NMDA-Rs are located in layer II/III pyramidal neurons of the rat visual cortex and that the glycine binding site of presynaptic NMDA-Rs tonically regulates glutamate release. SN - 0022-3077 UR - https://www.unboundmedicine.com/medline/citation/17093111/Glycine_binding_sites_of_presynaptic_NMDA_receptors_may_tonically_regulate_glutamate_release_in_the_rat_visual_cortex_ L2 - https://journals.physiology.org/doi/10.1152/jn.00980.2006?url_ver=Z39.88-2003&rfr_id=ori:rid:crossref.org&rfr_dat=cr_pub=pubmed DB - PRIME DP - Unbound Medicine ER -