Molecular and pharmacological evidence for a facilitatory functional role of pre‐synaptic GLUK 2/3 kainate receptors on GABA release in rat trigeminal caudal nucleus
Author:
Affiliation:
1. Institute of Pharmacology Catholic University of Sacred Heart Rome Italy
2. Division of Pharmacology University of Naples Federico II Naples Italy
3. Department of Health Sciences University of Molise Campobasso Italy
Publisher
Wiley
Subject
Anesthesiology and Pain Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/j.1532-2149.2012.00122.x
Reference50 articles.
1. Pharmacological characterization of glutamatergic agonists and antagonists at recombinant human homomeric and heteromeric kainate receptors in vitro
2. Trigeminal subnucleus caudalis: beyond homologies with the spinal dorsal horn
3. Cloning of a putative glutamate receptor: A low affinity kainate-binding subunit
4. (S)-2-Amino-3-(3-hydroxy-7,8-dihydro-6H-cyclohepta[d]isoxazol-4-yl)propionic Acid, a Potent and Selective Agonist at the GluR5 Subtype of Ionotropic Glutamate Receptors. Synthesis, Modeling, and Molecular Pharmacology
5. Heteromeric Kainate Receptors Formed by the Coassembly of GluR5, GluR6, and GluR7
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Kainate Receptor Antagonists: Recent Advances and Therapeutic Perspective;International Journal of Molecular Sciences;2023-01-18
2. Discovery of the First Highly Selective Antagonist of the GluK3 Kainate Receptor Subtype;International Journal of Molecular Sciences;2022-08-08
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