Glutamate Receptor Abnormalities in Schizophrenia: Implications for Innovative Treatments
Overview
Affiliations
Schizophrenia is a devastating psychiatric illness that afflicts 1% of the population worldwide, resulting in substantial impact to patients, their families, and health care delivery systems. For many years, schizophrenia has been felt to be associated with dysregulated dopaminergic neurotransmission as a key feature of the pathophysiology of the illness. Although numerous studies point to dopaminergic abnormalities in schizophrenia, dopamine dysfunction cannot completely account for all of the symptoms seen in schizophrenia, and dopamine-based treatments are often inadequate and can be associated with serious side effects. More recently, converging lines of evidence have suggested that there are abnormalities of glutamate transmission in schizophrenia. Glutamatergic neurotransmission involves numerous molecules that facilitate glutamate release, receptor activation, glutamate reuptake, and other synaptic activities. Evidence for glutamatergic abnormalities in schizophrenia primarily has implicated the NMDA and AMPA subtypes of the glutamate receptor. The expression of these receptors and other molecules associated with glutamate neurotransmission has been systematically studied in the brain in schizophrenia. These studies have generally revealed region- and molecule-specific changes in glutamate receptor transcript and protein expression in this illness. Given that glutamatergic neurotransmission has been implicated in the pathophysiology of schizophrenia, recent drug development efforts have targeted the glutamate system. Much effort to date has focused on modulation of the NMDA receptor, although more recently other glutamate receptors and transporters have been the targets of drug development. These efforts have been promising thus far, and ongoing efforts to develop additional drugs that modulate glutamatergic neurotransmission are underway that may hold the potential for novel classes of more effective treatments for this serious psychiatric illness.
Impact of neuroinflammation on brain glutamate and dopamine signalling in schizophrenia: an update.
Nayak U, Manikkath J, Arora D, Mudgal J Metab Brain Dis. 2025; 40(2):119.
PMID: 39907868 PMC: 11799129. DOI: 10.1007/s11011-025-01548-3.
Lucafo M, Bidoli C, Franzin M, Eitan E, Rau S, Amaddeo A Clin Pharmacol Ther. 2024; 117(1):174-183.
PMID: 39164873 PMC: 11652811. DOI: 10.1002/cpt.3420.
Potential Roles for the GluN2D NMDA Receptor Subunit in Schizophrenia.
Vinnakota C, Hudson M, Jones N, Sundram S, Hill R Int J Mol Sci. 2023; 24(14).
PMID: 37511595 PMC: 10380280. DOI: 10.3390/ijms241411835.
Dong B, Yue Y, Dong H, Wang Y Front Mol Neurosci. 2023; 16:1174738.
PMID: 37396784 PMC: 10308130. DOI: 10.3389/fnmol.2023.1174738.
The Difficult Path to the Discovery of Novel Treatments in Psychiatric Disorders.
Gribkoff V, Kaczmarek L Adv Neurobiol. 2023; 30:255-285.
PMID: 36928854 PMC: 10599454. DOI: 10.1007/978-3-031-21054-9_11.