About 74% of schizophrenia patients discontinue use within 18 months of therapy due to either poor tolerability of incomplete efficacy. This underscores the need for novel and more effective therapeutic targets for schizophrenia treatment. Recent clinical studies suggested that the metabotropic glutamate 2/3 receptor (mGlu2/3) agonist LY2140023 had antipsychotic properties, providing a new alternative for the treatment of schizophrenia. Unfortunately, follow-up studies with LY2140023 showed either inconclusive results, or clinical outcomes that were not different from placebo. Our published data demonstrated that chronic treatment with atypical antipsychotics, such as with clozapine or risperidone, but not with typical antipsychotics, such as haloperidol, induces repressive histone modifications at the mGlu2 (Grm2) promoter in mouse and human frontal cortex. Remarkably, the translational significance of our preclinical findings has been validated by a recent post-hoc analysis: patients previously treated with typical antipsychotics responded to LY2140023, whereas the effects of LY2140023 in patients previously exposed to atypical antipsychotics did not differ from placebo. Our published and preliminary data also suggest that these repressive epigenetic modifications occurred through a signaling mechanism that requires a serotonin 5-HT2A receptor (5HT2A)-dependent enhancement of NF-?B transcriptional function via I?B?, which is followed by NF-?B-dependent up-regulation and increased binding of histone deacetylase 2 (HDAC2) to the mGlu2 promoter. We have focused our investigation on the potential role of HDAC2 as the basic molecular mechanism underlying down-regulation of mGlu2 expression after chronic antipsychotic drug treatment. Our results are expected to provide a route to the identification of new and more effective epigenetic drugs to improve the currently limited response to treatment with glutamate antipsychotics.

Public Health Relevance

Schizophrenia is a chronic, debilitating psychotic mental disorder that affects about 1% of the population worldwide. We have discovered that administration of histone deacetylase inhibitors prevents repressive epigenetic changes induced by chronic treatment with atypical antipsychotic drugs, augmenting therapeutic- related effects in rodent models. A better understanding of the epigenetic mechanisms through which histone deacetylase inhibitors potentiate the biochemical and behavioral responses to antipsychotic drugs will help in discovering more effective treatments to improve the clinical efficacy of the currently available antipsychotic medications.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
5R01MH111940-02
Application #
9402660
Study Section
Pathophysiological Basis of Mental Disorders and Addictions Study Section (PMDA)
Program Officer
Nadler, Laurie S
Project Start
2017-01-01
Project End
2021-12-31
Budget Start
2018-01-01
Budget End
2018-12-31
Support Year
2
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Virginia Commonwealth University
Department
Physiology
Type
Schools of Medicine
DUNS #
105300446
City
Richmond
State
VA
Country
United States
Zip Code
23298
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López-Giménez, Juan F; González-Maeso, Javier (2017) Hallucinogens and Serotonin 5-HT2A Receptor-Mediated Signaling Pathways. Curr Top Behav Neurosci :
Fomsgaard, Luna; Moreno, Jose L; de la Fuente Revenga, Mario et al. (2017) Differences in 5-HT2A and mGlu2 Receptor Expression Levels and Repressive Epigenetic Modifications at the 5-HT2A Promoter Region in the Roman Low- (RLA-I) and High- (RHA-I) Avoidance Rat Strains. Mol Neurobiol :
Oliveras, Ignasi; Sánchez-González, Ana; Sampedro-Viana, Daniel et al. (2017) Differential effects of antipsychotic and propsychotic drugs on prepulse inhibition and locomotor activity in Roman high- (RHA) and low-avoidance (RLA) rats. Psychopharmacology (Berl) 234:957-975
Fribourg, Miguel; Logothetis, Diomedes E; González-Maeso, Javier et al. (2017) Elucidation of molecular kinetic schemes from macroscopic traces using system identification. PLoS Comput Biol 13:e1005376