Effects of antipsychotic drugs on energy metabolism

• Published in: European archives of psychiatry and clinical neuroscience Vol. 274; no. 5; pp. 1125 - 1135
• Main Authors: Panizzutti, Bruna, Bortolasci, Chiara C., Spolding, Briana, Kidnapillai, Srisaiyini, Connor, Timothy, Martin, Sheree D., Truong, Trang T. T., Liu, Zoe S. J., Gray, Laura, Kowalski, Greg M., McGee, Sean L., Kim, Jee Hyun, Berk, Michael, Walder, Ken
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Berlin Heidelberg 01.08.2024; Springer; Springer Nature B.V
• Subjects: Allosteric properties; Analysis; Antipsychotic drugs; Antipsychotics; Aripiprazole; Bioenergetics; Clozapine; Drug metabolism; Drugs; Energy metabolism; Enzymatic activity; Gas chromatography; Gene expression; Genes; Glycolysis; Health aspects; Mass spectrometry; Mass spectroscopy; Medicine; Medicine & Public Health; Mental disorders; Metabolism; Metabolites; Metabolomics; Mitochondria; Nervous system diseases; Neurosciences; Original Paper; Oxidative phosphorylation; Phosphorylation; Post-transcription; Post-translation; Psychiatry; Psychotropic drugs; Risperidone; Schizophrenia; Therapeutic applications; Tricarboxylic acid cycle; Antipsychotics; Energy metabolism; Mitochondria; Neuroscience; Neurons; Mental health; Schizophrenia; Psychiatry
• DOI: 10.1007/s00406-023-01727-2
• ISSN: 0940-1334; 1433-8491

Schizophrenia (SCZ) is a complex neuropsychiatric disorder associated with altered bioenergetic pathways and mitochondrial dysfunction. Antipsychotic medications, both first and second-generation, are commonly prescribed to manage SCZ symptoms, but their direct impact on mitochondrial function remains poorly understood. In this study, we investigated the effects of commonly prescribed antipsychotics on bioenergetic pathways in cultured neurons. We examined the impact of risperidone, aripiprazole, amisulpride, and clozapine on gene expression, mitochondrial bioenergetic profile, and targeted metabolomics after 24-h treatment, using RNA-seq, Seahorse XF24 Flux Analyser, and gas chromatography–mass spectrometry (GC–MS), respectively. Risperidone treatment reduced the expression of genes involved in oxidative phosphorylation, the tricarboxylic acid cycle, and glycolysis pathways, and it showed a tendency to decrease basal mitochondrial respiration. Aripiprazole led to dose-dependent reductions in various mitochondrial function parameters without significantly affecting gene expression. Aripiprazole, amisulpride and clozapine treatment showed an effect on the tricarboxylic acid cycle metabolism, leading to more abundant metabolite levels. Antipsychotic drug effects on mitochondrial function in SCZ are multifaceted. While some drugs have greater effects on gene expression, others appear to exert their effects through enzymatic post-translational or allosteric modification of enzymatic activity. Understanding these effects is crucial for optimising treatment strategies for SCZ. Novel therapeutic interventions targeting energy metabolism by post-transcriptional pathways might be more effective as these can more directly and efficiently regulate energy production.