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Olanzapine manipulates neuroactive signals and may onset metabolic disturbances
Pukar Khanal1, Farshid Zargari2,3, Yadu Nandan Dey4
1Department of Pharmacology, NGSM Institute of Pharmaceutical Sciences (NGSMIPS), Nitte (Deemed to be University), Mangalore, India.
Abstract:
Olanzapine is one of the most prescribed atypical antipsychotics to treat psychiatric illness and is associated with weight gain and metabolic disturbance. The present study investigated the olanzapine-regulated metabolic pathways using functional enrichent analysis including binding affinity with G-protein-coupled receptors (GPCRs). Proteins modulated by olanzapine were retrieved from SwissTargetPrediction, DIGEP-Pred, and BindingDB and then enriched in Search Tool for the Retrieval of Interacting Genes/Proteins (STRING) to assess molecular function, biological process, and cellular components including Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways. We used homology modeling to improve the 3D structure for GPCR synapse proteins including dopamine, serotonin, muscarinic, and histamine receptors which were then optimized using molecular dynamics (MD) simulations. The protein-olanzapine binding mechanisms for different GPCR binders were evaluated using molecular docking; later refined by MD simulations. Binding mechanism of olanzapine with D2, 5HT1A, 5HT2A, 5HT2B, 5HT2C, M1, and M2 receptors were created using homology modeling and optimized using MD simulations. In target identification, it was observed that olanzapine majority targeted G-protein coupled receptors. Further, enrichment analysis identified around 76% of the total genes regulated in molecular function, biological process, and cellular components were common including KEGG pathways. Moreover, it was observed that olanzapine had a major potency over the neurotransmitter synapse including neuroactive signals . Olanzapine-induced weight gain and metabolic alterations could be due to the deregulation of multiple synapses like dopamine, serotonin, muscarinic, and histamine at the feeding center followed by cGMP-PKG, cAMP, and PI3K-Akt signaling pathways. HIGHLIGHTSOlanzapine is used in the management of psychiatric illnesses.Olanzapine causes disturbance in lipids and glucosehomeostasis and manipulates energy expenditure.Olanzapine-induced weight gain may occur due to the deregulation of the multiple synapse and cGMP-PKG, cAMP, and PI3K-Akt signaling pathwayCommunicated by Ramaswamy H. Sarma.
Insights
Olanzapine, an antipsychotic, can cause weight gain by disrupting dopamine, serotonin, and histamine pathways. This deregulation affects key signaling pathways involved in energy balance and metabolism.
Area of Science:
- Pharmacology and Molecular Biology
- Neuroscience
- Metabolic Research
Background:
- Olanzapine is a widely prescribed atypical antipsychotic for psychiatric disorders.
- It is frequently associated with significant weight gain and metabolic disturbances, impacting patient adherence and outcomes.
Purpose of the Study:
- To investigate the molecular mechanisms underlying olanzapine-induced metabolic alterations.
- To identify the specific G-protein-coupled receptors (GPCRs) and signaling pathways targeted by olanzapine.
Main Methods:
- Functional enrichment analysis using STRING database.
- Protein-ligand binding affinity prediction and retrieval from SwissTargetPrediction, DIGEP-Pred, and BindingDB.
- Homology modeling, molecular docking, and molecular dynamics (MD) simulations for GPCR-olanzapine interactions.
- Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis.
Main Results:
- Olanzapine primarily targets G-protein coupled receptors, including dopamine, serotonin, muscarinic, and histamine receptors.
- Enrichment analysis revealed commonalities in molecular function, biological processes, and cellular components, including KEGG pathways.
- Olanzapine significantly impacts neurotransmitter synapses and neuroactive signaling.
- Deregulation of dopamine, serotonin, muscarinic, and histamine synapses at the feeding center, along with cGMP-PKG, cAMP, and PI3K-Akt signaling pathways, is linked to weight gain and metabolic changes.
Conclusions:
- Olanzapine-induced weight gain and metabolic disturbances are likely caused by the disruption of multiple neurotransmitter systems.
- Targeting specific GPCRs and associated signaling pathways offers potential avenues for mitigating olanzapine's side effects.
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