Serotonin-induced hyperactivity in SSRI-resistant major depressive disorder patient-derived neurons.
Krishna C VadodariaYuan JiMichelle SkimeApua PaquolaTimothy NelsonDaniel Hall-FlavinCallie FredlenderKelly J HeardYalin DengAmy T LeSonia DaveLianna FungXinyi LiMaria C MarchettoRichard WeinshilboumFred H GagePublished in: Molecular psychiatry (2019)
Selective serotonin reuptake inhibitors (SSRIs) are the most prescribed antidepressants. They regulate serotonergic neurotransmission, but it remains unclear how altered serotonergic neurotransmission may contribute to the SSRI resistance observed in approximately 30% of major depressive disorder (MDD) patients. Patient stratification based on pharmacological responsiveness and the use of patient-derived neurons may make possible the discovery of disease-relevant neural phenotypes. In our study from a large cohort of well-characterized MDD patients, we have generated induced pluripotent stem cells (iPSCs) from SSRI-remitters and SSRI-nonremitters. We studied serotonergic neurotransmission in patient forebrain neurons in vitro and observed that nonremitter patient-derived neurons displayed serotonin-induced hyperactivity downstream of upregulated excitatory serotonergic receptors, in contrast to what is seen in healthy and remitter patient-derived neurons. Our data suggest that postsynaptic forebrain hyperactivity downstream of SSRI treatment may play a role in SSRI resistance in MDD.
Keyphrases
- major depressive disorder
- bipolar disorder
- end stage renal disease
- spinal cord
- ejection fraction
- newly diagnosed
- chronic kidney disease
- induced pluripotent stem cells
- prognostic factors
- case report
- high glucose
- peritoneal dialysis
- magnetic resonance imaging
- magnetic resonance
- artificial intelligence
- diabetic rats
- high throughput
- endothelial cells
- oxidative stress
- deep learning
- smoking cessation