| Literature DB >> 30700803 |
Krishna C Vadodaria1, Yuan Ji2,3, Michelle Skime4, Apua Paquola1,5, Timothy Nelson3, Daniel Hall-Flavin4, Callie Fredlender1, Kelly J Heard1, Yalin Deng1, Amy T Le1, Sonia Dave1, Lianna Fung1, Xinyi Li1, Maria C Marchetto1, Richard Weinshilboum3, Fred H Gage6.
Abstract
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.Entities:
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Year: 2019 PMID: 30700803 DOI: 10.1038/s41380-019-0363-y
Source DB: PubMed Journal: Mol Psychiatry ISSN: 1359-4184 Impact factor: 13.437