5-羟色胺能
神经科学
神经传递
血清素
前脑
重性抑郁障碍
内科学
神经药理学
医学
心理学
再摄取抑制剂
受体
中枢神经系统
认知
作者
Krishna C. Vadodaria,Yuan Ji,Michelle Skime,Apuã C.M. Paquola,Timothy J. Nelson,Daniel K. Hall‐Flavin,Callie Fredlender,Kelly J. Heard,Yalin Deng,Amy Le,Sonia Dave,Lianna Fung,Xinyi Li,Maria C. Marchetto,Richard M. Weinshilboum,Fred H. Gage
标识
DOI:10.1038/s41380-019-0363-y
摘要
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI