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Our laboratory operates at the exciting interface between systems neuroscience and biological psychiatry. Our mission is to define the circuit mechanisms by which neurons in the prefrontal cortex contribute to cognitive and emotional processes and to understand how they are disrupted in neuropsychiatric disease states.
We are investigating how diverse neuronal cell types interact within prefrontal microcircuits to mediate various cognitive processes; how they are modulated by monoamines and neurosteroids; and how prefrontal circuits function within systems-level networks. We are particularly interested in how stress, sleep, and other circadian rhythms interact to regulate synaptic remodeling in corticolimbic circuits, especially during adolescence and young adulthood, when major psychiatric disorders most commonly emerge. Our studies leverage a variety of optogenetic tools, two-photon microscopy and other imaging modalities, behavioral assays, and functional MRI in rodent models, healthy humans subjects, and clinical populations.
In the long-term, our work may help to explain how dysregulated synaptic remodeling contributes to circuit dysfunction and ultimately, to the pathogenesis of affective disorders and other neurospsychiatric diseases. This, in turn, may facilitate the development of new treatment modalities and prognostic biomarkers derived from a systems-level understanding of circuit dysfunction in neuropsychiatic diseases.
We are investigating how diverse neuronal cell types interact within prefrontal microcircuits to mediate various cognitive processes; how they are modulated by monoamines and neurosteroids; and how prefrontal circuits function within systems-level networks. We are particularly interested in how stress, sleep, and other circadian rhythms interact to regulate synaptic remodeling in corticolimbic circuits, especially during adolescence and young adulthood, when major psychiatric disorders most commonly emerge. Our studies leverage a variety of optogenetic tools, two-photon microscopy and other imaging modalities, behavioral assays, and functional MRI in rodent models, healthy humans subjects, and clinical populations.
In the long-term, our work may help to explain how dysregulated synaptic remodeling contributes to circuit dysfunction and ultimately, to the pathogenesis of affective disorders and other neurospsychiatric diseases. This, in turn, may facilitate the development of new treatment modalities and prognostic biomarkers derived from a systems-level understanding of circuit dysfunction in neuropsychiatic diseases.
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论文共 170 篇作者统计合作学者相似作者
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Robert N. Fetcho,Puja K. Parekh, Jolin Chou,Margaux Kenwood, Laura Chalenc,David J. Estrin,Megan Johnson,Conor Liston
NEURONno. 3 (2024): 473-+
Biological Psychiatryno. 10 (2024): S51-S52
Nature biotechnologypp.1-11, (2024)
Biological Psychiatryno. 10 (2024): S39
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacologyno. 1 (2024): 343-344
Rachel Rahn,Conor Liston
Immunityno. 3 (2023): 469-471
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