Spencer K Cooke, Andrea J Martin, Robert C Spencer, Shannon E Nicol, Craig W Berridge
{"title":"Neurochemical and Circuit Heterogeneity of Cognition-Modulating Prefrontal Corticotropin-Releasing Factor Neurons.","authors":"Spencer K Cooke, Andrea J Martin, Robert C Spencer, Shannon E Nicol, Craig W Berridge","doi":"10.1016/j.biopsych.2025.03.011","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Impairment of prefrontal cortex (PFC)-dependent cognition is associated with multiple psychiatric disorders. Development of more effective treatments for this form of cognitive dysfunction is hindered by our limited understanding of the neurobiology underlying PFC-dependent cognition. We previously identified a robust population of corticotropin releasing factor (CRF) neurons in the caudal dorsomedial PFC (dmPFC) of rats that impair both working memory and sustained attention. Although the working memory actions of these neurons involved local CRF release, the sustained attention actions were not. These results suggest potential heterogeneity within this population of CRF neurons, including the potential existence of both GABAergic (CRF<sub>GABA</sub>) interneurons and glutamatergic (CRF<sub>Glu</sub>) CRF projection neurons.</p><p><strong>Methods: </strong>Immunohistochemical analyses first identified both CRF<sub>GABA</sub> and CRF<sub>Glu</sub> neurons in the caudal dmPFC. Intersectional viral vector chemogenetic approaches were then used to assess the effects of activating caudal dmPFC CRF<sub>Glu</sub> and CRF<sub>GABA</sub> neurons on working memory and sustained attention in males and females (tested outside of proestrus).</p><p><strong>Results: </strong>CRF<sub>Glu</sub> neurons comprised a majority (85%) of caudal dmPFC CRF neurons, while remaining were identified as CRF<sub>GABA</sub> neurons. For both females and males, activation of caudal dmPFC CRF<sub>GABA</sub> neurons impaired working memory but not sustained attention, while activation of CRF<sub>Glu</sub> neurons impaired both working memory and sustained attention. Interestingly, the working memory actions of both CRF<sub>GABA</sub> and CRF<sub>Glu</sub> neurons were dependent on local CRF receptors.</p><p><strong>Conclusion: </strong>These results advance our understanding of the neurobiology of PFC-dependent cognition and potential mechanisms through which cognitive dysfunction could arise.</p>","PeriodicalId":8918,"journal":{"name":"Biological Psychiatry","volume":" ","pages":""},"PeriodicalIF":9.6000,"publicationDate":"2025-03-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biological Psychiatry","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.biopsych.2025.03.011","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Impairment of prefrontal cortex (PFC)-dependent cognition is associated with multiple psychiatric disorders. Development of more effective treatments for this form of cognitive dysfunction is hindered by our limited understanding of the neurobiology underlying PFC-dependent cognition. We previously identified a robust population of corticotropin releasing factor (CRF) neurons in the caudal dorsomedial PFC (dmPFC) of rats that impair both working memory and sustained attention. Although the working memory actions of these neurons involved local CRF release, the sustained attention actions were not. These results suggest potential heterogeneity within this population of CRF neurons, including the potential existence of both GABAergic (CRFGABA) interneurons and glutamatergic (CRFGlu) CRF projection neurons.
Methods: Immunohistochemical analyses first identified both CRFGABA and CRFGlu neurons in the caudal dmPFC. Intersectional viral vector chemogenetic approaches were then used to assess the effects of activating caudal dmPFC CRFGlu and CRFGABA neurons on working memory and sustained attention in males and females (tested outside of proestrus).
Results: CRFGlu neurons comprised a majority (85%) of caudal dmPFC CRF neurons, while remaining were identified as CRFGABA neurons. For both females and males, activation of caudal dmPFC CRFGABA neurons impaired working memory but not sustained attention, while activation of CRFGlu neurons impaired both working memory and sustained attention. Interestingly, the working memory actions of both CRFGABA and CRFGlu neurons were dependent on local CRF receptors.
Conclusion: These results advance our understanding of the neurobiology of PFC-dependent cognition and potential mechanisms through which cognitive dysfunction could arise.
期刊介绍:
Biological Psychiatry is an official journal of the Society of Biological Psychiatry and was established in 1969. It is the first journal in the Biological Psychiatry family, which also includes Biological Psychiatry: Cognitive Neuroscience and Neuroimaging and Biological Psychiatry: Global Open Science. The Society's main goal is to promote excellence in scientific research and education in the fields related to the nature, causes, mechanisms, and treatments of disorders pertaining to thought, emotion, and behavior. To fulfill this mission, Biological Psychiatry publishes peer-reviewed, rapid-publication articles that present new findings from original basic, translational, and clinical mechanistic research, ultimately advancing our understanding of psychiatric disorders and their treatment. The journal also encourages the submission of reviews and commentaries on current research and topics of interest.