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Article: Ventromedial prefrontal cortex stimulation enhances memory and hippocampal neurogenesis in the middle-aged rats

TitleVentromedial prefrontal cortex stimulation enhances memory and hippocampal neurogenesis in the middle-aged rats
Authors
KeywordsNeurogenesis
Learning and memory
High-frequency stimulation
Hippocampus
Ventromedial prefrontal cortex
Issue Date2015
PublishereLife Sciences Publications Ltd.
Citation
eLife, 2015, v. 2015, n. 4 How to Cite?
Abstract© 2015, eLife Sciences Publications Ltd. All Rights Reserved. Memory dysfunction is a key symptom of age-related dementia. Although recent studies have suggested positive effects of electrical stimulation for memory enhancement, its potential targets remain largely unknown. In this study, we hypothesized that spatially targeted deep brain stimulation of ventromedial prefrontal cortex enhanced memory functions in a middle-aged rat model. Our results show that acute stimulation enhanced the short-, but not the long-term memory in the novel-object recognition task. Interestingly, after chronic high-frequency stimulation, both the short- and long-term memories were robustly improved in the novel-object recognition test and Morris water-maze spatial task compared to sham. Our results also demonstrated that chronic ventromedial prefrontal cortex high-frequency stimulation upregulated neurogenesis-associated genes along with enhanced hippocampal cell proliferation. Importantly, these memory behaviors were strongly correlated with the hippocampal neurogenesis. Overall, these findings suggest that chronic ventromedial prefrontal cortex high-frequency stimulation may serve as a novel effective therapeutic target for dementia-related disorders.
Persistent Identifierhttp://hdl.handle.net/10722/219890
ISSN
2023 Impact Factor: 6.4
2023 SCImago Journal Rankings: 3.932
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLiu, Albert-
dc.contributor.authorJain, Neeraj-
dc.contributor.authorVyas, Ajai-
dc.contributor.authorLim, Lee Wei-
dc.date.accessioned2015-09-24T04:44:17Z-
dc.date.available2015-09-24T04:44:17Z-
dc.date.issued2015-
dc.identifier.citationeLife, 2015, v. 2015, n. 4-
dc.identifier.issn2050-084X-
dc.identifier.urihttp://hdl.handle.net/10722/219890-
dc.description.abstract© 2015, eLife Sciences Publications Ltd. All Rights Reserved. Memory dysfunction is a key symptom of age-related dementia. Although recent studies have suggested positive effects of electrical stimulation for memory enhancement, its potential targets remain largely unknown. In this study, we hypothesized that spatially targeted deep brain stimulation of ventromedial prefrontal cortex enhanced memory functions in a middle-aged rat model. Our results show that acute stimulation enhanced the short-, but not the long-term memory in the novel-object recognition task. Interestingly, after chronic high-frequency stimulation, both the short- and long-term memories were robustly improved in the novel-object recognition test and Morris water-maze spatial task compared to sham. Our results also demonstrated that chronic ventromedial prefrontal cortex high-frequency stimulation upregulated neurogenesis-associated genes along with enhanced hippocampal cell proliferation. Importantly, these memory behaviors were strongly correlated with the hippocampal neurogenesis. Overall, these findings suggest that chronic ventromedial prefrontal cortex high-frequency stimulation may serve as a novel effective therapeutic target for dementia-related disorders.-
dc.languageeng-
dc.publishereLife Sciences Publications Ltd.-
dc.relation.ispartofeLife-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectNeurogenesis-
dc.subjectLearning and memory-
dc.subjectHigh-frequency stimulation-
dc.subjectHippocampus-
dc.subjectVentromedial prefrontal cortex-
dc.titleVentromedial prefrontal cortex stimulation enhances memory and hippocampal neurogenesis in the middle-aged rats-
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.7554/eLife.04803-
dc.identifier.pmid25768425-
dc.identifier.scopuseid_2-s2.0-85003047471-
dc.identifier.volume2015-
dc.identifier.issue4-
dc.identifier.eissn2050-084X-
dc.identifier.isiWOS:000351865200001-
dc.identifier.issnl2050-084X-

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