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Article: Prelimbic cortical stimulation improves spatial memory through distinct patterns of hippocampal gene expression in aged rats

TitlePrelimbic cortical stimulation improves spatial memory through distinct patterns of hippocampal gene expression in aged rats
Authors
KeywordsDeep brain stimulation
Dementia
Memory
Microarray
Prelimbic cortex
Hippocampus
Issue Date2020
PublisherSpringer New York LLC. The Journal's web site is located at https://www.springer.com/journal/13311
Citation
Neurotherapeutics, 2020, v. 17 n. 4, p. 2054-2068 How to Cite?
AbstractDementia poses major health challenges worldwide, yet current treatments are faced with issues of efficacy and toxicity. Deep Brain Stimulation (DBS) is a promising nonpharmacological treatment for dementia, but most DBS studies use young healthy animals, which may not be aetiologically relevant. In this study, we used an aged rat model in which cognitive decline occurs through a natural ageing process. We used a Morris Water Maze (MWM) to determine the effects of prelimbic cortex (PrL) DBS on memory in aged rats. To investigate the underlying mechanisms of the effects of DBS, we carried out microarray, quantitative PCR analysis, and mass spectrometry to detect gene expression and neurotransmitter changes in the hippocampus. We showed PrL DBS improved the performance in MWM, with related distinct patterns of gene expression involving G-protein-coupled receptor pathways. We further found neurotransmitter changes in the dorsal hippocampus, which corroborated and extended the microarray findings. Our results suggest that non-neurogenesis pathways play roles in the effects of DBS. Further studies are needed to investigate the effects of DBS on memory beyond neurogenesis and to consider the highlighted pathways suggested by our data.
Persistent Identifierhttp://hdl.handle.net/10722/285231
ISSN
2023 Impact Factor: 5.6
2023 SCImago Journal Rankings: 1.625
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorTan, SZK-
dc.contributor.authorNeoh, J-
dc.contributor.authorLawrence, AJ-
dc.contributor.authorWu, EX-
dc.contributor.authorLim, LW-
dc.date.accessioned2020-08-18T03:51:29Z-
dc.date.available2020-08-18T03:51:29Z-
dc.date.issued2020-
dc.identifier.citationNeurotherapeutics, 2020, v. 17 n. 4, p. 2054-2068-
dc.identifier.issn1933-7213-
dc.identifier.urihttp://hdl.handle.net/10722/285231-
dc.description.abstractDementia poses major health challenges worldwide, yet current treatments are faced with issues of efficacy and toxicity. Deep Brain Stimulation (DBS) is a promising nonpharmacological treatment for dementia, but most DBS studies use young healthy animals, which may not be aetiologically relevant. In this study, we used an aged rat model in which cognitive decline occurs through a natural ageing process. We used a Morris Water Maze (MWM) to determine the effects of prelimbic cortex (PrL) DBS on memory in aged rats. To investigate the underlying mechanisms of the effects of DBS, we carried out microarray, quantitative PCR analysis, and mass spectrometry to detect gene expression and neurotransmitter changes in the hippocampus. We showed PrL DBS improved the performance in MWM, with related distinct patterns of gene expression involving G-protein-coupled receptor pathways. We further found neurotransmitter changes in the dorsal hippocampus, which corroborated and extended the microarray findings. Our results suggest that non-neurogenesis pathways play roles in the effects of DBS. Further studies are needed to investigate the effects of DBS on memory beyond neurogenesis and to consider the highlighted pathways suggested by our data.-
dc.languageeng-
dc.publisherSpringer New York LLC. The Journal's web site is located at https://www.springer.com/journal/13311-
dc.relation.ispartofNeurotherapeutics-
dc.subjectDeep brain stimulation-
dc.subjectDementia-
dc.subjectMemory-
dc.subjectMicroarray-
dc.subjectPrelimbic cortex-
dc.subjectHippocampus-
dc.titlePrelimbic cortical stimulation improves spatial memory through distinct patterns of hippocampal gene expression in aged rats-
dc.typeArticle-
dc.identifier.emailWu, EX: ewu@eee.hku.hk-
dc.identifier.emailLim, LW: limlw@hku.hk-
dc.identifier.authorityWu, EX=rp00193-
dc.identifier.authorityLim, LW=rp02088-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1007/s13311-020-00913-7-
dc.identifier.pmid32816221-
dc.identifier.scopuseid_2-s2.0-85089742135-
dc.identifier.hkuros312755-
dc.identifier.volume17-
dc.identifier.issue4-
dc.identifier.spage2054-
dc.identifier.epage2068-
dc.identifier.isiWOS:000561241800002-
dc.publisher.placeUnited States-
dc.identifier.issnl1878-7479-

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