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Identifying candidate genes associated with hippocampal dysfunction in a hemiparkinsonian rat model by transcriptomic profiling
Parkinson's disease (PD) often results in hippocampal dysfunction, which leads to cognitive and emotional challenges and synaptic irregularities. This study attempted to assess behavioral anomalies and identify differentially expressed genes (DEGs) within the hippocampus of a hemiparkinsonian r...
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Published in: | Animal cells and systems 2024, 28(1), , pp.198-215 |
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description | Parkinson's disease (PD) often results in hippocampal dysfunction, which leads to cognitive and emotional challenges and synaptic irregularities. This study attempted to assess behavioral anomalies and identify differentially expressed genes (DEGs) within the hippocampus of a hemiparkinsonian rat model to potentially uncover novel genetic candidates linked to hippocampal dysfunction. Striatal 6-hydroxydopamine (6-OHDA) infusions were performed unilaterally in the brains of adult SD rats, while dopaminergic impairments were verified in rats with 6-OHDA-lesioned striata. RNA sequencing and gene expression analysis unveiled 1018 DEGs in the ipsilateral rat hippocampus following 6-OHDA infusion: 631 genes exhibited upregulation, while 387 genes were downregulated (with FDR-adjusted p-value 1.5). Gene ontology analysis of DEGs indicated that alterations in the hippocampi of 6-OHDA-lesioned rats were primarily associated with synaptic signaling, axon development, behavior, postsynaptic membrane, synaptic membrane, neurotransmitter receptor activity, and peptide receptor activity. The Kyoto Encyclopedia of Genes and Genomes analysis of DEGs demonstrated significant enrichment of the neuroactive ligand-receptor interaction, calcium signaling pathway, cAMP signaling pathway, axon guidance, and notch signaling pathway in rat hippocampi that had been subjected to striatal 6-OHDA infusion. STRING analysis confirmed a notable upregulation of eight hub genes (Notch3, Gng4, Itga3, Grin2d, Hgf, Fgf11, Htr3a, and Col6a2), along with a significant downregulation of two hub genes (Itga11 and Plp1), as validated by reverse transcription-quantitative polymerase chain reaction. This study provides a comprehensive transcriptomic profile of the hippocampi in a hemiparkinsonian rat model, thereby offering insights into the signaling pathways underlying hippocampal dysfunction. |
doi_str_mv | 10.1080/19768354.2024.2348671 |
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This study attempted to assess behavioral anomalies and identify differentially expressed genes (DEGs) within the hippocampus of a hemiparkinsonian rat model to potentially uncover novel genetic candidates linked to hippocampal dysfunction. Striatal 6-hydroxydopamine (6-OHDA) infusions were performed unilaterally in the brains of adult SD rats, while dopaminergic impairments were verified in rats with 6-OHDA-lesioned striata. RNA sequencing and gene expression analysis unveiled 1018 DEGs in the ipsilateral rat hippocampus following 6-OHDA infusion: 631 genes exhibited upregulation, while 387 genes were downregulated (with FDR-adjusted p-value < 0.05 and absolute fold-change > 1.5). Gene ontology analysis of DEGs indicated that alterations in the hippocampi of 6-OHDA-lesioned rats were primarily associated with synaptic signaling, axon development, behavior, postsynaptic membrane, synaptic membrane, neurotransmitter receptor activity, and peptide receptor activity. The Kyoto Encyclopedia of Genes and Genomes analysis of DEGs demonstrated significant enrichment of the neuroactive ligand-receptor interaction, calcium signaling pathway, cAMP signaling pathway, axon guidance, and notch signaling pathway in rat hippocampi that had been subjected to striatal 6-OHDA infusion. STRING analysis confirmed a notable upregulation of eight hub genes (Notch3, Gng4, Itga3, Grin2d, Hgf, Fgf11, Htr3a, and Col6a2), along with a significant downregulation of two hub genes (Itga11 and Plp1), as validated by reverse transcription-quantitative polymerase chain reaction. This study provides a comprehensive transcriptomic profile of the hippocampi in a hemiparkinsonian rat model, thereby offering insights into the signaling pathways underlying hippocampal dysfunction.</description><identifier>ISSN: 1976-8354</identifier><identifier>EISSN: 2151-2485</identifier><identifier>DOI: 10.1080/19768354.2024.2348671</identifier><identifier>PMID: 38693920</identifier><language>eng</language><publisher>England: Taylor & Francis</publisher><subject>6-Hydroxydopamine ; Axon guidance ; Axonogenesis ; Calcium signalling ; Differentially expressed genes ; Dopamine receptors ; Down-regulation ; Emotional behavior ; Gene expression ; Gene sequencing ; Genes ; Hippocampus ; Membranes ; Movement disorders ; Myelin proteolipid protein ; Neostriatum ; Neurodegenerative diseases ; Parkinson's disease ; Polymerase chain reaction ; Receptors ; Reverse transcription ; RNA-sequencing ; Signal transduction ; Synaptogenesis ; Transcriptomics ; Up-regulation ; 생물학</subject><ispartof>Animal Cells and Systems, 2024, 28(1), , pp.198-215</ispartof><rights>2024 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group 2024</rights><rights>2024 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.</rights><rights>2024 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. This work is licensed under the Creative Commons Attribution – Non-Commercial License http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2024 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group 2024 The Author(s)</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c546t-44c77373502678296f372c6b7715b2756b39af425f314d6074af269008294fdc3</cites><orcidid>0000-0002-5557-4576 ; 0009-0007-3906-3526 ; 0000-0003-4689-5797 ; 0000-0002-0970-1079 ; 0000-0002-9851-4354 ; 0000-0002-4535-2312 ; 0000-0002-8010-519X ; 0000-0003-2451-0374 ; 0000-0003-2180-4860</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11062273/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3145362137?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27502,27924,27925,37012,37013,44590,53791,53793,59143,59144</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38693920$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART003147382$$DAccess content in National Research Foundation of Korea (NRF)$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, Bohye</creatorcontrib><creatorcontrib>Hong, Sungmoo</creatorcontrib><creatorcontrib>Lee, Jeongmin</creatorcontrib><creatorcontrib>Kang, Sohi</creatorcontrib><creatorcontrib>Kim, Joong-Sun</creatorcontrib><creatorcontrib>Jung, Chaeyong</creatorcontrib><creatorcontrib>Shin, Taekyun</creatorcontrib><creatorcontrib>Youn, BuHyun</creatorcontrib><creatorcontrib>Moon, Changjong</creatorcontrib><title>Identifying candidate genes associated with hippocampal dysfunction in a hemiparkinsonian rat model by transcriptomic profiling</title><title>Animal cells and systems</title><addtitle>Anim Cells Syst (Seoul)</addtitle><description>Parkinson's disease (PD) often results in hippocampal dysfunction, which leads to cognitive and emotional challenges and synaptic irregularities. This study attempted to assess behavioral anomalies and identify differentially expressed genes (DEGs) within the hippocampus of a hemiparkinsonian rat model to potentially uncover novel genetic candidates linked to hippocampal dysfunction. Striatal 6-hydroxydopamine (6-OHDA) infusions were performed unilaterally in the brains of adult SD rats, while dopaminergic impairments were verified in rats with 6-OHDA-lesioned striata. RNA sequencing and gene expression analysis unveiled 1018 DEGs in the ipsilateral rat hippocampus following 6-OHDA infusion: 631 genes exhibited upregulation, while 387 genes were downregulated (with FDR-adjusted p-value < 0.05 and absolute fold-change > 1.5). Gene ontology analysis of DEGs indicated that alterations in the hippocampi of 6-OHDA-lesioned rats were primarily associated with synaptic signaling, axon development, behavior, postsynaptic membrane, synaptic membrane, neurotransmitter receptor activity, and peptide receptor activity. The Kyoto Encyclopedia of Genes and Genomes analysis of DEGs demonstrated significant enrichment of the neuroactive ligand-receptor interaction, calcium signaling pathway, cAMP signaling pathway, axon guidance, and notch signaling pathway in rat hippocampi that had been subjected to striatal 6-OHDA infusion. STRING analysis confirmed a notable upregulation of eight hub genes (Notch3, Gng4, Itga3, Grin2d, Hgf, Fgf11, Htr3a, and Col6a2), along with a significant downregulation of two hub genes (Itga11 and Plp1), as validated by reverse transcription-quantitative polymerase chain reaction. This study provides a comprehensive transcriptomic profile of the hippocampi in a hemiparkinsonian rat model, thereby offering insights into the signaling pathways underlying hippocampal dysfunction.</description><subject>6-Hydroxydopamine</subject><subject>Axon guidance</subject><subject>Axonogenesis</subject><subject>Calcium signalling</subject><subject>Differentially expressed genes</subject><subject>Dopamine receptors</subject><subject>Down-regulation</subject><subject>Emotional behavior</subject><subject>Gene expression</subject><subject>Gene sequencing</subject><subject>Genes</subject><subject>Hippocampus</subject><subject>Membranes</subject><subject>Movement disorders</subject><subject>Myelin proteolipid protein</subject><subject>Neostriatum</subject><subject>Neurodegenerative diseases</subject><subject>Parkinson's disease</subject><subject>Polymerase chain reaction</subject><subject>Receptors</subject><subject>Reverse transcription</subject><subject>RNA-sequencing</subject><subject>Signal transduction</subject><subject>Synaptogenesis</subject><subject>Transcriptomics</subject><subject>Up-regulation</subject><subject>생물학</subject><issn>1976-8354</issn><issn>2151-2485</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>0YH</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp9kltrFDEUx4Motq5-BCXgiwhbc8_Mky3Fy0JBkPocMrnsZncmGZNZyz751c1eWqwPvuSQ5Hf-5-TkD8BrjC4watAH3ErRUM4uCCJ1oawREj8B5wRzPCes4U_B-Z6Z76Ez8KKUNUKCoKZ9Ds5oI1raEnQOfi-si1PwuxCX0Ohog9WTg0sXXYG6lGRC3Vt4F6YVXIVxTEYPo-6h3RW_jWYKKcIQoYYrN4RR502IJcWgI8x6gkOyrofdDk5Zx2JyGKc0BAPHnHzoa82X4JnXfXGvTnEGfnz-dHv9dX7z7cvi-upmbjgT05wxIyWVlCMiZENa4akkRnRSYt4RyUVHW-0Z4Z5iZgWSTHsiWoQqy7w1dAbeH3Vj9mpjgko6HOIyqU1WV99vFwojwTkmqMKLI2yTXqsxh0Hn3SHjcJDyUuk8BdM7hVqHG-Ek884yY5uWaWyN9p0WtEOeVK2PR61x2w3OmjrtrPtHoo9vYljVpn4pXNshRNKq8O6kkNPPrSuTGkIxru91dGlbFEUcYcl4_dIZePsPuk7bHOtgVZ0Lp4LgOsQZ4EfK5FRKdv6hG4zU3lzq3lxqby51MlfNe_P3Ux6y7t1UgcsjEKJPedB3KfdWTXrXp-yrAUzY9_HfGn8A-mLfrA</recordid><startdate>20241231</startdate><enddate>20241231</enddate><creator>Kim, Bohye</creator><creator>Hong, Sungmoo</creator><creator>Lee, Jeongmin</creator><creator>Kang, Sohi</creator><creator>Kim, Joong-Sun</creator><creator>Jung, Chaeyong</creator><creator>Shin, Taekyun</creator><creator>Youn, BuHyun</creator><creator>Moon, Changjong</creator><general>Taylor & Francis</general><general>Taylor & Francis Ltd</general><general>Taylor & Francis Group</general><general>한국통합생물학회</general><scope>0YH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7SN</scope><scope>7TK</scope><scope>7TM</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M7P</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><scope>ACYCR</scope><orcidid>https://orcid.org/0000-0002-5557-4576</orcidid><orcidid>https://orcid.org/0009-0007-3906-3526</orcidid><orcidid>https://orcid.org/0000-0003-4689-5797</orcidid><orcidid>https://orcid.org/0000-0002-0970-1079</orcidid><orcidid>https://orcid.org/0000-0002-9851-4354</orcidid><orcidid>https://orcid.org/0000-0002-4535-2312</orcidid><orcidid>https://orcid.org/0000-0002-8010-519X</orcidid><orcidid>https://orcid.org/0000-0003-2451-0374</orcidid><orcidid>https://orcid.org/0000-0003-2180-4860</orcidid></search><sort><creationdate>20241231</creationdate><title>Identifying candidate genes associated with hippocampal dysfunction in a hemiparkinsonian rat model by transcriptomic profiling</title><author>Kim, Bohye ; Hong, Sungmoo ; Lee, Jeongmin ; Kang, Sohi ; Kim, Joong-Sun ; Jung, Chaeyong ; Shin, Taekyun ; Youn, BuHyun ; Moon, Changjong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c546t-44c77373502678296f372c6b7715b2756b39af425f314d6074af269008294fdc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>6-Hydroxydopamine</topic><topic>Axon guidance</topic><topic>Axonogenesis</topic><topic>Calcium signalling</topic><topic>Differentially expressed genes</topic><topic>Dopamine receptors</topic><topic>Down-regulation</topic><topic>Emotional behavior</topic><topic>Gene expression</topic><topic>Gene sequencing</topic><topic>Genes</topic><topic>Hippocampus</topic><topic>Membranes</topic><topic>Movement disorders</topic><topic>Myelin proteolipid protein</topic><topic>Neostriatum</topic><topic>Neurodegenerative diseases</topic><topic>Parkinson's disease</topic><topic>Polymerase chain reaction</topic><topic>Receptors</topic><topic>Reverse transcription</topic><topic>RNA-sequencing</topic><topic>Signal transduction</topic><topic>Synaptogenesis</topic><topic>Transcriptomics</topic><topic>Up-regulation</topic><topic>생물학</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Bohye</creatorcontrib><creatorcontrib>Hong, Sungmoo</creatorcontrib><creatorcontrib>Lee, Jeongmin</creatorcontrib><creatorcontrib>Kang, Sohi</creatorcontrib><creatorcontrib>Kim, Joong-Sun</creatorcontrib><creatorcontrib>Jung, Chaeyong</creatorcontrib><creatorcontrib>Shin, Taekyun</creatorcontrib><creatorcontrib>Youn, BuHyun</creatorcontrib><creatorcontrib>Moon, Changjong</creatorcontrib><collection>Taylor & Francis Open Access Journals</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Ecology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>Biological Sciences</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><collection>Korean Citation Index</collection><jtitle>Animal cells and systems</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Bohye</au><au>Hong, Sungmoo</au><au>Lee, Jeongmin</au><au>Kang, Sohi</au><au>Kim, Joong-Sun</au><au>Jung, Chaeyong</au><au>Shin, Taekyun</au><au>Youn, BuHyun</au><au>Moon, Changjong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identifying candidate genes associated with hippocampal dysfunction in a hemiparkinsonian rat model by transcriptomic profiling</atitle><jtitle>Animal cells and systems</jtitle><addtitle>Anim Cells Syst (Seoul)</addtitle><date>2024-12-31</date><risdate>2024</risdate><volume>28</volume><issue>1</issue><spage>198</spage><epage>215</epage><pages>198-215</pages><issn>1976-8354</issn><eissn>2151-2485</eissn><abstract>Parkinson's disease (PD) often results in hippocampal dysfunction, which leads to cognitive and emotional challenges and synaptic irregularities. This study attempted to assess behavioral anomalies and identify differentially expressed genes (DEGs) within the hippocampus of a hemiparkinsonian rat model to potentially uncover novel genetic candidates linked to hippocampal dysfunction. Striatal 6-hydroxydopamine (6-OHDA) infusions were performed unilaterally in the brains of adult SD rats, while dopaminergic impairments were verified in rats with 6-OHDA-lesioned striata. RNA sequencing and gene expression analysis unveiled 1018 DEGs in the ipsilateral rat hippocampus following 6-OHDA infusion: 631 genes exhibited upregulation, while 387 genes were downregulated (with FDR-adjusted p-value < 0.05 and absolute fold-change > 1.5). Gene ontology analysis of DEGs indicated that alterations in the hippocampi of 6-OHDA-lesioned rats were primarily associated with synaptic signaling, axon development, behavior, postsynaptic membrane, synaptic membrane, neurotransmitter receptor activity, and peptide receptor activity. The Kyoto Encyclopedia of Genes and Genomes analysis of DEGs demonstrated significant enrichment of the neuroactive ligand-receptor interaction, calcium signaling pathway, cAMP signaling pathway, axon guidance, and notch signaling pathway in rat hippocampi that had been subjected to striatal 6-OHDA infusion. STRING analysis confirmed a notable upregulation of eight hub genes (Notch3, Gng4, Itga3, Grin2d, Hgf, Fgf11, Htr3a, and Col6a2), along with a significant downregulation of two hub genes (Itga11 and Plp1), as validated by reverse transcription-quantitative polymerase chain reaction. 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subjects | 6-Hydroxydopamine Axon guidance Axonogenesis Calcium signalling Differentially expressed genes Dopamine receptors Down-regulation Emotional behavior Gene expression Gene sequencing Genes Hippocampus Membranes Movement disorders Myelin proteolipid protein Neostriatum Neurodegenerative diseases Parkinson's disease Polymerase chain reaction Receptors Reverse transcription RNA-sequencing Signal transduction Synaptogenesis Transcriptomics Up-regulation 생물학 |
title | Identifying candidate genes associated with hippocampal dysfunction in a hemiparkinsonian rat model by transcriptomic profiling |
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