Revision to psychopharmacology mRNA and microRNA profiles are associated with stress susceptibility and resilience induced by psychological stress in the prefrontal cortex

Objectives The prefrontal cortex is associated with many mental neurological diseases. The mRNA and microRNA profiles of stress susceptibility and resilience induced by psychological stress in the prefrontal cortex remain to be elucidated. Methods The C57 observer was placed in the cage next to the...

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Veröffentlicht in:Psychopharmacology 2020-10, Vol.237 (10), p.3067-3093
Hauptverfasser: Yang, Jiuyong, Sun, Jinyan, Lu, Yanjun, An, Tingting, Lu, Wei, Wang, Jin-Hui
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container_issue 10
container_start_page 3067
container_title Psychopharmacology
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creator Yang, Jiuyong
Sun, Jinyan
Lu, Yanjun
An, Tingting
Lu, Wei
Wang, Jin-Hui
description Objectives The prefrontal cortex is associated with many mental neurological diseases. The mRNA and microRNA profiles of stress susceptibility and resilience induced by psychological stress in the prefrontal cortex remain to be elucidated. Methods The C57 observer was placed in the cage next to the CD1 mouse and suffered psychological stress by watching the CD1 attacking another C57 mouse. After 5 days of psychological stress, the degree of fear memory and anxiety of mice were measured by social interaction test and elevated plus maze (EPM). The prefrontal cortex was extracted and mRNA and microRNA profiles were analyzed by high-throughput sequencing. Results In susceptible mice versus resilient mice, the downregulation of genes involved in serotonergic synapse may be related to the susceptibility to psychological stress. The imbalanced regulation of genes involved in VEGF, p53, chemokine, Ras, sphingolipid, GnRH, MAPK, and NOD-like receptor signaling pathways may be related to the susceptibility to psychological stress. Compared with control mice, susceptible mice and resilient mice have changed genes involved in serotonergic synapse, neuroactive ligand-receptor interaction, axon guidance, calcium, cAMP, GnRH, estrogen, PI3K-Akt, MAPK, Rap1, and Ras signaling pathways, these changes may be related to psychological stress processing. The sequencing results of mRNAs and microRNAs were verified by qRT-PCR and dual-luciferase reporter assay. Conclusions The downregulation of genes involved in serotonergic synapse and imbalance of signaling pathways in the prefrontal cortex may be related to susceptibility to psychological stress.
doi_str_mv 10.1007/s00213-020-05593-x
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The mRNA and microRNA profiles of stress susceptibility and resilience induced by psychological stress in the prefrontal cortex remain to be elucidated. Methods The C57 observer was placed in the cage next to the CD1 mouse and suffered psychological stress by watching the CD1 attacking another C57 mouse. After 5 days of psychological stress, the degree of fear memory and anxiety of mice were measured by social interaction test and elevated plus maze (EPM). The prefrontal cortex was extracted and mRNA and microRNA profiles were analyzed by high-throughput sequencing. Results In susceptible mice versus resilient mice, the downregulation of genes involved in serotonergic synapse may be related to the susceptibility to psychological stress. The imbalanced regulation of genes involved in VEGF, p53, chemokine, Ras, sphingolipid, GnRH, MAPK, and NOD-like receptor signaling pathways may be related to the susceptibility to psychological stress. Compared with control mice, susceptible mice and resilient mice have changed genes involved in serotonergic synapse, neuroactive ligand-receptor interaction, axon guidance, calcium, cAMP, GnRH, estrogen, PI3K-Akt, MAPK, Rap1, and Ras signaling pathways, these changes may be related to psychological stress processing. The sequencing results of mRNAs and microRNAs were verified by qRT-PCR and dual-luciferase reporter assay. Conclusions The downregulation of genes involved in serotonergic synapse and imbalance of signaling pathways in the prefrontal cortex may be related to susceptibility to psychological stress.</description><identifier>ISSN: 0033-3158</identifier><identifier>EISSN: 1432-2072</identifier><identifier>DOI: 10.1007/s00213-020-05593-x</identifier><identifier>PMID: 32591938</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>1-Phosphatidylinositol 3-kinase ; AKT protein ; Analysis ; Animals ; Anxiety ; Anxiety - genetics ; Anxiety - metabolism ; Anxiety - psychology ; Axon guidance ; Biomedical and Life Sciences ; Biomedicine ; Calcium ; Chemokines ; Fear - physiology ; Fear - psychology ; Gene regulation ; Gonadotropin-releasing hormone ; Male ; MAP kinase ; Memory - physiology ; Messenger RNA ; Mice ; Mice, Inbred C57BL ; MicroRNA ; MicroRNAs ; MicroRNAs - genetics ; MicroRNAs - metabolism ; miRNA ; mRNA ; Nervous system diseases ; Neurological diseases ; Neurosciences ; Next-generation sequencing ; Original Investigation ; p53 Protein ; Pharmacology/Toxicology ; Prefrontal cortex ; Prefrontal Cortex - metabolism ; Psychiatry ; Psychopharmacology ; Rap1 protein ; Resilience, Psychological ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; Signal transduction ; Social aspects ; Species Specificity ; Stress (Psychology) ; Stress, Psychological - genetics ; Stress, Psychological - metabolism ; Stress, Psychological - psychology ; Susceptibility ; Synapses ; Tumor proteins ; Vascular endothelial growth factor</subject><ispartof>Psychopharmacology, 2020-10, Vol.237 (10), p.3067-3093</ispartof><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2020</rights><rights>COPYRIGHT 2020 Springer</rights><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2020.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c442t-f7ddd274839e7bbf24e847d9c64525b72d3a4ba3176f6f1c531a93d9d2a5ffd03</citedby><cites>FETCH-LOGICAL-c442t-f7ddd274839e7bbf24e847d9c64525b72d3a4ba3176f6f1c531a93d9d2a5ffd03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00213-020-05593-x$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00213-020-05593-x$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32591938$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yang, Jiuyong</creatorcontrib><creatorcontrib>Sun, Jinyan</creatorcontrib><creatorcontrib>Lu, Yanjun</creatorcontrib><creatorcontrib>An, Tingting</creatorcontrib><creatorcontrib>Lu, Wei</creatorcontrib><creatorcontrib>Wang, Jin-Hui</creatorcontrib><title>Revision to psychopharmacology mRNA and microRNA profiles are associated with stress susceptibility and resilience induced by psychological stress in the prefrontal cortex</title><title>Psychopharmacology</title><addtitle>Psychopharmacology</addtitle><addtitle>Psychopharmacology (Berl)</addtitle><description>Objectives The prefrontal cortex is associated with many mental neurological diseases. The mRNA and microRNA profiles of stress susceptibility and resilience induced by psychological stress in the prefrontal cortex remain to be elucidated. Methods The C57 observer was placed in the cage next to the CD1 mouse and suffered psychological stress by watching the CD1 attacking another C57 mouse. After 5 days of psychological stress, the degree of fear memory and anxiety of mice were measured by social interaction test and elevated plus maze (EPM). The prefrontal cortex was extracted and mRNA and microRNA profiles were analyzed by high-throughput sequencing. Results In susceptible mice versus resilient mice, the downregulation of genes involved in serotonergic synapse may be related to the susceptibility to psychological stress. The imbalanced regulation of genes involved in VEGF, p53, chemokine, Ras, sphingolipid, GnRH, MAPK, and NOD-like receptor signaling pathways may be related to the susceptibility to psychological stress. Compared with control mice, susceptible mice and resilient mice have changed genes involved in serotonergic synapse, neuroactive ligand-receptor interaction, axon guidance, calcium, cAMP, GnRH, estrogen, PI3K-Akt, MAPK, Rap1, and Ras signaling pathways, these changes may be related to psychological stress processing. The sequencing results of mRNAs and microRNAs were verified by qRT-PCR and dual-luciferase reporter assay. Conclusions The downregulation of genes involved in serotonergic synapse and imbalance of signaling pathways in the prefrontal cortex may be related to susceptibility to psychological stress.</description><subject>1-Phosphatidylinositol 3-kinase</subject><subject>AKT protein</subject><subject>Analysis</subject><subject>Animals</subject><subject>Anxiety</subject><subject>Anxiety - genetics</subject><subject>Anxiety - metabolism</subject><subject>Anxiety - psychology</subject><subject>Axon guidance</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Calcium</subject><subject>Chemokines</subject><subject>Fear - physiology</subject><subject>Fear - psychology</subject><subject>Gene regulation</subject><subject>Gonadotropin-releasing hormone</subject><subject>Male</subject><subject>MAP kinase</subject><subject>Memory - physiology</subject><subject>Messenger RNA</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>MicroRNA</subject><subject>MicroRNAs</subject><subject>MicroRNAs - genetics</subject><subject>MicroRNAs - metabolism</subject><subject>miRNA</subject><subject>mRNA</subject><subject>Nervous system diseases</subject><subject>Neurological diseases</subject><subject>Neurosciences</subject><subject>Next-generation sequencing</subject><subject>Original Investigation</subject><subject>p53 Protein</subject><subject>Pharmacology/Toxicology</subject><subject>Prefrontal cortex</subject><subject>Prefrontal Cortex - metabolism</subject><subject>Psychiatry</subject><subject>Psychopharmacology</subject><subject>Rap1 protein</subject><subject>Resilience, Psychological</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>Signal transduction</subject><subject>Social aspects</subject><subject>Species Specificity</subject><subject>Stress (Psychology)</subject><subject>Stress, Psychological - genetics</subject><subject>Stress, Psychological - metabolism</subject><subject>Stress, Psychological - psychology</subject><subject>Susceptibility</subject><subject>Synapses</subject><subject>Tumor proteins</subject><subject>Vascular endothelial growth factor</subject><issn>0033-3158</issn><issn>1432-2072</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9UstuEzEUtRCIhsAPsECW2LCZ4te8llHFS6pAqmBteew7iauZcbA9Jfmm_mRvmpQKhLAX1rXPuY_jQ8hrzs45Y_X7xJjgsmCCFawsW1nsnpAFV1IUgtXiKVkwJmUhedmckRcpXTNcqlHPyZkUZctb2SzI7RXc-OTDRHOg27S3m7DdmDgaG4aw3tPx6uuKmsnR0dsYDsE2ht4PkKiJQE1KwXqTwdFfPm9oyhFSomlOFrbZd37weX_Px3sMYLJA_eRmi4xuf6qIlbw1wwPbYzMbwELQxzBlfLAhZti9JM96MyR4dTqX5MfHD98vPheX3z59uVhdFlYpkYu-ds6JWjWyhbrreqGgUbVrbaVKUXa1cNKozkheV33Vc1tKblrpWidM2feOySV5d8yLo_6cIWU9epxnGMwEYU5aKN5wIRVKviRv_4JehzlO2J0WZaWqtilV9YhamwG0n_qQo7GHpHpVyaqtG97UiDr_Bwq3AxQ_THCQ_U-COBLwZ1JCtfQ2-tHEveZMHxyijw7R6BB97xC9Q9KbU8dzN4L7TXmwBALkEZDwaVpDfBzpP2nvAN7Uygs</recordid><startdate>20201001</startdate><enddate>20201001</enddate><creator>Yang, Jiuyong</creator><creator>Sun, Jinyan</creator><creator>Lu, Yanjun</creator><creator>An, Tingting</creator><creator>Lu, Wei</creator><creator>Wang, Jin-Hui</creator><general>Springer Berlin Heidelberg</general><general>Springer</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QG</scope><scope>7QR</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8AO</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20201001</creationdate><title>Revision to psychopharmacology mRNA and microRNA profiles are associated with stress susceptibility and resilience induced by psychological stress in the prefrontal cortex</title><author>Yang, Jiuyong ; 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The mRNA and microRNA profiles of stress susceptibility and resilience induced by psychological stress in the prefrontal cortex remain to be elucidated. Methods The C57 observer was placed in the cage next to the CD1 mouse and suffered psychological stress by watching the CD1 attacking another C57 mouse. After 5 days of psychological stress, the degree of fear memory and anxiety of mice were measured by social interaction test and elevated plus maze (EPM). The prefrontal cortex was extracted and mRNA and microRNA profiles were analyzed by high-throughput sequencing. Results In susceptible mice versus resilient mice, the downregulation of genes involved in serotonergic synapse may be related to the susceptibility to psychological stress. The imbalanced regulation of genes involved in VEGF, p53, chemokine, Ras, sphingolipid, GnRH, MAPK, and NOD-like receptor signaling pathways may be related to the susceptibility to psychological stress. Compared with control mice, susceptible mice and resilient mice have changed genes involved in serotonergic synapse, neuroactive ligand-receptor interaction, axon guidance, calcium, cAMP, GnRH, estrogen, PI3K-Akt, MAPK, Rap1, and Ras signaling pathways, these changes may be related to psychological stress processing. The sequencing results of mRNAs and microRNAs were verified by qRT-PCR and dual-luciferase reporter assay. Conclusions The downregulation of genes involved in serotonergic synapse and imbalance of signaling pathways in the prefrontal cortex may be related to susceptibility to psychological stress.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>32591938</pmid><doi>10.1007/s00213-020-05593-x</doi><tpages>27</tpages></addata></record>
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subjects 1-Phosphatidylinositol 3-kinase
AKT protein
Analysis
Animals
Anxiety
Anxiety - genetics
Anxiety - metabolism
Anxiety - psychology
Axon guidance
Biomedical and Life Sciences
Biomedicine
Calcium
Chemokines
Fear - physiology
Fear - psychology
Gene regulation
Gonadotropin-releasing hormone
Male
MAP kinase
Memory - physiology
Messenger RNA
Mice
Mice, Inbred C57BL
MicroRNA
MicroRNAs
MicroRNAs - genetics
MicroRNAs - metabolism
miRNA
mRNA
Nervous system diseases
Neurological diseases
Neurosciences
Next-generation sequencing
Original Investigation
p53 Protein
Pharmacology/Toxicology
Prefrontal cortex
Prefrontal Cortex - metabolism
Psychiatry
Psychopharmacology
Rap1 protein
Resilience, Psychological
RNA, Messenger - genetics
RNA, Messenger - metabolism
Signal transduction
Social aspects
Species Specificity
Stress (Psychology)
Stress, Psychological - genetics
Stress, Psychological - metabolism
Stress, Psychological - psychology
Susceptibility
Synapses
Tumor proteins
Vascular endothelial growth factor
title Revision to psychopharmacology mRNA and microRNA profiles are associated with stress susceptibility and resilience induced by psychological stress in the prefrontal cortex
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