Neurogenic hypothesis of positive psychology in stress-induced depression: Adult hippocampal neurogenesis, neuroinflammation, and stress resilience
•Stress-induced neuroinflammation affects AHN related pattern separation.•Neuroprotection is a self-protection measure of the brain against neuroinflammation.•Therapeutic potential of AHN may be a new direction of antidepressant therapy. Stress is an important risk factor for depression. Emerging ev...
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description | •Stress-induced neuroinflammation affects AHN related pattern separation.•Neuroprotection is a self-protection measure of the brain against neuroinflammation.•Therapeutic potential of AHN may be a new direction of antidepressant therapy.
Stress is an important risk factor for depression. Emerging evidence supports the hypothesis that stress-mediated neuroinflammation destroys brain function and leads to anxiety-like and depression-like behaviors. Previous studies of stress-induced depression have mainly focused on pathological damage; however, the rise of positive psychology has attracted the interest of many researchers in environmental enrichment to promote stress resilience. The hippocampus is one of the most severely damaged brain regions in stress-induced depression. In addition, the hippocampus is one of the most unique regions in the brain, as new neurons are produced in the adult hippocampus, a process known as adult hippocampal neurogenesis (AHN). AHN is an important core component of the neurogenic hypothesis and has also become a major innovative breakthrough in positive psychology, in which environmental enrichment mediates stress resilience. Neuroinflammation, by activating microglia and releasing some proinflammatory cytokines, is increasingly shown to be one of the key determinant pathophysiological factors that negatively affects AHNand cognitive reserve. AHN is mainly related to remodeling stress response mechanisms, such as memory clearing, emotional control, and pattern separation, suggesting that a correlation may exist between neuroinflammation and AHN in stress resilience. Therefore, we summarized the previous research results to systematically expound on the relationship between AHN, stress resilience, and neuroinflammation. We hope this neurogenic hypothesis of positive psychology in stress-induced depression will provide a new perspective for the study of depression and antidepressant therapy. |
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Stress is an important risk factor for depression. Emerging evidence supports the hypothesis that stress-mediated neuroinflammation destroys brain function and leads to anxiety-like and depression-like behaviors. Previous studies of stress-induced depression have mainly focused on pathological damage; however, the rise of positive psychology has attracted the interest of many researchers in environmental enrichment to promote stress resilience. The hippocampus is one of the most severely damaged brain regions in stress-induced depression. In addition, the hippocampus is one of the most unique regions in the brain, as new neurons are produced in the adult hippocampus, a process known as adult hippocampal neurogenesis (AHN). AHN is an important core component of the neurogenic hypothesis and has also become a major innovative breakthrough in positive psychology, in which environmental enrichment mediates stress resilience. Neuroinflammation, by activating microglia and releasing some proinflammatory cytokines, is increasingly shown to be one of the key determinant pathophysiological factors that negatively affects AHNand cognitive reserve. AHN is mainly related to remodeling stress response mechanisms, such as memory clearing, emotional control, and pattern separation, suggesting that a correlation may exist between neuroinflammation and AHN in stress resilience. Therefore, we summarized the previous research results to systematically expound on the relationship between AHN, stress resilience, and neuroinflammation. We hope this neurogenic hypothesis of positive psychology in stress-induced depression will provide a new perspective for the study of depression and antidepressant therapy.</description><identifier>ISSN: 1567-5769</identifier><identifier>EISSN: 1878-1705</identifier><identifier>DOI: 10.1016/j.intimp.2021.107653</identifier><identifier>PMID: 33915495</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Adult ; Adult hippocampal neurogenesis ; Antidepressant therapy ; Antidepressants ; Anxiety ; Brain ; Brain damage ; Cognitive ability ; Cytokines ; Depression - immunology ; Depression - psychology ; Enrichment ; Hippocampus ; Hippocampus - growth & development ; Hippocampus - immunology ; Humans ; Hypotheses ; Inflammation ; Mental depression ; Microglia ; Neurogenesis ; Neurogenesis - immunology ; Neuroinflammation ; Neuroinflammatory Diseases - etiology ; Neuroinflammatory Diseases - immunology ; Neuroinflammatory Diseases - psychology ; Neurons ; Pattern separation ; Psychology ; Psychology, Positive ; Resilience ; Resilience, Psychological ; Risk analysis ; Risk factors ; Stress resilience ; Stress, Psychological - complications ; Stress, Psychological - immunology ; Stress, Psychological - psychology</subject><ispartof>International immunopharmacology, 2021-08, Vol.97, p.107653-107653, Article 107653</ispartof><rights>2021 Elsevier B.V.</rights><rights>Copyright © 2021 Elsevier B.V. All rights reserved.</rights><rights>Copyright Elsevier BV Aug 2021</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c390t-1101ec63ce69cdf415b4c5ccff70fe18fc62e8850f51fa412fb0e44ad26167523</citedby><cites>FETCH-LOGICAL-c390t-1101ec63ce69cdf415b4c5ccff70fe18fc62e8850f51fa412fb0e44ad26167523</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1567576921002897$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33915495$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wu, Zuotian</creatorcontrib><creatorcontrib>Xiao, Ling</creatorcontrib><creatorcontrib>Wang, Huiling</creatorcontrib><creatorcontrib>Wang, Gaohua</creatorcontrib><title>Neurogenic hypothesis of positive psychology in stress-induced depression: Adult hippocampal neurogenesis, neuroinflammation, and stress resilience</title><title>International immunopharmacology</title><addtitle>Int Immunopharmacol</addtitle><description>•Stress-induced neuroinflammation affects AHN related pattern separation.•Neuroprotection is a self-protection measure of the brain against neuroinflammation.•Therapeutic potential of AHN may be a new direction of antidepressant therapy.
Stress is an important risk factor for depression. Emerging evidence supports the hypothesis that stress-mediated neuroinflammation destroys brain function and leads to anxiety-like and depression-like behaviors. Previous studies of stress-induced depression have mainly focused on pathological damage; however, the rise of positive psychology has attracted the interest of many researchers in environmental enrichment to promote stress resilience. The hippocampus is one of the most severely damaged brain regions in stress-induced depression. In addition, the hippocampus is one of the most unique regions in the brain, as new neurons are produced in the adult hippocampus, a process known as adult hippocampal neurogenesis (AHN). AHN is an important core component of the neurogenic hypothesis and has also become a major innovative breakthrough in positive psychology, in which environmental enrichment mediates stress resilience. Neuroinflammation, by activating microglia and releasing some proinflammatory cytokines, is increasingly shown to be one of the key determinant pathophysiological factors that negatively affects AHNand cognitive reserve. AHN is mainly related to remodeling stress response mechanisms, such as memory clearing, emotional control, and pattern separation, suggesting that a correlation may exist between neuroinflammation and AHN in stress resilience. Therefore, we summarized the previous research results to systematically expound on the relationship between AHN, stress resilience, and neuroinflammation. We hope this neurogenic hypothesis of positive psychology in stress-induced depression will provide a new perspective for the study of depression and antidepressant therapy.</description><subject>Adult</subject><subject>Adult hippocampal neurogenesis</subject><subject>Antidepressant therapy</subject><subject>Antidepressants</subject><subject>Anxiety</subject><subject>Brain</subject><subject>Brain damage</subject><subject>Cognitive ability</subject><subject>Cytokines</subject><subject>Depression - immunology</subject><subject>Depression - psychology</subject><subject>Enrichment</subject><subject>Hippocampus</subject><subject>Hippocampus - growth & development</subject><subject>Hippocampus - immunology</subject><subject>Humans</subject><subject>Hypotheses</subject><subject>Inflammation</subject><subject>Mental depression</subject><subject>Microglia</subject><subject>Neurogenesis</subject><subject>Neurogenesis - immunology</subject><subject>Neuroinflammation</subject><subject>Neuroinflammatory Diseases - etiology</subject><subject>Neuroinflammatory Diseases - immunology</subject><subject>Neuroinflammatory Diseases - psychology</subject><subject>Neurons</subject><subject>Pattern separation</subject><subject>Psychology</subject><subject>Psychology, Positive</subject><subject>Resilience</subject><subject>Resilience, Psychological</subject><subject>Risk analysis</subject><subject>Risk factors</subject><subject>Stress resilience</subject><subject>Stress, Psychological - complications</subject><subject>Stress, Psychological - immunology</subject><subject>Stress, Psychological - psychology</subject><issn>1567-5769</issn><issn>1878-1705</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kcGOFCEQhonRuOvqGxhD4sXD9gjdDXR72GSzcdVkoxc9EwaKHSbdgEBvMs_hC8vYsx48eAGq8tVf5P8Rek3JhhLK3-83zhc3x01LWlpbgrPuCTqngxgaKgh7Wt-Mi4YJPp6hFznvCan9nj5HZ103UtaP7Bz9-gpLCvfgnca7QwxlB9llHCyOIbviHgDHfNC7MIX7A3Ye55Ig58Z5s2gw2EA81i74D_jaLFPBOxdj0GqOasL-JH7UvFwr5-2k5lmVOnKJlTcnRVwPNznwGl6iZ1ZNGV6d7gv04_bj95vPzd23T19uru8a3Y2kNLTaAJp3Gvioje0p2_aaaW2tIBboYDVvYRgYsYxa1dPWbgn0vTItp1ywtrtA71bdmMLPBXKRs8sapkl5CEuWLWvJIKpPQ0Xf_oPuw5J8_V2l-EA6OjJRqX6ldAo5J7AyJjerdJCUyGNoci_X0OQxNLmGVsfenMSX7Qzm79BjShW4WgGobjw4SDLrP04Zl0AXaYL7_4bfgK-uYA</recordid><startdate>202108</startdate><enddate>202108</enddate><creator>Wu, Zuotian</creator><creator>Xiao, Ling</creator><creator>Wang, Huiling</creator><creator>Wang, Gaohua</creator><general>Elsevier B.V</general><general>Elsevier BV</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>7QO</scope><scope>7T5</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>202108</creationdate><title>Neurogenic hypothesis of positive psychology in stress-induced depression: Adult hippocampal neurogenesis, neuroinflammation, and stress resilience</title><author>Wu, Zuotian ; Xiao, Ling ; Wang, Huiling ; Wang, Gaohua</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c390t-1101ec63ce69cdf415b4c5ccff70fe18fc62e8850f51fa412fb0e44ad26167523</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adult</topic><topic>Adult hippocampal neurogenesis</topic><topic>Antidepressant therapy</topic><topic>Antidepressants</topic><topic>Anxiety</topic><topic>Brain</topic><topic>Brain damage</topic><topic>Cognitive ability</topic><topic>Cytokines</topic><topic>Depression - immunology</topic><topic>Depression - psychology</topic><topic>Enrichment</topic><topic>Hippocampus</topic><topic>Hippocampus - growth & development</topic><topic>Hippocampus - immunology</topic><topic>Humans</topic><topic>Hypotheses</topic><topic>Inflammation</topic><topic>Mental depression</topic><topic>Microglia</topic><topic>Neurogenesis</topic><topic>Neurogenesis - immunology</topic><topic>Neuroinflammation</topic><topic>Neuroinflammatory Diseases - etiology</topic><topic>Neuroinflammatory Diseases - immunology</topic><topic>Neuroinflammatory Diseases - psychology</topic><topic>Neurons</topic><topic>Pattern separation</topic><topic>Psychology</topic><topic>Psychology, Positive</topic><topic>Resilience</topic><topic>Resilience, Psychological</topic><topic>Risk analysis</topic><topic>Risk factors</topic><topic>Stress resilience</topic><topic>Stress, Psychological - complications</topic><topic>Stress, Psychological - immunology</topic><topic>Stress, Psychological - psychology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wu, Zuotian</creatorcontrib><creatorcontrib>Xiao, Ling</creatorcontrib><creatorcontrib>Wang, Huiling</creatorcontrib><creatorcontrib>Wang, Gaohua</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Immunology Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>International immunopharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wu, Zuotian</au><au>Xiao, Ling</au><au>Wang, Huiling</au><au>Wang, Gaohua</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neurogenic hypothesis of positive psychology in stress-induced depression: Adult hippocampal neurogenesis, neuroinflammation, and stress resilience</atitle><jtitle>International immunopharmacology</jtitle><addtitle>Int Immunopharmacol</addtitle><date>2021-08</date><risdate>2021</risdate><volume>97</volume><spage>107653</spage><epage>107653</epage><pages>107653-107653</pages><artnum>107653</artnum><issn>1567-5769</issn><eissn>1878-1705</eissn><abstract>•Stress-induced neuroinflammation affects AHN related pattern separation.•Neuroprotection is a self-protection measure of the brain against neuroinflammation.•Therapeutic potential of AHN may be a new direction of antidepressant therapy.
Stress is an important risk factor for depression. Emerging evidence supports the hypothesis that stress-mediated neuroinflammation destroys brain function and leads to anxiety-like and depression-like behaviors. Previous studies of stress-induced depression have mainly focused on pathological damage; however, the rise of positive psychology has attracted the interest of many researchers in environmental enrichment to promote stress resilience. The hippocampus is one of the most severely damaged brain regions in stress-induced depression. In addition, the hippocampus is one of the most unique regions in the brain, as new neurons are produced in the adult hippocampus, a process known as adult hippocampal neurogenesis (AHN). AHN is an important core component of the neurogenic hypothesis and has also become a major innovative breakthrough in positive psychology, in which environmental enrichment mediates stress resilience. Neuroinflammation, by activating microglia and releasing some proinflammatory cytokines, is increasingly shown to be one of the key determinant pathophysiological factors that negatively affects AHNand cognitive reserve. AHN is mainly related to remodeling stress response mechanisms, such as memory clearing, emotional control, and pattern separation, suggesting that a correlation may exist between neuroinflammation and AHN in stress resilience. Therefore, we summarized the previous research results to systematically expound on the relationship between AHN, stress resilience, and neuroinflammation. We hope this neurogenic hypothesis of positive psychology in stress-induced depression will provide a new perspective for the study of depression and antidepressant therapy.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>33915495</pmid><doi>10.1016/j.intimp.2021.107653</doi><tpages>1</tpages></addata></record> |
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subjects | Adult Adult hippocampal neurogenesis Antidepressant therapy Antidepressants Anxiety Brain Brain damage Cognitive ability Cytokines Depression - immunology Depression - psychology Enrichment Hippocampus Hippocampus - growth & development Hippocampus - immunology Humans Hypotheses Inflammation Mental depression Microglia Neurogenesis Neurogenesis - immunology Neuroinflammation Neuroinflammatory Diseases - etiology Neuroinflammatory Diseases - immunology Neuroinflammatory Diseases - psychology Neurons Pattern separation Psychology Psychology, Positive Resilience Resilience, Psychological Risk analysis Risk factors Stress resilience Stress, Psychological - complications Stress, Psychological - immunology Stress, Psychological - psychology |
title | Neurogenic hypothesis of positive psychology in stress-induced depression: Adult hippocampal neurogenesis, neuroinflammation, and stress resilience |
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