Wistar-Kyoto rats and chronically stressed Wistar rats present similar depression- and anxiety-like behaviors but different corticosterone and endocannabinoid system modulation

The interplay of social, psychological, and biological stresses can trigger mental health conditions such as major depressive disorder (MDD), adjustment disorder, and posttraumatic stress disorder (PTSD). The endocannabinoid system (ECS), comprising endocannabinoids and cannabinoid receptors, is the...

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Veröffentlicht in:Progress in neuro-psychopharmacology & biological psychiatry 2023-12, Vol.127, p.110825-110825, Article 110825
Hauptverfasser: Wang, Zitong, van Bruggen, Rebekah, Sandini, Thaisa, Hagen, Ethan V., Li, Xin-Min, Zhang, Yanbo
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container_title Progress in neuro-psychopharmacology & biological psychiatry
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creator Wang, Zitong
van Bruggen, Rebekah
Sandini, Thaisa
Hagen, Ethan V.
Li, Xin-Min
Zhang, Yanbo
description The interplay of social, psychological, and biological stresses can trigger mental health conditions such as major depressive disorder (MDD), adjustment disorder, and posttraumatic stress disorder (PTSD). The endocannabinoid system (ECS), comprising endocannabinoids and cannabinoid receptors, is the critical pathway that mediates responses to stress stimuli. This study aimed to investigate the ECS's impact on responding to chronic social instability stress (SIS). Wistar (WIS) rats and an endogenously depressed rat model, Wistar-Kyoto (WKY), were used to evaluate depression- and anxiety-like behavioral responses, cognitive function, hormone levels, and ECS function. The animals in the stress group (WIS-STS and WKY-STS) were exposed to TMT (predator odor) for 10 mins (two exposures in total: one in light cycle and one in dark cycle) and daily roommate changes (30 days in total), while the control group (CTL) rats were exposed to a sham odor stimulus (distilled water) and did not undergo roommate changes. The results in the open field test suggest that WKY rats had significantly lower locomotor activity than WIS rats. In contrast, WKY rats and chronically stressed WIS rats presented similar depression- and anxiety-like behaviors and impaired cognitive function in the elevated plus maze, forced swimming test, and novel objective recognition test. However, chronic SIS did not exacerbate these behavioral changes in WKY rats. ELISA and Western blot analysis indicated that chronic SIS did not induce further upregulation of endocannabinoids and CB1R downregulation in WKY rats compared to WIS rats. In addition, the Luminex assay revealed that WKY rats showed a higher resilience on the HPA-axis modulation towards chronic SIS, distinguished by the hyperactivity of the HPA-axis modulation in WIS rats. Overall, the study revealed that the chronic SIS animal model (stressed WIS rats) and an animal model of endogenous depression (WKY rats) can generate similar behavioral changes in anxious behavior, behavioral despair, and cognitive impairment. Both animal models present hyperactivity of the ACTH modulation and ECS activity, while WKY rats are more resilient on CORT modulation towards chronic SIS. [Display omitted] •Wistar-Kyoto and stressed Wistar rats showed similar behavioral outcomes.•Social instability does not exacerbate behavioral changes in Wistar-Kyoto rats.•Wistar-Kyoto rats are more resilient to HPA-axis modulation under social instability.•Wistar-Kyoto rats ar
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The endocannabinoid system (ECS), comprising endocannabinoids and cannabinoid receptors, is the critical pathway that mediates responses to stress stimuli. This study aimed to investigate the ECS's impact on responding to chronic social instability stress (SIS). Wistar (WIS) rats and an endogenously depressed rat model, Wistar-Kyoto (WKY), were used to evaluate depression- and anxiety-like behavioral responses, cognitive function, hormone levels, and ECS function. The animals in the stress group (WIS-STS and WKY-STS) were exposed to TMT (predator odor) for 10 mins (two exposures in total: one in light cycle and one in dark cycle) and daily roommate changes (30 days in total), while the control group (CTL) rats were exposed to a sham odor stimulus (distilled water) and did not undergo roommate changes. The results in the open field test suggest that WKY rats had significantly lower locomotor activity than WIS rats. In contrast, WKY rats and chronically stressed WIS rats presented similar depression- and anxiety-like behaviors and impaired cognitive function in the elevated plus maze, forced swimming test, and novel objective recognition test. However, chronic SIS did not exacerbate these behavioral changes in WKY rats. ELISA and Western blot analysis indicated that chronic SIS did not induce further upregulation of endocannabinoids and CB1R downregulation in WKY rats compared to WIS rats. In addition, the Luminex assay revealed that WKY rats showed a higher resilience on the HPA-axis modulation towards chronic SIS, distinguished by the hyperactivity of the HPA-axis modulation in WIS rats. Overall, the study revealed that the chronic SIS animal model (stressed WIS rats) and an animal model of endogenous depression (WKY rats) can generate similar behavioral changes in anxious behavior, behavioral despair, and cognitive impairment. Both animal models present hyperactivity of the ACTH modulation and ECS activity, while WKY rats are more resilient on CORT modulation towards chronic SIS. [Display omitted] •Wistar-Kyoto and stressed Wistar rats showed similar behavioral outcomes.•Social instability does not exacerbate behavioral changes in Wistar-Kyoto rats.•Wistar-Kyoto rats are more resilient to HPA-axis modulation under social instability.•Wistar-Kyoto rats are more resilient to 2-AG regulation following social instability.•CB1R downregulation recorded in stressed Wistar rats was absent in Wistar-Kyoto rats.</description><identifier>ISSN: 0278-5846</identifier><identifier>EISSN: 1878-4216</identifier><identifier>DOI: 10.1016/j.pnpbp.2023.110825</identifier><identifier>PMID: 37437836</identifier><language>eng</language><publisher>England: Elsevier Inc</publisher><subject>Anxiety ; Chronic stress ; Depression ; Endocannabinoid system ; Wistar ; Wistar-Kyoto</subject><ispartof>Progress in neuro-psychopharmacology &amp; biological psychiatry, 2023-12, Vol.127, p.110825-110825, Article 110825</ispartof><rights>2023 Elsevier Inc.</rights><rights>Copyright © 2023. 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The endocannabinoid system (ECS), comprising endocannabinoids and cannabinoid receptors, is the critical pathway that mediates responses to stress stimuli. This study aimed to investigate the ECS's impact on responding to chronic social instability stress (SIS). Wistar (WIS) rats and an endogenously depressed rat model, Wistar-Kyoto (WKY), were used to evaluate depression- and anxiety-like behavioral responses, cognitive function, hormone levels, and ECS function. The animals in the stress group (WIS-STS and WKY-STS) were exposed to TMT (predator odor) for 10 mins (two exposures in total: one in light cycle and one in dark cycle) and daily roommate changes (30 days in total), while the control group (CTL) rats were exposed to a sham odor stimulus (distilled water) and did not undergo roommate changes. The results in the open field test suggest that WKY rats had significantly lower locomotor activity than WIS rats. In contrast, WKY rats and chronically stressed WIS rats presented similar depression- and anxiety-like behaviors and impaired cognitive function in the elevated plus maze, forced swimming test, and novel objective recognition test. However, chronic SIS did not exacerbate these behavioral changes in WKY rats. ELISA and Western blot analysis indicated that chronic SIS did not induce further upregulation of endocannabinoids and CB1R downregulation in WKY rats compared to WIS rats. In addition, the Luminex assay revealed that WKY rats showed a higher resilience on the HPA-axis modulation towards chronic SIS, distinguished by the hyperactivity of the HPA-axis modulation in WIS rats. Overall, the study revealed that the chronic SIS animal model (stressed WIS rats) and an animal model of endogenous depression (WKY rats) can generate similar behavioral changes in anxious behavior, behavioral despair, and cognitive impairment. Both animal models present hyperactivity of the ACTH modulation and ECS activity, while WKY rats are more resilient on CORT modulation towards chronic SIS. [Display omitted] •Wistar-Kyoto and stressed Wistar rats showed similar behavioral outcomes.•Social instability does not exacerbate behavioral changes in Wistar-Kyoto rats.•Wistar-Kyoto rats are more resilient to HPA-axis modulation under social instability.•Wistar-Kyoto rats are more resilient to 2-AG regulation following social instability.•CB1R downregulation recorded in stressed Wistar rats was absent in Wistar-Kyoto rats.</description><subject>Anxiety</subject><subject>Chronic stress</subject><subject>Depression</subject><subject>Endocannabinoid system</subject><subject>Wistar</subject><subject>Wistar-Kyoto</subject><issn>0278-5846</issn><issn>1878-4216</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9kc1u1DAUhS0EotPCEyAhL9lk8E9-PAsWqCpQUYkNiKXl2Deqh8QOvk5F3opHxDMpLFnZuv7OObo-hLzibM8Zb98e93OY-3kvmJB7zpkSzROy46pTVS14-5TsmCj3RtXtBblEPDLGuGTyObmQXS07Jdsd-f3dYzap-rzGHGkyGakJjtr7FIO3ZhxXijkBIji6oRs0lxmETNFPfixDB6cJ-hiqs4EJvzzktRr9D6A93JsHHxPSfsnU-WGAdBLbmLK3ETOUNDjrILhoTQim9yF6R3EtrxOdoltGk4v9C_JsMCPCy8fzinz7cPP1-lN19-Xj7fX7u8rK5pArceAcBHeK14p1NRua2rph6BoprBpErRorZS3c0BdAtX0vlOgkNJ3oHDRCyCvyZvOdU_y5AGY9ebQwjiZAXFCL8n2qaw5cFlRuqE0RMcGg5-Qnk1bNmT5VpY_6XJU-VaW3qorq9WPA0k_g_mn-dlOAdxsAZc0HD0mj9RAsOJ_AZu2i_2_AHySJqr0</recordid><startdate>20231220</startdate><enddate>20231220</enddate><creator>Wang, Zitong</creator><creator>van Bruggen, Rebekah</creator><creator>Sandini, Thaisa</creator><creator>Hagen, Ethan V.</creator><creator>Li, Xin-Min</creator><creator>Zhang, Yanbo</creator><general>Elsevier Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20231220</creationdate><title>Wistar-Kyoto rats and chronically stressed Wistar rats present similar depression- and anxiety-like behaviors but different corticosterone and endocannabinoid system modulation</title><author>Wang, Zitong ; van Bruggen, Rebekah ; Sandini, Thaisa ; Hagen, Ethan V. ; Li, Xin-Min ; Zhang, Yanbo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c359t-2911e21d81480740f54cdff7532c8f2485c3342dfb14886bb28273e5727de5223</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Anxiety</topic><topic>Chronic stress</topic><topic>Depression</topic><topic>Endocannabinoid system</topic><topic>Wistar</topic><topic>Wistar-Kyoto</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Zitong</creatorcontrib><creatorcontrib>van Bruggen, Rebekah</creatorcontrib><creatorcontrib>Sandini, Thaisa</creatorcontrib><creatorcontrib>Hagen, Ethan V.</creatorcontrib><creatorcontrib>Li, Xin-Min</creatorcontrib><creatorcontrib>Zhang, Yanbo</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Progress in neuro-psychopharmacology &amp; biological psychiatry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Zitong</au><au>van Bruggen, Rebekah</au><au>Sandini, Thaisa</au><au>Hagen, Ethan V.</au><au>Li, Xin-Min</au><au>Zhang, Yanbo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Wistar-Kyoto rats and chronically stressed Wistar rats present similar depression- and anxiety-like behaviors but different corticosterone and endocannabinoid system modulation</atitle><jtitle>Progress in neuro-psychopharmacology &amp; biological psychiatry</jtitle><addtitle>Prog Neuropsychopharmacol Biol Psychiatry</addtitle><date>2023-12-20</date><risdate>2023</risdate><volume>127</volume><spage>110825</spage><epage>110825</epage><pages>110825-110825</pages><artnum>110825</artnum><issn>0278-5846</issn><eissn>1878-4216</eissn><abstract>The interplay of social, psychological, and biological stresses can trigger mental health conditions such as major depressive disorder (MDD), adjustment disorder, and posttraumatic stress disorder (PTSD). The endocannabinoid system (ECS), comprising endocannabinoids and cannabinoid receptors, is the critical pathway that mediates responses to stress stimuli. This study aimed to investigate the ECS's impact on responding to chronic social instability stress (SIS). Wistar (WIS) rats and an endogenously depressed rat model, Wistar-Kyoto (WKY), were used to evaluate depression- and anxiety-like behavioral responses, cognitive function, hormone levels, and ECS function. The animals in the stress group (WIS-STS and WKY-STS) were exposed to TMT (predator odor) for 10 mins (two exposures in total: one in light cycle and one in dark cycle) and daily roommate changes (30 days in total), while the control group (CTL) rats were exposed to a sham odor stimulus (distilled water) and did not undergo roommate changes. The results in the open field test suggest that WKY rats had significantly lower locomotor activity than WIS rats. In contrast, WKY rats and chronically stressed WIS rats presented similar depression- and anxiety-like behaviors and impaired cognitive function in the elevated plus maze, forced swimming test, and novel objective recognition test. However, chronic SIS did not exacerbate these behavioral changes in WKY rats. ELISA and Western blot analysis indicated that chronic SIS did not induce further upregulation of endocannabinoids and CB1R downregulation in WKY rats compared to WIS rats. In addition, the Luminex assay revealed that WKY rats showed a higher resilience on the HPA-axis modulation towards chronic SIS, distinguished by the hyperactivity of the HPA-axis modulation in WIS rats. Overall, the study revealed that the chronic SIS animal model (stressed WIS rats) and an animal model of endogenous depression (WKY rats) can generate similar behavioral changes in anxious behavior, behavioral despair, and cognitive impairment. Both animal models present hyperactivity of the ACTH modulation and ECS activity, while WKY rats are more resilient on CORT modulation towards chronic SIS. [Display omitted] •Wistar-Kyoto and stressed Wistar rats showed similar behavioral outcomes.•Social instability does not exacerbate behavioral changes in Wistar-Kyoto rats.•Wistar-Kyoto rats are more resilient to HPA-axis modulation under social instability.•Wistar-Kyoto rats are more resilient to 2-AG regulation following social instability.•CB1R downregulation recorded in stressed Wistar rats was absent in Wistar-Kyoto rats.</abstract><cop>England</cop><pub>Elsevier Inc</pub><pmid>37437836</pmid><doi>10.1016/j.pnpbp.2023.110825</doi><tpages>1</tpages></addata></record>
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source Elsevier ScienceDirect Journals
subjects Anxiety
Chronic stress
Depression
Endocannabinoid system
Wistar
Wistar-Kyoto
title Wistar-Kyoto rats and chronically stressed Wistar rats present similar depression- and anxiety-like behaviors but different corticosterone and endocannabinoid system modulation
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