Ferulic acid reverses depression-like behavior and oxidative stress induced by chronic corticosterone treatment in mice
•Chronic administration of corticosterone elicits depressive-like behavior and oxidative stress.•Ferulic acid abolishes the depressive phenotype induced by corticosterone.•Corticosterone administration increases the levels of oxidative stress markers in mice.•Ferulic acid reverses the corticosterone...
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description | •Chronic administration of corticosterone elicits depressive-like behavior and oxidative stress.•Ferulic acid abolishes the depressive phenotype induced by corticosterone.•Corticosterone administration increases the levels of oxidative stress markers in mice.•Ferulic acid reverses the corticosterone –induced oxidative stress in the mice’s serum and brain.
Corticosterone (CORT) treatment has been evidenced to develop a depression-like state in animals, that mimic hypothalamic–pituitary–adrenal (HPA)-axis dysregulation implicated in the development of depression. The present study aimed to examine the ferulic acid (FA), a natural phenolic compound, antidepressant and antioxidant activities on the CORT chronic model. Mice orally treated with 20mg/kg of CORT for 21days were connsidered control group, while mice treated with FA (1mg/kg) or fluoxetine (10mg/kg) for the last week of CORT treatment, as drug groups. Three weeks of CORT treatment resulted in depressive-like behavior, as indicated by the increase on the immobility time in the tail suspension test, grooming in the splash test and an increase in the oxidative stress markers in the brain. It was observed that FA ameliorated the behavioral and oxidative stress alterations induced by CORT, which may plausibly suggest a mode of action for the FA antidepressant effect. The involvement of FA repairing the stress caused by HPA-axis dysfunction evidenced that this phenolic acid could be further investigated as a novel potential agent to improve the management of depression. |
doi_str_mv | 10.1016/j.steroids.2017.07.006 |
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Corticosterone (CORT) treatment has been evidenced to develop a depression-like state in animals, that mimic hypothalamic–pituitary–adrenal (HPA)-axis dysregulation implicated in the development of depression. The present study aimed to examine the ferulic acid (FA), a natural phenolic compound, antidepressant and antioxidant activities on the CORT chronic model. Mice orally treated with 20mg/kg of CORT for 21days were connsidered control group, while mice treated with FA (1mg/kg) or fluoxetine (10mg/kg) for the last week of CORT treatment, as drug groups. Three weeks of CORT treatment resulted in depressive-like behavior, as indicated by the increase on the immobility time in the tail suspension test, grooming in the splash test and an increase in the oxidative stress markers in the brain. It was observed that FA ameliorated the behavioral and oxidative stress alterations induced by CORT, which may plausibly suggest a mode of action for the FA antidepressant effect. The involvement of FA repairing the stress caused by HPA-axis dysfunction evidenced that this phenolic acid could be further investigated as a novel potential agent to improve the management of depression.</description><identifier>ISSN: 0039-128X</identifier><identifier>EISSN: 1878-5867</identifier><identifier>DOI: 10.1016/j.steroids.2017.07.006</identifier><identifier>PMID: 28733038</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Antidepressive Agents - pharmacology ; Antidepressive Agents - therapeutic use ; Behavior, Animal - drug effects ; Biomarkers - metabolism ; Corticosterone ; Corticosterone - adverse effects ; Coumaric Acids - pharmacology ; Coumaric Acids - therapeutic use ; Depression ; Depression - chemically induced ; Depression - drug therapy ; Depression - metabolism ; Emotions - drug effects ; Exploratory Behavior - drug effects ; Ferulic acid ; Grooming - drug effects ; Locomotion - drug effects ; Male ; Mice ; Oxidative stress ; Oxidative Stress - drug effects ; Time Factors</subject><ispartof>Steroids, 2017-09, Vol.125, p.131-136</ispartof><rights>2017 Elsevier Inc.</rights><rights>Copyright © 2017 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c368t-9c968e99d852e44441074d25d9eb7193d1209bfb15de6f5abd0ff8a6ad6814553</citedby><cites>FETCH-LOGICAL-c368t-9c968e99d852e44441074d25d9eb7193d1209bfb15de6f5abd0ff8a6ad6814553</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.steroids.2017.07.006$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28733038$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zeni, Ana Lúcia Bertarello</creatorcontrib><creatorcontrib>Camargo, Anderson</creatorcontrib><creatorcontrib>Dalmagro, Ana Paula</creatorcontrib><title>Ferulic acid reverses depression-like behavior and oxidative stress induced by chronic corticosterone treatment in mice</title><title>Steroids</title><addtitle>Steroids</addtitle><description>•Chronic administration of corticosterone elicits depressive-like behavior and oxidative stress.•Ferulic acid abolishes the depressive phenotype induced by corticosterone.•Corticosterone administration increases the levels of oxidative stress markers in mice.•Ferulic acid reverses the corticosterone –induced oxidative stress in the mice’s serum and brain.
Corticosterone (CORT) treatment has been evidenced to develop a depression-like state in animals, that mimic hypothalamic–pituitary–adrenal (HPA)-axis dysregulation implicated in the development of depression. The present study aimed to examine the ferulic acid (FA), a natural phenolic compound, antidepressant and antioxidant activities on the CORT chronic model. Mice orally treated with 20mg/kg of CORT for 21days were connsidered control group, while mice treated with FA (1mg/kg) or fluoxetine (10mg/kg) for the last week of CORT treatment, as drug groups. Three weeks of CORT treatment resulted in depressive-like behavior, as indicated by the increase on the immobility time in the tail suspension test, grooming in the splash test and an increase in the oxidative stress markers in the brain. It was observed that FA ameliorated the behavioral and oxidative stress alterations induced by CORT, which may plausibly suggest a mode of action for the FA antidepressant effect. The involvement of FA repairing the stress caused by HPA-axis dysfunction evidenced that this phenolic acid could be further investigated as a novel potential agent to improve the management of depression.</description><subject>Animals</subject><subject>Antidepressive Agents - pharmacology</subject><subject>Antidepressive Agents - therapeutic use</subject><subject>Behavior, Animal - drug effects</subject><subject>Biomarkers - metabolism</subject><subject>Corticosterone</subject><subject>Corticosterone - adverse effects</subject><subject>Coumaric Acids - pharmacology</subject><subject>Coumaric Acids - therapeutic use</subject><subject>Depression</subject><subject>Depression - chemically induced</subject><subject>Depression - drug therapy</subject><subject>Depression - metabolism</subject><subject>Emotions - drug effects</subject><subject>Exploratory Behavior - drug effects</subject><subject>Ferulic acid</subject><subject>Grooming - drug effects</subject><subject>Locomotion - drug effects</subject><subject>Male</subject><subject>Mice</subject><subject>Oxidative stress</subject><subject>Oxidative Stress - drug effects</subject><subject>Time Factors</subject><issn>0039-128X</issn><issn>1878-5867</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtv1DAQgC0EotuFv1D5yCVb29n4cQNV9CFV4gISN8uxJ-osSbzYztL--3rZliujkebyzesj5IKzDWdcXu42uUCKGPJGMK42rCaTb8iKa6WbTkv1lqwYa03Dhf55Rs5z3rFKtEa8J2dCq7ZlrV6RP9eQlhE9dR4DTXCAlCHTAPsEOWOcmxF_Ae3hwR0wJurmQOMjBlfwADSXI0VxDouHQPsn6h9SnOs4H1NBH_8eOQOtnCsTzKWydEIPH8i7wY0ZPr7UNflx_fX71W1z_-3m7urLfeNbqUtjvJEajAm6E7CtwZnaBtEFA73ipg1cMNMPPe8CyKFzfWDDoJ10QWq-7bp2TT6d5u5T_L1ALnbC7GEc3QxxyZYbITqmtFIVlSfUp5hzgsHuE04uPVnO7FG63dlX6fYo3bKaVemaXLzsWPoJwr-2V8sV-HwCoH56QEg2e4S5KsMEvtgQ8X87ngFxxJnH</recordid><startdate>20170901</startdate><enddate>20170901</enddate><creator>Zeni, Ana Lúcia Bertarello</creator><creator>Camargo, Anderson</creator><creator>Dalmagro, Ana Paula</creator><general>Elsevier Inc</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></search><sort><creationdate>20170901</creationdate><title>Ferulic acid reverses depression-like behavior and oxidative stress induced by chronic corticosterone treatment in mice</title><author>Zeni, Ana Lúcia Bertarello ; Camargo, Anderson ; Dalmagro, Ana Paula</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c368t-9c968e99d852e44441074d25d9eb7193d1209bfb15de6f5abd0ff8a6ad6814553</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Animals</topic><topic>Antidepressive Agents - pharmacology</topic><topic>Antidepressive Agents - therapeutic use</topic><topic>Behavior, Animal - drug effects</topic><topic>Biomarkers - metabolism</topic><topic>Corticosterone</topic><topic>Corticosterone - adverse effects</topic><topic>Coumaric Acids - pharmacology</topic><topic>Coumaric Acids - therapeutic use</topic><topic>Depression</topic><topic>Depression - chemically induced</topic><topic>Depression - drug therapy</topic><topic>Depression - metabolism</topic><topic>Emotions - drug effects</topic><topic>Exploratory Behavior - drug effects</topic><topic>Ferulic acid</topic><topic>Grooming - drug effects</topic><topic>Locomotion - drug effects</topic><topic>Male</topic><topic>Mice</topic><topic>Oxidative stress</topic><topic>Oxidative Stress - drug effects</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zeni, Ana Lúcia Bertarello</creatorcontrib><creatorcontrib>Camargo, Anderson</creatorcontrib><creatorcontrib>Dalmagro, Ana Paula</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Steroids</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zeni, Ana Lúcia Bertarello</au><au>Camargo, Anderson</au><au>Dalmagro, Ana Paula</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ferulic acid reverses depression-like behavior and oxidative stress induced by chronic corticosterone treatment in mice</atitle><jtitle>Steroids</jtitle><addtitle>Steroids</addtitle><date>2017-09-01</date><risdate>2017</risdate><volume>125</volume><spage>131</spage><epage>136</epage><pages>131-136</pages><issn>0039-128X</issn><eissn>1878-5867</eissn><abstract>•Chronic administration of corticosterone elicits depressive-like behavior and oxidative stress.•Ferulic acid abolishes the depressive phenotype induced by corticosterone.•Corticosterone administration increases the levels of oxidative stress markers in mice.•Ferulic acid reverses the corticosterone –induced oxidative stress in the mice’s serum and brain.
Corticosterone (CORT) treatment has been evidenced to develop a depression-like state in animals, that mimic hypothalamic–pituitary–adrenal (HPA)-axis dysregulation implicated in the development of depression. The present study aimed to examine the ferulic acid (FA), a natural phenolic compound, antidepressant and antioxidant activities on the CORT chronic model. Mice orally treated with 20mg/kg of CORT for 21days were connsidered control group, while mice treated with FA (1mg/kg) or fluoxetine (10mg/kg) for the last week of CORT treatment, as drug groups. Three weeks of CORT treatment resulted in depressive-like behavior, as indicated by the increase on the immobility time in the tail suspension test, grooming in the splash test and an increase in the oxidative stress markers in the brain. It was observed that FA ameliorated the behavioral and oxidative stress alterations induced by CORT, which may plausibly suggest a mode of action for the FA antidepressant effect. The involvement of FA repairing the stress caused by HPA-axis dysfunction evidenced that this phenolic acid could be further investigated as a novel potential agent to improve the management of depression.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>28733038</pmid><doi>10.1016/j.steroids.2017.07.006</doi><tpages>6</tpages></addata></record> |
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subjects | Animals Antidepressive Agents - pharmacology Antidepressive Agents - therapeutic use Behavior, Animal - drug effects Biomarkers - metabolism Corticosterone Corticosterone - adverse effects Coumaric Acids - pharmacology Coumaric Acids - therapeutic use Depression Depression - chemically induced Depression - drug therapy Depression - metabolism Emotions - drug effects Exploratory Behavior - drug effects Ferulic acid Grooming - drug effects Locomotion - drug effects Male Mice Oxidative stress Oxidative Stress - drug effects Time Factors |
title | Ferulic acid reverses depression-like behavior and oxidative stress induced by chronic corticosterone treatment in mice |
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