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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Veröffentlicht in:Steroids 2017-09, Vol.125, p.131-136
Hauptverfasser: Zeni, Ana Lúcia Bertarello, Camargo, Anderson, Dalmagro, Ana Paula
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Camargo, Anderson
Dalmagro, Ana Paula
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.
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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. 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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. 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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. 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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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