Curcumin reverses the effects of chronic stress on behavior, the HPA axis, BDNF expression and phosphorylation of CREB
Curcuma longa is a major constituent of the traditional Chinese medicine Xiaoyao-san, which has been used to effectively manage stress and depression-related disorders in China. Curcumin is the active component of curcuma longa, and its antidepressant effects were described in our prior studies in m...
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description | Curcuma longa is a major constituent of the traditional Chinese medicine Xiaoyao-san, which has been used to effectively manage stress and depression-related disorders in China. Curcumin is the active component of curcuma longa, and its antidepressant effects were described in our prior studies in mouse models of behavioral despair. We hypothesized that curcumin may also alleviate stress-induced depressive-like behaviors and hypothalamic–pituitary–adrenal (HPA) axis dysfunction. Thus in present study we assessed whether curcumin treatment (2.5, 5 and 10 mg/kg, p.o.) affects behavior in a chronic unpredictable stress model of depression in rats and examined what its molecular targets may be. We found that subjecting animals to the chronic stress protocol for 20
days resulted in performance deficits in the shuttle-box task and several physiological effects, such as an abnormal adrenal gland weight to body weight (AG/B) ratio and increased thickness of the adrenal cortex as well as elevated serum corticosterone levels and reduced glucocorticoid receptor (GR) mRNA expression. These changes were reversed by chronic curcumin administration (5 or 10 mg/kg, p.o.). In addition, we also found that the chronic stress procedure induced a down-regulation of brain-derived neurotrophic factor (BDNF) protein levels and reduced the ratio of phosphorylated cAMP response element-binding protein (pCREB) to CREB levels (pCREB/CREB) in the hippocampus and frontal cortex of stressed rats. Furthermore, these stress-induced decreases in BDNF and pCREB/CREB were also blocked by chronic curcumin administration (5 or 10 mg/kg, p.o.). These results provide compelling evidence that the behavioral effects of curcumin in chronically stressed animals, and by extension humans, may be related to their modulating effects on the HPA axis and neurotrophin factor expressions. |
doi_str_mv | 10.1016/j.brainres.2006.09.009 |
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days resulted in performance deficits in the shuttle-box task and several physiological effects, such as an abnormal adrenal gland weight to body weight (AG/B) ratio and increased thickness of the adrenal cortex as well as elevated serum corticosterone levels and reduced glucocorticoid receptor (GR) mRNA expression. These changes were reversed by chronic curcumin administration (5 or 10 mg/kg, p.o.). In addition, we also found that the chronic stress procedure induced a down-regulation of brain-derived neurotrophic factor (BDNF) protein levels and reduced the ratio of phosphorylated cAMP response element-binding protein (pCREB) to CREB levels (pCREB/CREB) in the hippocampus and frontal cortex of stressed rats. Furthermore, these stress-induced decreases in BDNF and pCREB/CREB were also blocked by chronic curcumin administration (5 or 10 mg/kg, p.o.). These results provide compelling evidence that the behavioral effects of curcumin in chronically stressed animals, and by extension humans, may be related to their modulating effects on the HPA axis and neurotrophin factor expressions.</description><identifier>ISSN: 0006-8993</identifier><identifier>EISSN: 1872-6240</identifier><identifier>DOI: 10.1016/j.brainres.2006.09.009</identifier><identifier>PMID: 17022948</identifier><identifier>CODEN: BRREAP</identifier><language>eng</language><publisher>London: Elsevier B.V</publisher><subject>Adrenal Glands - anatomy & histology ; Adrenal Glands - drug effects ; Adult and adolescent clinical studies ; Analysis of Variance ; Animals ; BDNF ; Biological and medical sciences ; Body Weight - drug effects ; Brain-Derived Neurotrophic Factor - drug effects ; Brain-Derived Neurotrophic Factor - genetics ; Brain-Derived Neurotrophic Factor - metabolism ; Chronic unpredictable stress ; Corticosterone - blood ; Curcuma ; Curcuma longa ; Curcumin ; Curcumin - administration & dosage ; Cyclic AMP Response Element-Binding Protein - drug effects ; Cyclic AMP Response Element-Binding Protein - metabolism ; Depression ; Depressive Disorder - drug therapy ; Depressive Disorder - etiology ; Depressive Disorder - metabolism ; Dose-Response Relationship, Drug ; Down-Regulation ; Drugs, Chinese Herbal - administration & dosage ; Escape Reaction - drug effects ; Exploratory Behavior - drug effects ; Exploratory Behavior - physiology ; Frontal Lobe - drug effects ; Frontal Lobe - metabolism ; Hippocampus - drug effects ; Hippocampus - metabolism ; HPA axis ; Hypothalamo-Hypophyseal System - drug effects ; Hypothalamo-Hypophyseal System - metabolism ; Hypothalamo-Hypophyseal System - physiopathology ; Male ; Medical sciences ; Mood disorders ; Organ Size ; pCREB/CREB ; Phosphorylation ; Pituitary-Adrenal System - drug effects ; Pituitary-Adrenal System - metabolism ; Pituitary-Adrenal System - physiopathology ; Psychology. Psychoanalysis. Psychiatry ; Psychopathology. Psychiatry ; Rat ; Rats ; Rats, Sprague-Dawley ; RNA, Messenger - analysis ; Shuttle box ; Statistics, Nonparametric ; Stress, Psychological - complications ; Stress, Psychological - drug therapy ; Stress, Psychological - metabolism</subject><ispartof>Brain research, 2006-11, Vol.1122 (1), p.56-64</ispartof><rights>2006 Elsevier B.V.</rights><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c493t-b2496a452191c71bb75500d5432e825ea7c86b1a1e647c7f117858bdbb2797af3</citedby><cites>FETCH-LOGICAL-c493t-b2496a452191c71bb75500d5432e825ea7c86b1a1e647c7f117858bdbb2797af3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0006899306027144$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18294784$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17022948$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xu, Ying</creatorcontrib><creatorcontrib>Ku, Baoshan</creatorcontrib><creatorcontrib>Tie, Lu</creatorcontrib><creatorcontrib>Yao, Haiyan</creatorcontrib><creatorcontrib>Jiang, Wengao</creatorcontrib><creatorcontrib>Ma, Xing</creatorcontrib><creatorcontrib>Li, Xuejun</creatorcontrib><title>Curcumin reverses the effects of chronic stress on behavior, the HPA axis, BDNF expression and phosphorylation of CREB</title><title>Brain research</title><addtitle>Brain Res</addtitle><description>Curcuma longa is a major constituent of the traditional Chinese medicine Xiaoyao-san, which has been used to effectively manage stress and depression-related disorders in China. Curcumin is the active component of curcuma longa, and its antidepressant effects were described in our prior studies in mouse models of behavioral despair. We hypothesized that curcumin may also alleviate stress-induced depressive-like behaviors and hypothalamic–pituitary–adrenal (HPA) axis dysfunction. Thus in present study we assessed whether curcumin treatment (2.5, 5 and 10 mg/kg, p.o.) affects behavior in a chronic unpredictable stress model of depression in rats and examined what its molecular targets may be. We found that subjecting animals to the chronic stress protocol for 20
days resulted in performance deficits in the shuttle-box task and several physiological effects, such as an abnormal adrenal gland weight to body weight (AG/B) ratio and increased thickness of the adrenal cortex as well as elevated serum corticosterone levels and reduced glucocorticoid receptor (GR) mRNA expression. These changes were reversed by chronic curcumin administration (5 or 10 mg/kg, p.o.). In addition, we also found that the chronic stress procedure induced a down-regulation of brain-derived neurotrophic factor (BDNF) protein levels and reduced the ratio of phosphorylated cAMP response element-binding protein (pCREB) to CREB levels (pCREB/CREB) in the hippocampus and frontal cortex of stressed rats. Furthermore, these stress-induced decreases in BDNF and pCREB/CREB were also blocked by chronic curcumin administration (5 or 10 mg/kg, p.o.). These results provide compelling evidence that the behavioral effects of curcumin in chronically stressed animals, and by extension humans, may be related to their modulating effects on the HPA axis and neurotrophin factor expressions.</description><subject>Adrenal Glands - anatomy & histology</subject><subject>Adrenal Glands - drug effects</subject><subject>Adult and adolescent clinical studies</subject><subject>Analysis of Variance</subject><subject>Animals</subject><subject>BDNF</subject><subject>Biological and medical sciences</subject><subject>Body Weight - drug effects</subject><subject>Brain-Derived Neurotrophic Factor - drug effects</subject><subject>Brain-Derived Neurotrophic Factor - genetics</subject><subject>Brain-Derived Neurotrophic Factor - metabolism</subject><subject>Chronic unpredictable stress</subject><subject>Corticosterone - blood</subject><subject>Curcuma</subject><subject>Curcuma longa</subject><subject>Curcumin</subject><subject>Curcumin - administration & dosage</subject><subject>Cyclic AMP Response Element-Binding Protein - drug effects</subject><subject>Cyclic AMP Response Element-Binding Protein - metabolism</subject><subject>Depression</subject><subject>Depressive Disorder - drug therapy</subject><subject>Depressive Disorder - etiology</subject><subject>Depressive Disorder - metabolism</subject><subject>Dose-Response Relationship, Drug</subject><subject>Down-Regulation</subject><subject>Drugs, Chinese Herbal - administration & dosage</subject><subject>Escape Reaction - drug effects</subject><subject>Exploratory Behavior - drug effects</subject><subject>Exploratory Behavior - physiology</subject><subject>Frontal Lobe - drug effects</subject><subject>Frontal Lobe - metabolism</subject><subject>Hippocampus - drug effects</subject><subject>Hippocampus - metabolism</subject><subject>HPA axis</subject><subject>Hypothalamo-Hypophyseal System - drug effects</subject><subject>Hypothalamo-Hypophyseal System - metabolism</subject><subject>Hypothalamo-Hypophyseal System - physiopathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mood disorders</subject><subject>Organ Size</subject><subject>pCREB/CREB</subject><subject>Phosphorylation</subject><subject>Pituitary-Adrenal System - drug effects</subject><subject>Pituitary-Adrenal System - metabolism</subject><subject>Pituitary-Adrenal System - physiopathology</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychopathology. Psychiatry</subject><subject>Rat</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>RNA, Messenger - analysis</subject><subject>Shuttle box</subject><subject>Statistics, Nonparametric</subject><subject>Stress, Psychological - complications</subject><subject>Stress, Psychological - drug therapy</subject><subject>Stress, Psychological - metabolism</subject><issn>0006-8993</issn><issn>1872-6240</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcFu3CAQQFHVqtkk_YWIS3uKXcDYwK3JNmkqRW0VtWcEeKxl5bW3jL1K_r5sdqsccxihGd7MIB4hF5yVnPHm87r0ycUhAZaCsaZkpmTMvCELrpUoGiHZW7Jg-abQxlQn5BRxndOqMuw9OeGKCWGkXpDdck5h3sSBJthBQkA6rYBC10GYkI4dDas0DjFQnPKyXBmoh5XbxTFdPqN3v66oe4x4Sa-__ril8LjdczFzbmjpdjVijvTUu2lfywOXDzfX5-Rd53qED8fzjPy5vfm9vCvuf377vry6L4I01VR4IU3jZC244UFx71VdM9bWshKgRQ1OBd147jg0UgXVca50rX3rvVBGua46I58Oc7dp_DsDTnYTMUDfuwHGGW2juay0FK-C3NSsllpnsDmAIY2ICTq7TXHj0pPlzO7V2LX9r8bu1VhmbFaTGy-OG2a_gfal7egiAx-PgMPg-i65IUR84XSmlJaZ-3LgIH_cLkKyGCIMAdqYsjTbjvG1t_wDIdmvyA</recordid><startdate>20061129</startdate><enddate>20061129</enddate><creator>Xu, Ying</creator><creator>Ku, Baoshan</creator><creator>Tie, Lu</creator><creator>Yao, Haiyan</creator><creator>Jiang, Wengao</creator><creator>Ma, Xing</creator><creator>Li, Xuejun</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><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>7TK</scope><scope>7X8</scope></search><sort><creationdate>20061129</creationdate><title>Curcumin reverses the effects of chronic stress on behavior, the HPA axis, BDNF expression and phosphorylation of CREB</title><author>Xu, Ying ; Ku, Baoshan ; Tie, Lu ; Yao, Haiyan ; Jiang, Wengao ; Ma, Xing ; Li, Xuejun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c493t-b2496a452191c71bb75500d5432e825ea7c86b1a1e647c7f117858bdbb2797af3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Adrenal Glands - anatomy & histology</topic><topic>Adrenal Glands - drug effects</topic><topic>Adult and adolescent clinical studies</topic><topic>Analysis of Variance</topic><topic>Animals</topic><topic>BDNF</topic><topic>Biological and medical sciences</topic><topic>Body Weight - drug effects</topic><topic>Brain-Derived Neurotrophic Factor - drug effects</topic><topic>Brain-Derived Neurotrophic Factor - genetics</topic><topic>Brain-Derived Neurotrophic Factor - metabolism</topic><topic>Chronic unpredictable stress</topic><topic>Corticosterone - blood</topic><topic>Curcuma</topic><topic>Curcuma longa</topic><topic>Curcumin</topic><topic>Curcumin - administration & dosage</topic><topic>Cyclic AMP Response Element-Binding Protein - drug effects</topic><topic>Cyclic AMP Response Element-Binding Protein - metabolism</topic><topic>Depression</topic><topic>Depressive Disorder - drug therapy</topic><topic>Depressive Disorder - etiology</topic><topic>Depressive Disorder - metabolism</topic><topic>Dose-Response Relationship, Drug</topic><topic>Down-Regulation</topic><topic>Drugs, Chinese Herbal - administration & dosage</topic><topic>Escape Reaction - drug effects</topic><topic>Exploratory Behavior - drug effects</topic><topic>Exploratory Behavior - physiology</topic><topic>Frontal Lobe - drug effects</topic><topic>Frontal Lobe - metabolism</topic><topic>Hippocampus - drug effects</topic><topic>Hippocampus - metabolism</topic><topic>HPA axis</topic><topic>Hypothalamo-Hypophyseal System - drug effects</topic><topic>Hypothalamo-Hypophyseal System - metabolism</topic><topic>Hypothalamo-Hypophyseal System - physiopathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mood disorders</topic><topic>Organ Size</topic><topic>pCREB/CREB</topic><topic>Phosphorylation</topic><topic>Pituitary-Adrenal System - drug effects</topic><topic>Pituitary-Adrenal System - metabolism</topic><topic>Pituitary-Adrenal System - physiopathology</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychopathology. Psychiatry</topic><topic>Rat</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>RNA, Messenger - analysis</topic><topic>Shuttle box</topic><topic>Statistics, Nonparametric</topic><topic>Stress, Psychological - complications</topic><topic>Stress, Psychological - drug therapy</topic><topic>Stress, Psychological - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xu, Ying</creatorcontrib><creatorcontrib>Ku, Baoshan</creatorcontrib><creatorcontrib>Tie, Lu</creatorcontrib><creatorcontrib>Yao, Haiyan</creatorcontrib><creatorcontrib>Jiang, Wengao</creatorcontrib><creatorcontrib>Ma, Xing</creatorcontrib><creatorcontrib>Li, Xuejun</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Brain research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xu, Ying</au><au>Ku, Baoshan</au><au>Tie, Lu</au><au>Yao, Haiyan</au><au>Jiang, Wengao</au><au>Ma, Xing</au><au>Li, Xuejun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Curcumin reverses the effects of chronic stress on behavior, the HPA axis, BDNF expression and phosphorylation of CREB</atitle><jtitle>Brain research</jtitle><addtitle>Brain Res</addtitle><date>2006-11-29</date><risdate>2006</risdate><volume>1122</volume><issue>1</issue><spage>56</spage><epage>64</epage><pages>56-64</pages><issn>0006-8993</issn><eissn>1872-6240</eissn><coden>BRREAP</coden><abstract>Curcuma longa is a major constituent of the traditional Chinese medicine Xiaoyao-san, which has been used to effectively manage stress and depression-related disorders in China. Curcumin is the active component of curcuma longa, and its antidepressant effects were described in our prior studies in mouse models of behavioral despair. We hypothesized that curcumin may also alleviate stress-induced depressive-like behaviors and hypothalamic–pituitary–adrenal (HPA) axis dysfunction. Thus in present study we assessed whether curcumin treatment (2.5, 5 and 10 mg/kg, p.o.) affects behavior in a chronic unpredictable stress model of depression in rats and examined what its molecular targets may be. We found that subjecting animals to the chronic stress protocol for 20
days resulted in performance deficits in the shuttle-box task and several physiological effects, such as an abnormal adrenal gland weight to body weight (AG/B) ratio and increased thickness of the adrenal cortex as well as elevated serum corticosterone levels and reduced glucocorticoid receptor (GR) mRNA expression. These changes were reversed by chronic curcumin administration (5 or 10 mg/kg, p.o.). In addition, we also found that the chronic stress procedure induced a down-regulation of brain-derived neurotrophic factor (BDNF) protein levels and reduced the ratio of phosphorylated cAMP response element-binding protein (pCREB) to CREB levels (pCREB/CREB) in the hippocampus and frontal cortex of stressed rats. Furthermore, these stress-induced decreases in BDNF and pCREB/CREB were also blocked by chronic curcumin administration (5 or 10 mg/kg, p.o.). These results provide compelling evidence that the behavioral effects of curcumin in chronically stressed animals, and by extension humans, may be related to their modulating effects on the HPA axis and neurotrophin factor expressions.</abstract><cop>London</cop><cop>Amsterdam</cop><cop>New York, NY</cop><pub>Elsevier B.V</pub><pmid>17022948</pmid><doi>10.1016/j.brainres.2006.09.009</doi><tpages>9</tpages></addata></record> |
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subjects | Adrenal Glands - anatomy & histology Adrenal Glands - drug effects Adult and adolescent clinical studies Analysis of Variance Animals BDNF Biological and medical sciences Body Weight - drug effects Brain-Derived Neurotrophic Factor - drug effects Brain-Derived Neurotrophic Factor - genetics Brain-Derived Neurotrophic Factor - metabolism Chronic unpredictable stress Corticosterone - blood Curcuma Curcuma longa Curcumin Curcumin - administration & dosage Cyclic AMP Response Element-Binding Protein - drug effects Cyclic AMP Response Element-Binding Protein - metabolism Depression Depressive Disorder - drug therapy Depressive Disorder - etiology Depressive Disorder - metabolism Dose-Response Relationship, Drug Down-Regulation Drugs, Chinese Herbal - administration & dosage Escape Reaction - drug effects Exploratory Behavior - drug effects Exploratory Behavior - physiology Frontal Lobe - drug effects Frontal Lobe - metabolism Hippocampus - drug effects Hippocampus - metabolism HPA axis Hypothalamo-Hypophyseal System - drug effects Hypothalamo-Hypophyseal System - metabolism Hypothalamo-Hypophyseal System - physiopathology Male Medical sciences Mood disorders Organ Size pCREB/CREB Phosphorylation Pituitary-Adrenal System - drug effects Pituitary-Adrenal System - metabolism Pituitary-Adrenal System - physiopathology Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry Rat Rats Rats, Sprague-Dawley RNA, Messenger - analysis Shuttle box Statistics, Nonparametric Stress, Psychological - complications Stress, Psychological - drug therapy Stress, Psychological - metabolism |
title | Curcumin reverses the effects of chronic stress on behavior, the HPA axis, BDNF expression and phosphorylation of CREB |
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