Effects of Curcumin on Lung Histopathology and Fungal Burden in a Mouse Model of Chronic Asthma and Oropharyngeal Candidiasis
Background and Aims Oropharyngeal candidiasis (OPC) is one of the most common local side effects of current therapy in chronic asthma. New therapeutic options with fewer side effects and reverse chronic changes are needed. Curcumin, as a promising antiinflammatory and antifungal agent, could be a ca...
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description | Background and Aims Oropharyngeal candidiasis (OPC) is one of the most common local side effects of current therapy in chronic asthma. New therapeutic options with fewer side effects and reverse chronic changes are needed. Curcumin, as a promising antiinflammatory and antifungal agent, could be a candidate of alternative therapy in asthma. This study aimed to determine the efficacy of orally administrated curcumin on lung histopathology, serum nitric oxide levels and fungal burden in a murine model of asthma and OPC. Methods Thirty five BALB/c mice were divided into five groups: I, II, III, IV (placebo) and V (control). All groups except the control were sensitized and challenged with ovalbumin. OPC model was established after the model of chronic asthma. Lung histology, serum nitric oxide levels and fungal burden were evaluated after 5 days of treatment with curcumin, dexamethasone, curcumin-dexamethasone combination and placebo. Evaluation of lung histology included subepithelial smooth muscle and epithelial thickness and number of goblet and mast cells by using light microscopy. Results All histological parameters improved in curcumin group similar to dexamethasone group. Curcumin and dexamethasone-curcumin combination were also as effective as dexamethasone on decreasing nitric oxide levels. Oral fungal burden was significantly lower in curcumin-treated group than dexamethasone. Conclusions In our study we demonstrated that curcumin administration alleviates the pathological changes in asthma and decreases the fungal burden. Curcumin may have a potential effect on treating chronic asthma and decreasing the frequency of the OPC. |
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New therapeutic options with fewer side effects and reverse chronic changes are needed. Curcumin, as a promising antiinflammatory and antifungal agent, could be a candidate of alternative therapy in asthma. This study aimed to determine the efficacy of orally administrated curcumin on lung histopathology, serum nitric oxide levels and fungal burden in a murine model of asthma and OPC. Methods Thirty five BALB/c mice were divided into five groups: I, II, III, IV (placebo) and V (control). All groups except the control were sensitized and challenged with ovalbumin. OPC model was established after the model of chronic asthma. Lung histology, serum nitric oxide levels and fungal burden were evaluated after 5 days of treatment with curcumin, dexamethasone, curcumin-dexamethasone combination and placebo. Evaluation of lung histology included subepithelial smooth muscle and epithelial thickness and number of goblet and mast cells by using light microscopy. Results All histological parameters improved in curcumin group similar to dexamethasone group. Curcumin and dexamethasone-curcumin combination were also as effective as dexamethasone on decreasing nitric oxide levels. Oral fungal burden was significantly lower in curcumin-treated group than dexamethasone. Conclusions In our study we demonstrated that curcumin administration alleviates the pathological changes in asthma and decreases the fungal burden. Curcumin may have a potential effect on treating chronic asthma and decreasing the frequency of the OPC.</description><identifier>ISSN: 0188-4409</identifier><identifier>EISSN: 1873-5487</identifier><identifier>DOI: 10.1016/j.arcmed.2011.01.011</identifier><identifier>PMID: 21565619</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Anti-Inflammatory Agents - pharmacology ; Asthma - chemically induced ; Asthma - drug therapy ; Asthma - pathology ; C. albicans colonization ; Candidiasis, Oral - drug therapy ; Candidiasis, Oral - microbiology ; Chronic asthma ; Colony Count, Microbial ; Curcumin ; Curcumin - pharmacology ; Dexamethasone - pharmacology ; Disease Models, Animal ; Drug Combinations ; Drug Evaluation, Preclinical ; Internal Medicine ; Lung - drug effects ; Lung - pathology ; Male ; Mice ; Mice, Inbred BALB C ; Mouse ; Nitric Oxide - blood ; Oropharyngeal candidiasis ; Ovalbumin ; Tongue - microbiology ; Tongue - pathology</subject><ispartof>Archives of medical research, 2011-02, Vol.42 (2), p.79-87</ispartof><rights>IMSS</rights><rights>2011 IMSS</rights><rights>Copyright © 2011 IMSS. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c448t-ed08e4659c1d693377e6e3f1f182007ee232b5129d64e5dd6bf0b9643ed7f7073</citedby><cites>FETCH-LOGICAL-c448t-ed08e4659c1d693377e6e3f1f182007ee232b5129d64e5dd6bf0b9643ed7f7073</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.arcmed.2011.01.011$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,782,786,3554,27933,27934,46004</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21565619$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Karaman, Meral</creatorcontrib><creatorcontrib>Arkan Ayyldz, Zeynep</creatorcontrib><creatorcontrib>Frnc, Fatih</creatorcontrib><creatorcontrib>Kiray, Müge</creatorcontrib><creatorcontrib>Bağryank, Alper</creatorcontrib><creatorcontrib>Yilmaz, Osman</creatorcontrib><creatorcontrib>Uzuner, Nevin</creatorcontrib><creatorcontrib>Karaman, Özkan</creatorcontrib><title>Effects of Curcumin on Lung Histopathology and Fungal Burden in a Mouse Model of Chronic Asthma and Oropharyngeal Candidiasis</title><title>Archives of medical research</title><addtitle>Arch Med Res</addtitle><description>Background and Aims Oropharyngeal candidiasis (OPC) is one of the most common local side effects of current therapy in chronic asthma. New therapeutic options with fewer side effects and reverse chronic changes are needed. Curcumin, as a promising antiinflammatory and antifungal agent, could be a candidate of alternative therapy in asthma. This study aimed to determine the efficacy of orally administrated curcumin on lung histopathology, serum nitric oxide levels and fungal burden in a murine model of asthma and OPC. Methods Thirty five BALB/c mice were divided into five groups: I, II, III, IV (placebo) and V (control). All groups except the control were sensitized and challenged with ovalbumin. OPC model was established after the model of chronic asthma. Lung histology, serum nitric oxide levels and fungal burden were evaluated after 5 days of treatment with curcumin, dexamethasone, curcumin-dexamethasone combination and placebo. Evaluation of lung histology included subepithelial smooth muscle and epithelial thickness and number of goblet and mast cells by using light microscopy. Results All histological parameters improved in curcumin group similar to dexamethasone group. Curcumin and dexamethasone-curcumin combination were also as effective as dexamethasone on decreasing nitric oxide levels. Oral fungal burden was significantly lower in curcumin-treated group than dexamethasone. Conclusions In our study we demonstrated that curcumin administration alleviates the pathological changes in asthma and decreases the fungal burden. Curcumin may have a potential effect on treating chronic asthma and decreasing the frequency of the OPC.</description><subject>Animals</subject><subject>Anti-Inflammatory Agents - pharmacology</subject><subject>Asthma - chemically induced</subject><subject>Asthma - drug therapy</subject><subject>Asthma - pathology</subject><subject>C. albicans colonization</subject><subject>Candidiasis, Oral - drug therapy</subject><subject>Candidiasis, Oral - microbiology</subject><subject>Chronic asthma</subject><subject>Colony Count, Microbial</subject><subject>Curcumin</subject><subject>Curcumin - pharmacology</subject><subject>Dexamethasone - pharmacology</subject><subject>Disease Models, Animal</subject><subject>Drug Combinations</subject><subject>Drug Evaluation, Preclinical</subject><subject>Internal Medicine</subject><subject>Lung - drug effects</subject><subject>Lung - pathology</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mouse</subject><subject>Nitric Oxide - blood</subject><subject>Oropharyngeal candidiasis</subject><subject>Ovalbumin</subject><subject>Tongue - microbiology</subject><subject>Tongue - pathology</subject><issn>0188-4409</issn><issn>1873-5487</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUsFuEzEQtRCIhsIfIOQbpw2etdf2XpBK1FKkoB6As-XYs4nDZh3s3Uo58O94m_bCpdLIlsbvvRnPG0LeA1sCA_lpv7TJHdAvawawZHPAC7IArXjVCK1ekgUDrSshWHtB3uS8Z4xpIdVrclFDIxsJ7YL8ve46dGOmsaOrKbnpEAYaB7qehi29DXmMRzvuYh-3J2oHT29K3vb0y5Q8DrRgLf0ep4zl9Ng_qOxSHIKjV3ncHewD6S7F486m07DFwl2VVPDB5pDfkled7TO-e7wvya-b65-r22p99_Xb6mpdOSH0WKFnGoVsWgdetpwrhRJ5Bx3omjGFWPN600Ddeimw8V5uOrZppeDoVaeY4pfk41n3mOKfCfNoDiE77Hs7YOneaCVrDqD480gpG17rRhSkOCNdijkn7MwxhUP5pQFmZofM3pwdMrNDhs0BhfbhscC0md-eSE-WFMDnMwDLQO4DJpNdwMGhD6k4ZXwMz1X4X8D1oThi-994wryPUxrKsA2YXBtmfsxbMi8JQFmQMkT-DzOkuEU</recordid><startdate>20110201</startdate><enddate>20110201</enddate><creator>Karaman, Meral</creator><creator>Arkan Ayyldz, Zeynep</creator><creator>Frnc, Fatih</creator><creator>Kiray, Müge</creator><creator>Bağryank, Alper</creator><creator>Yilmaz, Osman</creator><creator>Uzuner, Nevin</creator><creator>Karaman, Özkan</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><scope>7X8</scope><scope>M7N</scope></search><sort><creationdate>20110201</creationdate><title>Effects of Curcumin on Lung Histopathology and Fungal Burden in a Mouse Model of Chronic Asthma and Oropharyngeal Candidiasis</title><author>Karaman, Meral ; Arkan Ayyldz, Zeynep ; Frnc, Fatih ; Kiray, Müge ; Bağryank, Alper ; Yilmaz, Osman ; Uzuner, Nevin ; Karaman, Özkan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c448t-ed08e4659c1d693377e6e3f1f182007ee232b5129d64e5dd6bf0b9643ed7f7073</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Animals</topic><topic>Anti-Inflammatory Agents - pharmacology</topic><topic>Asthma - chemically induced</topic><topic>Asthma - drug therapy</topic><topic>Asthma - pathology</topic><topic>C. albicans colonization</topic><topic>Candidiasis, Oral - drug therapy</topic><topic>Candidiasis, Oral - microbiology</topic><topic>Chronic asthma</topic><topic>Colony Count, Microbial</topic><topic>Curcumin</topic><topic>Curcumin - pharmacology</topic><topic>Dexamethasone - pharmacology</topic><topic>Disease Models, Animal</topic><topic>Drug Combinations</topic><topic>Drug Evaluation, Preclinical</topic><topic>Internal Medicine</topic><topic>Lung - drug effects</topic><topic>Lung - pathology</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mouse</topic><topic>Nitric Oxide - blood</topic><topic>Oropharyngeal candidiasis</topic><topic>Ovalbumin</topic><topic>Tongue - microbiology</topic><topic>Tongue - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Karaman, Meral</creatorcontrib><creatorcontrib>Arkan Ayyldz, Zeynep</creatorcontrib><creatorcontrib>Frnc, Fatih</creatorcontrib><creatorcontrib>Kiray, Müge</creatorcontrib><creatorcontrib>Bağryank, Alper</creatorcontrib><creatorcontrib>Yilmaz, Osman</creatorcontrib><creatorcontrib>Uzuner, Nevin</creatorcontrib><creatorcontrib>Karaman, Özkan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><jtitle>Archives of medical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Karaman, Meral</au><au>Arkan Ayyldz, Zeynep</au><au>Frnc, Fatih</au><au>Kiray, Müge</au><au>Bağryank, Alper</au><au>Yilmaz, Osman</au><au>Uzuner, Nevin</au><au>Karaman, Özkan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of Curcumin on Lung Histopathology and Fungal Burden in a Mouse Model of Chronic Asthma and Oropharyngeal Candidiasis</atitle><jtitle>Archives of medical research</jtitle><addtitle>Arch Med Res</addtitle><date>2011-02-01</date><risdate>2011</risdate><volume>42</volume><issue>2</issue><spage>79</spage><epage>87</epage><pages>79-87</pages><issn>0188-4409</issn><eissn>1873-5487</eissn><abstract>Background and Aims Oropharyngeal candidiasis (OPC) is one of the most common local side effects of current therapy in chronic asthma. New therapeutic options with fewer side effects and reverse chronic changes are needed. Curcumin, as a promising antiinflammatory and antifungal agent, could be a candidate of alternative therapy in asthma. This study aimed to determine the efficacy of orally administrated curcumin on lung histopathology, serum nitric oxide levels and fungal burden in a murine model of asthma and OPC. Methods Thirty five BALB/c mice were divided into five groups: I, II, III, IV (placebo) and V (control). All groups except the control were sensitized and challenged with ovalbumin. OPC model was established after the model of chronic asthma. Lung histology, serum nitric oxide levels and fungal burden were evaluated after 5 days of treatment with curcumin, dexamethasone, curcumin-dexamethasone combination and placebo. Evaluation of lung histology included subepithelial smooth muscle and epithelial thickness and number of goblet and mast cells by using light microscopy. Results All histological parameters improved in curcumin group similar to dexamethasone group. Curcumin and dexamethasone-curcumin combination were also as effective as dexamethasone on decreasing nitric oxide levels. Oral fungal burden was significantly lower in curcumin-treated group than dexamethasone. Conclusions In our study we demonstrated that curcumin administration alleviates the pathological changes in asthma and decreases the fungal burden. Curcumin may have a potential effect on treating chronic asthma and decreasing the frequency of the OPC.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>21565619</pmid><doi>10.1016/j.arcmed.2011.01.011</doi><tpages>9</tpages></addata></record> |
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subjects | Animals Anti-Inflammatory Agents - pharmacology Asthma - chemically induced Asthma - drug therapy Asthma - pathology C. albicans colonization Candidiasis, Oral - drug therapy Candidiasis, Oral - microbiology Chronic asthma Colony Count, Microbial Curcumin Curcumin - pharmacology Dexamethasone - pharmacology Disease Models, Animal Drug Combinations Drug Evaluation, Preclinical Internal Medicine Lung - drug effects Lung - pathology Male Mice Mice, Inbred BALB C Mouse Nitric Oxide - blood Oropharyngeal candidiasis Ovalbumin Tongue - microbiology Tongue - pathology |
title | Effects of Curcumin on Lung Histopathology and Fungal Burden in a Mouse Model of Chronic Asthma and Oropharyngeal Candidiasis |
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