Ethanolic leaf extract of neem (Azadirachta indica) inhibits buccal pouch carcinogenesis in hamsters
We evaluated the chemopreventive effects of ethanolic neem leaf extract in the initiation and post‐initiation phases of 7,12‐dimethylbenz[a]anthracene (DMBA)‐induced hamster buccal pouch (HBP) carcinogenesis. The frequency of bone marrow micronuclei as well as the concentrations of lipid peroxides,...
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Veröffentlicht in: | Cell biochemistry and function 2005-07, Vol.23 (4), p.229-238 |
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description | We evaluated the chemopreventive effects of ethanolic neem leaf extract in the initiation and post‐initiation phases of 7,12‐dimethylbenz[a]anthracene (DMBA)‐induced hamster buccal pouch (HBP) carcinogenesis. The frequency of bone marrow micronuclei as well as the concentrations of lipid peroxides, ratio of reduced to oxidized glutathione (GSH/GSSG), and the activities of the GSH‐dependent enzymes glutathione peroxidase (GPx) and glutathione‐S‐transferase (GST) in the buccal pouch, liver and erythrocytes were used as biomarkers of chemoprevention. All the hamsters painted with DMBA alone for 14 weeks developed buccal pouch carcinomas that showed diminished lipid peroxidation and enhanced antioxidant status associated with increased frequencies of bone marrow micronuclei. In the liver and erythrocytes of tumour‐bearing animals, enhanced lipid peroxidation was accompanied by compromised antioxidant defences. Administration of ethanolic neem leaf extract effectively suppressed DMBA‐induced HBP carcinogenesis as revealed by the absence of tumours in the initiation phase and reduced tumour incidence in the post‐initiation phase. In addition, ethanolic neem leaf extract modulated lipid peroxidation and enhanced antioxidant status in the pouch, liver and erythrocytes and reduced the incidence of bone marrow micronuclei. The results of the present study, demonstrate that ethanolic neem leaf extract inhibits the development of DMBA‐induced HBP tumours by protecting against oxidative stress. Copyright © 2004 John Wiley & Sons, Ltd. |
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The frequency of bone marrow micronuclei as well as the concentrations of lipid peroxides, ratio of reduced to oxidized glutathione (GSH/GSSG), and the activities of the GSH‐dependent enzymes glutathione peroxidase (GPx) and glutathione‐S‐transferase (GST) in the buccal pouch, liver and erythrocytes were used as biomarkers of chemoprevention. All the hamsters painted with DMBA alone for 14 weeks developed buccal pouch carcinomas that showed diminished lipid peroxidation and enhanced antioxidant status associated with increased frequencies of bone marrow micronuclei. In the liver and erythrocytes of tumour‐bearing animals, enhanced lipid peroxidation was accompanied by compromised antioxidant defences. Administration of ethanolic neem leaf extract effectively suppressed DMBA‐induced HBP carcinogenesis as revealed by the absence of tumours in the initiation phase and reduced tumour incidence in the post‐initiation phase. In addition, ethanolic neem leaf extract modulated lipid peroxidation and enhanced antioxidant status in the pouch, liver and erythrocytes and reduced the incidence of bone marrow micronuclei. The results of the present study, demonstrate that ethanolic neem leaf extract inhibits the development of DMBA‐induced HBP tumours by protecting against oxidative stress. Copyright © 2004 John Wiley & Sons, Ltd.</description><identifier>ISSN: 0263-6484</identifier><identifier>EISSN: 1099-0844</identifier><identifier>DOI: 10.1002/cbf.1143</identifier><identifier>PMID: 15473007</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>9,10-Dimethyl-1,2-benzanthracene - toxicity ; Animals ; Antineoplastic Agents, Phytogenic - therapeutic use ; antioxidants ; Antioxidants - metabolism ; Azadirachta ; Azadirachta indica ; Carcinogens - toxicity ; Carcinoma, Squamous Cell - chemically induced ; Carcinoma, Squamous Cell - pathology ; Carcinoma, Squamous Cell - prevention & control ; chemoprevention ; Cricetinae ; Erythrocytes - drug effects ; Erythrocytes - metabolism ; Ethanol - pharmacology ; Glutathione - drug effects ; Glutathione Peroxidase - metabolism ; Glutathione Transferase - metabolism ; lipid peroxidation ; Lipid Peroxidation - drug effects ; Liver - drug effects ; Liver - metabolism ; Male ; Mesocricetus ; Micronuclei, Chromosome-Defective - drug effects ; Mouth Neoplasms - chemically induced ; Mouth Neoplasms - pathology ; Mouth Neoplasms - prevention & control ; neem leaf ; oral cancer ; oxidative stress ; Phytotherapy ; Plant Extracts - therapeutic use ; Plant Leaves</subject><ispartof>Cell biochemistry and function, 2005-07, Vol.23 (4), p.229-238</ispartof><rights>Copyright © 2004 John Wiley & Sons, Ltd.</rights><rights>Copyright 2004 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3883-6854dba59883e04b23c4d13508fbe6ce8d7eff6f812662bea8b99af76f84f8643</citedby><cites>FETCH-LOGICAL-c3883-6854dba59883e04b23c4d13508fbe6ce8d7eff6f812662bea8b99af76f84f8643</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fcbf.1143$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fcbf.1143$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15473007$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Subapriya, R.</creatorcontrib><creatorcontrib>Bhuvaneswari, V.</creatorcontrib><creatorcontrib>Ramesh, V.</creatorcontrib><creatorcontrib>Nagini, S.</creatorcontrib><title>Ethanolic leaf extract of neem (Azadirachta indica) inhibits buccal pouch carcinogenesis in hamsters</title><title>Cell biochemistry and function</title><addtitle>Cell Biochem. Funct</addtitle><description>We evaluated the chemopreventive effects of ethanolic neem leaf extract in the initiation and post‐initiation phases of 7,12‐dimethylbenz[a]anthracene (DMBA)‐induced hamster buccal pouch (HBP) carcinogenesis. The frequency of bone marrow micronuclei as well as the concentrations of lipid peroxides, ratio of reduced to oxidized glutathione (GSH/GSSG), and the activities of the GSH‐dependent enzymes glutathione peroxidase (GPx) and glutathione‐S‐transferase (GST) in the buccal pouch, liver and erythrocytes were used as biomarkers of chemoprevention. All the hamsters painted with DMBA alone for 14 weeks developed buccal pouch carcinomas that showed diminished lipid peroxidation and enhanced antioxidant status associated with increased frequencies of bone marrow micronuclei. In the liver and erythrocytes of tumour‐bearing animals, enhanced lipid peroxidation was accompanied by compromised antioxidant defences. Administration of ethanolic neem leaf extract effectively suppressed DMBA‐induced HBP carcinogenesis as revealed by the absence of tumours in the initiation phase and reduced tumour incidence in the post‐initiation phase. In addition, ethanolic neem leaf extract modulated lipid peroxidation and enhanced antioxidant status in the pouch, liver and erythrocytes and reduced the incidence of bone marrow micronuclei. The results of the present study, demonstrate that ethanolic neem leaf extract inhibits the development of DMBA‐induced HBP tumours by protecting against oxidative stress. Copyright © 2004 John Wiley & Sons, Ltd.</description><subject>9,10-Dimethyl-1,2-benzanthracene - toxicity</subject><subject>Animals</subject><subject>Antineoplastic Agents, Phytogenic - therapeutic use</subject><subject>antioxidants</subject><subject>Antioxidants - metabolism</subject><subject>Azadirachta</subject><subject>Azadirachta indica</subject><subject>Carcinogens - toxicity</subject><subject>Carcinoma, Squamous Cell - chemically induced</subject><subject>Carcinoma, Squamous Cell - pathology</subject><subject>Carcinoma, Squamous Cell - prevention & control</subject><subject>chemoprevention</subject><subject>Cricetinae</subject><subject>Erythrocytes - drug effects</subject><subject>Erythrocytes - metabolism</subject><subject>Ethanol - pharmacology</subject><subject>Glutathione - drug effects</subject><subject>Glutathione Peroxidase - metabolism</subject><subject>Glutathione Transferase - metabolism</subject><subject>lipid peroxidation</subject><subject>Lipid Peroxidation - drug effects</subject><subject>Liver - drug effects</subject><subject>Liver - metabolism</subject><subject>Male</subject><subject>Mesocricetus</subject><subject>Micronuclei, Chromosome-Defective - drug effects</subject><subject>Mouth Neoplasms - chemically induced</subject><subject>Mouth Neoplasms - pathology</subject><subject>Mouth Neoplasms - prevention & control</subject><subject>neem leaf</subject><subject>oral cancer</subject><subject>oxidative stress</subject><subject>Phytotherapy</subject><subject>Plant Extracts - therapeutic use</subject><subject>Plant Leaves</subject><issn>0263-6484</issn><issn>1099-0844</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kEtr3DAUhUVp6EyTQn9B0aqkC08kS5blZTrkxQwJgYQshSRf1Wr9mEg2TfrrqzAmWWV1uIePw-VD6CslK0pIfmKNW1HK2Qe0pKSqMiI5_4iWJBcsE1zyBfoc429CSCUY-YQWtOAlI6RcovpsbHQ_tN7iFrTD8DQGbUc8ONwDdPj49J-ufaqaUWPf197qHykbb_wYsZms1S3eDZNtsNXB-n74BT1EHxOEG93FEUI8QgdOtxG-zHmI7s_P7taX2fbm4mp9us0skzJ9KgteG11U6QDCTc4srykriHQGhAVZl-CccJLmQuQGtDRVpV2ZGu6k4OwQfd_v7sLwOEEcVeejhbbVPQxTVLSSlApBEni8B20YYgzg1C74TodnRYl6MaqSUfViNKHf5s3JdFC_gbPCBGR74K9v4fndIbX-eT4PzrxPbp5eeR3-KFGyslAP1xeK3m7Y5eaWq4L9B1CGjrw</recordid><startdate>200507</startdate><enddate>200507</enddate><creator>Subapriya, R.</creator><creator>Bhuvaneswari, V.</creator><creator>Ramesh, V.</creator><creator>Nagini, S.</creator><general>John Wiley & Sons, Ltd</general><scope>BSCLL</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>7U7</scope><scope>C1K</scope></search><sort><creationdate>200507</creationdate><title>Ethanolic leaf extract of neem (Azadirachta indica) inhibits buccal pouch carcinogenesis in hamsters</title><author>Subapriya, R. ; Bhuvaneswari, V. ; Ramesh, V. ; Nagini, S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3883-6854dba59883e04b23c4d13508fbe6ce8d7eff6f812662bea8b99af76f84f8643</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>9,10-Dimethyl-1,2-benzanthracene - toxicity</topic><topic>Animals</topic><topic>Antineoplastic Agents, Phytogenic - therapeutic use</topic><topic>antioxidants</topic><topic>Antioxidants - metabolism</topic><topic>Azadirachta</topic><topic>Azadirachta indica</topic><topic>Carcinogens - toxicity</topic><topic>Carcinoma, Squamous Cell - chemically induced</topic><topic>Carcinoma, Squamous Cell - pathology</topic><topic>Carcinoma, Squamous Cell - prevention & control</topic><topic>chemoprevention</topic><topic>Cricetinae</topic><topic>Erythrocytes - drug effects</topic><topic>Erythrocytes - metabolism</topic><topic>Ethanol - pharmacology</topic><topic>Glutathione - drug effects</topic><topic>Glutathione Peroxidase - metabolism</topic><topic>Glutathione Transferase - metabolism</topic><topic>lipid peroxidation</topic><topic>Lipid Peroxidation - drug effects</topic><topic>Liver - drug effects</topic><topic>Liver - metabolism</topic><topic>Male</topic><topic>Mesocricetus</topic><topic>Micronuclei, Chromosome-Defective - drug effects</topic><topic>Mouth Neoplasms - chemically induced</topic><topic>Mouth Neoplasms - pathology</topic><topic>Mouth Neoplasms - prevention & control</topic><topic>neem leaf</topic><topic>oral cancer</topic><topic>oxidative stress</topic><topic>Phytotherapy</topic><topic>Plant Extracts - therapeutic use</topic><topic>Plant Leaves</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Subapriya, R.</creatorcontrib><creatorcontrib>Bhuvaneswari, V.</creatorcontrib><creatorcontrib>Ramesh, V.</creatorcontrib><creatorcontrib>Nagini, S.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Cell biochemistry and function</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Subapriya, R.</au><au>Bhuvaneswari, V.</au><au>Ramesh, V.</au><au>Nagini, S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ethanolic leaf extract of neem (Azadirachta indica) inhibits buccal pouch carcinogenesis in hamsters</atitle><jtitle>Cell biochemistry and function</jtitle><addtitle>Cell Biochem. Funct</addtitle><date>2005-07</date><risdate>2005</risdate><volume>23</volume><issue>4</issue><spage>229</spage><epage>238</epage><pages>229-238</pages><issn>0263-6484</issn><eissn>1099-0844</eissn><abstract>We evaluated the chemopreventive effects of ethanolic neem leaf extract in the initiation and post‐initiation phases of 7,12‐dimethylbenz[a]anthracene (DMBA)‐induced hamster buccal pouch (HBP) carcinogenesis. The frequency of bone marrow micronuclei as well as the concentrations of lipid peroxides, ratio of reduced to oxidized glutathione (GSH/GSSG), and the activities of the GSH‐dependent enzymes glutathione peroxidase (GPx) and glutathione‐S‐transferase (GST) in the buccal pouch, liver and erythrocytes were used as biomarkers of chemoprevention. All the hamsters painted with DMBA alone for 14 weeks developed buccal pouch carcinomas that showed diminished lipid peroxidation and enhanced antioxidant status associated with increased frequencies of bone marrow micronuclei. In the liver and erythrocytes of tumour‐bearing animals, enhanced lipid peroxidation was accompanied by compromised antioxidant defences. Administration of ethanolic neem leaf extract effectively suppressed DMBA‐induced HBP carcinogenesis as revealed by the absence of tumours in the initiation phase and reduced tumour incidence in the post‐initiation phase. In addition, ethanolic neem leaf extract modulated lipid peroxidation and enhanced antioxidant status in the pouch, liver and erythrocytes and reduced the incidence of bone marrow micronuclei. The results of the present study, demonstrate that ethanolic neem leaf extract inhibits the development of DMBA‐induced HBP tumours by protecting against oxidative stress. Copyright © 2004 John Wiley & Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><pmid>15473007</pmid><doi>10.1002/cbf.1143</doi><tpages>10</tpages></addata></record> |
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subjects | 9,10-Dimethyl-1,2-benzanthracene - toxicity Animals Antineoplastic Agents, Phytogenic - therapeutic use antioxidants Antioxidants - metabolism Azadirachta Azadirachta indica Carcinogens - toxicity Carcinoma, Squamous Cell - chemically induced Carcinoma, Squamous Cell - pathology Carcinoma, Squamous Cell - prevention & control chemoprevention Cricetinae Erythrocytes - drug effects Erythrocytes - metabolism Ethanol - pharmacology Glutathione - drug effects Glutathione Peroxidase - metabolism Glutathione Transferase - metabolism lipid peroxidation Lipid Peroxidation - drug effects Liver - drug effects Liver - metabolism Male Mesocricetus Micronuclei, Chromosome-Defective - drug effects Mouth Neoplasms - chemically induced Mouth Neoplasms - pathology Mouth Neoplasms - prevention & control neem leaf oral cancer oxidative stress Phytotherapy Plant Extracts - therapeutic use Plant Leaves |
title | Ethanolic leaf extract of neem (Azadirachta indica) inhibits buccal pouch carcinogenesis in hamsters |
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