Protective Effects of Ethanolic Neem Leaf Extract on N-Methyl-N′-nitro-N-nitrosoguanidine-Induced Genotoxicity and Oxidative Stress in Mice
We evaluated the effects of pretreatment with ethanolic neem leaf extract on N-methyl-N′-nitro-N-nitrosoguanidine (MNNG)-induced genotoxicity and oxidative stress in male Swiss albino mice. The frequency of micronuclei (MN), concentrations of lipid peroxides and the status of the antioxidants, reduc...
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description | We evaluated the effects of pretreatment with ethanolic neem leaf extract on N-methyl-N′-nitro-N-nitrosoguanidine (MNNG)-induced genotoxicity and oxidative stress in male Swiss albino mice. The frequency of micronuclei (MN), concentrations of lipid peroxides and the status of the antioxidants, reduced glutathione (GSH), glutathione peroxidase (GPx) and glutathione-S-transferase (GST) were used as intermediate biomarkers of chemoprotection. Animals were divided into four groups of five animals each. Animals in group 1 were given MNNG (40 mg kg body weight) by intragastric intubation. Animals in group 2 received intragastric administration of ethanolic neem leaf extract at a concentration of 200 mg kg body weight for 5 days followed by MNNG 1.5 h after the final feeding. Group 3 animals received ethanolic neem leaf extract alone for five days. Group 4 received the same volume of normal saline and served as control. The animals were sacrificed by cervical dislocation 27 h after the carcinogen exposure. In MNNG-treated mice, enhanced lipid peroxidation with compromised antioxidant defences in the stomach, liver and erythrocytes was accompanied by increase in bone marrow micronuclei. Pretreatment with ethanolic neem leaf extract significantly reduced MNNG-induced micronuclei and lipid peroxides and enhanced GSH-dependent antioxidant activities. The results of the present study demonstrate that ethanolic neem leaf extract exerts protective effects against MNNG-induced genotoxicity and oxidative stress by augmenting host antioxidant defence mechanisms. |
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K. ; Nagini, S.</creator><creatorcontrib>Subapriya, R. ; Kumaraguruparan, R. ; Abraham, S. K. ; Nagini, S.</creatorcontrib><description>We evaluated the effects of pretreatment with ethanolic neem leaf extract on N-methyl-N′-nitro-N-nitrosoguanidine (MNNG)-induced genotoxicity and oxidative stress in male Swiss albino mice. The frequency of micronuclei (MN), concentrations of lipid peroxides and the status of the antioxidants, reduced glutathione (GSH), glutathione peroxidase (GPx) and glutathione-S-transferase (GST) were used as intermediate biomarkers of chemoprotection. Animals were divided into four groups of five animals each. Animals in group 1 were given MNNG (40 mg kg body weight) by intragastric intubation. Animals in group 2 received intragastric administration of ethanolic neem leaf extract at a concentration of 200 mg kg body weight for 5 days followed by MNNG 1.5 h after the final feeding. Group 3 animals received ethanolic neem leaf extract alone for five days. Group 4 received the same volume of normal saline and served as control. The animals were sacrificed by cervical dislocation 27 h after the carcinogen exposure. In MNNG-treated mice, enhanced lipid peroxidation with compromised antioxidant defences in the stomach, liver and erythrocytes was accompanied by increase in bone marrow micronuclei. Pretreatment with ethanolic neem leaf extract significantly reduced MNNG-induced micronuclei and lipid peroxides and enhanced GSH-dependent antioxidant activities. The results of the present study demonstrate that ethanolic neem leaf extract exerts protective effects against MNNG-induced genotoxicity and oxidative stress by augmenting host antioxidant defence mechanisms.</description><identifier>ISSN: 0148-0545</identifier><identifier>EISSN: 1525-6014</identifier><identifier>DOI: 10.1081/DCT-120027894</identifier><identifier>PMID: 15038245</identifier><language>eng</language><publisher>New York, NY: Informa UK Ltd</publisher><subject>Administration, Oral ; Animals ; Antimutagenic Agents - pharmacology ; Antioxidants ; Azadirachta - chemistry ; Biological and medical sciences ; Bone Marrow Cells - cytology ; Bone Marrow Cells - drug effects ; Carcinogenesis, carcinogens and anticarcinogens ; Chemical agents ; Drug Therapy, Combination ; Glutathione ; Glutathione - metabolism ; Lipid Peroxidation - drug effects ; Male ; Medical sciences ; Methylnitronitrosoguanidine - toxicity ; Mice ; Micronuclei ; Micronucleus Tests ; MNNG ; Mutagens - toxicity ; Neem ; Oxidative stress ; Oxidative Stress - drug effects ; Plant Extracts - administration & dosage ; Plant Extracts - pharmacology ; Plant Leaves - chemistry ; Plants, Medicinal ; Tumors</subject><ispartof>Drug and chemical toxicology (New York, N.Y. 1978), 2005-01, Vol.27 (1), p.15-26</ispartof><rights>2004 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2004</rights><rights>2004 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c416t-93962dec6b50ca95f94ca900a3e8d10388b8a2131d680b92cf671c94fc33079c3</citedby><cites>FETCH-LOGICAL-c416t-93962dec6b50ca95f94ca900a3e8d10388b8a2131d680b92cf671c94fc33079c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.tandfonline.com/doi/pdf/10.1081/DCT-120027894$$EPDF$$P50$$Ginformaworld$$H</linktopdf><linktohtml>$$Uhttps://www.tandfonline.com/doi/full/10.1081/DCT-120027894$$EHTML$$P50$$Ginformaworld$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,59620,59726,60409,60515,61194,61229,61375,61410</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15543739$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15038245$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Subapriya, R.</creatorcontrib><creatorcontrib>Kumaraguruparan, R.</creatorcontrib><creatorcontrib>Abraham, S. K.</creatorcontrib><creatorcontrib>Nagini, S.</creatorcontrib><title>Protective Effects of Ethanolic Neem Leaf Extract on N-Methyl-N′-nitro-N-nitrosoguanidine-Induced Genotoxicity and Oxidative Stress in Mice</title><title>Drug and chemical toxicology (New York, N.Y. 1978)</title><addtitle>Drug Chem Toxicol</addtitle><description>We evaluated the effects of pretreatment with ethanolic neem leaf extract on N-methyl-N′-nitro-N-nitrosoguanidine (MNNG)-induced genotoxicity and oxidative stress in male Swiss albino mice. The frequency of micronuclei (MN), concentrations of lipid peroxides and the status of the antioxidants, reduced glutathione (GSH), glutathione peroxidase (GPx) and glutathione-S-transferase (GST) were used as intermediate biomarkers of chemoprotection. Animals were divided into four groups of five animals each. Animals in group 1 were given MNNG (40 mg kg body weight) by intragastric intubation. Animals in group 2 received intragastric administration of ethanolic neem leaf extract at a concentration of 200 mg kg body weight for 5 days followed by MNNG 1.5 h after the final feeding. Group 3 animals received ethanolic neem leaf extract alone for five days. Group 4 received the same volume of normal saline and served as control. The animals were sacrificed by cervical dislocation 27 h after the carcinogen exposure. In MNNG-treated mice, enhanced lipid peroxidation with compromised antioxidant defences in the stomach, liver and erythrocytes was accompanied by increase in bone marrow micronuclei. Pretreatment with ethanolic neem leaf extract significantly reduced MNNG-induced micronuclei and lipid peroxides and enhanced GSH-dependent antioxidant activities. The results of the present study demonstrate that ethanolic neem leaf extract exerts protective effects against MNNG-induced genotoxicity and oxidative stress by augmenting host antioxidant defence mechanisms.</description><subject>Administration, Oral</subject><subject>Animals</subject><subject>Antimutagenic Agents - pharmacology</subject><subject>Antioxidants</subject><subject>Azadirachta - chemistry</subject><subject>Biological and medical sciences</subject><subject>Bone Marrow Cells - cytology</subject><subject>Bone Marrow Cells - drug effects</subject><subject>Carcinogenesis, carcinogens and anticarcinogens</subject><subject>Chemical agents</subject><subject>Drug Therapy, Combination</subject><subject>Glutathione</subject><subject>Glutathione - metabolism</subject><subject>Lipid Peroxidation - drug effects</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Methylnitronitrosoguanidine - toxicity</subject><subject>Mice</subject><subject>Micronuclei</subject><subject>Micronucleus Tests</subject><subject>MNNG</subject><subject>Mutagens - toxicity</subject><subject>Neem</subject><subject>Oxidative stress</subject><subject>Oxidative Stress - drug effects</subject><subject>Plant Extracts - administration & dosage</subject><subject>Plant Extracts - pharmacology</subject><subject>Plant Leaves - chemistry</subject><subject>Plants, Medicinal</subject><subject>Tumors</subject><issn>0148-0545</issn><issn>1525-6014</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kMFuVCEUhonR2LG6dGvYuKSFy-VeWJpxbJtMpybW9Q0DB4fmDjTA6MzOF_BlfCSfROyM1i664SfkO_DzIfSa0RNGJTt9P70mrKG06aVqn6AJE40gHWXtUzSpqyRUtOIIvcj5hlLWKMGfoyMmKJdNKybox8cUC5jivwKeOVd3GUeHZ2WlQxy9wQuANZ6DrmfbkrQpOAa8IJdQVruRLH59_0mCLymSxT5z_LLRwVsfgFwEuzFg8RmEWOLWG192WAeLr7be6rs3P5UEOWMf8KU38BI9c3rM8OqQx-jzh9n19JzMr84upu_mxLSsK0Rx1TUWTLcU1GglnGprUKo5SMvq1-RS6oZxZjtJl6oxruuZUa0znNNeGX6MyP5eUwvnBG64TX6t025gdPijdahah39aK_9mz99ulmuw9_TBYwXeHgCdjR5d0sH4_B8nWt5zVTm553xwMa31t5hGOxS9G2P6O8Qf69A_GF2BHsvK6ATDTdykUH090v43qn6mfg</recordid><startdate>20050101</startdate><enddate>20050101</enddate><creator>Subapriya, R.</creator><creator>Kumaraguruparan, R.</creator><creator>Abraham, S. K.</creator><creator>Nagini, S.</creator><general>Informa UK Ltd</general><general>Taylor & Francis</general><general>Informa Healthcare</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></search><sort><creationdate>20050101</creationdate><title>Protective Effects of Ethanolic Neem Leaf Extract on N-Methyl-N′-nitro-N-nitrosoguanidine-Induced Genotoxicity and Oxidative Stress in Mice</title><author>Subapriya, R. ; Kumaraguruparan, R. ; Abraham, S. K. ; Nagini, S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c416t-93962dec6b50ca95f94ca900a3e8d10388b8a2131d680b92cf671c94fc33079c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Administration, Oral</topic><topic>Animals</topic><topic>Antimutagenic Agents - pharmacology</topic><topic>Antioxidants</topic><topic>Azadirachta - chemistry</topic><topic>Biological and medical sciences</topic><topic>Bone Marrow Cells - cytology</topic><topic>Bone Marrow Cells - drug effects</topic><topic>Carcinogenesis, carcinogens and anticarcinogens</topic><topic>Chemical agents</topic><topic>Drug Therapy, Combination</topic><topic>Glutathione</topic><topic>Glutathione - metabolism</topic><topic>Lipid Peroxidation - drug effects</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Methylnitronitrosoguanidine - toxicity</topic><topic>Mice</topic><topic>Micronuclei</topic><topic>Micronucleus Tests</topic><topic>MNNG</topic><topic>Mutagens - toxicity</topic><topic>Neem</topic><topic>Oxidative stress</topic><topic>Oxidative Stress - drug effects</topic><topic>Plant Extracts - administration & dosage</topic><topic>Plant Extracts - pharmacology</topic><topic>Plant Leaves - chemistry</topic><topic>Plants, Medicinal</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Subapriya, R.</creatorcontrib><creatorcontrib>Kumaraguruparan, R.</creatorcontrib><creatorcontrib>Abraham, S. K.</creatorcontrib><creatorcontrib>Nagini, S.</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><jtitle>Drug and chemical toxicology (New York, N.Y. 1978)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Subapriya, R.</au><au>Kumaraguruparan, R.</au><au>Abraham, S. K.</au><au>Nagini, S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Protective Effects of Ethanolic Neem Leaf Extract on N-Methyl-N′-nitro-N-nitrosoguanidine-Induced Genotoxicity and Oxidative Stress in Mice</atitle><jtitle>Drug and chemical toxicology (New York, N.Y. 1978)</jtitle><addtitle>Drug Chem Toxicol</addtitle><date>2005-01-01</date><risdate>2005</risdate><volume>27</volume><issue>1</issue><spage>15</spage><epage>26</epage><pages>15-26</pages><issn>0148-0545</issn><eissn>1525-6014</eissn><abstract>We evaluated the effects of pretreatment with ethanolic neem leaf extract on N-methyl-N′-nitro-N-nitrosoguanidine (MNNG)-induced genotoxicity and oxidative stress in male Swiss albino mice. The frequency of micronuclei (MN), concentrations of lipid peroxides and the status of the antioxidants, reduced glutathione (GSH), glutathione peroxidase (GPx) and glutathione-S-transferase (GST) were used as intermediate biomarkers of chemoprotection. Animals were divided into four groups of five animals each. Animals in group 1 were given MNNG (40 mg kg body weight) by intragastric intubation. Animals in group 2 received intragastric administration of ethanolic neem leaf extract at a concentration of 200 mg kg body weight for 5 days followed by MNNG 1.5 h after the final feeding. Group 3 animals received ethanolic neem leaf extract alone for five days. Group 4 received the same volume of normal saline and served as control. The animals were sacrificed by cervical dislocation 27 h after the carcinogen exposure. In MNNG-treated mice, enhanced lipid peroxidation with compromised antioxidant defences in the stomach, liver and erythrocytes was accompanied by increase in bone marrow micronuclei. Pretreatment with ethanolic neem leaf extract significantly reduced MNNG-induced micronuclei and lipid peroxides and enhanced GSH-dependent antioxidant activities. The results of the present study demonstrate that ethanolic neem leaf extract exerts protective effects against MNNG-induced genotoxicity and oxidative stress by augmenting host antioxidant defence mechanisms.</abstract><cop>New York, NY</cop><pub>Informa UK Ltd</pub><pmid>15038245</pmid><doi>10.1081/DCT-120027894</doi><tpages>12</tpages></addata></record> |
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subjects | Administration, Oral Animals Antimutagenic Agents - pharmacology Antioxidants Azadirachta - chemistry Biological and medical sciences Bone Marrow Cells - cytology Bone Marrow Cells - drug effects Carcinogenesis, carcinogens and anticarcinogens Chemical agents Drug Therapy, Combination Glutathione Glutathione - metabolism Lipid Peroxidation - drug effects Male Medical sciences Methylnitronitrosoguanidine - toxicity Mice Micronuclei Micronucleus Tests MNNG Mutagens - toxicity Neem Oxidative stress Oxidative Stress - drug effects Plant Extracts - administration & dosage Plant Extracts - pharmacology Plant Leaves - chemistry Plants, Medicinal Tumors |
title | Protective Effects of Ethanolic Neem Leaf Extract on N-Methyl-N′-nitro-N-nitrosoguanidine-Induced Genotoxicity and Oxidative Stress in Mice |
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