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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Veröffentlicht in:Drug and chemical toxicology (New York, N.Y. 1978) N.Y. 1978), 2005-01, Vol.27 (1), p.15-26
Hauptverfasser: Subapriya, R., Kumaraguruparan, R., Abraham, S. K., Nagini, S.
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container_title Drug and chemical toxicology (New York, N.Y. 1978)
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creator Subapriya, R.
Kumaraguruparan, R.
Abraham, S. K.
Nagini, S.
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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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. 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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. 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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 &amp; 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. 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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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ispartof Drug and chemical toxicology (New York, N.Y. 1978), 2005-01, Vol.27 (1), p.15-26
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source Taylor & Francis; MEDLINE; Taylor & Francis Medical Library - CRKN
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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