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Tinospora cordifolia, a safety evaluation
Tinospora cordifolia is one of the indispensable medicinal plants used in veterinary folk medicine/Ayurvedic system of medicine for the treatment of diverse diseases and recommended for improving the immune system by means of body resistance. In the current study, we evaluated the genotoxic risk of...
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Published in: | Toxicology in vitro 2009-10, Vol.23 (7), p.1220-1226 |
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container_title | Toxicology in vitro |
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creator | Chandrasekaran, C.V. Mathuram, L.N. Daivasigamani, Prabhu Bhatnagar, Upendra |
description | Tinospora cordifolia is one of the indispensable medicinal plants used in veterinary folk medicine/Ayurvedic system of medicine for the treatment of diverse diseases and recommended for improving the immune system by means of body resistance. In the current study, we evaluated the genotoxic risk of the aqueous extract of
T. cordifolia (TC) in a battery of four different genotoxicity tests viz., Ames, in vitro chromosome aberration (CA), rodent bone marrow micronucleus (MN), and Comet assay. Experimental results confirmed that in Ames test up to 5000
μg/plate of TC did not exhibit any mutagenic effect in
Salmonella typhimurium mutant strains (TA97a, TA98, TA100, TA102, and TA1535). In CA assay, TC was not clastogenic to human peripheral blood lymphocytes up to a concentration of 3000
μg/ml. In MN and Comet assays, TC was pre-treated for 7
days at three dose levels (150, 200 and 250
mg/kg body weight) orally to male Balb/c mice. The results showed that TC treatment did not display clastogenicity and DNA damaging effect in bone marrow erythrocytes and peripheral blood lymphocytes respectively. |
doi_str_mv | 10.1016/j.tiv.2009.07.030 |
format | article |
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T. cordifolia (TC) in a battery of four different genotoxicity tests viz., Ames, in vitro chromosome aberration (CA), rodent bone marrow micronucleus (MN), and Comet assay. Experimental results confirmed that in Ames test up to 5000
μg/plate of TC did not exhibit any mutagenic effect in
Salmonella typhimurium mutant strains (TA97a, TA98, TA100, TA102, and TA1535). In CA assay, TC was not clastogenic to human peripheral blood lymphocytes up to a concentration of 3000
μg/ml. In MN and Comet assays, TC was pre-treated for 7
days at three dose levels (150, 200 and 250
mg/kg body weight) orally to male Balb/c mice. The results showed that TC treatment did not display clastogenicity and DNA damaging effect in bone marrow erythrocytes and peripheral blood lymphocytes respectively.</description><identifier>ISSN: 0887-2333</identifier><identifier>EISSN: 1879-3177</identifier><identifier>DOI: 10.1016/j.tiv.2009.07.030</identifier><identifier>PMID: 19651204</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Ames test ; Animals ; Bone Marrow - drug effects ; Chromosome aberration assay ; Chromosome Aberrations - chemically induced ; Comet assay ; DNA Damage ; Humans ; Lymphocytes - drug effects ; Male ; Mice ; Mice, Inbred BALB C ; Micronucleus assay ; Mutagenicity Tests - methods ; Mutagens - toxicity ; Plant Extracts - toxicity ; Salmonella typhimurium ; Salmonella typhimurium - drug effects ; Tinospora ; Tinospora - toxicity ; Tinospora cordifolia</subject><ispartof>Toxicology in vitro, 2009-10, Vol.23 (7), p.1220-1226</ispartof><rights>2009 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c383t-2673e4577792c6c50b90242381bb36024d890f8f09efd12ced365736bcfa32b13</citedby><cites>FETCH-LOGICAL-c383t-2673e4577792c6c50b90242381bb36024d890f8f09efd12ced365736bcfa32b13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19651204$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chandrasekaran, C.V.</creatorcontrib><creatorcontrib>Mathuram, L.N.</creatorcontrib><creatorcontrib>Daivasigamani, Prabhu</creatorcontrib><creatorcontrib>Bhatnagar, Upendra</creatorcontrib><title>Tinospora cordifolia, a safety evaluation</title><title>Toxicology in vitro</title><addtitle>Toxicol In Vitro</addtitle><description>Tinospora cordifolia is one of the indispensable medicinal plants used in veterinary folk medicine/Ayurvedic system of medicine for the treatment of diverse diseases and recommended for improving the immune system by means of body resistance. In the current study, we evaluated the genotoxic risk of the aqueous extract of
T. cordifolia (TC) in a battery of four different genotoxicity tests viz., Ames, in vitro chromosome aberration (CA), rodent bone marrow micronucleus (MN), and Comet assay. Experimental results confirmed that in Ames test up to 5000
μg/plate of TC did not exhibit any mutagenic effect in
Salmonella typhimurium mutant strains (TA97a, TA98, TA100, TA102, and TA1535). In CA assay, TC was not clastogenic to human peripheral blood lymphocytes up to a concentration of 3000
μg/ml. In MN and Comet assays, TC was pre-treated for 7
days at three dose levels (150, 200 and 250
mg/kg body weight) orally to male Balb/c mice. The results showed that TC treatment did not display clastogenicity and DNA damaging effect in bone marrow erythrocytes and peripheral blood lymphocytes respectively.</description><subject>Ames test</subject><subject>Animals</subject><subject>Bone Marrow - drug effects</subject><subject>Chromosome aberration assay</subject><subject>Chromosome Aberrations - chemically induced</subject><subject>Comet assay</subject><subject>DNA Damage</subject><subject>Humans</subject><subject>Lymphocytes - drug effects</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Micronucleus assay</subject><subject>Mutagenicity Tests - methods</subject><subject>Mutagens - toxicity</subject><subject>Plant Extracts - toxicity</subject><subject>Salmonella typhimurium</subject><subject>Salmonella typhimurium - drug effects</subject><subject>Tinospora</subject><subject>Tinospora - toxicity</subject><subject>Tinospora cordifolia</subject><issn>0887-2333</issn><issn>1879-3177</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNp9kE1LAzEQhoMotlZ_gBfZkyC46yTp5gNPUvyCgpd6DtlsAinbTU12C_33prTgzdPM4XlfZh6EbjFUGDB7WleD31UEQFbAK6BwhqZYcFlSzPk5moIQvCSU0gm6SmkNALUgcIkmWLIaE5hP0cPK9yFtQ9SFCbH1LnRePxa6SNrZYV_Yne5GPfjQX6MLp7tkb05zhr7fXleLj3L59f65eFmWhgo6lIRxauc151wSw0wNjQQyJ1TgpqEsr62Q4IQDaV2LibEtZTWnrDFOU9JgOkP3x95tDD-jTYPa-GRs1-nehjEpgoHJWtYZxEfQxJBStE5to9_ouFcY1MGPWqvsRx38KOAq-8mZu1P52Gxs-5c4CcnA8xGw-cWdt1El422fz_TRmkG1wf9T_wsZsXQO</recordid><startdate>20091001</startdate><enddate>20091001</enddate><creator>Chandrasekaran, C.V.</creator><creator>Mathuram, L.N.</creator><creator>Daivasigamani, Prabhu</creator><creator>Bhatnagar, Upendra</creator><general>Elsevier Ltd</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>7QL</scope><scope>7U7</scope><scope>C1K</scope></search><sort><creationdate>20091001</creationdate><title>Tinospora cordifolia, a safety evaluation</title><author>Chandrasekaran, C.V. ; Mathuram, L.N. ; Daivasigamani, Prabhu ; Bhatnagar, Upendra</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c383t-2673e4577792c6c50b90242381bb36024d890f8f09efd12ced365736bcfa32b13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Ames test</topic><topic>Animals</topic><topic>Bone Marrow - drug effects</topic><topic>Chromosome aberration assay</topic><topic>Chromosome Aberrations - chemically induced</topic><topic>Comet assay</topic><topic>DNA Damage</topic><topic>Humans</topic><topic>Lymphocytes - drug effects</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Micronucleus assay</topic><topic>Mutagenicity Tests - methods</topic><topic>Mutagens - toxicity</topic><topic>Plant Extracts - toxicity</topic><topic>Salmonella typhimurium</topic><topic>Salmonella typhimurium - drug effects</topic><topic>Tinospora</topic><topic>Tinospora - toxicity</topic><topic>Tinospora cordifolia</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chandrasekaran, C.V.</creatorcontrib><creatorcontrib>Mathuram, L.N.</creatorcontrib><creatorcontrib>Daivasigamani, Prabhu</creatorcontrib><creatorcontrib>Bhatnagar, Upendra</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Toxicology in vitro</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chandrasekaran, C.V.</au><au>Mathuram, L.N.</au><au>Daivasigamani, Prabhu</au><au>Bhatnagar, Upendra</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tinospora cordifolia, a safety evaluation</atitle><jtitle>Toxicology in vitro</jtitle><addtitle>Toxicol In Vitro</addtitle><date>2009-10-01</date><risdate>2009</risdate><volume>23</volume><issue>7</issue><spage>1220</spage><epage>1226</epage><pages>1220-1226</pages><issn>0887-2333</issn><eissn>1879-3177</eissn><abstract>Tinospora cordifolia is one of the indispensable medicinal plants used in veterinary folk medicine/Ayurvedic system of medicine for the treatment of diverse diseases and recommended for improving the immune system by means of body resistance. In the current study, we evaluated the genotoxic risk of the aqueous extract of
T. cordifolia (TC) in a battery of four different genotoxicity tests viz., Ames, in vitro chromosome aberration (CA), rodent bone marrow micronucleus (MN), and Comet assay. Experimental results confirmed that in Ames test up to 5000
μg/plate of TC did not exhibit any mutagenic effect in
Salmonella typhimurium mutant strains (TA97a, TA98, TA100, TA102, and TA1535). In CA assay, TC was not clastogenic to human peripheral blood lymphocytes up to a concentration of 3000
μg/ml. In MN and Comet assays, TC was pre-treated for 7
days at three dose levels (150, 200 and 250
mg/kg body weight) orally to male Balb/c mice. The results showed that TC treatment did not display clastogenicity and DNA damaging effect in bone marrow erythrocytes and peripheral blood lymphocytes respectively.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>19651204</pmid><doi>10.1016/j.tiv.2009.07.030</doi><tpages>7</tpages></addata></record> |
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subjects | Ames test Animals Bone Marrow - drug effects Chromosome aberration assay Chromosome Aberrations - chemically induced Comet assay DNA Damage Humans Lymphocytes - drug effects Male Mice Mice, Inbred BALB C Micronucleus assay Mutagenicity Tests - methods Mutagens - toxicity Plant Extracts - toxicity Salmonella typhimurium Salmonella typhimurium - drug effects Tinospora Tinospora - toxicity Tinospora cordifolia |
title | Tinospora cordifolia, a safety evaluation |
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