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Antihepatotoxic activity of Saussurea lappa extract on D-galactosamine and lipopolysaccharide-induced hepatitis in mice
The effects of aqueous-methanol extract of Saussurea lappa Clarke root (Sl.Cr) was investigated against D-galactosamine (D-GalN) and lipopolysaccharide (LPS)-induced hepatitis in mice. Co-administration of D-GalN (700 mg/kg) and LPS (1 μg/kg) significantly raised the plasma transaminase levels (ALT/...
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Published in: | Phytotherapy research 2010-06, Vol.24 (S2), p.S229-S232 |
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description | The effects of aqueous-methanol extract of Saussurea lappa Clarke root (Sl.Cr) was investigated against D-galactosamine (D-GalN) and lipopolysaccharide (LPS)-induced hepatitis in mice. Co-administration of D-GalN (700 mg/kg) and LPS (1 μg/kg) significantly raised the plasma transaminase levels (ALT/AST) as compared to the control group (p < 0.05). Pretreatment of mice with different doses of Sl.Cr (150, 300 and 600 mg/kg) significantly prevented the D-GalN and LPS-induced rise in plasma levels of ALT and AST in a dose-dependent manner (p < 0.05). Post-treatment with Sl.Cr (600 mg/kg) significantly restricted the progression of hepatic damage induced by D-GalN and LPS (p < 0.05). The improvement in plasma enzyme levels was further verified by histopathology of the liver, which showed improved architecture, absence of parenchyma congestion, decreased cellular swelling and apoptotic cells in treatment groups as compared to the toxin group of animals. These data indicate that the Sl.Cr exhibits hepatoprotective effect in mice and this study rationalize the traditional use of this plant in liver disorders. Copyright © 2009 John Wiley & Sons, Ltd. |
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Co-administration of D-GalN (700 mg/kg) and LPS (1 μg/kg) significantly raised the plasma transaminase levels (ALT/AST) as compared to the control group (p < 0.05). Pretreatment of mice with different doses of Sl.Cr (150, 300 and 600 mg/kg) significantly prevented the D-GalN and LPS-induced rise in plasma levels of ALT and AST in a dose-dependent manner (p < 0.05). Post-treatment with Sl.Cr (600 mg/kg) significantly restricted the progression of hepatic damage induced by D-GalN and LPS (p < 0.05). The improvement in plasma enzyme levels was further verified by histopathology of the liver, which showed improved architecture, absence of parenchyma congestion, decreased cellular swelling and apoptotic cells in treatment groups as compared to the toxin group of animals. These data indicate that the Sl.Cr exhibits hepatoprotective effect in mice and this study rationalize the traditional use of this plant in liver disorders. Copyright © 2009 John Wiley & Sons, Ltd.</description><identifier>ISSN: 0951-418X</identifier><identifier>ISSN: 1099-1573</identifier><identifier>EISSN: 1099-1573</identifier><identifier>DOI: 10.1002/ptr.3089</identifier><identifier>PMID: 20041433</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>Alanine Transaminase - blood ; Animals ; antihepatotoxic ; Apoptosis ; Chemical and Drug Induced Liver Injury - drug therapy ; D-Galactosamine ; Data processing ; Enzymes ; Female ; Galactosamine - toxicity ; Hepatitis ; hepatoprotective ; lipopolysaccharide ; lipopolysaccharide, hepatoprotective ; Lipopolysaccharides ; Lipopolysaccharides - toxicity ; Liver ; Liver - drug effects ; Liver - pathology ; Liver diseases ; Male ; Mice ; Mice, Inbred BALB C ; Parenchyma ; Phytotherapy ; Plant Extracts - pharmacology ; Plant Roots - chemistry ; Plasma levels ; Protective Agents - pharmacology ; Roots ; Saussurea ; Saussurea - chemistry ; Saussurea lappa ; Toxicity Tests, Acute ; Toxins ; transaminase</subject><ispartof>Phytotherapy research, 2010-06, Vol.24 (S2), p.S229-S232</ispartof><rights>Copyright © 2009 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4479-c9e257173649b9c74d5d3a6326e1f6f6f600f12c719d35ec46e8d80fea6442403</citedby><cites>FETCH-LOGICAL-c4479-c9e257173649b9c74d5d3a6326e1f6f6f600f12c719d35ec46e8d80fea6442403</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20041433$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yaeesh, Sheikh</creatorcontrib><creatorcontrib>Jamal, Qamar</creatorcontrib><creatorcontrib>Shah, Abdul Jabbar</creatorcontrib><creatorcontrib>Gilani, Anwarul Hassan</creatorcontrib><title>Antihepatotoxic activity of Saussurea lappa extract on D-galactosamine and lipopolysaccharide-induced hepatitis in mice</title><title>Phytotherapy research</title><addtitle>Phytother. Res</addtitle><description>The effects of aqueous-methanol extract of Saussurea lappa Clarke root (Sl.Cr) was investigated against D-galactosamine (D-GalN) and lipopolysaccharide (LPS)-induced hepatitis in mice. Co-administration of D-GalN (700 mg/kg) and LPS (1 μg/kg) significantly raised the plasma transaminase levels (ALT/AST) as compared to the control group (p < 0.05). Pretreatment of mice with different doses of Sl.Cr (150, 300 and 600 mg/kg) significantly prevented the D-GalN and LPS-induced rise in plasma levels of ALT and AST in a dose-dependent manner (p < 0.05). Post-treatment with Sl.Cr (600 mg/kg) significantly restricted the progression of hepatic damage induced by D-GalN and LPS (p < 0.05). The improvement in plasma enzyme levels was further verified by histopathology of the liver, which showed improved architecture, absence of parenchyma congestion, decreased cellular swelling and apoptotic cells in treatment groups as compared to the toxin group of animals. These data indicate that the Sl.Cr exhibits hepatoprotective effect in mice and this study rationalize the traditional use of this plant in liver disorders. Copyright © 2009 John Wiley & Sons, Ltd.</description><subject>Alanine Transaminase - blood</subject><subject>Animals</subject><subject>antihepatotoxic</subject><subject>Apoptosis</subject><subject>Chemical and Drug Induced Liver Injury - drug therapy</subject><subject>D-Galactosamine</subject><subject>Data processing</subject><subject>Enzymes</subject><subject>Female</subject><subject>Galactosamine - toxicity</subject><subject>Hepatitis</subject><subject>hepatoprotective</subject><subject>lipopolysaccharide</subject><subject>lipopolysaccharide, hepatoprotective</subject><subject>Lipopolysaccharides</subject><subject>Lipopolysaccharides - toxicity</subject><subject>Liver</subject><subject>Liver - drug effects</subject><subject>Liver - pathology</subject><subject>Liver diseases</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Parenchyma</subject><subject>Phytotherapy</subject><subject>Plant Extracts - pharmacology</subject><subject>Plant Roots - chemistry</subject><subject>Plasma levels</subject><subject>Protective Agents - pharmacology</subject><subject>Roots</subject><subject>Saussurea</subject><subject>Saussurea - chemistry</subject><subject>Saussurea lappa</subject><subject>Toxicity Tests, Acute</subject><subject>Toxins</subject><subject>transaminase</subject><issn>0951-418X</issn><issn>1099-1573</issn><issn>1099-1573</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNqF0cFu1DAUBVALgehQkPgC8A42Ke_FThwvqyktoBFUtIXuLNdxWkMSB9uhM39PwgyzA2TJfpKPrxeXkOcIRwiQvxlSOGJQyQdkgSBlhoVgD8kCZIEZx-r6gDyJ8RsAyBz4Y3KQA3DkjC3I_XGf3J0ddPLJr52h2iT306UN9Q290GOMY7CatnoYNLXrFKZ76nt6kt3qdpp91J3rLdV9TVs3-MG3m6iNudPB1TZzfT0aW9PfP7jkInU97ZyxT8mjRrfRPtudh-Tq9O3l8l22-nT2fnm8ygznQmZG2rwQKFjJ5Y00gtdFzXTJ8tJiU84LoMHcCJQ1K6zhpa3qChqrS85zDuyQvNrmDsH_GG1MqnPR2LbVvfVjVBIRi1wK8V8pGJsZ4iRf_1Mi5FCxat721AQfY7CNGoLrdNhMSM3Vqak6NVc30Re71PGms_Ue_ulqAtkW3LvWbv4apM4vP-8Cd97FZNd7r8N3VQomCvX145m6Xn1Znn84LRWf_Mutb7RX-ja4qK4uckAGWJUMpze_AH9ou8w</recordid><startdate>201006</startdate><enddate>201006</enddate><creator>Yaeesh, Sheikh</creator><creator>Jamal, Qamar</creator><creator>Shah, Abdul Jabbar</creator><creator>Gilani, Anwarul Hassan</creator><general>John Wiley & Sons, Ltd</general><scope>FBQ</scope><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>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>201006</creationdate><title>Antihepatotoxic activity of Saussurea lappa extract on D-galactosamine and lipopolysaccharide-induced hepatitis in mice</title><author>Yaeesh, Sheikh ; Jamal, Qamar ; Shah, Abdul Jabbar ; Gilani, Anwarul Hassan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4479-c9e257173649b9c74d5d3a6326e1f6f6f600f12c719d35ec46e8d80fea6442403</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Alanine Transaminase - blood</topic><topic>Animals</topic><topic>antihepatotoxic</topic><topic>Apoptosis</topic><topic>Chemical and Drug Induced Liver Injury - drug therapy</topic><topic>D-Galactosamine</topic><topic>Data processing</topic><topic>Enzymes</topic><topic>Female</topic><topic>Galactosamine - toxicity</topic><topic>Hepatitis</topic><topic>hepatoprotective</topic><topic>lipopolysaccharide</topic><topic>lipopolysaccharide, hepatoprotective</topic><topic>Lipopolysaccharides</topic><topic>Lipopolysaccharides - toxicity</topic><topic>Liver</topic><topic>Liver - drug effects</topic><topic>Liver - pathology</topic><topic>Liver diseases</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Parenchyma</topic><topic>Phytotherapy</topic><topic>Plant Extracts - pharmacology</topic><topic>Plant Roots - chemistry</topic><topic>Plasma levels</topic><topic>Protective Agents - pharmacology</topic><topic>Roots</topic><topic>Saussurea</topic><topic>Saussurea - chemistry</topic><topic>Saussurea lappa</topic><topic>Toxicity Tests, Acute</topic><topic>Toxins</topic><topic>transaminase</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yaeesh, Sheikh</creatorcontrib><creatorcontrib>Jamal, Qamar</creatorcontrib><creatorcontrib>Shah, Abdul Jabbar</creatorcontrib><creatorcontrib>Gilani, Anwarul Hassan</creatorcontrib><collection>AGRIS</collection><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>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Phytotherapy research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yaeesh, Sheikh</au><au>Jamal, Qamar</au><au>Shah, Abdul Jabbar</au><au>Gilani, Anwarul Hassan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antihepatotoxic activity of Saussurea lappa extract on D-galactosamine and lipopolysaccharide-induced hepatitis in mice</atitle><jtitle>Phytotherapy research</jtitle><addtitle>Phytother. Res</addtitle><date>2010-06</date><risdate>2010</risdate><volume>24</volume><issue>S2</issue><spage>S229</spage><epage>S232</epage><pages>S229-S232</pages><issn>0951-418X</issn><issn>1099-1573</issn><eissn>1099-1573</eissn><abstract>The effects of aqueous-methanol extract of Saussurea lappa Clarke root (Sl.Cr) was investigated against D-galactosamine (D-GalN) and lipopolysaccharide (LPS)-induced hepatitis in mice. Co-administration of D-GalN (700 mg/kg) and LPS (1 μg/kg) significantly raised the plasma transaminase levels (ALT/AST) as compared to the control group (p < 0.05). Pretreatment of mice with different doses of Sl.Cr (150, 300 and 600 mg/kg) significantly prevented the D-GalN and LPS-induced rise in plasma levels of ALT and AST in a dose-dependent manner (p < 0.05). Post-treatment with Sl.Cr (600 mg/kg) significantly restricted the progression of hepatic damage induced by D-GalN and LPS (p < 0.05). The improvement in plasma enzyme levels was further verified by histopathology of the liver, which showed improved architecture, absence of parenchyma congestion, decreased cellular swelling and apoptotic cells in treatment groups as compared to the toxin group of animals. These data indicate that the Sl.Cr exhibits hepatoprotective effect in mice and this study rationalize the traditional use of this plant in liver disorders. Copyright © 2009 John Wiley & Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><pmid>20041433</pmid><doi>10.1002/ptr.3089</doi><tpages>4</tpages></addata></record> |
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subjects | Alanine Transaminase - blood Animals antihepatotoxic Apoptosis Chemical and Drug Induced Liver Injury - drug therapy D-Galactosamine Data processing Enzymes Female Galactosamine - toxicity Hepatitis hepatoprotective lipopolysaccharide lipopolysaccharide, hepatoprotective Lipopolysaccharides Lipopolysaccharides - toxicity Liver Liver - drug effects Liver - pathology Liver diseases Male Mice Mice, Inbred BALB C Parenchyma Phytotherapy Plant Extracts - pharmacology Plant Roots - chemistry Plasma levels Protective Agents - pharmacology Roots Saussurea Saussurea - chemistry Saussurea lappa Toxicity Tests, Acute Toxins transaminase |
title | Antihepatotoxic activity of Saussurea lappa extract on D-galactosamine and lipopolysaccharide-induced hepatitis in mice |
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