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Protective effects of polydatin from Polygonum cuspidatum against carbon tetrachloride-induced liver injury in mice
Polydatin is one of main compounds in Polygonum cuspidatum, a plant with both medicinal and nutritional value. The possible hepatoprotective effects of polydatin on acute liver injury mice induced by carbon tetrachloride (CCl(4)) and the mechanisms involved were investigated. Intraperitoneal injecti...
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Published in: | PloS one 2012-09, Vol.7 (9), p.e46574 |
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description | Polydatin is one of main compounds in Polygonum cuspidatum, a plant with both medicinal and nutritional value. The possible hepatoprotective effects of polydatin on acute liver injury mice induced by carbon tetrachloride (CCl(4)) and the mechanisms involved were investigated. Intraperitoneal injection of CCl(4) (50 µl/kg) resulted in a significant increase in the levels of serum aspartate aminotransferase (AST), alanine aminotransferase (ALT) and hepatic malondialdehyde (MDA), also a marked enhancement in the expression of hepatic tumor necrosis factor-alpha (TNF-α), interleukin-1 beta (IL-1β), cyclooxygenase-2 (COX-2), inducible nitric oxide synthase (iNOS) and nuclearfactor-kappa B (NF-κB). On the other hand, decreased glutathione (GSH) content and activities of glutathione transferase (GST), superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GPx) were observed following CCl(4) exposure. Nevertheless, all of these phenotypes were evidently reversed by preadministration of polydatin for 5 continuous days. The mRNA and protein expression levels of hepatic growth factor-beta1 (TGF-β(1)) were enhanced further by polydatin. These results suggest that polydatin protects mice against CCl(4)-induced liver injury through antioxidant stress and antiinflammatory effects. Polydatin may be an effective hepatoprotective agent and a promising candidate for the treatment of oxidative stress- and inflammation-related diseases. |
doi_str_mv | 10.1371/journal.pone.0046574 |
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The possible hepatoprotective effects of polydatin on acute liver injury mice induced by carbon tetrachloride (CCl(4)) and the mechanisms involved were investigated. Intraperitoneal injection of CCl(4) (50 µl/kg) resulted in a significant increase in the levels of serum aspartate aminotransferase (AST), alanine aminotransferase (ALT) and hepatic malondialdehyde (MDA), also a marked enhancement in the expression of hepatic tumor necrosis factor-alpha (TNF-α), interleukin-1 beta (IL-1β), cyclooxygenase-2 (COX-2), inducible nitric oxide synthase (iNOS) and nuclearfactor-kappa B (NF-κB). On the other hand, decreased glutathione (GSH) content and activities of glutathione transferase (GST), superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GPx) were observed following CCl(4) exposure. Nevertheless, all of these phenotypes were evidently reversed by preadministration of polydatin for 5 continuous days. The mRNA and protein expression levels of hepatic growth factor-beta1 (TGF-β(1)) were enhanced further by polydatin. These results suggest that polydatin protects mice against CCl(4)-induced liver injury through antioxidant stress and antiinflammatory effects. Polydatin may be an effective hepatoprotective agent and a promising candidate for the treatment of oxidative stress- and inflammation-related diseases.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0046574</identifier><identifier>PMID: 23029551</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Alanine ; Alanine transaminase ; Alanine Transaminase - blood ; Analysis ; Animals ; Anti-Inflammatory Agents - pharmacology ; Anti-Inflammatory Agents - therapeutic use ; Antioxidants ; Antioxidants - pharmacology ; Antioxidants - therapeutic use ; Aquatic plants ; Aspartate aminotransferase ; Aspartate Aminotransferases - blood ; Biology ; Carbon Tetrachloride ; Care and treatment ; Catalase ; Catalase - metabolism ; CCL4 protein ; Chemical and Drug Induced Liver Injury - blood ; Chemical and Drug Induced Liver Injury - drug therapy ; Chemical and Drug Induced Liver Injury - pathology ; Chemical properties ; Chinese medicine ; Cyclooxygenase-2 ; Drugs, Chinese Herbal - pharmacology ; Drugs, Chinese Herbal - therapeutic use ; Fallopia japonica - chemistry ; Gene Expression ; Glucosides - pharmacology ; Glucosides - therapeutic use ; Glutathione ; Glutathione - metabolism ; Glutathione peroxidase ; Glutathione Peroxidase - metabolism ; Glutathione transferase ; Glutathione Transferase - metabolism ; Health aspects ; Herbal medicine ; Inflammation Mediators - metabolism ; Injuries ; Interleukin 1 ; Kinases ; Liver ; Liver - drug effects ; Liver - enzymology ; Liver - metabolism ; Liver diseases ; Male ; Malondialdehyde ; Medical treatment ; Medicinal plants ; Medicine ; Mice ; Mice, Inbred ICR ; mRNA ; NF-kappa B - metabolism ; NF-κB protein ; Nitric oxide ; Nitric-oxide synthase ; Nutritive value ; Oxidative stress ; Oxidative Stress - drug effects ; Peroxidase ; Polygonum cuspidatum ; Rodents ; Stilbenes - pharmacology ; Stilbenes - therapeutic use ; Superoxide dismutase ; Superoxide Dismutase - metabolism ; Transforming Growth Factor beta1 - genetics ; Transforming Growth Factor beta1 - metabolism ; Transforming growth factor-b1 ; Tumor necrosis factor ; Up-Regulation</subject><ispartof>PloS one, 2012-09, Vol.7 (9), p.e46574</ispartof><rights>COPYRIGHT 2012 Public Library of Science</rights><rights>Zhang et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2012 Zhang et al 2012 Zhang et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c758t-1fc98131af77a2c3f85d2e500a1c4059156a2942092a830b0bb8c2ec5bf4fc293</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1326552947/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1326552947?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23029551$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Khan, Firoze</contributor><creatorcontrib>Zhang, Hong</creatorcontrib><creatorcontrib>Yu, Cheng-Hao</creatorcontrib><creatorcontrib>Jiang, Yi-Ping</creatorcontrib><creatorcontrib>Peng, Cheng</creatorcontrib><creatorcontrib>He, Kun</creatorcontrib><creatorcontrib>Tang, Jian-Yuan</creatorcontrib><creatorcontrib>Xin, Hai-Liang</creatorcontrib><title>Protective effects of polydatin from Polygonum cuspidatum against carbon tetrachloride-induced liver injury in mice</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Polydatin is one of main compounds in Polygonum cuspidatum, a plant with both medicinal and nutritional value. The possible hepatoprotective effects of polydatin on acute liver injury mice induced by carbon tetrachloride (CCl(4)) and the mechanisms involved were investigated. Intraperitoneal injection of CCl(4) (50 µl/kg) resulted in a significant increase in the levels of serum aspartate aminotransferase (AST), alanine aminotransferase (ALT) and hepatic malondialdehyde (MDA), also a marked enhancement in the expression of hepatic tumor necrosis factor-alpha (TNF-α), interleukin-1 beta (IL-1β), cyclooxygenase-2 (COX-2), inducible nitric oxide synthase (iNOS) and nuclearfactor-kappa B (NF-κB). On the other hand, decreased glutathione (GSH) content and activities of glutathione transferase (GST), superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GPx) were observed following CCl(4) exposure. Nevertheless, all of these phenotypes were evidently reversed by preadministration of polydatin for 5 continuous days. The mRNA and protein expression levels of hepatic growth factor-beta1 (TGF-β(1)) were enhanced further by polydatin. These results suggest that polydatin protects mice against CCl(4)-induced liver injury through antioxidant stress and antiinflammatory effects. Polydatin may be an effective hepatoprotective agent and a promising candidate for the treatment of oxidative stress- and inflammation-related diseases.</description><subject>Alanine</subject><subject>Alanine transaminase</subject><subject>Alanine Transaminase - blood</subject><subject>Analysis</subject><subject>Animals</subject><subject>Anti-Inflammatory Agents - pharmacology</subject><subject>Anti-Inflammatory Agents - therapeutic use</subject><subject>Antioxidants</subject><subject>Antioxidants - pharmacology</subject><subject>Antioxidants - therapeutic use</subject><subject>Aquatic plants</subject><subject>Aspartate aminotransferase</subject><subject>Aspartate Aminotransferases - blood</subject><subject>Biology</subject><subject>Carbon Tetrachloride</subject><subject>Care and treatment</subject><subject>Catalase</subject><subject>Catalase - metabolism</subject><subject>CCL4 protein</subject><subject>Chemical and Drug Induced Liver Injury - blood</subject><subject>Chemical and Drug Induced Liver Injury - drug therapy</subject><subject>Chemical and Drug Induced Liver Injury - pathology</subject><subject>Chemical properties</subject><subject>Chinese medicine</subject><subject>Cyclooxygenase-2</subject><subject>Drugs, Chinese Herbal - pharmacology</subject><subject>Drugs, Chinese Herbal - therapeutic use</subject><subject>Fallopia japonica - chemistry</subject><subject>Gene Expression</subject><subject>Glucosides - pharmacology</subject><subject>Glucosides - therapeutic use</subject><subject>Glutathione</subject><subject>Glutathione - metabolism</subject><subject>Glutathione peroxidase</subject><subject>Glutathione Peroxidase - metabolism</subject><subject>Glutathione transferase</subject><subject>Glutathione Transferase - metabolism</subject><subject>Health aspects</subject><subject>Herbal medicine</subject><subject>Inflammation Mediators - metabolism</subject><subject>Injuries</subject><subject>Interleukin 1</subject><subject>Kinases</subject><subject>Liver</subject><subject>Liver - drug effects</subject><subject>Liver - enzymology</subject><subject>Liver - metabolism</subject><subject>Liver diseases</subject><subject>Male</subject><subject>Malondialdehyde</subject><subject>Medical treatment</subject><subject>Medicinal plants</subject><subject>Medicine</subject><subject>Mice</subject><subject>Mice, Inbred ICR</subject><subject>mRNA</subject><subject>NF-kappa B - metabolism</subject><subject>NF-κB protein</subject><subject>Nitric oxide</subject><subject>Nitric-oxide synthase</subject><subject>Nutritive value</subject><subject>Oxidative stress</subject><subject>Oxidative Stress - drug effects</subject><subject>Peroxidase</subject><subject>Polygonum cuspidatum</subject><subject>Rodents</subject><subject>Stilbenes - pharmacology</subject><subject>Stilbenes - therapeutic use</subject><subject>Superoxide dismutase</subject><subject>Superoxide Dismutase - metabolism</subject><subject>Transforming Growth Factor beta1 - genetics</subject><subject>Transforming Growth Factor beta1 - metabolism</subject><subject>Transforming growth factor-b1</subject><subject>Tumor necrosis factor</subject><subject>Up-Regulation</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNkllrGzEUhYfS0iztPyitoBDog12ts7wUQuhiCCR0exUaLWOZGcmRNKH-95XrSfBAC0UPupK-cySOblG8QnCJSIXeb_wYnOiXW-_0EkJasoo-KU5RQ_CixJA8PapPirMYNxAyUpfl8-IEE4gbxtBpEW-DT1ome6-BNiZXEXgDtr7fKZGsAyb4AdzmZefdOAA5xq3NJ7kUnbAuJiBFaL0DSacg5Lr3wSq9sE6NUivQZ-MArNuMYZcnMFipXxTPjOijfjnN58WPTx-_X31ZXN98Xl1dXi9kxeq0QEY2NSJImKoSWBJTM4U1g1AgSSFrECsFbiiGDRY1gS1s21piLVlrqJG4IefFm4PvtveRT3lFjgguGcvKKhOrA6G82PBtsIMIO-6F5X82fOi4CMnKXnOsRKXzBapVmmJcti1EdSuMYUQpBWn2-jDdNraDVlK7nEc_M52fOLvmnb_nhJYIIpgN3k4Gwd-NOqZ_PHmiOpFfZZ3x-9gHGyW_pE2NKWVlmanlX6g8lM4_kDvG2Lw_E7ybCTKT9K_UiTFGvvr29f_Zm59z9uKIXWvRp3X0_Zisd3EO0gMog48xaPOYHIJ83_APafB9w_Op4bPs9XHqj6KHDie_AeWs_kk</recordid><startdate>20120928</startdate><enddate>20120928</enddate><creator>Zhang, Hong</creator><creator>Yu, Cheng-Hao</creator><creator>Jiang, Yi-Ping</creator><creator>Peng, Cheng</creator><creator>He, Kun</creator><creator>Tang, Jian-Yuan</creator><creator>Xin, Hai-Liang</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20120928</creationdate><title>Protective effects of polydatin from Polygonum cuspidatum against carbon tetrachloride-induced liver injury in mice</title><author>Zhang, Hong ; Yu, Cheng-Hao ; Jiang, Yi-Ping ; Peng, Cheng ; He, Kun ; Tang, Jian-Yuan ; Xin, Hai-Liang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c758t-1fc98131af77a2c3f85d2e500a1c4059156a2942092a830b0bb8c2ec5bf4fc293</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Alanine</topic><topic>Alanine transaminase</topic><topic>Alanine Transaminase - blood</topic><topic>Analysis</topic><topic>Animals</topic><topic>Anti-Inflammatory Agents - pharmacology</topic><topic>Anti-Inflammatory Agents - therapeutic use</topic><topic>Antioxidants</topic><topic>Antioxidants - pharmacology</topic><topic>Antioxidants - therapeutic use</topic><topic>Aquatic plants</topic><topic>Aspartate aminotransferase</topic><topic>Aspartate Aminotransferases - blood</topic><topic>Biology</topic><topic>Carbon Tetrachloride</topic><topic>Care and treatment</topic><topic>Catalase</topic><topic>Catalase - metabolism</topic><topic>CCL4 protein</topic><topic>Chemical and Drug Induced Liver Injury - blood</topic><topic>Chemical and Drug Induced Liver Injury - drug therapy</topic><topic>Chemical and Drug Induced Liver Injury - pathology</topic><topic>Chemical properties</topic><topic>Chinese medicine</topic><topic>Cyclooxygenase-2</topic><topic>Drugs, Chinese Herbal - pharmacology</topic><topic>Drugs, Chinese Herbal - therapeutic use</topic><topic>Fallopia japonica - chemistry</topic><topic>Gene Expression</topic><topic>Glucosides - pharmacology</topic><topic>Glucosides - therapeutic use</topic><topic>Glutathione</topic><topic>Glutathione - metabolism</topic><topic>Glutathione peroxidase</topic><topic>Glutathione Peroxidase - metabolism</topic><topic>Glutathione transferase</topic><topic>Glutathione Transferase - metabolism</topic><topic>Health aspects</topic><topic>Herbal medicine</topic><topic>Inflammation Mediators - metabolism</topic><topic>Injuries</topic><topic>Interleukin 1</topic><topic>Kinases</topic><topic>Liver</topic><topic>Liver - drug effects</topic><topic>Liver - enzymology</topic><topic>Liver - metabolism</topic><topic>Liver diseases</topic><topic>Male</topic><topic>Malondialdehyde</topic><topic>Medical treatment</topic><topic>Medicinal plants</topic><topic>Medicine</topic><topic>Mice</topic><topic>Mice, Inbred ICR</topic><topic>mRNA</topic><topic>NF-kappa B - metabolism</topic><topic>NF-κB protein</topic><topic>Nitric oxide</topic><topic>Nitric-oxide synthase</topic><topic>Nutritive value</topic><topic>Oxidative stress</topic><topic>Oxidative Stress - 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The possible hepatoprotective effects of polydatin on acute liver injury mice induced by carbon tetrachloride (CCl(4)) and the mechanisms involved were investigated. Intraperitoneal injection of CCl(4) (50 µl/kg) resulted in a significant increase in the levels of serum aspartate aminotransferase (AST), alanine aminotransferase (ALT) and hepatic malondialdehyde (MDA), also a marked enhancement in the expression of hepatic tumor necrosis factor-alpha (TNF-α), interleukin-1 beta (IL-1β), cyclooxygenase-2 (COX-2), inducible nitric oxide synthase (iNOS) and nuclearfactor-kappa B (NF-κB). On the other hand, decreased glutathione (GSH) content and activities of glutathione transferase (GST), superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GPx) were observed following CCl(4) exposure. Nevertheless, all of these phenotypes were evidently reversed by preadministration of polydatin for 5 continuous days. The mRNA and protein expression levels of hepatic growth factor-beta1 (TGF-β(1)) were enhanced further by polydatin. These results suggest that polydatin protects mice against CCl(4)-induced liver injury through antioxidant stress and antiinflammatory effects. Polydatin may be an effective hepatoprotective agent and a promising candidate for the treatment of oxidative stress- and inflammation-related diseases.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>23029551</pmid><doi>10.1371/journal.pone.0046574</doi><tpages>e46574</tpages><oa>free_for_read</oa></addata></record> |
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identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2012-09, Vol.7 (9), p.e46574 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_1326552947 |
source | Open Access: PubMed Central; Publicly Available Content Database (Proquest) (PQ_SDU_P3) |
subjects | Alanine Alanine transaminase Alanine Transaminase - blood Analysis Animals Anti-Inflammatory Agents - pharmacology Anti-Inflammatory Agents - therapeutic use Antioxidants Antioxidants - pharmacology Antioxidants - therapeutic use Aquatic plants Aspartate aminotransferase Aspartate Aminotransferases - blood Biology Carbon Tetrachloride Care and treatment Catalase Catalase - metabolism CCL4 protein Chemical and Drug Induced Liver Injury - blood Chemical and Drug Induced Liver Injury - drug therapy Chemical and Drug Induced Liver Injury - pathology Chemical properties Chinese medicine Cyclooxygenase-2 Drugs, Chinese Herbal - pharmacology Drugs, Chinese Herbal - therapeutic use Fallopia japonica - chemistry Gene Expression Glucosides - pharmacology Glucosides - therapeutic use Glutathione Glutathione - metabolism Glutathione peroxidase Glutathione Peroxidase - metabolism Glutathione transferase Glutathione Transferase - metabolism Health aspects Herbal medicine Inflammation Mediators - metabolism Injuries Interleukin 1 Kinases Liver Liver - drug effects Liver - enzymology Liver - metabolism Liver diseases Male Malondialdehyde Medical treatment Medicinal plants Medicine Mice Mice, Inbred ICR mRNA NF-kappa B - metabolism NF-κB protein Nitric oxide Nitric-oxide synthase Nutritive value Oxidative stress Oxidative Stress - drug effects Peroxidase Polygonum cuspidatum Rodents Stilbenes - pharmacology Stilbenes - therapeutic use Superoxide dismutase Superoxide Dismutase - metabolism Transforming Growth Factor beta1 - genetics Transforming Growth Factor beta1 - metabolism Transforming growth factor-b1 Tumor necrosis factor Up-Regulation |
title | Protective effects of polydatin from Polygonum cuspidatum against carbon tetrachloride-induced liver injury in mice |
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