Effect of matrine on transforming growth factor β1 and hepatocyte growth factor in rat liver fibrosis model
Objective:To observe the preventive and control effect of matrine on transforming growth factor(TCF- β1) and hepatocyte.growth factor(HCF) of liver fibrosis tissue in rals.Methods:A total of48 SD rats were randomly divided into A,B,C,D groups with 12 in each,group A as the normal control group and g...
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description | Objective:To observe the preventive and control effect of matrine on transforming growth factor(TCF- β1) and hepatocyte.growth factor(HCF) of liver fibrosis tissue in rals.Methods:A total of48 SD rats were randomly divided into A,B,C,D groups with 12 in each,group A as the normal control group and groups B.C,D as liver fibrosis models using composite modulus method with carbon tetrachloride(CCL4).Group B was the model group,group C adopted γ— interferon lavage therapy in the second day of modeling,and group D adopted matrine lavage treatment,at 4 and8 weeks after treatment.Six rats were executed for detection of TGF- β1 and HGF,liver tissue histology and comparison fibrosis degree changes of rat liver tissue between groups.Results:Croups B,C,D showed a more significantly increased TCF- β1 at each time point compared with group A(P<0.05);Group B showed a more significantly increased TGF- β1 than groups C and D at weeks 4 and 8(P<0.05);group D showed a lowest level of TGF-β1,followed by groups C and B.HGF of group B decreased more significantly than A group at weeks 4 and 8(P<0.05);HGF of groups C and D was significantly elevated at 4 and 8 weeks than groups A and B(P<0.05),in which the group D showed the highest level of HGF.According to tissue histologic observation,rat liver tissue structure of group A was clear and normal,tissue structure of group B was destroyed with obvious fibrous tissue hyperplasia and fatty change of hepatic cells;groups C and D showed a slighter liver tissue damage,cell necrosis and connective tissue hyperplasia in collect abbacy than group B with a trend of obvious improvement.Conclusions:Matrine can reduce TGF- β1expression and enhance the activity of HGF,so as to realize the inhibition effect on liver fibrosis in rats. |
doi_str_mv | 10.1016/S1995-7645(14)60062-6 |
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fullrecord | <record><control><sourceid>wanfang_jour_proqu</sourceid><recordid>TN_cdi_wanfang_journals_yrdyyzz_e201405011</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><cqvip_id>1003036776</cqvip_id><wanfj_id>yrdyyzz_e201405011</wanfj_id><els_id>S1995764514600626</els_id><sourcerecordid>yrdyyzz_e201405011</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4421-30c6f603241a5955d8ecdab38b6953a10b76966b4cb7524e356b04459597d6333</originalsourceid><addsrcrecordid>eNqFkctuEzEUhi0EolHpI4AssSlIA76eyaxQVZWLVIkFsLY8nuPE1Yyd2pNW6WPxIDwTbhMqxAZvvPmO_9_nI-QlZ-844_D-G-863bSg9ClXb4AxEA08IQshtWgUV_CULB6RI3JSyhWrR4qua-VzciQ0A8mgXZDxwnt0M02eTnbOISJNkc7ZxuJTnkJc0VVOt_OaeuvmlOmvn5zaONA1buyc3G7Gf4AQabYzHcMNZupDn1MJhU5pwPEFeebtWPDkcB-THx8vvp9_bi6_fvpyfnbZOKUEbyRz4KG2VdzqTuthiW6wvVz20GlpOetb6AB65fpWC4VSQ8-UqmjXDiClPCZv9-_e2uhtXJmrtM2xJppdHna7uzuDgnHFNOO8wqd7eJPT9RbLbKZQHI6jjZi2xXCtliCXQrQV1XvU1U-VjN5scphs3hnOzL0Y8yDG3G_dcGUexBioc68OEdt-wuFx6o-GCnzYA1i3chMwm-ICRodDyNWOGVL4b8TrQ7V1iqvr6u2vbkwyCW0L8jfcgKih</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1548638227</pqid></control><display><type>article</type><title>Effect of matrine on transforming growth factor β1 and hepatocyte growth factor in rat liver fibrosis model</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>Yu, Jian-Lan ; Li, Jun-Hua ; Chengz, Rong-Gui ; Ma, Yan-Mei ; Wang, Xiao-Juan ; Liu, Jing-Chun</creator><creatorcontrib>Yu, Jian-Lan ; Li, Jun-Hua ; Chengz, Rong-Gui ; Ma, Yan-Mei ; Wang, Xiao-Juan ; Liu, Jing-Chun</creatorcontrib><description>Objective:To observe the preventive and control effect of matrine on transforming growth factor(TCF- β1) and hepatocyte.growth factor(HCF) of liver fibrosis tissue in rals.Methods:A total of48 SD rats were randomly divided into A,B,C,D groups with 12 in each,group A as the normal control group and groups B.C,D as liver fibrosis models using composite modulus method with carbon tetrachloride(CCL4).Group B was the model group,group C adopted γ— interferon lavage therapy in the second day of modeling,and group D adopted matrine lavage treatment,at 4 and8 weeks after treatment.Six rats were executed for detection of TGF- β1 and HGF,liver tissue histology and comparison fibrosis degree changes of rat liver tissue between groups.Results:Croups B,C,D showed a more significantly increased TCF- β1 at each time point compared with group A(P&lt;0.05);Group B showed a more significantly increased TGF- β1 than groups C and D at weeks 4 and 8(P&lt;0.05);group D showed a lowest level of TGF-β1,followed by groups C and B.HGF of group B decreased more significantly than A group at weeks 4 and 8(P&lt;0.05);HGF of groups C and D was significantly elevated at 4 and 8 weeks than groups A and B(P&lt;0.05),in which the group D showed the highest level of HGF.According to tissue histologic observation,rat liver tissue structure of group A was clear and normal,tissue structure of group B was destroyed with obvious fibrous tissue hyperplasia and fatty change of hepatic cells;groups C and D showed a slighter liver tissue damage,cell necrosis and connective tissue hyperplasia in collect abbacy than group B with a trend of obvious improvement.Conclusions:Matrine can reduce TGF- β1expression and enhance the activity of HGF,so as to realize the inhibition effect on liver fibrosis in rats.</description><identifier>ISSN: 1995-7645</identifier><identifier>EISSN: 2352-4146</identifier><identifier>DOI: 10.1016/S1995-7645(14)60062-6</identifier><identifier>PMID: 25063067</identifier><language>eng</language><publisher>India: Elsevier B.V</publisher><subject>Alkaloids - pharmacology ; Animals ; factor ; fibrosis ; Gene Expression - drug effects ; growth ; Hepatocyte ; Hepatocyte growth factor ; Hepatocyte Growth Factor - analysis ; Hepatocyte Growth Factor - genetics ; Hepatocyte Growth Factor - metabolism ; Liver ; Liver - chemistry ; Liver - drug effects ; Liver - metabolism ; Liver - pathology ; Liver Cirrhosis - metabolism ; Liver Cirrhosis - pathology ; Liver fibrosis ; Male ; Matrine ; Protective Agents - pharmacology ; Quinolizines - pharmacology ; Rats ; Rats, Sprague-Dawley ; RNA, Messenger - analysis ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; Transforming ; Transforming Growth Factor beta1 - analysis ; Transforming Growth Factor beta1 - genetics ; Transforming Growth Factor beta1 - metabolism ; Transforming growth factor β1</subject><ispartof>Asian Pacific journal of tropical medicine, 2014-05, Vol.7 (5), p.390-393</ispartof><rights>2014 Hainan Medical College</rights><rights>Copyright © 2014 Hainan Medical College. Published by Elsevier B.V. All rights reserved.</rights><rights>Copyright © Wanfang Data Co. Ltd. All Rights Reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4421-30c6f603241a5955d8ecdab38b6953a10b76966b4cb7524e356b04459597d6333</citedby><cites>FETCH-LOGICAL-c4421-30c6f603241a5955d8ecdab38b6953a10b76966b4cb7524e356b04459597d6333</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/71792X/71792X.jpg</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S1995-7645(14)60062-6$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25063067$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yu, Jian-Lan</creatorcontrib><creatorcontrib>Li, Jun-Hua</creatorcontrib><creatorcontrib>Chengz, Rong-Gui</creatorcontrib><creatorcontrib>Ma, Yan-Mei</creatorcontrib><creatorcontrib>Wang, Xiao-Juan</creatorcontrib><creatorcontrib>Liu, Jing-Chun</creatorcontrib><title>Effect of matrine on transforming growth factor β1 and hepatocyte growth factor in rat liver fibrosis model</title><title>Asian Pacific journal of tropical medicine</title><addtitle>Asian Pacific Journal of Tropical Medicine</addtitle><description>Objective:To observe the preventive and control effect of matrine on transforming growth factor(TCF- β1) and hepatocyte.growth factor(HCF) of liver fibrosis tissue in rals.Methods:A total of48 SD rats were randomly divided into A,B,C,D groups with 12 in each,group A as the normal control group and groups B.C,D as liver fibrosis models using composite modulus method with carbon tetrachloride(CCL4).Group B was the model group,group C adopted γ— interferon lavage therapy in the second day of modeling,and group D adopted matrine lavage treatment,at 4 and8 weeks after treatment.Six rats were executed for detection of TGF- β1 and HGF,liver tissue histology and comparison fibrosis degree changes of rat liver tissue between groups.Results:Croups B,C,D showed a more significantly increased TCF- β1 at each time point compared with group A(P&lt;0.05);Group B showed a more significantly increased TGF- β1 than groups C and D at weeks 4 and 8(P&lt;0.05);group D showed a lowest level of TGF-β1,followed by groups C and B.HGF of group B decreased more significantly than A group at weeks 4 and 8(P&lt;0.05);HGF of groups C and D was significantly elevated at 4 and 8 weeks than groups A and B(P&lt;0.05),in which the group D showed the highest level of HGF.According to tissue histologic observation,rat liver tissue structure of group A was clear and normal,tissue structure of group B was destroyed with obvious fibrous tissue hyperplasia and fatty change of hepatic cells;groups C and D showed a slighter liver tissue damage,cell necrosis and connective tissue hyperplasia in collect abbacy than group B with a trend of obvious improvement.Conclusions:Matrine can reduce TGF- β1expression and enhance the activity of HGF,so as to realize the inhibition effect on liver fibrosis in rats.</description><subject>Alkaloids - pharmacology</subject><subject>Animals</subject><subject>factor</subject><subject>fibrosis</subject><subject>Gene Expression - drug effects</subject><subject>growth</subject><subject>Hepatocyte</subject><subject>Hepatocyte growth factor</subject><subject>Hepatocyte Growth Factor - analysis</subject><subject>Hepatocyte Growth Factor - genetics</subject><subject>Hepatocyte Growth Factor - metabolism</subject><subject>Liver</subject><subject>Liver - chemistry</subject><subject>Liver - drug effects</subject><subject>Liver - metabolism</subject><subject>Liver - pathology</subject><subject>Liver Cirrhosis - metabolism</subject><subject>Liver Cirrhosis - pathology</subject><subject>Liver fibrosis</subject><subject>Male</subject><subject>Matrine</subject><subject>Protective Agents - pharmacology</subject><subject>Quinolizines - pharmacology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>RNA, Messenger - analysis</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>Transforming</subject><subject>Transforming Growth Factor beta1 - analysis</subject><subject>Transforming Growth Factor beta1 - genetics</subject><subject>Transforming Growth Factor beta1 - metabolism</subject><subject>Transforming growth factor β1</subject><issn>1995-7645</issn><issn>2352-4146</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkctuEzEUhi0EolHpI4AssSlIA76eyaxQVZWLVIkFsLY8nuPE1Yyd2pNW6WPxIDwTbhMqxAZvvPmO_9_nI-QlZ-844_D-G-863bSg9ClXb4AxEA08IQshtWgUV_CULB6RI3JSyhWrR4qua-VzciQ0A8mgXZDxwnt0M02eTnbOISJNkc7ZxuJTnkJc0VVOt_OaeuvmlOmvn5zaONA1buyc3G7Gf4AQabYzHcMNZupDn1MJhU5pwPEFeebtWPDkcB-THx8vvp9_bi6_fvpyfnbZOKUEbyRz4KG2VdzqTuthiW6wvVz20GlpOetb6AB65fpWC4VSQ8-UqmjXDiClPCZv9-_e2uhtXJmrtM2xJppdHna7uzuDgnHFNOO8wqd7eJPT9RbLbKZQHI6jjZi2xXCtliCXQrQV1XvU1U-VjN5scphs3hnOzL0Y8yDG3G_dcGUexBioc68OEdt-wuFx6o-GCnzYA1i3chMwm-ICRodDyNWOGVL4b8TrQ7V1iqvr6u2vbkwyCW0L8jfcgKih</recordid><startdate>201405</startdate><enddate>201405</enddate><creator>Yu, Jian-Lan</creator><creator>Li, Jun-Hua</creator><creator>Chengz, Rong-Gui</creator><creator>Ma, Yan-Mei</creator><creator>Wang, Xiao-Juan</creator><creator>Liu, Jing-Chun</creator><general>Elsevier B.V</general><general>Heji Hospital affiliated to Changzhi Medical School, Changzhi 046011, China%Tumor Hospital of Shanxi Province, Taiyuan 030013, China%Shanxi Medical School, Taiyuan 030001, China%The First Clinical Hospital of Shanxi Medical School, Taiyuan 030001, China</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W91</scope><scope>~WA</scope><scope>6I.</scope><scope>AAFTH</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>7X8</scope><scope>2B.</scope><scope>4A8</scope><scope>92I</scope><scope>93N</scope><scope>PSX</scope><scope>TCJ</scope></search><sort><creationdate>201405</creationdate><title>Effect of matrine on transforming growth factor β1 and hepatocyte growth factor in rat liver fibrosis model</title><author>Yu, Jian-Lan ; Li, Jun-Hua ; Chengz, Rong-Gui ; Ma, Yan-Mei ; Wang, Xiao-Juan ; Liu, Jing-Chun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4421-30c6f603241a5955d8ecdab38b6953a10b76966b4cb7524e356b04459597d6333</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Alkaloids - pharmacology</topic><topic>Animals</topic><topic>factor</topic><topic>fibrosis</topic><topic>Gene Expression - drug effects</topic><topic>growth</topic><topic>Hepatocyte</topic><topic>Hepatocyte growth factor</topic><topic>Hepatocyte Growth Factor - analysis</topic><topic>Hepatocyte Growth Factor - genetics</topic><topic>Hepatocyte Growth Factor - metabolism</topic><topic>Liver</topic><topic>Liver - chemistry</topic><topic>Liver - drug effects</topic><topic>Liver - metabolism</topic><topic>Liver - pathology</topic><topic>Liver Cirrhosis - metabolism</topic><topic>Liver Cirrhosis - pathology</topic><topic>Liver fibrosis</topic><topic>Male</topic><topic>Matrine</topic><topic>Protective Agents - pharmacology</topic><topic>Quinolizines - pharmacology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>RNA, Messenger - analysis</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>Transforming</topic><topic>Transforming Growth Factor beta1 - analysis</topic><topic>Transforming Growth Factor beta1 - genetics</topic><topic>Transforming Growth Factor beta1 - metabolism</topic><topic>Transforming growth factor β1</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yu, Jian-Lan</creatorcontrib><creatorcontrib>Li, Jun-Hua</creatorcontrib><creatorcontrib>Chengz, Rong-Gui</creatorcontrib><creatorcontrib>Ma, Yan-Mei</creatorcontrib><creatorcontrib>Wang, Xiao-Juan</creatorcontrib><creatorcontrib>Liu, Jing-Chun</creatorcontrib><collection>中文科技期刊数据库</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库-医药卫生</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Wanfang Data Journals - Hong Kong</collection><collection>WANFANG Data Centre</collection><collection>Wanfang Data Journals</collection><collection>万方数据期刊 - 香港版</collection><collection>China Online Journals (COJ)</collection><collection>China Online Journals (COJ)</collection><jtitle>Asian Pacific journal of tropical medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yu, Jian-Lan</au><au>Li, Jun-Hua</au><au>Chengz, Rong-Gui</au><au>Ma, Yan-Mei</au><au>Wang, Xiao-Juan</au><au>Liu, Jing-Chun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of matrine on transforming growth factor β1 and hepatocyte growth factor in rat liver fibrosis model</atitle><jtitle>Asian Pacific journal of tropical medicine</jtitle><addtitle>Asian Pacific Journal of Tropical Medicine</addtitle><date>2014-05</date><risdate>2014</risdate><volume>7</volume><issue>5</issue><spage>390</spage><epage>393</epage><pages>390-393</pages><issn>1995-7645</issn><eissn>2352-4146</eissn><abstract>Objective:To observe the preventive and control effect of matrine on transforming growth factor(TCF- β1) and hepatocyte.growth factor(HCF) of liver fibrosis tissue in rals.Methods:A total of48 SD rats were randomly divided into A,B,C,D groups with 12 in each,group A as the normal control group and groups B.C,D as liver fibrosis models using composite modulus method with carbon tetrachloride(CCL4).Group B was the model group,group C adopted γ— interferon lavage therapy in the second day of modeling,and group D adopted matrine lavage treatment,at 4 and8 weeks after treatment.Six rats were executed for detection of TGF- β1 and HGF,liver tissue histology and comparison fibrosis degree changes of rat liver tissue between groups.Results:Croups B,C,D showed a more significantly increased TCF- β1 at each time point compared with group A(P&lt;0.05);Group B showed a more significantly increased TGF- β1 than groups C and D at weeks 4 and 8(P&lt;0.05);group D showed a lowest level of TGF-β1,followed by groups C and B.HGF of group B decreased more significantly than A group at weeks 4 and 8(P&lt;0.05);HGF of groups C and D was significantly elevated at 4 and 8 weeks than groups A and B(P&lt;0.05),in which the group D showed the highest level of HGF.According to tissue histologic observation,rat liver tissue structure of group A was clear and normal,tissue structure of group B was destroyed with obvious fibrous tissue hyperplasia and fatty change of hepatic cells;groups C and D showed a slighter liver tissue damage,cell necrosis and connective tissue hyperplasia in collect abbacy than group B with a trend of obvious improvement.Conclusions:Matrine can reduce TGF- β1expression and enhance the activity of HGF,so as to realize the inhibition effect on liver fibrosis in rats.</abstract><cop>India</cop><pub>Elsevier B.V</pub><pmid>25063067</pmid><doi>10.1016/S1995-7645(14)60062-6</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Alkaloids - pharmacology Animals factor fibrosis Gene Expression - drug effects growth Hepatocyte Hepatocyte growth factor Hepatocyte Growth Factor - analysis Hepatocyte Growth Factor - genetics Hepatocyte Growth Factor - metabolism Liver Liver - chemistry Liver - drug effects Liver - metabolism Liver - pathology Liver Cirrhosis - metabolism Liver Cirrhosis - pathology Liver fibrosis Male Matrine Protective Agents - pharmacology Quinolizines - pharmacology Rats Rats, Sprague-Dawley RNA, Messenger - analysis RNA, Messenger - genetics RNA, Messenger - metabolism Transforming Transforming Growth Factor beta1 - analysis Transforming Growth Factor beta1 - genetics Transforming Growth Factor beta1 - metabolism Transforming growth factor β1 |
title | Effect of matrine on transforming growth factor β1 and hepatocyte growth factor in rat liver fibrosis model |
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