Inhibitory effects of emodin on the proliferation of cultured rat vascular smooth muscle cell-induced by angiotensin II

Rhubarb, used as a traditional Chinese medicine for centuries, offers therapeutic potential for cardiovascular and other diseases. Emodin, extracted from the root extract of rhubarb has sparked increasing interest for therapeutic application. The main objective was to study the effect of emodin on c...

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Veröffentlicht in:Phytotherapy research 2008-02, Vol.22 (2), p.247-251
Hauptverfasser: Wang, ShiJun, Liu, YunYing, Fan, FangHua, Yan, Jie, Wang, XingXiang, Chen, JunZhu
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container_issue 2
container_start_page 247
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creator Wang, ShiJun
Liu, YunYing
Fan, FangHua
Yan, Jie
Wang, XingXiang
Chen, JunZhu
description Rhubarb, used as a traditional Chinese medicine for centuries, offers therapeutic potential for cardiovascular and other diseases. Emodin, extracted from the root extract of rhubarb has sparked increasing interest for therapeutic application. The main objective was to study the effect of emodin on cultured vascular smooth muscle cells (VSMCs) proliferation induced by angiotensin II (Ang II) and the expression of proto-oncogene c-myc. VSMCs were cultured by the explant method, then incubated for 24, 48 and 72 h with emodin (10-80 μm) and Ang II, or were left untreated (control). Cell proliferation was measured by MTT assay and immunohistochemical staining for proliferating cell nuclear antigen (PCNA), respectively. The expression of c-myc was measured by immunohistochemical staining and image analysis technique. Ang II increased the cell proliferation compared with the control group (p < 0.01). The expression of PCNA and c-myc was increased compared with the control group (p < 0.01). After pretreatment with emodin, the above indexes were obviously reduced compared with the Ang II group (p < 0.01). These findings suggested that emodin inhibited VSMCs proliferation induced by Ang II. Inhibition of the expression of c-myc might be correlated with the inhibitory effects. Copyright © 2007 John Wiley & Sons, Ltd.
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Emodin, extracted from the root extract of rhubarb has sparked increasing interest for therapeutic application. The main objective was to study the effect of emodin on cultured vascular smooth muscle cells (VSMCs) proliferation induced by angiotensin II (Ang II) and the expression of proto-oncogene c-myc. VSMCs were cultured by the explant method, then incubated for 24, 48 and 72 h with emodin (10-80 μm) and Ang II, or were left untreated (control). Cell proliferation was measured by MTT assay and immunohistochemical staining for proliferating cell nuclear antigen (PCNA), respectively. The expression of c-myc was measured by immunohistochemical staining and image analysis technique. Ang II increased the cell proliferation compared with the control group (p &lt; 0.01). The expression of PCNA and c-myc was increased compared with the control group (p &lt; 0.01). After pretreatment with emodin, the above indexes were obviously reduced compared with the Ang II group (p &lt; 0.01). 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Res</addtitle><description>Rhubarb, used as a traditional Chinese medicine for centuries, offers therapeutic potential for cardiovascular and other diseases. Emodin, extracted from the root extract of rhubarb has sparked increasing interest for therapeutic application. The main objective was to study the effect of emodin on cultured vascular smooth muscle cells (VSMCs) proliferation induced by angiotensin II (Ang II) and the expression of proto-oncogene c-myc. VSMCs were cultured by the explant method, then incubated for 24, 48 and 72 h with emodin (10-80 μm) and Ang II, or were left untreated (control). Cell proliferation was measured by MTT assay and immunohistochemical staining for proliferating cell nuclear antigen (PCNA), respectively. The expression of c-myc was measured by immunohistochemical staining and image analysis technique. Ang II increased the cell proliferation compared with the control group (p &lt; 0.01). The expression of PCNA and c-myc was increased compared with the control group (p &lt; 0.01). After pretreatment with emodin, the above indexes were obviously reduced compared with the Ang II group (p &lt; 0.01). These findings suggested that emodin inhibited VSMCs proliferation induced by Ang II. Inhibition of the expression of c-myc might be correlated with the inhibitory effects. Copyright © 2007 John Wiley &amp; Sons, Ltd.</description><subject>angiotensin II</subject><subject>Angiotensin II - pharmacology</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>c-myc</subject><subject>Cell Proliferation - drug effects</subject><subject>Cell Survival - drug effects</subject><subject>Cells, Cultured</subject><subject>emodin</subject><subject>Emodin - chemistry</subject><subject>Emodin - pharmacology</subject><subject>General pharmacology</subject><subject>Immunohistochemistry</subject><subject>L-Lactate Dehydrogenase - metabolism</subject><subject>Medical sciences</subject><subject>Muscle, Smooth, Vascular - cytology</subject><subject>Muscle, Smooth, Vascular - drug effects</subject><subject>Muscle, Smooth, Vascular - metabolism</subject><subject>Pharmacognosy. Homeopathy. Health food</subject><subject>Pharmacology. Drug treatments</subject><subject>proliferating cell nuclear antigen</subject><subject>Proliferating Cell Nuclear Antigen - metabolism</subject><subject>Proto-Oncogene Proteins c-myc - metabolism</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Rheum - chemistry</subject><subject>vascular smooth muscle cells</subject><issn>0951-418X</issn><issn>1099-1573</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10FFv1SAUB3BiXNx1mvgJlBeNL50caKE8LotuN9vUzC36RmgLu2hbrkCd99vLTZvtyScC_Djn8EfoFZBjIIR-2KZwTBmBJ2gFRMoCKsGeohWRFRQl1D8O0fMYfxJCJCXlM3QIoq55frBC9-tx4xqXfNhhY61pU8TeYjP4zo3YjzhtDN4G3ztrgk4un-TrdurTFEyH8xH-o2Pe64Dj4H3a4GGKbW9wa_q-cGM3tdk1O6zHO-eTGWOuu16_QAdW99G8XNYjdPvp483peXH55Wx9enJZtCUAFIzTruQ1GMtLTmtOBICVnGoBgjBpJUjgRtQV19oQVrNS19A0uuo6KoUGdoTezXXzH35PJiY1uLgfTY_GT1EJQrksCcvw_Qzb4GMMxqptcIMOOwVE7UNWOWS1DznT10vNqRlM9wiXVDN4u4Acje5t0GPr4oOjBCifexazu3e92f23ofp6c700XryLyfx98Dr8UlwwUanvn8-UEFf8HPi1usj-zeyt9krfhTzD7bfcnRFSVwIoZf8Atd6rEA</recordid><startdate>200802</startdate><enddate>200802</enddate><creator>Wang, ShiJun</creator><creator>Liu, YunYing</creator><creator>Fan, FangHua</creator><creator>Yan, Jie</creator><creator>Wang, XingXiang</creator><creator>Chen, JunZhu</creator><general>John Wiley &amp; Sons, Ltd</general><general>Wiley</general><scope>FBQ</scope><scope>BSCLL</scope><scope>IQODW</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></search><sort><creationdate>200802</creationdate><title>Inhibitory effects of emodin on the proliferation of cultured rat vascular smooth muscle cell-induced by angiotensin II</title><author>Wang, ShiJun ; Liu, YunYing ; Fan, FangHua ; Yan, Jie ; Wang, XingXiang ; Chen, JunZhu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4111-362d4681ef6462860711f962a717039f91916e7856aae03834a81bba5dd297a13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>angiotensin II</topic><topic>Angiotensin II - pharmacology</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>c-myc</topic><topic>Cell Proliferation - drug effects</topic><topic>Cell Survival - drug effects</topic><topic>Cells, Cultured</topic><topic>emodin</topic><topic>Emodin - chemistry</topic><topic>Emodin - pharmacology</topic><topic>General pharmacology</topic><topic>Immunohistochemistry</topic><topic>L-Lactate Dehydrogenase - metabolism</topic><topic>Medical sciences</topic><topic>Muscle, Smooth, Vascular - cytology</topic><topic>Muscle, Smooth, Vascular - drug effects</topic><topic>Muscle, Smooth, Vascular - metabolism</topic><topic>Pharmacognosy. Homeopathy. Health food</topic><topic>Pharmacology. Drug treatments</topic><topic>proliferating cell nuclear antigen</topic><topic>Proliferating Cell Nuclear Antigen - metabolism</topic><topic>Proto-Oncogene Proteins c-myc - metabolism</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Rheum - chemistry</topic><topic>vascular smooth muscle cells</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, ShiJun</creatorcontrib><creatorcontrib>Liu, YunYing</creatorcontrib><creatorcontrib>Fan, FangHua</creatorcontrib><creatorcontrib>Yan, Jie</creatorcontrib><creatorcontrib>Wang, XingXiang</creatorcontrib><creatorcontrib>Chen, JunZhu</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>Pascal-Francis</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><jtitle>Phytotherapy research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, ShiJun</au><au>Liu, YunYing</au><au>Fan, FangHua</au><au>Yan, Jie</au><au>Wang, XingXiang</au><au>Chen, JunZhu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inhibitory effects of emodin on the proliferation of cultured rat vascular smooth muscle cell-induced by angiotensin II</atitle><jtitle>Phytotherapy research</jtitle><addtitle>Phytother. 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The expression of c-myc was measured by immunohistochemical staining and image analysis technique. Ang II increased the cell proliferation compared with the control group (p &lt; 0.01). The expression of PCNA and c-myc was increased compared with the control group (p &lt; 0.01). After pretreatment with emodin, the above indexes were obviously reduced compared with the Ang II group (p &lt; 0.01). These findings suggested that emodin inhibited VSMCs proliferation induced by Ang II. Inhibition of the expression of c-myc might be correlated with the inhibitory effects. Copyright © 2007 John Wiley &amp; Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley &amp; Sons, Ltd</pub><pmid>17886230</pmid><doi>10.1002/ptr.2301</doi><tpages>5</tpages></addata></record>
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subjects angiotensin II
Angiotensin II - pharmacology
Animals
Biological and medical sciences
c-myc
Cell Proliferation - drug effects
Cell Survival - drug effects
Cells, Cultured
emodin
Emodin - chemistry
Emodin - pharmacology
General pharmacology
Immunohistochemistry
L-Lactate Dehydrogenase - metabolism
Medical sciences
Muscle, Smooth, Vascular - cytology
Muscle, Smooth, Vascular - drug effects
Muscle, Smooth, Vascular - metabolism
Pharmacognosy. Homeopathy. Health food
Pharmacology. Drug treatments
proliferating cell nuclear antigen
Proliferating Cell Nuclear Antigen - metabolism
Proto-Oncogene Proteins c-myc - metabolism
Rats
Rats, Sprague-Dawley
Rheum - chemistry
vascular smooth muscle cells
title Inhibitory effects of emodin on the proliferation of cultured rat vascular smooth muscle cell-induced by angiotensin II
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