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Expression and bioactivities of endothelin-1 in gingiva during cyclosporine A treatment.

Identifieur interne : 001E29 ( PubMed/Corpus ); précédent : 001E28; suivant : 001E30

Expression and bioactivities of endothelin-1 in gingiva during cyclosporine A treatment.

Auteurs : Y-T Chin ; H-P Tu ; Y-T Chen ; N-T Dai ; E-C Shen ; C-Y Chiang ; M M-J Fu ; E. Fu

Source :

RBID : pubmed:18973526

English descriptors

Abstract

This study aimed to evaluate the expression and bioactivities of endothelin-1 (ET-1) in gingiva during cyclosporine A (CsA) treatment.

DOI: 10.1111/j.1600-0765.2007.01058.x
PubMed: 18973526

Links to Exploration step

pubmed:18973526

Le document en format XML

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<title xml:lang="en">Expression and bioactivities of endothelin-1 in gingiva during cyclosporine A treatment.</title>
<author>
<name sortKey="Chin, Y T" sort="Chin, Y T" uniqKey="Chin Y" first="Y-T" last="Chin">Y-T Chin</name>
<affiliation>
<nlm:affiliation>Graduate Institute of Life Sciences, National Defense Medical Center, Taipei, Taiwan, ROC.</nlm:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Tu, H P" sort="Tu, H P" uniqKey="Tu H" first="H-P" last="Tu">H-P Tu</name>
</author>
<author>
<name sortKey="Chen, Y T" sort="Chen, Y T" uniqKey="Chen Y" first="Y-T" last="Chen">Y-T Chen</name>
</author>
<author>
<name sortKey="Dai, N T" sort="Dai, N T" uniqKey="Dai N" first="N-T" last="Dai">N-T Dai</name>
</author>
<author>
<name sortKey="Shen, E C" sort="Shen, E C" uniqKey="Shen E" first="E-C" last="Shen">E-C Shen</name>
</author>
<author>
<name sortKey="Chiang, C Y" sort="Chiang, C Y" uniqKey="Chiang C" first="C-Y" last="Chiang">C-Y Chiang</name>
</author>
<author>
<name sortKey="Fu, M M J" sort="Fu, M M J" uniqKey="Fu M" first="M M-J" last="Fu">M M-J Fu</name>
</author>
<author>
<name sortKey="Fu, E" sort="Fu, E" uniqKey="Fu E" first="E" last="Fu">E. Fu</name>
</author>
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<idno type="wicri:source">PubMed</idno>
<date when="2009">2009</date>
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<title xml:lang="en">Expression and bioactivities of endothelin-1 in gingiva during cyclosporine A treatment.</title>
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<name sortKey="Chin, Y T" sort="Chin, Y T" uniqKey="Chin Y" first="Y-T" last="Chin">Y-T Chin</name>
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<nlm:affiliation>Graduate Institute of Life Sciences, National Defense Medical Center, Taipei, Taiwan, ROC.</nlm:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Tu, H P" sort="Tu, H P" uniqKey="Tu H" first="H-P" last="Tu">H-P Tu</name>
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<author>
<name sortKey="Chen, Y T" sort="Chen, Y T" uniqKey="Chen Y" first="Y-T" last="Chen">Y-T Chen</name>
</author>
<author>
<name sortKey="Dai, N T" sort="Dai, N T" uniqKey="Dai N" first="N-T" last="Dai">N-T Dai</name>
</author>
<author>
<name sortKey="Shen, E C" sort="Shen, E C" uniqKey="Shen E" first="E-C" last="Shen">E-C Shen</name>
</author>
<author>
<name sortKey="Chiang, C Y" sort="Chiang, C Y" uniqKey="Chiang C" first="C-Y" last="Chiang">C-Y Chiang</name>
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<author>
<name sortKey="Fu, M M J" sort="Fu, M M J" uniqKey="Fu M" first="M M-J" last="Fu">M M-J Fu</name>
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<name sortKey="Fu, E" sort="Fu, E" uniqKey="Fu E" first="E" last="Fu">E. Fu</name>
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</analytic>
<series>
<title level="j">Journal of periodontal research</title>
<idno type="eISSN">1600-0765</idno>
<imprint>
<date when="2009" type="published">2009</date>
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<keywords scheme="KwdEn" xml:lang="en">
<term>Animals</term>
<term>Cell Proliferation (drug effects)</term>
<term>Cells, Cultured</term>
<term>Cyclosporine (pharmacology)</term>
<term>Endothelin A Receptor Antagonists</term>
<term>Endothelin B Receptor Antagonists</term>
<term>Endothelin-1 (analysis)</term>
<term>Endothelin-1 (metabolism)</term>
<term>Fibroblasts (drug effects)</term>
<term>Fibroblasts (pathology)</term>
<term>Gingiva (drug effects)</term>
<term>Gingiva (pathology)</term>
<term>Humans</term>
<term>Immunosuppressive Agents (pharmacology)</term>
<term>Male</term>
<term>Mouth, Edentulous (pathology)</term>
<term>Nitric Oxide Synthase Type II (analysis)</term>
<term>Proliferating Cell Nuclear Antigen (analysis)</term>
<term>Rats</term>
<term>Receptor, Endothelin A (analysis)</term>
<term>Receptor, Endothelin B (analysis)</term>
<term>Up-Regulation</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="analysis" xml:lang="en">
<term>Endothelin-1</term>
<term>Nitric Oxide Synthase Type II</term>
<term>Proliferating Cell Nuclear Antigen</term>
<term>Receptor, Endothelin A</term>
<term>Receptor, Endothelin B</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en">
<term>Endothelin-1</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en">
<term>Cyclosporine</term>
<term>Immunosuppressive Agents</term>
</keywords>
<keywords scheme="MESH" qualifier="drug effects" xml:lang="en">
<term>Cell Proliferation</term>
<term>Fibroblasts</term>
<term>Gingiva</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en">
<term>Fibroblasts</term>
<term>Gingiva</term>
<term>Mouth, Edentulous</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Animals</term>
<term>Cells, Cultured</term>
<term>Endothelin A Receptor Antagonists</term>
<term>Endothelin B Receptor Antagonists</term>
<term>Humans</term>
<term>Male</term>
<term>Rats</term>
<term>Up-Regulation</term>
</keywords>
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<front>
<div type="abstract" xml:lang="en">This study aimed to evaluate the expression and bioactivities of endothelin-1 (ET-1) in gingiva during cyclosporine A (CsA) treatment.</div>
</front>
</TEI>
<pubmed>
<MedlineCitation Status="MEDLINE" Owner="NLM">
<PMID Version="1">18973526</PMID>
<DateCompleted>
<Year>2009</Year>
<Month>09</Month>
<Day>15</Day>
</DateCompleted>
<DateRevised>
<Year>2014</Year>
<Month>11</Month>
<Day>20</Day>
</DateRevised>
<Article PubModel="Print-Electronic">
<Journal>
<ISSN IssnType="Electronic">1600-0765</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>44</Volume>
<Issue>1</Issue>
<PubDate>
<Year>2009</Year>
<Month>Feb</Month>
</PubDate>
</JournalIssue>
<Title>Journal of periodontal research</Title>
<ISOAbbreviation>J. Periodont. Res.</ISOAbbreviation>
</Journal>
<ArticleTitle>Expression and bioactivities of endothelin-1 in gingiva during cyclosporine A treatment.</ArticleTitle>
<Pagination>
<MedlinePgn>35-42</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1111/j.1600-0765.2007.01058.x</ELocationID>
<Abstract>
<AbstractText Label="BACKGROUND AND OBJECTIVE" NlmCategory="OBJECTIVE">This study aimed to evaluate the expression and bioactivities of endothelin-1 (ET-1) in gingiva during cyclosporine A (CsA) treatment.</AbstractText>
<AbstractText Label="MATERIAL AND METHODS" NlmCategory="METHODS">After establishing edentulous ridges, experimental rats were fed 30 mg/kg/day CsA while control animals received mineral oil for 4 weeks, after which a reverse transcription-polymerase chain reaction (RT-PCR) and/or immunohistochemistry was used to examine the expression of ET-1, its receptors, proliferating cell nuclear antigen (PCNA) and inducible nitric oxide synthase (iNOS) in gingivae. The roles of the endothelin receptors A and B (ET(A) and ET(B)) in CsA-enhanced expression of PCNA and iNOS were examined in cultured human gingival fibroblasts pretreated with receptor antagonists, by immunocytochemistry and RT-PCR, respectively.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">The mRNA expression of ET-1, ET(A) and ET(B), as well as of PCNA and iNOS, was significantly greater in edentulous gingiva that received CsA compared with control gingiva. Immunohistochemistry revealed more cells positively stained for ET-1 and its receptors in the tissues of CsA-treated rats than in those of control rats. In fibroblast cultures, enhanced mRNA expression of ET-1, ET(A) and ET(B) was observed after CsA treatment at the concentrations of 10 and 100 ng/mL. Cyclosporine A-enhanced PCNA expression was somewhat reduced by blockade of ET(A), but not ET(B), whereas iNOS expression was somewhat reduced by blockade of ET(B).</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">Based on the present findings, we suggest that: (1) CsA upregulates the gingival expression of ET-1 and its receptors; and (2) ET(A) and ET(B) have different bioactivities, ET(A) being involved in cell proliferation and ET(B) being associated with iNOS expression.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y">
<Author ValidYN="Y">
<LastName>Chin</LastName>
<ForeName>Y-T</ForeName>
<Initials>YT</Initials>
<AffiliationInfo>
<Affiliation>Graduate Institute of Life Sciences, National Defense Medical Center, Taipei, Taiwan, ROC.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Tu</LastName>
<ForeName>H-P</ForeName>
<Initials>HP</Initials>
</Author>
<Author ValidYN="Y">
<LastName>Chen</LastName>
<ForeName>Y-T</ForeName>
<Initials>YT</Initials>
</Author>
<Author ValidYN="Y">
<LastName>Dai</LastName>
<ForeName>N-T</ForeName>
<Initials>NT</Initials>
</Author>
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<LastName>Shen</LastName>
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<Initials>CY</Initials>
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<LastName>Fu</LastName>
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</Author>
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<Language>eng</Language>
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<PublicationType UI="D003160">Comparative Study</PublicationType>
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<PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType>
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<Year>2008</Year>
<Month>10</Month>
<Day>07</Day>
</ArticleDate>
</Article>
<MedlineJournalInfo>
<Country>United States</Country>
<MedlineTA>J Periodontal Res</MedlineTA>
<NlmUniqueID>0055107</NlmUniqueID>
<ISSNLinking>0022-3484</ISSNLinking>
</MedlineJournalInfo>
<ChemicalList>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D065130">Endothelin A Receptor Antagonists</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D065131">Endothelin B Receptor Antagonists</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D019332">Endothelin-1</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D007166">Immunosuppressive Agents</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D018809">Proliferating Cell Nuclear Antigen</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D044022">Receptor, Endothelin A</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D044023">Receptor, Endothelin B</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>83HN0GTJ6D</RegistryNumber>
<NameOfSubstance UI="D016572">Cyclosporine</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>EC 1.14.13.39</RegistryNumber>
<NameOfSubstance UI="C496319">NOS2 protein, human</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>EC 1.14.13.39</RegistryNumber>
<NameOfSubstance UI="D052247">Nitric Oxide Synthase Type II</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>EC 1.14.13.39</RegistryNumber>
<NameOfSubstance UI="C496318">Nos2 protein, rat</NameOfSubstance>
</Chemical>
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<CitationSubset>D</CitationSubset>
<CitationSubset>IM</CitationSubset>
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<DescriptorName UI="D000818" MajorTopicYN="N">Animals</DescriptorName>
</MeshHeading>
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<DescriptorName UI="D049109" MajorTopicYN="N">Cell Proliferation</DescriptorName>
<QualifierName UI="Q000187" MajorTopicYN="N">drug effects</QualifierName>
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<MeshHeading>
<DescriptorName UI="D002478" MajorTopicYN="N">Cells, Cultured</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D016572" MajorTopicYN="N">Cyclosporine</DescriptorName>
<QualifierName UI="Q000494" MajorTopicYN="Y">pharmacology</QualifierName>
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<DescriptorName UI="D065130" MajorTopicYN="N">Endothelin A Receptor Antagonists</DescriptorName>
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<DescriptorName UI="D005347" MajorTopicYN="N">Fibroblasts</DescriptorName>
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<MeshHeading>
<DescriptorName UI="D005881" MajorTopicYN="N">Gingiva</DescriptorName>
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</MeshHeading>
<MeshHeading>
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<QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName>
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