The role of macrophages on the expression of sex difference in the susceptibility to Brugia pahangi infection in C57BL/6 mice.
Identifieur interne : 005F39 ( PubMed/Corpus ); précédent : 005F38; suivant : 005F40The role of macrophages on the expression of sex difference in the susceptibility to Brugia pahangi infection in C57BL/6 mice.
Auteurs : H. Nakanishi ; Y. Horii ; K. FujitaSource :
- Journal of helminthology [ 0022-149X ] ; 1989.
English descriptors
- KwdEn :
- Animals, Brugia (immunology), Brugia (isolation & purification), Carbon (pharmacology), Cell Count, Disease Susceptibility, Elephantiasis, Filarial (immunology), Eosinophils (drug effects), Eosinophils (immunology), Female, Filariasis (immunology), Macrophages (drug effects), Macrophages (immunology), Male, Mice, Mice, Inbred C57BL, Promethazine (pharmacology), Sex Factors.
- MESH :
- chemical , pharmacology : Carbon, Promethazine.
- drug effects : Eosinophils, Macrophages.
- immunology : Brugia, Elephantiasis, Filarial, Eosinophils, Filariasis, Macrophages.
- isolation & purification : Brugia.
- Animals, Cell Count, Disease Susceptibility, Female, Male, Mice, Mice, Inbred C57BL, Sex Factors.
Abstract
The role of macrophages or eosinophils on the expression of sex difference in the susceptibility to a primary Brugia pahangi infection in C57BL/6 mice was investigated by using a macrophage blockade technique (carbon treatment) or a histamine type 1 (H1) receptor antagonist (promethazine). Carbon treatment remarkably inhibited macrophage exudation, reduced the resistance of female mice, and completely abolished sex difference in the susceptibility to B. pahangi infection. Although promethazine treatment inhibited eosinophil exudation, it caused only a little increase (not significant) in the recovery rate of worms. These results suggest that macrophages have more important role(s) than do eosinophils on the expression of sex difference in the susceptibility to a primary B. pahangi infection in C57BL/6 mice.
PubMed: 2794454
Links to Exploration step
pubmed:2794454Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">The role of macrophages on the expression of sex difference in the susceptibility to Brugia pahangi infection in C57BL/6 mice.</title>
<author><name sortKey="Nakanishi, H" sort="Nakanishi, H" uniqKey="Nakanishi H" first="H" last="Nakanishi">H. Nakanishi</name>
<affiliation><nlm:affiliation>Department of Medical Zoology, Nagasaki University School of Medicine, Japan.</nlm:affiliation>
</affiliation>
</author>
<author><name sortKey="Horii, Y" sort="Horii, Y" uniqKey="Horii Y" first="Y" last="Horii">Y. Horii</name>
</author>
<author><name sortKey="Fujita, K" sort="Fujita, K" uniqKey="Fujita K" first="K" last="Fujita">K. Fujita</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">The role of macrophages on the expression of sex difference in the susceptibility to Brugia pahangi infection in C57BL/6 mice.</title>
<author><name sortKey="Nakanishi, H" sort="Nakanishi, H" uniqKey="Nakanishi H" first="H" last="Nakanishi">H. Nakanishi</name>
<affiliation><nlm:affiliation>Department of Medical Zoology, Nagasaki University School of Medicine, Japan.</nlm:affiliation>
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<author><name sortKey="Horii, Y" sort="Horii, Y" uniqKey="Horii Y" first="Y" last="Horii">Y. Horii</name>
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<author><name sortKey="Fujita, K" sort="Fujita, K" uniqKey="Fujita K" first="K" last="Fujita">K. Fujita</name>
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<series><title level="j">Journal of helminthology</title>
<idno type="ISSN">0022-149X</idno>
<imprint><date when="1989" type="published">1989</date>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Animals</term>
<term>Brugia (immunology)</term>
<term>Brugia (isolation & purification)</term>
<term>Carbon (pharmacology)</term>
<term>Cell Count</term>
<term>Disease Susceptibility</term>
<term>Elephantiasis, Filarial (immunology)</term>
<term>Eosinophils (drug effects)</term>
<term>Eosinophils (immunology)</term>
<term>Female</term>
<term>Filariasis (immunology)</term>
<term>Macrophages (drug effects)</term>
<term>Macrophages (immunology)</term>
<term>Male</term>
<term>Mice</term>
<term>Mice, Inbred C57BL</term>
<term>Promethazine (pharmacology)</term>
<term>Sex Factors</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en"><term>Carbon</term>
<term>Promethazine</term>
</keywords>
<keywords scheme="MESH" qualifier="drug effects" xml:lang="en"><term>Eosinophils</term>
<term>Macrophages</term>
</keywords>
<keywords scheme="MESH" qualifier="immunology" xml:lang="en"><term>Brugia</term>
<term>Elephantiasis, Filarial</term>
<term>Eosinophils</term>
<term>Filariasis</term>
<term>Macrophages</term>
</keywords>
<keywords scheme="MESH" qualifier="isolation & purification" xml:lang="en"><term>Brugia</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Animals</term>
<term>Cell Count</term>
<term>Disease Susceptibility</term>
<term>Female</term>
<term>Male</term>
<term>Mice</term>
<term>Mice, Inbred C57BL</term>
<term>Sex Factors</term>
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<front><div type="abstract" xml:lang="en">The role of macrophages or eosinophils on the expression of sex difference in the susceptibility to a primary Brugia pahangi infection in C57BL/6 mice was investigated by using a macrophage blockade technique (carbon treatment) or a histamine type 1 (H1) receptor antagonist (promethazine). Carbon treatment remarkably inhibited macrophage exudation, reduced the resistance of female mice, and completely abolished sex difference in the susceptibility to B. pahangi infection. Although promethazine treatment inhibited eosinophil exudation, it caused only a little increase (not significant) in the recovery rate of worms. These results suggest that macrophages have more important role(s) than do eosinophils on the expression of sex difference in the susceptibility to a primary B. pahangi infection in C57BL/6 mice.</div>
</front>
</TEI>
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<DateCreated><Year>1989</Year>
<Month>11</Month>
<Day>22</Day>
</DateCreated>
<DateCompleted><Year>1989</Year>
<Month>11</Month>
<Day>22</Day>
</DateCompleted>
<DateRevised><Year>2013</Year>
<Month>11</Month>
<Day>21</Day>
</DateRevised>
<Article PubModel="Print"><Journal><ISSN IssnType="Print">0022-149X</ISSN>
<JournalIssue CitedMedium="Print"><Volume>63</Volume>
<Issue>3</Issue>
<PubDate><Year>1989</Year>
<Month>Sep</Month>
</PubDate>
</JournalIssue>
<Title>Journal of helminthology</Title>
<ISOAbbreviation>J. Helminthol.</ISOAbbreviation>
</Journal>
<ArticleTitle>The role of macrophages on the expression of sex difference in the susceptibility to Brugia pahangi infection in C57BL/6 mice.</ArticleTitle>
<Pagination><MedlinePgn>213-7</MedlinePgn>
</Pagination>
<Abstract><AbstractText>The role of macrophages or eosinophils on the expression of sex difference in the susceptibility to a primary Brugia pahangi infection in C57BL/6 mice was investigated by using a macrophage blockade technique (carbon treatment) or a histamine type 1 (H1) receptor antagonist (promethazine). Carbon treatment remarkably inhibited macrophage exudation, reduced the resistance of female mice, and completely abolished sex difference in the susceptibility to B. pahangi infection. Although promethazine treatment inhibited eosinophil exudation, it caused only a little increase (not significant) in the recovery rate of worms. These results suggest that macrophages have more important role(s) than do eosinophils on the expression of sex difference in the susceptibility to a primary B. pahangi infection in C57BL/6 mice.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Nakanishi</LastName>
<ForeName>H</ForeName>
<Initials>H</Initials>
<AffiliationInfo><Affiliation>Department of Medical Zoology, Nagasaki University School of Medicine, Japan.</Affiliation>
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<Author ValidYN="Y"><LastName>Horii</LastName>
<ForeName>Y</ForeName>
<Initials>Y</Initials>
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<Author ValidYN="Y"><LastName>Fujita</LastName>
<ForeName>K</ForeName>
<Initials>K</Initials>
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<Language>eng</Language>
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<MedlineJournalInfo><Country>England</Country>
<MedlineTA>J Helminthol</MedlineTA>
<NlmUniqueID>2985115R</NlmUniqueID>
<ISSNLinking>0022-149X</ISSNLinking>
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<ChemicalList><Chemical><RegistryNumber>7440-44-0</RegistryNumber>
<NameOfSubstance UI="D002244">Carbon</NameOfSubstance>
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<Chemical><RegistryNumber>FF28EJQ494</RegistryNumber>
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<MeshHeadingList><MeshHeading><DescriptorName UI="D000818" MajorTopicYN="N">Animals</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D002009" MajorTopicYN="N">Brugia</DescriptorName>
<QualifierName UI="Q000276" MajorTopicYN="N">immunology</QualifierName>
<QualifierName UI="Q000302" MajorTopicYN="N">isolation & purification</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D002244" MajorTopicYN="N">Carbon</DescriptorName>
<QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D002452" MajorTopicYN="N">Cell Count</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D004198" MajorTopicYN="N">Disease Susceptibility</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D004605" MajorTopicYN="N">Elephantiasis, Filarial</DescriptorName>
<QualifierName UI="Q000276" MajorTopicYN="Y">immunology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D004804" MajorTopicYN="N">Eosinophils</DescriptorName>
<QualifierName UI="Q000187" MajorTopicYN="N">drug effects</QualifierName>
<QualifierName UI="Q000276" MajorTopicYN="N">immunology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D005368" MajorTopicYN="N">Filariasis</DescriptorName>
<QualifierName UI="Q000276" MajorTopicYN="Y">immunology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008264" MajorTopicYN="N">Macrophages</DescriptorName>
<QualifierName UI="Q000187" MajorTopicYN="N">drug effects</QualifierName>
<QualifierName UI="Q000276" MajorTopicYN="Y">immunology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D051379" MajorTopicYN="N">Mice</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008810" MajorTopicYN="N">Mice, Inbred C57BL</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D011398" MajorTopicYN="N">Promethazine</DescriptorName>
<QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D012737" MajorTopicYN="N">Sex Factors</DescriptorName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>1989</Year>
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