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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
1997-9-19
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pubmed:abstractText |
A large number of eosinophils were recruited to the intestinal villi after infection with Hymenolepis nana. Eosinophil numbers were increased more rapidly in challenged mice than in primary infected mice. Local intestinal eosinophils from challenged mice showed more extracellular oxygen radical release, as assessed by histochemical methods using nitro blue tetrazolium, accompanied with tissue injury and larval degradation. Intestinal eosinophils isolated from the lamina propria induced specific oxygen radical generation in response to H. nana oncosphere extract as measured by luminol-dependent chemiluminescence. This response was stronger in challenged mice than in primary infected mice. Radical generation from uninfected mice was negligible. Lipid peroxidation in the small intestine, as measured by formation of malondialdehyde, was increased during H. nana challenge infection, the peak activity coinciding with the elimination of challenge larvae. Continuous administration of a NADPH oxidase inhibitor to sensitized mice interfered with the degeneration of challenge larvae. These results suggest that intestinal eosinophils may be the major contributor to oxygen radical production in response to H. nana and that reactive oxygen species may play a part of effector molecule in the resistance to reinfection with H. nana.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Acetophenones,
http://linkedlifedata.com/resource/pubmed/chemical/Enzyme Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/Malondialdehyde,
http://linkedlifedata.com/resource/pubmed/chemical/NADPH Oxidase,
http://linkedlifedata.com/resource/pubmed/chemical/Reactive Oxygen Species,
http://linkedlifedata.com/resource/pubmed/chemical/acetovanillone
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0141-9838
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
18
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
285-95
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:9229381-Acetophenones,
pubmed-meshheading:9229381-Animals,
pubmed-meshheading:9229381-Enzyme Inhibitors,
pubmed-meshheading:9229381-Eosinophils,
pubmed-meshheading:9229381-Female,
pubmed-meshheading:9229381-Hymenolepiasis,
pubmed-meshheading:9229381-Hymenolepis,
pubmed-meshheading:9229381-Intestines,
pubmed-meshheading:9229381-Lipid Peroxidation,
pubmed-meshheading:9229381-Luminescent Measurements,
pubmed-meshheading:9229381-Malondialdehyde,
pubmed-meshheading:9229381-Mice,
pubmed-meshheading:9229381-Mice, Inbred BALB C,
pubmed-meshheading:9229381-NADPH Oxidase,
pubmed-meshheading:9229381-Reactive Oxygen Species
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pubmed:year |
1996
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pubmed:articleTitle |
Reactive oxygen intermediates from eosinophils in mice infected with Hymenolepis nana.
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pubmed:affiliation |
Department of Parasitology, Kinki University School of Medicine, Osaka, Japan.
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pubmed:publicationType |
Journal Article,
In Vitro
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