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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1990-6-14
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pubmed:abstractText |
Natural killer cell activity was compared in the Long-Sleep and Short-Sleep mouse lines. These mice, initially selected for their sensitivities to a hypnotic dose of ethanol, are also differentially sensitive to other agents which act through the benzodiazepine/GABA receptor chloride ionophore complex. Natural killer cell activity was 40-59% lower in Short-Sleep when compared to Long-Sleep mice. Flow cytofluorometric analysis demonstrated that the number of Nk-1+ cells was also lower in the spleens of Short-Sleep than Long-Sleep mice. In addition, the incidence of 3-methylcholanthrene-induced tumors was significantly greater in Short-Sleep (85.7%) than in Long-Sleep (14.3%) mice. These results suggest that the Long-Sleep and Short-Sleep mouse lines may represent a unique model to assess the physiological role of the benzodiazepine/GABA receptor chloride ionophore complex in the neural modulation of immune function.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0889-1591
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
4
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
39-49
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:2334815-Animals,
pubmed-meshheading:2334815-Cell Count,
pubmed-meshheading:2334815-Ethanol,
pubmed-meshheading:2334815-Flow Cytometry,
pubmed-meshheading:2334815-Immune System,
pubmed-meshheading:2334815-Killer Cells, Natural,
pubmed-meshheading:2334815-Methylcholanthrene,
pubmed-meshheading:2334815-Mice,
pubmed-meshheading:2334815-Mice, Inbred C3H,
pubmed-meshheading:2334815-Neoplasms, Experimental,
pubmed-meshheading:2334815-Sleep,
pubmed-meshheading:2334815-Spleen
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pubmed:year |
1990
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pubmed:articleTitle |
Differential immune responsiveness in mouse lines selectively bred for high and low sensitivity to ethanol.
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pubmed:affiliation |
Laboratory of Neuroscience, National Institute of Diabetes, Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.
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