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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
1994-3-31
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pubmed:abstractText |
1. In a concentration-dependent manner neuropeptide Y was found to be a potent inhibitor of the spontaneous activation of human granulocytes and macrophages as well as Mytilus edulis immunocytes. 2. Neuropeptide Y also inhibited the chemotaxic response of these immunocytes to the chemoattractant f-MLP. 3. Incubation of both the human and the invertebrate immunocytes in f-MLP (10(-9) M) causes "activation" as noted by random locomotion (chemokinesis). Neuropeptide Y also blocked f-MLP-induced chemokinesis. 4. The results suggest that neuropeptide Y may, in addition to other functions, serve as an endogenous regulator of immunocyte function.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Oct
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pubmed:issn |
0272-4340
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
13
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
541-6
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:8111825-Animals,
pubmed-meshheading:8111825-Bivalvia,
pubmed-meshheading:8111825-Chemotaxis,
pubmed-meshheading:8111825-Chemotaxis, Leukocyte,
pubmed-meshheading:8111825-Dose-Response Relationship, Drug,
pubmed-meshheading:8111825-Granulocytes,
pubmed-meshheading:8111825-Lymphocytes,
pubmed-meshheading:8111825-Macrophages,
pubmed-meshheading:8111825-N-Formylmethionine Leucyl-Phenylalanine,
pubmed-meshheading:8111825-Neuropeptide Y
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pubmed:year |
1993
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pubmed:articleTitle |
Neuropeptide Y inhibits human and invertebrate immunocyte chemotaxis, chemokinesis, and spontaneous activation.
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pubmed:affiliation |
Multidisciplinary Center for the Study of Aging, Old Westbury Neuroscience Research Institute, State University of New York/College at Old Westbury 11568.
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pubmed:publicationType |
Journal Article,
In Vitro,
Research Support, U.S. Gov't, P.H.S.,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, Non-U.S. Gov't
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