|
rdf:type |
|
|
lifeskim:mentions |
umls-concept:C0019944,
umls-concept:C0033268,
umls-concept:C0142528,
umls-concept:C0206190,
umls-concept:C0332157,
umls-concept:C0392756,
umls-concept:C0441655,
umls-concept:C1158360,
umls-concept:C1456820,
umls-concept:C1554184,
umls-concept:C1879725,
umls-concept:C1999216
|
|
pubmed:issue |
2
|
|
pubmed:dateCreated |
1992-7-1
|
|
pubmed:abstractText |
The purpose of this study was to determine if a structurally novel dual inhibitor of arachidonic acid metabolism, SK & F 86002, would inhibit the endotoxin-induced production of tumor necrosis factor (TNF) activity by equine peritoneal macrophages. Equine peritoneal macrophages were variously pretreated for 0, 0.5 and 2 h with SK & F 86002 at 10(-9) to 10(-4) molar final concentrations or were left untreated. Then, the macrophages were cultured in vitro in the presence of endotoxin (5 ng/mL). Supernatant media were collected after 4 h and stored at -70 degrees C until assayed for TNF activity and immunoreactive thromboxane B2 (iTxB2). Macrophage supernatant TNF activities were estimated by an in vitro cytotoxicity bioassay using the murine fibrosarcoma cell line, WEHI 164 clone 13. Concentrations of iTxB2 were quantitated by radioimmunoassay. Coincubation of macrophages with SK & F 86002 significantly decreased the subsequent supernatant TNF activity. Concentrations of SK & F 86002 from 10(-7) to 10(-4) molar effectively reduced TNF production when added to macrophages 0 and 0.5 h prior to endotoxin. After 2 h of preincubation, SK & F 86002 significantly reduced supernatant TNF activity at 10(-5) and 10(-4) M concentrations. Supernatant concentrations of iTxB2 were reduced when SK & F 86002 was added at 10(-6) to 10(-4) M concentrations, 0 and 0.5 h prior to endotoxin, and at all concentrations (10(-9) to 10(-4)) when preincubated with macrophages for 2 h.(ABSTRACT TRUNCATED AT 250 WORDS)
|
|
pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/1591653-1767972,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1591653-1778741,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1591653-2085219,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1591653-2108507,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1591653-2178798,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1591653-2178801,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1591653-2182227,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1591653-2492908,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1591653-2499232,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1591653-2559032,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1591653-2565207,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1591653-2678952,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1591653-2823821,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1591653-2835680,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1591653-2880163,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1591653-3108157,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1591653-3121207,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1591653-3142488,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1591653-3148560,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1591653-3289691,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1591653-3543677,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1591653-3555304,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1591653-3576418,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1591653-3782828,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1591653-3828981,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1591653-6479139,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1591653-6606682,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1591653-6690686
|
|
pubmed:language |
eng
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Apr
|
|
pubmed:issn |
0830-9000
|
|
pubmed:author |
|
|
pubmed:issnType |
Print
|
|
pubmed:volume |
56
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
110-4
|
|
pubmed:dateRevised |
2009-11-18
|
|
pubmed:meshHeading |
pubmed-meshheading:1591653-Animals,
pubmed-meshheading:1591653-Anti-Inflammatory Agents, Non-Steroidal,
pubmed-meshheading:1591653-Arachidonic Acids,
pubmed-meshheading:1591653-Cells, Cultured,
pubmed-meshheading:1591653-Female,
pubmed-meshheading:1591653-Horses,
pubmed-meshheading:1591653-Imidazoles,
pubmed-meshheading:1591653-Lipopolysaccharides,
pubmed-meshheading:1591653-Macrophages,
pubmed-meshheading:1591653-Male,
pubmed-meshheading:1591653-Peritoneal Cavity,
pubmed-meshheading:1591653-Thiazoles,
pubmed-meshheading:1591653-Tumor Necrosis Factor-alpha
|
|
pubmed:year |
1992
|
|
pubmed:articleTitle |
Reduced endotoxin-induced production of tumor necrosis factor activity by equine peritoneal macrophages exposed to the dual inhibitor of arachidonic acid metabolism, SK & F 86002.
|
|
pubmed:affiliation |
Department of Large Animal Medicine, College of Veterinary Medicine, University of Georgia, Athens 30602.
|
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|
