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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1999-2-5
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pubmed:abstractText |
The in vitro actions were investigated of LY293111, a potent and selective leukotriene B4 (LTB4) receptor antagonist, on human neutrophils, human blood fractions, guinea pig lung membranes, and guinea pig parenchymal and tracheal strips. The IC50 for inhibiting [3H]LTB4 binding to human neutrophils was 17.6 +/- 4.8 nM. LY293111 inhibited LTB4-induced human neutrophil aggregation (IC50 = 32 +/- 5 nM), luminol-dependent chemiluminescence (IC50 = 20 +/- 2 nM), chemotaxis (IC50 = 6.3 +/- 1.7 nM), and superoxide production by adherent cells (IC50 = 0.5 nM). Corresponding responses induced by N-formyl-L-methionyl-L-leucyl-L-phenylalanine were inhibited by 100-fold higher concentrations of LY293111. LTB4 binding to guinea pig tissues and subsequent activation were also inhibited. The Ki for inhibition of [3H]LTB4 binding to lung membranes was 7.1 +/- 0.8 nM; IC50 for preventing binding of [3H]LTB4 to spleen membranes was 65 nM. The compound inhibited LTB4-induced contraction of guinea pig lung parenchyma. At 10 nM, LY293111 caused a parallel rightward shift of the LTB4 concentration-response curve. At higher concentrations, plots were shifted in a nonparallel manner, and maximum responses were depressed. LY293111 did not prevent antigen-stimulated contraction of sensitized trachea strips. At micromolar concentrations, LY293111 inhibited production of LTB4 and thromboxane B2 by plasma-depleted human blood stimulated with N-formyl-L-methionyl-L-leucyl-L-phenylalanine and thrombin. In addition, at these higher concentrations, formation of LTB4 by A23187-activated whole blood and conversion of arachidonic acid to LTB4 by a human neutrophil cytosolic fraction were inhibited. In summary, LY293111 is a second-generation LTB4 receptor antagonist with much improved potency in a variety of functional assay systems.
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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/Benzoic Acids,
http://linkedlifedata.com/resource/pubmed/chemical/Eicosanoids,
http://linkedlifedata.com/resource/pubmed/chemical/LY 293111,
http://linkedlifedata.com/resource/pubmed/chemical/Leukotriene Antagonists,
http://linkedlifedata.com/resource/pubmed/chemical/Leukotriene B4,
http://linkedlifedata.com/resource/pubmed/chemical/Oxidants,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Leukotriene B4
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
0022-3565
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pubmed:author |
pubmed-author:BoydR JRJ,
pubmed-author:FleischJ HJH,
pubmed-author:FroelichL LLL,
pubmed-author:GoodsonTTJr,
pubmed-author:HerronD KDK,
pubmed-author:JacksonW TWT,
pubmed-author:PechousP APA,
pubmed-author:RomanC RCR,
pubmed-author:SaussyD LDLJr,
pubmed-author:SawyerJ SJS,
pubmed-author:SchrementiJ PJP,
pubmed-author:SchultzR MRM,
pubmed-author:SnyderD WDW,
pubmed-author:SofiaM JMJ,
pubmed-author:SpaetheS MSM
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pubmed:issnType |
Print
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pubmed:volume |
288
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
286-94
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:9862783-Animals,
pubmed-meshheading:9862783-Benzoic Acids,
pubmed-meshheading:9862783-Binding, Competitive,
pubmed-meshheading:9862783-Cell Aggregation,
pubmed-meshheading:9862783-Cell Membrane,
pubmed-meshheading:9862783-Chemotaxis, Leukocyte,
pubmed-meshheading:9862783-Eicosanoids,
pubmed-meshheading:9862783-Guinea Pigs,
pubmed-meshheading:9862783-Humans,
pubmed-meshheading:9862783-Leukotriene Antagonists,
pubmed-meshheading:9862783-Leukotriene B4,
pubmed-meshheading:9862783-Lung,
pubmed-meshheading:9862783-Male,
pubmed-meshheading:9862783-Neutrophils,
pubmed-meshheading:9862783-Oxidants,
pubmed-meshheading:9862783-Receptors, Leukotriene B4,
pubmed-meshheading:9862783-Spleen,
pubmed-meshheading:9862783-Trachea
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pubmed:year |
1999
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pubmed:articleTitle |
Pharmacologic actions of the second-generation leukotriene B4 receptor antagonist LY293111: in vitro studies.
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pubmed:affiliation |
Lilly Research Laboratories, Lilly Corporate Center, Indianapolis, Indiana, USA.
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pubmed:publicationType |
Journal Article
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