Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
|
pubmed:dateCreated |
1988-12-30
|
pubmed:abstractText |
The IgE-mediated hypersensitivity to Ascaris antigen in reactor rhesus primates was used to assess the pharmacologic profile of U-66,858 (1-acetoxy-2-n-butyl-4-methoxy-naphthalene). When the compound was given by the oral route, it showed dose-related inhibition of resistance (RL) and compliance (Cdyn) changes. When the compound was given by the aerosol route, it showed dose independent inhibition. In 15 animals, aerosols (52 +/- 32 to 53 +/- 10% for RL, p = 0.05 and 45 +/- 19 to 28 +/- 19% Cdyn inhibitions, p = 0.05) for 5.0-0.1% aerosol. By the oral route, inhibition was seen at 1-4 h following administration. In 5 animals, oral doses of 10 and 5 mg/kg inhibited (RL by 98 +/- 2 to 78 +/- 1.5%, p = 0.01 and Cdyn by 75 +/- 17 to 60.9 +/- 9.1%, p = 0.05) by 10 and 5 mg/kg U-66,858, respectively. The in vivo demonstration of inhibition of pulmonary bronchoconstriction by this compound, in a model known to be leukotriene sensitive, coupled with its potent in vitro inhibition of 5-lipoxygenase enzymes, suggests this compound may be of use in 5-lypoxygenase-mediated models of asthma.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Aerosols,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Helminth,
http://linkedlifedata.com/resource/pubmed/chemical/Arachidonate Lipoxygenases,
http://linkedlifedata.com/resource/pubmed/chemical/Hydroquinones,
http://linkedlifedata.com/resource/pubmed/chemical/Lipoxygenase Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/Naphthols
|
pubmed:status |
MEDLINE
|
pubmed:issn |
0020-5915
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
87
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
204-7
|
pubmed:dateRevised |
2010-11-18
|
pubmed:meshHeading |
pubmed-meshheading:3192307-Administration, Inhalation,
pubmed-meshheading:3192307-Administration, Oral,
pubmed-meshheading:3192307-Aerosols,
pubmed-meshheading:3192307-Animals,
pubmed-meshheading:3192307-Antigens, Helminth,
pubmed-meshheading:3192307-Arachidonate Lipoxygenases,
pubmed-meshheading:3192307-Ascaris,
pubmed-meshheading:3192307-Bronchial Spasm,
pubmed-meshheading:3192307-Disease Models, Animal,
pubmed-meshheading:3192307-Dose-Response Relationship, Immunologic,
pubmed-meshheading:3192307-Female,
pubmed-meshheading:3192307-Hydroquinones,
pubmed-meshheading:3192307-Intubation, Intratracheal,
pubmed-meshheading:3192307-Lipoxygenase Inhibitors,
pubmed-meshheading:3192307-Macaca mulatta,
pubmed-meshheading:3192307-Male,
pubmed-meshheading:3192307-Naphthols
|
pubmed:year |
1988
|
pubmed:articleTitle |
Activity of a novel hydroquinone inhibitor of leukotriene synthesis (U-66,858) in the rhesus monkey Ascaris reactor.
|
pubmed:affiliation |
Hypersensitivity Diseases Research, Upjohn Company, Kalamazoo, Mich.
|
pubmed:publicationType |
Journal Article
|