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Invest Ophthalmol Vis Sci ; 24(8): 1079-85, 1983 Aug.
Article in English | MEDLINE | ID: mdl-6135672

ABSTRACT

The ability of rabbit conjunctiva and anterior uvea to synthesize lipoxygenase products was assessed. Using autoradiographic techniques, we demonstrate that rabbit anterior uvea synthesizes 5 and 12 lipoxygenase products such as 12-HETE, 5-HETE and 5,12-DiHETE and cyclooxygenase product HHT from 14C-arachidonic acid. Indomethacin pretreated conjunctiva and anterior uvea generated slow reacting substance (SRS)-like activity from arachidonic acid in the presence of reduced glutathione and A23187. This SRS-like activity contracted guinea pig ileum. Specific SRS-like activity antagonist FPL-55712 inhibited the contractions of guinea pig ileum induced by SRS-like substance generated by either conjunctiva or anterior uvea. The activity was still present in the sample following extraction with organic solvents. SRS-like activity was destroyed by arylsulfatase and its generation was prevented by either boiling or pretreatment with cyclooxygenase/lipoxygenase inhibitors, BW755 and nordihydroguaiacetic acid. These results indicate that following cyclooxygenase inhibition by indomethacin rabbit conjunctiva and anterior uvea generate SRS-like activity from arachidonic acid via lipoxygenase pathways.


Subject(s)
Autacoids/biosynthesis , Conjunctiva/metabolism , Uvea/metabolism , 4,5-Dihydro-1-(3-(trifluoromethyl)phenyl)-1H-pyrazol-3-amine , Animals , Arachidonic Acids/metabolism , Autacoids/antagonists & inhibitors , Catechols/pharmacology , Chromones/pharmacology , Conjunctiva/analysis , Enzyme Activation , Guinea Pigs , Ileum/drug effects , Lipoxygenase/metabolism , Lipoxygenase Inhibitors , Masoprocol , Muscle Contraction/drug effects , Pyrazoles/pharmacology , Rabbits , Tissue Extracts/pharmacology
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