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Prostaglandins, leukotrienes, and medicine.

Discontinued
Periodical
Endocrinology
Arachidonic Acids
Fatty Acids
Unsaturated
Medicine
Prostaglandins
Publisher:
Churchill Livingstone,. Edinburgh : Churchill Livingstone
Frequency: Monthly
Country: Scotland
Language: English
Start Year:1982 - 1987
Identifiers
ISSN:0262-1746 (Print)
0262-1746 (Linking)
NLM ID:8206868
(DNLM):P50270000(s)
(OCoLC):08241724
Coden:PLMEDD
Classification:W1 PR77TM
Effects of multiple low doses of flunixin meglumine on repeated endotoxin challenge in the horse.
Prostaglandins, leukotrienes, and medicine    May 1, 1987   Volume 27, Issue 2-3 169-181 doi: 10.1016/0262-1746(87)90069-2
Semrad SD, Moore JN.Previous work has shown repeated low doses of flunixin meglumine (FM) inhibit thromboxane production in normal horses. Enhanced concentrations of thromboxane in serum occurred after the drug therapy was discontinued. Our study was performed to evaluate the effects of low doses of FM in horses repeatedly challenged with endotoxin. Group I horses received E. coli endotoxin (0.1 microgram/kg IV) at 0 and 90 h. Group II horses received endotoxin and were also treated with FM (0.25 mg/kg IV) at 2, 10, 18, 26, 34, and 42 h after the initial administration of endotoxin. Clinical signs of endotoxemia ...
Enhanced prostacyclin biosynthesis and decreased thromboxane formation by 3-dimethylamino 5-(2′,6′-dichlorobenzylidene) 6-methyl (4H)-pyridazine (PC 89).
Prostaglandins, leukotrienes, and medicine    July 1, 1985   Volume 19, Issue 1 37-49 doi: 10.1016/0262-1746(85)90159-3
Pham HC, Lasserre B, Tronche P, Couquelet J, Dossou-Gbete V, Palhares de Miranda AL.The effects of 3-dimethylamino 5-(2',6'-dichlorobenzylidene) 6-methyl (4H)-pyridazine (PC 89) on the biosynthesis of PG I2 and TX A2 using horse aorta and horse platelet microsomes as sources of enzymes and arachidonic acid as substrate, were investigated. PC 89 (1.10(-6) M- 1.10(-3) M) dose-dependently - enhanced the biosynthesis of PG I2: the AD50 was 6.8 X 10(-6) M +/- 1.2 X 10(-9) M, the Vmax did not vary significantly with concentrations: PC 89 increased the affinity of enzyme for substrate - but inhibited TX A2 biosynthesis (ID50 = 3.31 X 10(-3) M +/- 4.8 X 10(-7) M): this inhibiting act...
Characteristics of receptors for prostaglandin F-2 alpha in bovine and equine corpora lutea.
Prostaglandins, leukotrienes, and medicine    July 1, 1983   Volume 11, Issue 3 259-268 doi: 10.1016/0262-1746(83)90039-2
Mattioli M, Galeati G, Seren E.Prostaglandin F-2 alpha (PGF-2 alpha) receptors of bovine and equine corpora lutea (C.L.) were studied. From both the equilibrium binding data and the dissociation kinetics behaviour, two affinity classes of receptors are evident in the mare, with apparent dissociation constants (Kd) of 1,5 x 10(-9) M and 3.5 x 10(-8) M. Bovine PGF-2 alpha receptors present a homogeneous population of binding sites with Kd = 1 x 10(-8) M. Both bovine and equine C.L. receptors bind PGF-2 alpha in a specific manner; only 13, 14-dihydro-PGF-2 alpha considerably cross-reacts with these receptors. Since in the mare...
The effects of dipyridamole on TXA2 formation by horse platelet microsomes.
Prostaglandins, leukotrienes, and medicine    February 1, 1983   Volume 10, Issue 2 179-185 doi: 10.1016/s0262-1746(83)80008-0
Katano Y, Imai S.The effects of dipyridamole on thromboxane A2 formation by horse platelet microsomes were studied in comparison with those of imidazole, a prototype inhibitor of TXA2 synthetase and nifedipine, a calcium antagonistic vasodilator. Thromboxane A2 was synthesized by incubating PGH2 with horse platelet microsomes and was assayed on the superfused rabbit aorta. Dipyridamole induced as strong an inhibition of TXA2 synthesis as imidazole, while nifedipine was without effects. The possible beneficial clinical outcomes of this effect of dipyridamole are discussed.