dinoprost has been researched along with vitexin-rhamnoside* in 1 studies
1 other study(ies) available for dinoprost and vitexin-rhamnoside
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Functional and antiischaemic effects of Monoacetyl-vitexinrhamnoside in different in vitro models.
1. Functional and antiischaemic effects of monoacetyl-vitexinrhamnoside (AVR), a flavonoid with phosphodiesterase (PDE)-inhibitory properties contained in Crataegus species (Hawthorn, Rosaceae) were studied in several in-vitro models. 2. In rabbit isolated femoral artery rings, AVR concentration-dependently reduced developed tension. Vasodilation by AVR was reduced after inhibiting EDRF formation by L-NG-nitro arginine. 3. In spontaneously-beating Langendorff-guinea pig hearts, AVR concentration-dependently enhanced heart-rate, contractility, lusitropy and coronary flow. 4. In isolated electrically-driven Langendorff-rabbit hearts, acute regional ischemia (MI) was induced by coronary artery occlusion and quantified from epicardial NADH-fluorescence photography. AVR (5 x 10(-5) mol/l) induced a slight numerical increase of left ventricular pressure and coronary flow (p > 0.05). MI was reduced (p < 0.05). 5. Monoacetyl-vitexinrhamnoside is an inodilator whose vasodilatory action may be mediated in part by EDRF in addition to PDE-inhibition. Monoacetyl-vitexinrhamnoside does possess marked antiischemic properties even in isolated hearts, suggesting an improvement of myocardial perfusion. Topics: Abortifacient Agents; Animals; Apigenin; Dinoprost; Femoral Artery; Flavonoids; Guinea Pigs; Heart; In Vitro Techniques; Male; Myocardial Ischemia; Plant Extracts; Rabbits; Substance P; Vasoconstriction | 1995 |