Differential vasodilator properties of KRN2391, cromakalim, nitroglycerin and nifedipine in rabbit isolated femoral artery and vein
Author:
Publisher
Wiley
Subject
Pharmacology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1476-5381.1994.tb14056.x/fullpdf
Reference26 articles.
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2. Vasorelaxant effects of cromakalim in rats mediated in glibenclamide-sensitive potassium channels;CAVERO;J. Pharmacol. Exp. Ther.,1989
3. Specificity of action of the novel antihypertensive agent, BRL34915, as a potassium channel activator: comparison with nicorandil;COLDWELL;Biochem. Pharmacol.,1987
4. The pharmacology of potassium channels and their therapeutic potential;COOK;Trends Pharmacol. Sci.,1988
5. Glibenclamide is a competitive antagonist of cromakalim, pinacidil, and RP49356 in guinea-pig pulmonary artery;ELTZE;Eur. J. Pharmacol.,1989
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1. Relaxation of human placental arteries and veins by ATP-sensitive potassium channel openers;European Journal of Clinical Investigation;2007-01
2. Krn2391: Dual Action On Rat Pulmonary Artery And No Loss Of Potency In Pulmonary Hypertension;Clinical and Experimental Pharmacology and Physiology;2000-04-10
3. Haemodynamic effects of hypotension induced by KRN2391 and nicardipine in isoflurane anaesthetized dogs;Canadian Journal of Anaesthesia;1997-09
4. Possible evaluation of hemodynamic effects of the potassium channel opener KRN2391 on induced hypotension in dogs;Journal of Anesthesia;1997-06
5. Inhibition of contractile responses of human myometrium and intramyometrial arteries by potassium channel openers;Acta Obstetricia et Gynecologica Scandinavica;1996-01
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