Chloroethylclonidine and alpha-adrenoceptor agonist interaction in blood vessels following heart failure.
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[1] C. Forster. Interaction of 5-methyl-urapidil with alpha 1-adrenoceptors in canine blood vessels: impact of pacing-induced heart failure. , 1996, European journal of pharmacology.
[2] E. Daniel,et al. Unusual αadrenoceptor subtype in canine saphenous vein: comparison to mesenteric vein , 1996 .
[3] C. Forster,et al. Coronary β-adrenoceptor function is modified by the endothelium in heart failure , 1996 .
[4] J. Docherty,et al. Investigation of the actions of chloroethylclonidine in rat aorta , 1995, British journal of pharmacology.
[5] R. Lefkowitz,et al. International Union of Pharmacology. X. Recommendation for nomenclature of alpha 1-adrenoceptors: consensus update. , 1995, Pharmacological reviews.
[6] A. M. Low,et al. Interactions of chloroethylclonidine with rauwolscine‐ and prazosin‐sensitive adrenoceptors in dog saphenous vein , 1994, British journal of pharmacology.
[7] A. Ford,et al. α1-Adrenoceptor classification: sharpening Occam's razor , 1994 .
[8] D. Girdlestone,et al. TiPS receptor and ion channel nomenclature supplement 1994 , 1994 .
[9] T. Branchek,et al. Selective irreversible binding of chloroethylclonidine at alpha 1- and alpha 2-adrenoceptor subtypes. , 1993, Molecular pharmacology.
[10] J. Mironneau,et al. Relation between α1‐adrenoceptor subtypes and noradrenaline‐induced contraction in rat portal vein smooth muscle , 1993, British journal of pharmacology.
[11] H. Hartman,et al. Cardiovascular effects of chloroethylclonidine, an irreversible alpha 1B-adrenoceptor antagonist, in the unanesthetized rat: a pharmacological analysis in vivo and in vitro. , 1993, The Journal of pharmacology and experimental therapeutics.
[12] J. Docherty,et al. Investigation of the subtypes of α1‐adrenoceptor mediating contractions of rat aorta, vas deferens and spleen , 1993, British journal of pharmacology.
[13] P. Armstrong,et al. Temporal Alterations in Peripheral Vascular Responsiveness During Both the Development and Recovery from Pacing‐Induced Heart Failure , 1992, Journal of cardiovascular pharmacology.
[14] W. Parmley,et al. Pathophysiology of congestive heart failure. , 1985, Clinical cardiology.
[15] M. Oriowo,et al. Activation of a single alpha-1-adrenoceptor subtype in rat aorta mobilizes intracellular and extracellular pools of calcium. , 1992, Pharmacology.
[16] R. Graham,et al. Solution-phase library screening for the identification of rare clones: isolation of an alpha 1D-adrenergic receptor cDNA. , 1991, Molecular pharmacology.
[17] M. Caron,et al. Molecular biology of α-adrenergic receptors: implications for receptor classification and for structure-function relationships , 1991 .
[18] P. Armstrong,et al. Novel vascular effects of isoprenaline following pacing-induced heart failure in the dog. , 1991, European journal of pharmacology.
[19] M. Piascik,et al. Evidence for a complex interaction between the subtypes of the alpha 1-adrenoceptor. , 1991, European journal of pharmacology.
[20] M. Barras,et al. α‐Adrenoceptor subtypes in dog saphenous vein that mediate contraction and inositol phosphate production , 1991, British journal of pharmacology.
[21] P. Armstrong,et al. Pacing-Induced Heart Failure in the Dog: Evaluation of Peripheral Vascular α-Adrenoceptor Subtypes , 1990, Journal of cardiovascular pharmacology.
[22] M. Caron,et al. Molecular cloning and expression of the cDNA for a novel alpha 1-adrenergic receptor subtype. , 1990, The Journal of biological chemistry.
[23] J. Bevan,et al. Chloroethylclonidine unmasks a non-α-adrenoceptor noradrenaline binding site in the rat aorta , 1990 .
[24] P. Armstrong,et al. Vascular smooth muscle responsiveness to noradrenaline and phenylephrine following experimental heart failure in dogs. , 1989, Cardiovascular research.
[25] P. Armstrong,et al. α1-Adrenoceptor activity in arterial smooth muscle following congestive heart failure , 1989 .
[26] J. Docherty. The pharmacology of α1- and α2-adrenoceptors: Evidence for and against a further subdivision , 1989 .
[27] M. Caron,et al. Molecular cloning and expression of the cDNA for the hamster alpha 1-adrenergic receptor. , 1988, Proceedings of the National Academy of Sciences of the United States of America.
[28] G. Gross,et al. 5-Methyl-urapidil discriminates between subtypes of the α1-adrenoceptor , 1988 .
[29] P. Abel,et al. Heterogeneity of alpha 1-adrenergic receptors revealed by chlorethylclonidine. , 1987, Molecular pharmacology.
[30] P. Abel,et al. α1Adrenoceptor subtypes linked to different mechanisms for increasing intracellular Ca2+ in smooth muscle , 1987, Nature.
[31] P. Armstrong,et al. Rapid ventricular pacing in the dog: pathophysiologic studies of heart failure. , 1986, Circulation.
[32] R. Coleman,et al. Tachycardia-induced cardiomyopathy: a reversible form of left ventricular dysfunction. , 1986, The American journal of cardiology.
[33] I. Creese,et al. Characterization of alpha 1-adrenergic receptor subtypes in rat brain: a reevaluation of [3H]WB4104 and [3H]prazosin binding. , 1986, Molecular pharmacology.
[34] J. T. Herlihy,et al. Effect of preload on rat aortic smooth muscle sensitivity to vasoactive agents. , 1986, Pharmacology.
[35] C. Dollery,et al. Drug treatment of heart failure. , 1985, British heart journal.
[36] R. B. Parker,et al. Pharmacological estimation of drug-receptor dissociation constants. Statistical evaluation. I. Agonists. , 1971, The Journal of pharmacology and experimental therapeutics.