Discrimination by SZL49 between contractions evoked by noradrenaline in longitudinal and circular muscle of human vas deferens
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J. Guillebaud | E. Turner | I. Smith | N. Amobi | A. Kaisary | A V. Kaisary
[1] J. Docherty,et al. Investigation of the subtypes of α1‐adrenoceptor mediating contractions of rat vas deferens , 1999 .
[2] P. H. van der Graaf,et al. Analysis of α1L‐adrenoceptor pharmacology in rat small mesenteric artery , 1999 .
[3] J. Gever,et al. Human cloned α1A-adrenoceptor isoforms display α1L-adrenoceptor pharmacology in functional studies , 1999 .
[4] J. Guillebaud,et al. Functional characterization of alpha1-adrenoceptor subtypes in longitudinal and circular muscle of human vas deferens. , 1999, European journal of pharmacology.
[5] Y. Watanabe,et al. Binding and functional characterization of alpha1-adrenoceptor subtypes in the rat prostate. , 1999, European journal of pharmacology.
[6] N. Flavahan,et al. α1l-adrenoceptors in Canine Pulmonary Artery , 1998 .
[7] A. Ford,et al. α1L‐Adrenoceptor mediation of smooth muscle contraction in rabbit bladder neck: a model for lower urinary tract tissues of man , 1998, British journal of pharmacology.
[8] C. Chapple,et al. α1A‐Adrenoceptor mediated contraction of rat prostatic vas deferens and the involvement of ryanodine stores and Ca2+ influx stimulated by diacylglycerol and PKC , 1998, British journal of pharmacology.
[9] H. Nishimatsu,et al. Quantification and distribution of α1‐adrenoceptor subtype mRNAs in human vas deferens: comparison with those of epididymal and pelvic portions , 1997, British Journal of Pharmacology.
[10] J. Gever,et al. Pharmacological pleiotropism of the human recombinant α1A‐adrenoceptor: implications for α1‐adrenoceptor classification , 1997 .
[11] J. Hieble,et al. Pharmacological characterization of the uroselective alpha-1 antagonist Rec 15/2739 (SB 216469): role of the alpha-1L adrenoceptor in tissue selectivity, part II. , 1997, The Journal of pharmacology and experimental therapeutics.
[12] A. Ford,et al. Pharmacological characterization of an α1A‐adrenoceptor mediating contractile responses to noradrenaline in isolated caudal artery of rat , 1997, British journal of pharmacology.
[13] J. Hieble,et al. Pharmacological characterization of the uroselective alpha-1 antagonist Rec 15/2739 (SB 216469): role of the alpha-1L adrenoceptor in tissue selectivity, part I. , 1997, The Journal of pharmacology and experimental therapeutics.
[14] A. Noble,et al. The effects of SB 216469, an antagonist which discriminates between the α1A‐adrenoceptor and the human prostatic α1‐adrenoceptor , 1996 .
[15] C. Chapple,et al. Different subtypes of α1A‐adrenoceptor mediating contraction of rat epididymal vas deferens, rat hepatic portal vein and human prostate distinguished by the antagonist RS 17053 , 1996, British journal of pharmacology.
[16] A. Naylor,et al. Evaluation of the pharmacological selectivity profile of α1 adrenoceptor antagonists at prostatic α1 adrenoceptors: binding, functional and in vivo studies , 1996 .
[17] S. Meretyk,et al. Functional antagonistic activity of Rec 15/2739, a novel alpha-1 antagonist selective for the lower urinary tract, on noradrenaline-induced contraction of human prostate and mesenteric artery. , 1996, The Journal of pharmacology and experimental therapeutics.
[18] T. Stamey,et al. RS-17053 (N-[2-(2-cyclopropylmethoxyphenoxy)ethyl]-5-chloro-alpha, alpha-dimethyl-1H-indole-3-ethanamine hydrochloride), a selective alpha 1A-adrenoceptor antagonist, displays low affinity for functional alpha 1-adrenoceptors in human prostate: implications for adrenoceptor classification. , 1996, Molecular pharmacology.
[19] R. Chess-Williams,et al. α1A‐Adrenoceptor‐mediated contractile responses of the human vas deferens , 1995, British journal of pharmacology.
[20] I. Muramatsu,et al. Identification of alpha 1-adrenoceptor subtypes in the rabbit prostate. , 1995, Journal of autonomic pharmacology.
[21] I. Marshall,et al. Noradrenaline contractions of human prostate mediated by α1c‐(α1c‐) adrenoceptor subtype , 1995 .
[22] C. Chapple,et al. Evidence for a functional α1A‐ (α1C‐) adrenoceptor mediating contraction of the rat epididymal vas deferens and an α1B‐adrenoceptor mediating contraction of the rat spleen , 1995 .
[23] R. Lefkowitz,et al. International Union of Pharmacology. X. Recommendation for nomenclature of alpha 1-adrenoceptors: consensus update. , 1995, Pharmacological reviews.
[24] A. Ford,et al. Functional evidence equating the pharmacologically‐defined α1A‐ and cloned α1C‐adrenoceptor: studies in the isolated perfused kidney of rat , 1995 .
[25] N. Amobi,et al. The human vas deferens: correlation of response pattern to noradrenaline and histological structure. , 1995, European journal of pharmacology.
[26] C. Chapple,et al. Noradrenaline contractions of human prostate mediated by alpha 1A-(alpha 1c-) adrenoceptor subtype. , 1995, British journal of pharmacology.
[27] H. Akino,et al. Pharmacological characterization of alpha 1-adrenoceptor subtypes in the human prostate: functional and binding studies. , 1994, British journal of urology.
[28] J. Hieble,et al. New directions in adrenoceptor pharmacology. , 1994, Trends in pharmacological sciences.
[29] I. Muramatsu,et al. Heterogeneity of α1‐adrenoceptor subtypes involved in adrenergic contractions of dog blood vessels , 1994, British journal of pharmacology.
[30] A. Ford,et al. α1-Adrenoceptor classification: sharpening Occam's razor , 1994 .
[31] 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.
[32] I. Muramatsu,et al. Pharmacological characterization of two distinct α1‐adrenoceptor subtypes in rabbit thoracic aorta , 1993, British journal of pharmacology.
[33] I. Muramatsu,et al. Identification of α1‐adrenoceptor subtypes in the rat vas deferens: binding and functional studies , 1992 .
[34] J. Sallés,et al. Mechanisms underlying the differential sensitivity to a1‐adrenoceptor activation in the bisected rat vas deferens , 1991, British journal of pharmacology.
[35] I. Muramatsu,et al. Subtypes of alpha 1-adrenoceptors involved in noradrenaline-induced contractions of rat thoracic aorta and dog carotid artery. , 1991, Japanese journal of pharmacology.
[36] M. Piascik,et al. Agonist interaction with alkylation-sensitive and -resistant alpha-1 adrenoceptor subtypes. , 1990, The Journal of pharmacology and experimental therapeutics.
[37] I. Muramatsu,et al. Pharmacological subclassification of α1‐adrenoceptors in vascular smooth muscle , 1990 .
[38] I. Smith,et al. Direct and indirect contractile responses of the human vas deferens and actions of noradrenaline and of calcium antagonists , 1990, Experimental physiology.
[39] M. Martí,et al. Relationship between α-adrenoceptor occupancy and contractile response in rat vas deferens. Experimental and theoretical analysis☆ , 1988 .
[40] J. McGrath,et al. Alpha-adrenoceptor subclassification by classical and response-related methods: same question, different answers. , 1988, Trends in pharmacological sciences.
[41] N. Flavahan,et al. α1-Adrenoceptor subclassification in vascular smooth muscle , 1986 .
[42] K. Andersson,et al. Effect of drugs interacting with adrenoreceptors and muscarinic receptors in the epididymal and prostatic parts of the human isolated vas deferens. , 1985, Journal of autonomic pharmacology.
[43] P. Abel,et al. "Spare" alpha 1-adrenergic receptors and the potency of agonists in rat vas deferens. , 1984, Molecular pharmacology.
[44] P. Abel,et al. Occupancy of alpha 1-adrenergic receptors and contraction of rat vas deferens. , 1983, Molecular pharmacology.
[45] R. Ruffolo. IMPORTANT CONCEPTS OF RECEPTOR THEORY , 1982 .
[46] R. Furchgott,et al. COMPARISON OF DISSOCIATION CONSTANTS AND OF RELATIVE EFFICACIES OF SELECTED AGONISTS ACTING ON PARASYMPATHETIC RECEPTORS * , 1967 .