Selective agonists reveal α1A‐ and α1B‐adrenoceptor subtypes in caudal artery of the young rat
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R. Villalobos-Molina | J. Parés-Hipólito | I. Gallardo-Ortíz | M. Ibarra | J. López-Guerrero | J. Gómez-Zamudio | J. Santamaría-Ortiz
[1] A. Pupo,et al. Differential Distribution of Functional α1-Adrenergic Receptor Subtypes along the Rat Tail Artery , 2005, Journal of Pharmacology and Experimental Therapeutics.
[2] D. Barettino,et al. Correlation between mRNA levels and functional role of α1-adrenoceptor subtypes in arteries: evidence of α1L as a functional isoform of the α1A-adrenoceptor , 2005 .
[3] James A. Slattery,et al. Sympathectomy reveals α1A‐ and α1D‐adrenoceptor components to contractions to noradrenaline in rat vas deferens , 2004 .
[4] M. Kunitomo,et al. Alpha‐1D adrenoceptors are involved in reserpine‐induced supersensitivity of rat tail artery , 2004, British journal of pharmacology.
[5] H. Pertz,et al. Evidence that α1B-adrenoceptors are involved in noradrenaline-induced contractions of rat tail artery , 2004 .
[6] R. Villalobos-Molina,et al. Evidence for the role of α1D- and α1A-adrenoceptors in contraction of the rat mesenteric artery , 2003 .
[7] M. Noguera,et al. Functional evidence of a constitutively active population of alpha(1D)-adrenoceptors in rat aorta. , 2000, The Journal of pharmacology and experimental therapeutics.
[8] J. Pediani,et al. Quantitative imaging in live human cells reveals intracellular alpha(1)-adrenoceptor ligand-binding sites. , 2000, The Journal of pharmacology and experimental therapeutics.
[9] R. Villalobos-Molina,et al. Differential response to chloroethylclonidine in blood vessels of normotensive and spontaneously hypertensive rats: role of α1D‐ and α1A‐adrenoceptors in contraction , 2000 .
[10] C. Han,et al. Alpha(1)-adrenoceptor subtypes mediating inotropic responses in rat heart. , 1999, The Journal of pharmacology and experimental therapeutics.
[11] J. Docherty,et al. Investigation of the subtypes of α1‐adrenoceptor mediating contractions of rat vas deferens , 1999 .
[12] J. Gever,et al. In vitroα1‐adrenoceptor pharmacology of Ro 70–0004 and RS‐100329, novel α1A‐adrenoceptor selective antagonists , 1999 .
[13] M. Oriowo,et al. Heterogeneity of α1-Adrenoceptor Subtypes Mediating Noradrenaline-Induced Contractions of theRat Superior Mesenteric Artery , 1998, Pharmacology.
[14] M. Piascik,et al. Immunocytochemical localization of the alpha-1B adrenergic receptor and the contribution of this and the other subtypes to vascular smooth muscle contraction: analysis with selective ligands and antisense oligonucleotides. , 1997, The Journal of pharmacology and experimental therapeutics.
[15] J. Docherty,et al. Further investigation of the alpha-adrenoceptor-mediated actions of chloroethylclonidine in rat aorta. , 1997, European journal of pharmacology.
[16] J. Gever,et al. Pharmacological pleiotropism of the human recombinant α1A‐adrenoceptor: implications for α1‐adrenoceptor classification , 1997 .
[17] R. Villalobos-Molina,et al. Evidence for an age-dependent functional expression of α1D-adrenoceptors in the rat vasculature , 1997 .
[18] R. Villalobos-Molina,et al. α1D- and α1A-adrenoceptors mediate contraction in rat renal artery , 1997 .
[19] 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.
[20] 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.
[21] L. Zhou,et al. Vascular alpha 1D-adrenoceptors have a role in the pressor response to phenylephrine in the pithed rat. , 1996, European journal of pharmacology.
[22] R. Villalobos-Molina,et al. α1-Adrenoceptors mediating contraction in arteries of normotensive and spontaneously hypertensive rats are of the α1D or α1A subtypes , 1996 .
[23] 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.
[24] M. S. Smith,et al. The specific contribution of the novel alpha-1D adrenoceptor to the contraction of vascular smooth muscle. , 1995, The Journal of pharmacology and experimental therapeutics.
[25] W. B. Jeffries,et al. Quantification of steady state expression of mRNA for alpha-1 adrenergic receptor subtypes using reverse transcription and a competitive polymerase chain reaction. , 1995, The Journal of pharmacology and experimental therapeutics.
[26] A. Goetz,et al. BMY 7378 is a selective antagonist of the D subtype of α1-adrenoceptors , 1995 .
[27] I. Muramatsu,et al. Two distinct α1‐adrenoceptor subtypes involved in noradrenaline contraction of the rabbit thoracic aorta , 1990, British journal of pharmacology.
[28] K. Minneman. Alpha 1-adrenergic receptor subtypes, inositol phosphates, and sources of cell Ca2+. , 1988, Pharmacological reviews.
[29] R. Furchgott,et al. The obligatory role of endothelial cells in the relaxation of arterial smooth muscle by acetylcholine , 1980, Nature.