Publications by the researcher in collaboration with MARIA PILAR D'OCON NAVAZA (53)

2024

  1. Beyond lectures and practical courses: Teaching pharmacology using imaginative pedagogical tools

    Pharmacological Research, Vol. 202

2022

  1. Red de innovación docente interuniversitaria en farmacología: Un espacio común para mejorar el aprendizaje

    Actualidad en farmacología y terapéutica, Vol. 20, Núm. 3, pp. 214-220

2021

  1. NT3/TrkC Pathway Modulates the Expression of UCP-1 and Adipocyte Size in Human and Rodent Adipose Tissue

    Frontiers in Endocrinology, Vol. 12

2017

  1. Activation of α1A-adrenoceptors desensitizes the rat aorta response to phenylephrine through a neuronal NOS pathway, a mechanism lost with ageing

    British Journal of Pharmacology, Vol. 174, Núm. 13, pp. 2015-2030

2016

  1. Red de innovación docente interuniversitaria en Farmacología

    XIV Jornadas de Redes de Investigación en Docencia Universitaria: investigación, innovación y enseñanza universitaria: enfoques pluridisciplinares

2015

  1. β2-and β1-adrenoceptor expression exhibits a common regulatory pattern with GRK2 and GRK5 in human and animal models of cardiovascular diseases

    Journal of Cardiovascular Pharmacology, Vol. 66, Núm. 5, pp. 478-486

2014

  1. Action of an extract from the seeds of Fraxinus excelsior L. on metabolic disorders in hypertensive and obese animal models

    Food and Function, Vol. 5, Núm. 4, pp. 786-796

  2. Changes in adrenoceptors and G-protein-coupled receptor kinase 2 in L-NAME-induced hypertension compared to spontaneous hypertension in rats

    Journal of Vascular Research, Vol. 51, Núm. 3, pp. 209-220

  3. β-Adrenoceptors differentially regulate vascular tone and angiogenesis of rat aorta via ERK1/2 and p38

    Vascular Pharmacology, Vol. 61, Núm. 2-3, pp. 80-89

2013

  1. Different β-adrenoceptor subtypes coupling to cAMP or NO/cGMP pathways: Implications in the relaxant response of rat conductance and resistance vessels

    British Journal of Pharmacology, Vol. 169, Núm. 2, pp. 413-425

  2. α1D-Adrenoceptors are responsible for the high sensitivity and the slow time-course of noradrenaline-mediated contraction in conductance arteries

    Pharmacology Research and Perspectives, Vol. 1, Núm. 1

2012

  1. Different expression of adrenoceptors and GRKs in the human myocardium depends on heart failure ethiology and correlates to clinical variables

    American Journal of Physiology - Heart and Circulatory Physiology, Vol. 303, Núm. 3, pp. 368-376

2010

  1. The impact of α1-adrenoceptors up-regulation accompanied by the impairment of β-adrenergic vasodilatation in hypertension (The Journal of Pharmacology and Experimental Therapeutics (2009) 328, (982-990))

    Journal of Pharmacology and Experimental Therapeutics

  2. α1-Adrenoceptors in the rat cerebral cortex: New insights into the characterization of α1L- and α1D-adrenoceptors

    European Journal of Pharmacology, Vol. 641, Núm. 1, pp. 41-48

2009

  1. The Impact of α1-Adrenoceptors Up-regulation accompanied by the mpairment of β-adrenergic vasodilatation in hypertension

    Journal of Pharmacology and Experimental Therapeutics, Vol. 328, Núm. 3, pp. 982-990

2005

  1. 8-NH2-boldine, an antagonist of α1A and α1B adrenoceptors without affinity for the α1D subtype: Structural requirements for aporphines at α1- adrenoceptor subtypes

    Planta Medica, Vol. 71, Núm. 10, pp. 897-903

  2. Acute and chronic captopril, but not prazosin or nifedipine, normalize alterations in adrenergic intracellular Ca2+ handling observed in the mesenteric arterial tree of spontaneously hypertensive rats

    Journal of Pharmacology and Experimental Therapeutics, Vol. 313, Núm. 1, pp. 359-367

  3. Correlation between mRNA levels and functional role of α1- adrenoceptor subtypes in arteries: Evidence of α1L as a functional isoform of the α1A-adrenoceptor

    American Journal of Physiology - Heart and Circulatory Physiology, Vol. 289, Núm. 5 58-5

2004

  1. Vascular activity of (-)-anonaine, (-)-roemerine and (-)-pukateine, three natural 6a(R)-1,2-methylenedioxyaporphines with different affinities for α1-adrenoceptor subtypes

    Planta Medica, Vol. 70, Núm. 7, pp. 603-609

2003

  1. Cytosolic Ca2+ and phosphoinositide hydrolysis linked to constitutively active α1D-adrenoceptors in vascular smooth muscle

    Journal of Pharmacology and Experimental Therapeutics, Vol. 305, Núm. 3, pp. 1006-1014