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Title: Effect of vascular smooth muscle relaxants on the protein kinase C-mediated contraction in the rat pulmonary artery. Author: Savineau JP, Gonzalez De La Fuente P, Marthan R. Journal: Eur J Pharmacol; 1993 Nov 09; 249(2):191-8. PubMed ID: 8287900. Abstract: In the rat pulmonary artery, phorbol 12,13-dibutyrate induces a contraction due to the activation of the protein kinase C. We investigated the sensitivity of this protein kinase C-mediated contraction to a variety of vascular smooth muscle relaxants. Pretreatment of rat pulmonary artery with relaxant compounds altered the subsequent concentration-response curve to phorbol 12,13-dibutyrate (0.05-2 microM) in a variable manner. Isoprenaline (0.1-10 microM), nifedipine (0.01-1 microM) and cromakalim (0.1-10 microM) had no effect, whereas vasoactive intestinal peptide (VIP, 1-10 nM), forskolin (0.1-2 microM), theophylline (0.1-2.5 mM), 4-(3-butoxy-4-methoxybenzyl)-2-imidazolidinone (RO 20-1724, 2-20 microM), dipyridamole (10-100 microM), 8 bromo-cyclic GMP (8-br-cGMP, 5-500 microM) and dibutyryl cyclic AMP (db-cAMP, 100-500 microM) shifted the concentration-response curve to phorbol 12,13-dibutyrate to the right and decreased the maximal response. When cumulative concentrations of relaxants were applied on the plateau of the contraction induced by 0.2 or 2 microM phorbol 12,13-dibutyrate, again, isoprenaline, nifedipine and cromakalim failed to decrease the protein kinase C-mediated contraction, whereas the other agents produced concentration-dependent relaxation. From their inhibitory effect on the 0.2 microM phorbol 12,13-dibutyrate-induced contraction, the rank order of potency of these relaxants was: VIP >> forskolin > RO 20-1724 > 8-br-cGMP > theophylline > dipyridamole > db-cAMP. In chemically (beta escin) skinned preparations, cGMP (5-500 microM) and cAMP (50-1000 microM) antagonized in a concentration dependent manner the contraction induced by phorbol 12,13-dibutyrate at constant Ca2+ concentration.(ABSTRACT TRUNCATED AT 250 WORDS)[Abstract] [Full Text] [Related] [New Search]