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Activation of cyclic AMP-dependent protein kinases by vasoactive intestinal peptide (VIP) in isolated intestinal epithelial cells from rat.
Authors:M Laburthe  P Mangeat  G Marchis-Mouren  G Rosselin
Institution:1. Unité de Recherche de Diabétologie et d''Etudes Radio-Immunologiques des Hormones Protéiques (ERA 494, CNRS, U.55, INSERM) , hôpital Saint-Antoine, 75012 Paris, France
Abstract:VIP stimulates protein kinase activity in intestinal epithelial cells isolated from rat jejuno-ileum. The stimulation is time-dependent and is potentiated by the phosphodiesterase inhibitor 3-isobutyl-1-methylxanthine. The response occurs in the 0.1–10 nM range of VIP concentrations, half-maximal stimulation being observed with 0.7 nM VIP. The VIP-induced protien kinase activation is thus observed at concentrations similar to those promoting the accumulation of cyclic AMP (11). Secretin also stimulates protien kinase activity but with a 100-times lower potency than VIP, in agreement with the fact that secretin is a VIP agonist of 100-times lower potency with respect to cyclic AMP increase. Prostaglandins E1 and E2 (10?5 M), are also found to increase protein kinase activity.
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