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Research Article Free access | 10.1172/JCI117957
Department of Medicine, Emory University School of Medicine, Atlanta, Georgia 30322, USA.
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Department of Medicine, Emory University School of Medicine, Atlanta, Georgia 30322, USA.
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Department of Medicine, Emory University School of Medicine, Atlanta, Georgia 30322, USA.
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Department of Medicine, Emory University School of Medicine, Atlanta, Georgia 30322, USA.
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Department of Medicine, Emory University School of Medicine, Atlanta, Georgia 30322, USA.
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Department of Medicine, Emory University School of Medicine, Atlanta, Georgia 30322, USA.
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Department of Medicine, Emory University School of Medicine, Atlanta, Georgia 30322, USA.
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Published June 1, 1995 - More info
The effect of extracellular L-arginine and L-glutamine on nitric oxide (NO) release was studied in cultured bovine aortic endothelial cells and in rabbit aortic rings. Increasing L-arginine (0.01 to 10 mM) did not alter NO release from cultured endothelial cells or modify endothelium-dependent relaxation to acetylcholine in isolated vessels. L-Glutamine (0.6 and 2 mM) inhibited NO release from cultured cells (in response to bradykinin) and from aortic rings (in response to acetylcholine or ADP). L-Arginine (0.1-10 mM) dose-dependently reversed the L-glutamine inhibition of receptor-stimulated NO release in both models. In contrast to its inhibitory response to receptor-mediated stimuli, glutamine alone slightly potentiated NO release in both models when the calcium ionophore, A23187, was added. Furthermore, cultured cells incubated with L-arginine (0.01-10 mM), in the presence or absence of glutamine, released similar amounts of NO in response to A23187. L-Glutamine did not affect intracellular L-arginine levels. Neither D-glutamine nor D-arginine affected NO release or endothelium-dependent vascular relaxation. L-Glutamine had no effect on the activity of endothelial NOS assessed by L-arginine to L-citrulline conversion. These findings show that in the absence of L-glutamine, manipulating intracellular L-arginine levels over a wide range does not affect NO release. L-Glutamine in concentrations circulating in vivo may tonically inhibit receptor-mediated NO release by interfering with signal transduction. One mechanism by which L-arginine may enhance NO release is via reversal of the inhibitory effect of L-glutamine, but apparently independently of enhancing NO synthase substrate.
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