Stimulation of β- and β-adrenoceptors dilates retinal blood vessels in rats.

Naunyn Schmiedebergs Arch Pharmacol

Department of Molecular Pharmacology, Kitasato University School of Pharmaceutical Sciences, 5-9-1 Shirokane, Minato-ku, Tokyo, 108-8641, Japan.

Published: May 2017

Our previous studies have demonstrated that adrenaline dilates rat retinal arterioles by stimulating propranolol-sensitive β-adrenoceptors and β-adrenoceptors, and selective stimulation of β- or β-adrenoceptors causes retinal vasodilator responses. In the present study, we compared the effects of β- and β-adrenoceptor stimulation on rat retinal arterioles in vivo. Rat ocular fundus images were captured using an original high-resolution digital fundus camera. Diameters of retinal arterioles contained in the images were measured. Systemic blood pressure and heart rate were recorded continuously. Denopamine, a β-adrenoceptor agonist, increased the diameter of retinal arterioles and heart rate, and produced a small but statistically insignificant decrease in mean arterial pressure. CGP20712A, a β-adrenoceptor antagonist, but not ICI118551, a β-adrenoceptor antagonist, significantly prevented denopamine-induced retinal vasodilator and heart rate responses. Salbutamol, a β-adrenoceptor agonist, increased the diameter of retinal arterioles and decreased mean arterial pressure without significantly changing heart rate. The effects of salbutamol were significantly prevented by ICI118551, but not by CGP20712A. These results suggest that stimulation of β- and β-adrenoceptors dilates retinal blood vessels and indicate that all three β-adrenoceptor subtypes (β, β, and β) may be involved in the retinal vasodilator response to adrenaline in rats.

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Source
http://dx.doi.org/10.1007/s00210-017-1349-4DOI Listing

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