Role of Na+/K+-stimulated adenosine triphosphatase in the action of dopaminergic-D2 receptors of the liver in rats

Author:

Abu-Jayyab Abdulrahim1,Mahgoub Ahmed1

Affiliation:

1. Department of Pharmacology, College of Pharmacy, King Saud University, PO Box 2457, Riyadh-1145, Saudi Arabia

Abstract

The dopamine receptor agonist, bromocriptine, in a dose of 10 mg/kg i.p. for 14 days, in rats caused a significant increase in liver Na+/K+-ATPase activity, whereas sulpiride, a dopamine receptor antagonist, in a dose of 10 mg/kg, i.p. for 14 days, in rats, caused a significant decrease in liver Na+/K+-ATPase activity. Injection of bromocriptine and sulpiride simultaneously in a group of rats, under the same conditions and using the same doses caused a complete block of both stimulatory activity of bromocriptine and inhibitory activity of sulpiride on liver Na+/K+-ATPase activity. It is suggested that Na+/K+-ATPase may have a role in the action of dopaminergic-D2 receptors.

Publisher

Portland Press Ltd.

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference26 articles.

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3. Smythe, G. A., Brandstater, J. F., Compton, P. J. and Lazarus, L. (1977). In:Twentieth Annual Meeting of the Endocrine Society of Australia, Abst. No. 12; P. E. Harding, Adelaide.

4. Trabucchi, M., Hofmann, M., Montefusco, O. and Spani, P. F. (1978).Pharmacology 16 (Suppl. I) 150?155.

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