Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 1990;30 Suppl 1(Suppl 1):61S-68S.
doi: 10.1111/j.1365-2125.1990.tb05470.x.

The role of DA1- and DA2-receptors in the control of blood pressure

Affiliations
Review

The role of DA1- and DA2-receptors in the control of blood pressure

J P Hieble et al. Br J Clin Pharmacol. 1990.

Abstract

1. Endogenous dopamine, acting through specific receptors on blood vessels, renal tubules and adrenal cortical cells, may play a role in the development and maintenance of the hypertensive state. 2. In hypertensive patients, activation of the DA1-receptor with intravenous fenoldopam produces a rapid and sustained reduction in blood pressure, in contrast to the tachyphylaxis seen in some rat models. 3. Activation of the DA2-receptor also represents a viable antihypertensive approach, based on the chronic efficacy of hydergine. However, none of the recently developed selective DA2-receptor agonists has been shown to reduce blood pressure in man. 4. Since animal experiments suggest qualitatively different antihypertensive profiles for quinpirole and SK&F 101468, both presumed to be selective agonists at the DA2-receptor, it may be possible to design new DA2-receptor agonists more effective as antihypertensive drugs. 5. Dopamine receptors at different sites, even if of the same subtype, can be differentially regulated; this may be a consequence of activation of multiple second messenger systems by receptor occupation.

PubMed Disclaimer

References

    1. Br J Clin Pharmacol. 1986 Jan;21(1):53-61 - PubMed
    1. Int J Clin Pharmacol Ther Toxicol. 1985 Sep;23(9):506-9 - PubMed
    1. J Pharmacol Exp Ther. 1986 Nov;239(2):426-32 - PubMed
    1. J Pharm Sci. 1986 Oct;75(10):925-8 - PubMed
    1. J Clin Endocrinol Metab. 1987 Jul;65(1):203-7 - PubMed

LinkOut - more resources