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
. 1990 Jan;99(1):71-6.
doi: 10.1111/j.1476-5381.1990.tb14656.x.

Action of calcitonin gene-related peptide upon bovine vascular endothelial and smooth muscle cells grown in isolation and co-culture

Affiliations

Action of calcitonin gene-related peptide upon bovine vascular endothelial and smooth muscle cells grown in isolation and co-culture

D C Crossman et al. Br J Pharmacol. 1990 Jan.

Abstract

1. Bovine aortic endothelial cells (BAE) and smooth muscle cells (BASM) were grown separately and in co-culture. 2. Calcitonin gene-related peptide (CGRP) caused dose-dependent activation of adenylate cyclase in each cell type when grown in isolation. The concentration of CGRP causing half-maximal activation in BAE and BASM was 200 nM and 310 nM, respectively. 3. In cells grown in co-culture exposure to bradykinin produced dose-dependent elevations in cyclic GMP content which were maximal 1 min after application of the agonist. 4. CGRP (1 nM-1 microM) did not stimulate a rise in cyclic GMP in co-cultures. 5. Displaceable CGRP binding was identified throughout the wall of the bovine aorta. 6. We conclude that CGRP receptors coupled to adenylate cyclase are present on BAE and BASM, but there is no coupling of these receptors to the release of any agent (such as endothelium-derived relaxing factor) that activates guanylate cyclase.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Br J Clin Pharmacol. 1987 Aug;24(2):139-44 - PubMed
    1. Naunyn Schmiedebergs Arch Pharmacol. 1987 Jul;336(1):94-8 - PubMed
    1. Br J Pharmacol. 1987 Aug;91(4):729-33 - PubMed
    1. Br J Pharmacol. 1987 Oct;92(2):257-64 - PubMed
    1. Eur J Biochem. 1987 Dec 30;170(1-2):373-9 - PubMed

Publication types

MeSH terms

Substances