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
Comparative Study
. 1985 Jun;85(2):383-5.
doi: 10.1111/j.1476-5381.1985.tb08872.x.

Comparison of effects of a new dihydropyridine, Bay K 8644, and nifedipine on spontaneous mechanical activity in rat portal vein

Comparative Study

Comparison of effects of a new dihydropyridine, Bay K 8644, and nifedipine on spontaneous mechanical activity in rat portal vein

E Mikkelsen. Br J Pharmacol. 1985 Jun.

Abstract

In isolated portal veins from rats, Bay K 8644 (methyl-1, 4-dihydro-2, 6-dimethyl-3-nitro-4 (2-trifluoromethyl-phenyl) pyridine-5-carboxylate) increased the spontaneous mechanical activity in low but not in high concentrations. The Bay K 8644-induced increase in spontaneous mechanical activity was abolished in Ca-free medium and restored by readdition of Ca. Nifedipine abolished the augmenting effect of Bay K 8644 on the spontaneous mechanical activity; this effect of nifedipine could be eliminated by further increasing the concentration of Bay K 8644. The results are consistent with the conclusion that in rat portal vein, Bay K 8644 increases the entry of extracellular Ca by a mechanism antagonistic to that of nifedipine and in high concentration has a Ca-entry blocking effect.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Circ Res. 1967 Nov;21(5):609-18 - PubMed
    1. Blood Vessels. 1981;18(3):89-99 - PubMed
    1. Acta Pharmacol Toxicol (Copenh). 1985 Jan;56(1):44-9 - PubMed
    1. Arzneimittelforschung. 1983;33(9):1268-72 - PubMed
    1. Acta Pharmacol Toxicol (Copenh). 1984 Apr;54(4):258-64 - PubMed

Publication types

MeSH terms

Substances

LinkOut - more resources