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
. 1972 Mar;221(3):601-15.
doi: 10.1113/jphysiol.1972.sp009770.

Modification of the evoked release of noradrenaline from the perfused cat spleen by various ions and agents

Modification of the evoked release of noradrenaline from the perfused cat spleen by various ions and agents

S M Kirpekar et al. J Physiol. 1972 Mar.

Abstract

1. Cat spleens were perfused with Krebs-bicarbonate solution at a rate of about 7 ml./min at 33-35 degrees C. Noradrenaline release after splenic nerve stimulation at 10 or 30 Hz was measured. Effects of various ions and drugs on noradrenaline release were determined.2. Perfusion of phenoxybenzamine- and [(3)H]noradrenaline-treated spleens with 1, 2.5 and 5 mM cobalt or nickel-2 Krebs solution markedly reduced the release of noradrenaline by nerve stimulation. Lanthanum was the most potent inhibitor of noradrenaline release. Increasing the calcium concentration or adding tetraethylammonium chloride (TEA) partially counteracted the inhibitory effects of cobalt on release. Cobalt did not inhibit release induced by tyramine.3. Calcium did not cause spontaneous release of noradrenaline either when high concentrations were injected directly into the spleen or after first perfusing the spleen with calcium-free medium.4. Carbachol, protoveratrine and high potassium inhibit, whereas TEA, barium and rubidium enhance, the evoked release of noradrenaline.5. The relation of noradrenaline release to influx of calcium ions and its modification by various agents has been discussed.

PubMed Disclaimer

References

    1. J Physiol. 1968 Feb;194(3):595-608 - PubMed
    1. J Pharmacol Exp Ther. 1967 Sep;157(3):532-40 - PubMed
    1. J Pharmacol Exp Ther. 1970 Jul;174(1):72-6 - PubMed
    1. Nature. 1971 Feb 5;229(5284):410-1 - PubMed
    1. C R Acad Sci Hebd Seances Acad Sci D. 1967 Feb 20;264(8):1072-5 - PubMed

MeSH terms

LinkOut - more resources