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
. 1985 Jul;82(14):4857-61.
doi: 10.1073/pnas.82.14.4857.

Adenosine-activated potassium conductance in cultured striatal neurons

Adenosine-activated potassium conductance in cultured striatal neurons

L O Trussell et al. Proc Natl Acad Sci U S A. 1985 Jul.

Abstract

We have examined the effect of adenosine on the membrane properties of cultured embryonic mouse striatal neurons using patch electrode techniques. Adenosine at 50 microM effectively blocked spontaneous action potential activity. Adenosine or 2-chloroadenosine caused a slow hyperpolarization of the membrane potential and, under voltage clamp, an outward current that was blocked by 1 mM theophylline. ATP also caused a hyperpolarization that was slower and weaker than the adenosine response and could be blocked by 1 mM theophylline. The current induced by adenosine appears to be carried by potassium since (i) an inward current was generated by adenosine when the cells were internally perfused with cesium salts and (ii) the reversal potential of the outward current shifted 57 mV with a 10-fold change in extracellular potassium concentration. The adenosine response is voltage dependent in that the current evoked by adenosine is reduced at holding potentials more positive than -55 mV, despite a larger driving force. Though calcium influx is not required for adenosine to activate the potassium conductance, some components of the cytosol may be essential, since the response is lost during intracellular perfusion.

PubMed Disclaimer

References

    1. Science. 1984 Apr 13;224(4645):166-8 - PubMed
    1. J Physiol. 1984 Jan;346:243-56 - PubMed
    1. Nature. 1984 Sep 6-11;311(5981):62-5 - PubMed
    1. J Neurosci. 1984 Nov;4(11):2772-83 - PubMed
    1. Pflugers Arch. 1984 Nov;402(3):244-7 - PubMed

Publication types

MeSH terms