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
. 1970 Sep;56(3):309-21.
doi: 10.1085/jgp.56.3.309.

Influence of polyvalent cations on the activation of muscle end plate receptors

Influence of polyvalent cations on the activation of muscle end plate receptors

D H Lambert et al. J Gen Physiol. 1970 Sep.

Abstract

The influence of polyvalent cations on the activation of end plate receptors has been studied in vitro on the sartorius muscle of the frog. In the absence of extracellular calcium, the sensitivity of the receptors to depolarizing quaternary ammonium salts was markedly reduced. Maximum receptor activation occurred in those fibers equilibrated in 1.8 mM calcium Ringer solution, with the response being reduced as the calcium concentration was raised or lowered. Magnesium was less efficient than calcium in regulating the sensitivity of the end plate receptors, the maximum receptor response occurring in those fibers equilibrated in 8 mM magnesium Ringer solution. In the presence of lanthanum the end plate response to carbamylcholine or acetylcholine was enhanced. Lanthanum increased the conductance change produced by carbamylcholine both in polarized and in potassium-depolarized fibers. The application of 10(-2) mM lanthanum to the end plate increased MEPP's amplitude, rise time, and half-fall time by 19, 54, and 45%, respectively. The results suggest that polyvalent cations influence postjunctional membrane receptor processes in addition to their well-documented prejunctional action.

PubMed Disclaimer

References

    1. J Gen Physiol. 1966 Nov;50(2):461-71 - PubMed
    1. J Pharm Pharmacol. 1968 Dec;20(12):889-910 - PubMed
    1. J Physiol. 1952 May;117(1):109-28 - PubMed
    1. C R Seances Soc Biol Fil. 1964;158:1454-8 - PubMed
    1. Am J Physiol. 1969 Apr;216(4):925-31 - PubMed