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Potentiation of the Cardiac L-Type Ca(2+) Channel (α(1C)) by Dihydropyridine Agonist and Strong Depolarization Occur via Distinct Mechanisms

A defining property of L-type Ca(2+) channels is their potentiation by both 1,4-dihydropyridine agonists and strong depolarization. In contrast, non–L-type channels are potentiated by neither agonist nor depolarization, suggesting that these two processes may by linked. In this study, we have tested...

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Hlavní autoři: Wilkens, Christina M., Grabner, Manfred, Beam, Kurt G.
Médium: Artigo
Jazyk:Inglês
Vydáno: The Rockefeller University Press 2001
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2233833/
https://ncbi.nlm.nih.gov/pubmed/11696608
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