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Upregulation of the rat cardiac sodium channel by in vivo treatment with a class I antiarrhythmic drug.

Class I antiarrhythmic drugs inhibit the sodium channel by binding to a drug receptor associated with the channel. In this report we show that in vivo administration of the class I antiarrhythmic drug mexiletine to rats induces sodium channel upregulation in isolated cardiac myocytes. The number of...

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Pubblicato in:J Clin Invest
Autori principali: Taouis, M, Sheldon, R S, Duff, H J
Natura: Artigo
Lingua:Inglês
Pubblicazione: American Society for Clinical Investigation 1991
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Accesso online:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC295340/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1650791/
https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI115313
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