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Mechanistic link between lidocaine block and inactivation probed by outer pore mutations in the rat μ1 skeletal muscle sodium channel

1. Mutations that disrupt Na(+) channel fast inactivation attenuate lidocaine (lignocaine)-induced use dependence; however, the pharmacological role of slower inactivation processes remains unclear. In Xenopus oocytes, tryptophan substitution in the outer pore of the rat skeletal muscle channel (μ1-...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Kambouris, Nicholas G, Hastings, Laura A, Stepanovic, Svetlana, Marban, Eduardo, Tomaselli, Gordon F, Balser, Jeffrey R
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Blackwell Science Inc 1998
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2231251/
https://ncbi.nlm.nih.gov/pubmed/9769414
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1469-7793.1998.693bd.x
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