PMID: 8973385Sep 1, 1996Paper

The heart sodium channel phenotype for inactivation and lidocaine block

Japanese Heart Journal
J C Makielski

Abstract

The heart Na channel, although resembling other voltage-gated Na channels, has important functional and structural differences. For heart channels expressed in oocytes, the midpoint of the inactivation relationship was 13 mV negative to that of rat skeletal muscle Na channels, and sensitivity to tonic lidocaine block was approximately 5 times more sensitive for heart. Co-expression with the beta subunit increased the difference in inactivation midpoint to 24 mV, largely by changing the midpoint of the rat skeletal muscle channel by 10 mV in the positive direction. Co-expression with beta 1 decreased lidocaine sensitivity for heart but not for skeletal muscle Na channels, and decreased but did not eliminate the greater heart sensitivity to lidocaine block. The differences in inactivation are likely to account for some, but not all, of the differences in lidocaine sensitivity. This cardiac phenotype is important for the role the channel plays in cardiac physiology and pathophysiology, and also may lead to elucidation of structure-function relationships.

Citations

Jul 22, 1999·Annals of the New York Academy of Sciences·A L Goldin
Dec 6, 2005·Journal of Neurobiology·Christopher A CouttsDeclan W Ali
Sep 18, 2002·Journal of Molecular and Cellular Cardiology·Carmen R ValdiviaJonathan C Makielski
Feb 22, 2001·Annual Review of Physiology·A L Goldin

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