Differential interactions of Na+ channel toxins with T-type Ca2+ channels

Hui Sun, Diego Varela, Denis Chartier, Peter C. Ruben, Stanley Nattel, Gerald W. Zamponi, Normand Leblanc

Research output: Contribution to journalArticle

Abstract

Two types of voltage-dependent Ca2+ channels have been identified in heart: high (ICaL) and low (ICaT) voltage-activated Ca2+ channels. In guinea pig ventricular myocytes, low voltage-activated inward current consists of ICaT and a tetrodotoxin (TTX)-sensitive ICa component (ICa(TTX)). In this study, we reexamined the nature of low-threshold ICa in dog atrium, as well as whether it is affected by Na+ channel toxins. Ca2+ currents were recorded using the whole-cell patch clamp technique. In the absence of external Na+, a transient inward current activated near -50 mV, peaked at -30 mV, and reversed around +40 mV (HP = -90 mV). It was unaffected by 30 μM TTX or micromolar concentrations of external Na+, but was inhibited by 50 μM Ni2+ (by ∼90%) or 5 μM mibefradil (by ∼50%), consistent with the reported properties of ICaT. Addition of 30 μM TTX in the presence of Ni2+ increased the current approximately fourfold (41% of control), and shifted the dose-response curve of Ni2+ block to the right (IC50 from 7.6 to 30 μM). Saxitoxin (STX) at 1 μM abolished the current left in 50 μM Ni2+. In the absence of Ni2+, STX potently blocked ICaT (EC50 = 185 nM) and modestly reduced ICaL (EC50 = 1.6 μM). While TTX produced no direct effect on I CaT elicited by expression of hCaV3.1 and hCa V3.2 in HEK-293 cells, it significantly attenuated the block of this current by Ni2+ (IC50 increased to 550 μM Ni 2+ for CaV3.1 and 15 μM Ni2+ for Ca V3.2); in contrast, 30 μM TTX directly inhibited hCa V3.3-induced ICaT and the addition of 750 μM Ni 2+ to the TTX-containing medium led to greater block of the current that was not significantly different than that produced by Ni2+ alone. 1 μM STX directly inhibited CaV3.1-, CaV3.2-, and CaV3.3-mediated ICaT but did not enhance the ability of Ni2+ to block these currents. These findings provide important new implications for our understanding of structure-function relationships of ICaT in heart, and further extend the hypothesis of a parallel evolution of Na+ and Ca2+ channels from an ancestor with common structural motifs.

Original languageEnglish (US)
Pages (from-to)101-113
Number of pages13
JournalJournal of General Physiology
Volume132
Issue number1
DOIs
StatePublished - Jul 2008
Externally publishedYes

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Tetrodotoxin
Saxitoxin
Inhibitory Concentration 50
Mibefradil
HEK293 Cells
Patch-Clamp Techniques
Muscle Cells
Guinea Pigs
Dogs

ASJC Scopus subject areas

  • Physiology

Cite this

Sun, H., Varela, D., Chartier, D., Ruben, P. C., Nattel, S., Zamponi, G. W., & Leblanc, N. (2008). Differential interactions of Na+ channel toxins with T-type Ca2+ channels. Journal of General Physiology, 132(1), 101-113. https://doi.org/10.1085/jgp.200709883

Differential interactions of Na+ channel toxins with T-type Ca2+ channels. / Sun, Hui; Varela, Diego; Chartier, Denis; Ruben, Peter C.; Nattel, Stanley; Zamponi, Gerald W.; Leblanc, Normand.

In: Journal of General Physiology, Vol. 132, No. 1, 07.2008, p. 101-113.

Research output: Contribution to journalArticle

Sun, H, Varela, D, Chartier, D, Ruben, PC, Nattel, S, Zamponi, GW & Leblanc, N 2008, 'Differential interactions of Na+ channel toxins with T-type Ca2+ channels', Journal of General Physiology, vol. 132, no. 1, pp. 101-113. https://doi.org/10.1085/jgp.200709883
Sun, Hui ; Varela, Diego ; Chartier, Denis ; Ruben, Peter C. ; Nattel, Stanley ; Zamponi, Gerald W. ; Leblanc, Normand. / Differential interactions of Na+ channel toxins with T-type Ca2+ channels. In: Journal of General Physiology. 2008 ; Vol. 132, No. 1. pp. 101-113.
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