An antisense oligonucleotide against H1 inhibits the classical sodium current but not ICa(TTX) in rat ventricular cells

Qun Sha, Shawn W. Robinson, Stacey L. McCulle, Stephen R. Shorofsky, Paul A. Welling, L. Goldman, C. William Balke

Research output: Contribution to journalReview articlepeer-review

Abstract

ICa(TTX) is a sodium current component, functionally distinct from the main body of sodium current, seen in cardiac and other cells. To determine if ICa(TTX) channels are a separate isoform from the classical cardiac sodium channels, we exposed rat ventricular cells in primary culture to an antisense oligonucleotide (AON) directed against rH1 (rNav1.5): 5′-CTCCTCATACCCTCT-3′. The homologous human sequence has been identified (and confirmed by us on HEK 293 cells) as effective against hH1 expressed heterologously. Scrambled sequence (5′-CCCCCCTTATCTACT-3′) controls were also included. The AON (10 μM; day 2 of exposure) reduced the classical sodium current by 69.6% compared to untreated and 60.8% compared to scrambled sequence (10 μM; day 2 of exposure) controls (mean ± S.E.M. maximum peak inward current density of -8.23 ± 0.60 pA pF-1, 18 cells, for untreated; -6.37 ± 0.79 pA pF-1, 16 cells, for scrambled sequence; and -2.50 ± 0.31 pA pF-1, 18 cells, for AON-treated cells). The two control groups are not significantly different from each other, but are both significantly different from the AON-treated group (P < 0.001). The inhibition was specific for sodium channels, with no significant AON effect on the L-type calcium current. This confirms that H1 generates the classical cardiac sodium current. This same AON at the same concentration and time of exposure had no significant effect on ICa(TTX) (mean of -4.72 ± 0.55, 15 cells; -5.47 ± 0.53, 13 cells; and -5.04 ± 0.63 pA pF-1, 15 cells, for untreated controls, scrambled controls and AON treated, respectively). Hence, ICa(TTX), which is functionally distinct from the classical cardiac sodium current, is encoded by a distinct gene.

Original languageEnglish (US)
Pages (from-to)435-440
Number of pages6
JournalJournal of Physiology
Volume547
Issue number2
DOIs
StatePublished - Mar 1 2003
Externally publishedYes

ASJC Scopus subject areas

  • Physiology

Fingerprint Dive into the research topics of 'An antisense oligonucleotide against H1 inhibits the classical sodium current but not I<sub>Ca(TTX)</sub> in rat ventricular cells'. Together they form a unique fingerprint.

Cite this