Salvia miltiorrhiza (Danshen) inhibits L-type calcium current and attenuates calcium transient and contractility in rat ventricular myocytes

J Ethnopharmacol. 2014 Dec 2:158 Pt A:397-403. doi: 10.1016/j.jep.2014.10.049. Epub 2014 Oct 31.

Abstract

Ethnopharmacological relevance: Salvia miltiorrhiza (SM, Danshen), a traditional Chinese herbal drug, has been widely used for hundreds of years to treat coronary artery disease.

Materials and methods: We studied the effects of SM on the L-type Ca(2+) current (ICa-L) with whole-cell patch-clamp technique in rat ventricular myocytes, and its influence on Ca(2+) transient and contractility using video-based edge detection and dual excitation fluorescence photomultiplier systems as well.

Results: Exposure to SM solution caused a concentration- and voltage-dependent blockade of ICa-L, and the dose of SM solution (10g/l) decreased the maximal inhibitory effect of 35.2±1.2%. However, SM solution did not significantly change the current-voltage relationship or reversal potential of ICa-L, nor did it altered the activation and inactivation gating properties of cardiac Ca(2+) channels. Meanwhile, SM decreased the amplitude of myocyte shortening and the peak value of Ca(2+) transient with a significant decrease in the time to 90% of the baseline (Tr), but the time to 10% of the peak (Tp) was not dramatically prolonged.

Conclusions: The results indicated that SM significantly inhibited L-type Ca(2+) channels, decreased [Ca(2+)]i and contractility in adult rat cardiac myocytes. These findings may be relevant to the cardioprotective efficacy of SM.

Keywords: Calcium transient; L-type calcium current; Myocyte contractility; Patch clamp; SM; SM (PubChem CID: 105117); Verapamil hydrochloride (PubChem CID: 62969).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calcium / metabolism*
  • Calcium Channel Blockers / pharmacology*
  • Calcium Channels, L-Type / drug effects*
  • Chromatography, High Pressure Liquid
  • Dose-Response Relationship, Drug
  • Heart Ventricles / cytology
  • Heart Ventricles / drug effects*
  • Male
  • Myocytes, Cardiac / drug effects*
  • Plant Extracts / pharmacology*
  • Rats
  • Rats, Sprague-Dawley
  • Salvia miltiorrhiza / chemistry*
  • Spectrophotometry, Ultraviolet

Substances

  • Calcium Channel Blockers
  • Calcium Channels, L-Type
  • Plant Extracts
  • Calcium