Diclofenac a Non-steroidal Anti-inflammatory Drug Inhibits L-type Ca2+ Channels in Neonatal Rat Ventricular Cardiomyocytes

摘要

A non-steroidal anti-inflammatory drug (NSAID) has many adverse effects including cardiovascular (CV) risk. Diclofenac among the nonselective NSAIDs has the highest CV risk such as congestive heart failure, which resulted commonly from the impaired cardiac pumping due to a disrupted excitation-contraction (E-C) coupling. We investigated the effects of diclofenac on the L-type calcium channels which are essential to the E-C coupling at the level of single ventricular myocytes isolated from neonatal rat heart, using the whole-cell voltage-clamp technique. Only diclofenac of three NSAIDs, including naproxen and ibuprofen, significantly reduced inward whole cell currents. At concentrations higher than 3 µM, diclofenac inhibited reversibly the Na⁺ current and did irreversibly the L-type Ca²⁺ channels-mediated inward current (IC50=12.89±0.43 µM) in a dose-dependent manner. However, nifedipine, a well-known L-type channel blocker, effectively inhibited the L-type Ca²⁺ currents but not the Na⁺ current. Our finding may explain that diclofenac causes the CV risk by the inhibition of L-type Ca²⁺ channel, leading to the impairment of E-C coupling in cardiac myocytes.