SEA0400 is a selective inhibitor of the Na+/Ca2+ exchanger having equal potencies to suppress both the forward and reverse mode operation of the Na+/Ca2+ exchanger. Present experiments were designed to study the effect of partial blockade of Na+/Ca2+ exchanger on Ca2+ handling in isolated rat ventricular myocytes. Intracellular Ca2+ transient and cell shortening were measured in ventricular myocytes loaded with Fura-2-AM fluorescent dye. Partial blockade of Na+/Ca2+ exchanger was induced by superfusion of the cells with SEA0400 at a concentration of 0.3 mu M. Amplitude of the intracellular Ca2+ transient and cell shortening was significantly increased by SEA0400 in both field stimulated and voltage clamped myocytes, without significant elevation of diastolic Ca2+ level and the decay time constant of the Ca2+ transient. In patch clamped myocytes the SEA0400 induced increase in the Ca2+ transient and cell shortening was accompanied by significant reduction of peak L-type Ca2+ current. These effects can be explained by the autoregulative nature of cardiac Ca2+ handling, as the reduced Ca2+ efflux from the cell results in an increased Ca2+ load to the sarcoplasmic reticulum leading to increased Ca2+ release, which in turn may decrease the L-type Ca2+ current by accelaration of Ca2+ dependent inactivation of L-type Ca2+ Current. Our results suggest that complex changes in the Ca2+ cycling can occur after selective pharmacological inhibition of the Na+/Ca2+ exchanger. (c) 2007 Elsevier B.V. All rights reserved.
机构:
Kyushu Univ, Div Mol Cardiol, Angiocardiol Res Inst, Grad Sch Med Sci,Higashi Ku, Fukuoka 8128582, JapanKyushu Univ, Div Mol Cardiol, Angiocardiol Res Inst, Grad Sch Med Sci,Higashi Ku, Fukuoka 8128582, Japan