sodium-lactate and sodium-binding-benzofuran-isophthalate

The role of the Na+/H+ exchanger in rat hearts during ischemia and reperfusion was investigated by measurements of intracellular Na+ concentration ([Na+]i) and intracellular and extracellular pH. Under our standard conditions (2-Hz stimulation), 10 min of ischemia caused no significant rise in [Na+]i but an acidosis of 1.0 pH unit, suggesting that the Na+/H+ exchanger was inactive during ischemia. This was confirmed by showing that the Na+/H+ exchange inhibitor methylisobutyl amiloride (MIA) had no effect on [Na+]i or on intracellular pH during ischemia. However, there was a short-lived increase in [Na+]i of 8.2 +/- 0.6 mM on reperfusion, which was reduced by MIA, showing that the Na+/H+ exchanger became active on reperfusion. To investigate the role of metabolic changes, we measured [Na+]i during anoxia. The [Na+]i did not change during 10 min of anoxia, but there was a small, transient rise of [Na+]i on reoxygenation, which was inhibited by MIA. In addition, we show that the Na+/H+ exchanger, tested by sodium lactate exposure, was inhibited during anoxia. These results show that the Na+/H+ exchanger is inhibited during ischemia and anoxia, probably by an intracellular metabolic mechanism. The exchanger activates rapidly on reperfusion and can cause a rapid rise in [Na+]i.

Topics: Acidosis; Amiloride; Animals; Benzofurans; Benzopyrans; Ethers, Cyclic; Female; Fluorescent Dyes; Heart Ventricles; Hydrogen-Ion Concentration; Hypoxia; Muscle Fibers, Skeletal; Myocardial Ischemia; Myocardium; Naphthols; Organ Culture Techniques; Rats; Rats, Sprague-Dawley; Rhodamines; Sodium; Sodium Lactate; Sodium-Hydrogen Exchangers; Ventricular Function, Left