H2O2: a Ca2+ or Mg2+-sensing function in statin passive diffusion

In a previous paper Guillaume's group demonstrated that magnesium (Mg2+ concentration range 0.00-2.60 mm) increased the passive diffusion of statins and thus played a role in their potential toxicity. In order to confirm an increase in this passive diffusion by divalent salt cations, the role of calcium chloride (CaCl2) on the statin-immobilized artificial membrane (IAM) association was studied. It was demonstrated that calcium supplementation (Ca2+ concentration range 0.00-3.25 mm) increases the statin passive diffusion. In addition, it was shown that the Ca2+ effect on the statin-IAM association is higher than that of Mg2+. These results show that Ca2+ enhances the passive diffusion of drugs into biological membranes and thus their potential toxicity. Also, addition of H2O2 to the medium showed a hyperbolic response for the statin passive diffusion and this effect was enhanced for the highest Ca2+ or Mg2+ concentrations in the medium. H2O2 is likely to interact with the polar head groups of the IAM through dipole-dipole interactions. The conformational changes in H2O2-IAM result in a higher degree of exposure of hydrophobic areas, thus explaining why the binding of pravastatin, which showed the lowest logP value, was less affected by H2O2. This result shows the significant contribution of H2O2 and thus the oxidative stress on the statin passive diffusion. Much of the sensitivity derives from the action of Ca2+ or Mg2+, in turn supported the idea that H2O2 may serve a Ca2+ or Mg2+ sensing function in statin passive diffusion Copyright (c) 2015 John Wiley & Sons, Ltd.