Multiple binding sites for local anesthetics in membranes: characterization of the sites and their equilibria by deuterium NMR of specifically deuterated procaine and tetracaine

Abstract

Anesthetics bound to model membranes were observed directly by 2H NMR. The specifically deuterated local anesthetics, procaine and tetracaine, were synthesized, and their partition coefficients (water:phosphatidylcholine) and pKa values determined. The interaction of these anesthetics with lamellar dispersions of egg phosphatidylcholine was studied by 2H NMR, and by electron spin resonance (ESR) of a spin-labeled phospholipid at low (5.5) and high (9.5) pH. The ESR experiments suggest that tetracaine intercalates in the membrane, and that it equilibrates between water and the phospholipid bilayers of the multilamellar system. The NMR results are consistent with a model in which the anesthetic is free in water, weakly-bound to the membrane, and strongly-bound to it. A fast exchange exists between the 2 1st sites, but exchange is slow with the 3rd site. Binding of type 3 is observed only at high pH for procaine, whereas it is found both at low and high pH for tetracaine. Calculations of the partition coefficients for the charged and uncharged forms of tetracaine indicate that both sites, 2 and 3, are occupied by the charged form at low pH, and by the uncharged form at high pH. The partition coefficient for the weakly-bound species was estimated from an analysis of the dependence of line width on the lipid to water ratio. The NMR data suggest that the binding sites for the strongly-bound charged and uncharged species are different, the former probably being closer to the membrane-water interface. Estimates of molecular order parameters for the strongly-bound species indicate that it is located with its long molecular axis approximately parallel to the director for ordering of the fatty acyl chains. A small increase in lipid ordering by tetracaine is observed at low pH, as evidenced by 2H NMR of the deuterated N-methyl groups of phosphatidylcholine; the reverse occurs at high pH.