Surface activity of thymol: implications for an eventual pharmacological activity

SANCHEZ M.E.; TURINA A.DEL V.; GARCÍA D.A.; NOLAN M.V.; PERILLO M.A.

COLLOIDS AND SURFACES B-BIOINTERFACES

Elsevier

Año: 2004 vol. 34 p. 77 - 86

0927-7765

In the present work, we studied the ability of thymol to affect the organization of model membranes and the activity of an intrinsic membrane protein, the GABAA receptor (GABAA-R). In this last aspect, we tried to elucidate if the action mechanism of this terpene at the molecular level, involves its binding to the receptor protein, changes in the organization of the receptor molecular environment, or both. The self-aggregation of thymol in water with a critical micellar concentration (CMC)= 4uM and its ability to penetrate in monomolecular layers of soybean phosphatidylcholine (sPC) at the air–water interface, even at surface pressures above the equilibrium, lateral pressure of natural bilayers were demonstrated. Thymol affected the self-aggregation of Triton X-100 and the topology of sPC vesicles. It also increased the polarity of the membrane environment sensed by the electrochromic dye merocyanine. A dipolar moment of 1.341 Debye was calculated from its energy-minimized structure. Its effect on the binding of [3H]-flunitrazepam ([3H]-FNZ) to chick brain synaptosomal membranes changed qualitatively from a tendency to the inhibition to a clear activatory regime, up on changing the phase state of the terpene (from a monomeric to a self-aggregated state). Above its CMC, thymol increased the affinity of the binding of [3H]-FNZ (Kd-control = 2.9, Kd-thymol = 1.7 nM) without changing the receptor density (Bmax-control = 910, Bmax-thymol = 895 fmol/mg protein). The activatory effect of thymol on the binding of [3H]-FNZ was observed even in the presence of the allosteric activator gamma-aminobutyric acid (GABA) at a concentration of maximal activity, and was blocked by the GABA antagonist bicuculline. Changes in the dipolar arrangement and in the molecular packing of GABAA-R environment are discussed as possible mediators of the action mechanism of thymol