Journal of Neuroscience, Vol 4, 939-944, Copyright © 1984 by Society for Neuroscience
Thermodynamic parameters of end-plate channel blockade
JG McLarnon and DM Quastel
The reaction kinetics for drug blockade of postsynaptic channels at the
mouse neuromuscular junction were studied. The activation energies
associated with the onward and off-rate constants, from a sequential model,
were measured for procaine, scopolamine, octanol, and heptanol, and from
these the transition state thermodynamic parameters of free energy (delta
G++), enthalpy (delta H++), and entropy (delta S++) of activation were
determined. All agents showed positive entropies of activation for the
channel blocking rate constant kappa 2, with the values for the alcohols
significantly greater than those for the two positively charged local
anesthetics. No significant differences in the activation energies for the
off-rate constant kappa-2 were observed between any of the agents. The
magnitude of kappa-2 decreased as the hydrophobicity of the agent
increased. The large activation energies measured for kappa 2 and kappa-2
(in excess of 10 kcal/mol) are higher than expected for simple
rate-limiting diffusion, and the possibility exists that channel blockade
involves conformational changes in a protein segment, induced by a
hydrophobic interaction between agent and intrachannel site or sites. The
large entropy increase observed in the blocking step is indicative of the
agent replacing structured waters of hydration near a hydrophobic region of
a protein.