Acetylcholine-induced membrane currents and excitatory postsynaptic currents (EPSCs) were recorded from the neurons of rat superior cervical ganglion (SCG) using the whole-cell patch clamp and the two-electrode voltage clamp techniques, correspondingly. The EPSC decay was bi-exponential, with fast and slow components characterized by time constants 5.5 +/- 0.5 msec and 20.4 +/- 1.2 msec (mean +/- SEM; n = 23), respectively. Blocking of these currents by a series of newly synthesized bis-cationic ammonium compounds, the pentamethonium and pentaethonium derivatives, was analyzed. Blocking effects were due to a block of nicotinic acetylcholine receptor (nAChR) open channel, with mean blocker binding rate constants for the fast component three to five times higher than those for the slow component. Dimensions of a nAChR ionic channel were deduced from a relationship between blocking activity of the compounds and the size of the projections of their three-dimensional molecular models on the neuronal membrane plane. The results suggest that there are two populations of nAChRs in rat SCG neurons; while these polulations differ in the rate constants of the binding by the blocker to their open channels, they exhibit similar channel diameter, 11.8 A, at the level at which the blockers bind to the channel.

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The participation of definite molecular fragments of bis-cationic ammonium compounds in their blocking effect upon neuronal nicotinic acetylcholine receptors (nAChRs) was deduced from the relationship between the blocking efficacy and three-dimensional molecular models of such compounds that have different fragments. The data on the structure and activity of 15 channel blockers were used for this purpose; predicted blocking effects of the substances were calculated. The correlation coefficients between the blocking activity of the compounds and their predicted efficacy were statistically significant (P > 0.95). The results suggest that HCNCCCCCNCH and HCCNCCCCCNCH fragments (atom chains) with the dimensions of 1.42 and 1.36 nm, respectively, provide the most positive contribution, while a HCNCCCCCNCH fragment with the dimension of 1.36 nm corresponds to highly negative contribution to the blocking activity of compounds. Using the data obtained, we identified the optimum compound structures. The mechanism of the blocking effect upon nAChRs is discussed.Keywords: nicotinic acetylcholine receptor, channel blockers, open channel block, bis-quaternary ammonium compounds, quantitative structure/activity relationship (QSAR).

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