The Binding of Donepezil with External Mouth of K+-Channels of Molluscan Neurons

Springer Science and Business Media LLC - Tập 29 - Trang 219-224 - 2008
Elena I. Solntseva1, Julia V. Bukanova1, Evgeny V. Marchenko1, Alexey V. Rossokhin1, Vladimir G. Skrebitsky1
1Department of Brain Research, Center of Neurology RAMS, Moscow, Russia

Tóm tắt

Earlier, we have shown a strong inhibitory effect of donepezil on K+-current of molluscan neurons (Solntseva et al., Comp Biochem Physiol 144, 319–326, 2007). In the present work, a possible interaction of donepezil with the external mouth of the channel was examined using, as a tool, tetraethylammonium (TEA), a classical antagonist of potassium channels. Experiments were conducted in isolated neurons of snail Helix aspersa using the two-microelectrode voltage-clamp technique. A high-threshold slow-inactivating K+-current involving Ca2+-dependent (I C) and Ca2+-independent (I K) components was recorded. The I C was estimated at 30 mV, and I K at 100 mV. The IC50 values for blocking effect of donepezil on I C varied from 5.0 to 8.9 μM in different cells. Corresponding values for I K varied from 4.9 to 9.9 μM. The IC50 values for blocking effect of TEA on I C lied in the range of 200 to 910 μM, and on I K lied in the range of 100 to 990 μM. The comparison of the effects of donepezil and TEA on the same cells revealed significant correlation between IC50 values of these effects. The value of Spearman coefficient of correlation (r) was 0.77 for I C (P < 0.05), and 0.82 for I K (P < 0.05). In the presence of TEA, the effect of donepezil, both on I C and I K, appears significantly weaker than in control solution. Dose–response curves of donepezil effect both on I C and I K were shifted right along horizontal axis when donepezil was applied in combination with TEA. Results suggest that TEA interferes with donepezil and precludes the occupation by donepezil of its own site. We suppose that the site for donepezil is situated near the TEA site with possible overlap.

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Tập 29

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