Activation and inhibition of rat neuronal nicotinic receptors by ABT-418

Abstract

1. ABT-418 appeared to function as a relatively broad spectrum activator of neuronal nicotinic receptors, expressed in Xenopus oocytes, with little cross reactivity to the mammalian muscle receptor subtype. However, the relative potencies of ABT-418 at the various subtypes differed from those acetylcholine (ACh). For example, ACh was most potent at α3β2 (EC₅₀≈30 μM) and least potent at α2β2 (EC₅₀≈500 μM). ABT-418 was most potent at α4β2 and α2β2 (EC₅₀≈6 μM and 11 μM, respectively) and least potent at α3β4 (EC₅₀≈188 μM).

2. In addition to activating neuronal receptors, ABT-418 exhibited complex properties, including the inhibition of ACh responses.

3. The current responses elicited by relatively high concentrations of ABT-418 on the α4β2 receptor subtype were protracted beyond the application interval. The coapplication of ABT-418 with either of the use-dependent inhibitors bis(1,2,2,6,6-tetramethyl-4-pipendimyl)sebacate (BTMPS) or tetramethyl-pipenidine (TMP) eliminated the late protracted phase of the currents with only small effects on the initial activation phase. When the reversible inhibitor TMP was washed from the bath, the previously inhibited late current reappeared, suggesting that the observed mixed agonist-antagonist effects of ABT-418 and (±)-epibatidine on α₄β₂ were due to a concentration-dependent noncompetitive inhibition, an effect similar to that obtained for (−)-nicotine.

4. The inhibition of α4β2 receptors by ABT-418 was voltage-dependent. When high concentrations of ABT-418 were applied under depolarizing conditions, additional late currents could be observed under conditions which suggested that a build up of ABT-418 in an unstirred layer over the surface of the oocyte was occurring. This may have been due to the dissociation of the drug from channel blocking sites on the receptors themselves, or alternatively, from the plasma membrane of the cells.

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