Differential modulation of TWIK-related K+ channel (TREK) and TWIK-related acid-sensitive K+ channel 2 (TASK2) activity by pyrazole compounds

Abstract

Pyrazole derivatives were originally suggested as selective blockers of the transient receptor potential cation 3 (TRPC3) and channel. In particular, pyr3 and 10 selectively inhibit TRPC3, whereas pyr2 (BTP2) and 6 inhibit ORAI1. However, their effects on background K+ channel activity have not been elucidated. In this study, the effects of BTP2, pyr3, pyr6, and pyr10 were studied on cloned human TWIK-related K+ channels (TREKs) and TWIK-related acid-sensitive K+ channel 2 (TASK-2) channels, which modulate Ca2+ signaling by controlling membrane potential, in HEK293T-overexpressing cells by using a whole-cell patch clamp technique. Pyr3 potently inhibited TREK-1 (I-TREK1), TREK-2 (I-TREK2), and TASK2 current (ITASK-2) with half-maximal inhibitory concentrations (IC50) of 0.89 +/- 0.27, 1.95 +/- 1.44, and 2.42 +/- 0.39 mu M, respectively. BTP2 slightly inhibited ITASK-2 (80.3 +/- 2.5% at 100 mu M). In contrast, pyr6 at 100 mu M potentiated I-TREK1 and I-TREK2 by approximately 2.6- and 3.6-fold compared to the control and inhibited I-TASK2 (38.7 +/- 9.2%). Pyr10 showed a subtype-specific inhibition of I-TREK1 but not I-TREK2. It also inhibited I-TASK2 (70.9 +/- 3.1% at 100 mu M). To the best of our knowledge, this study is the first to describe the differential modulation of TREKs and TASK2 channels by pyrazole derivatives, previously used as inhibitors of TRPC3 and ORAI1. Therefore, studies using these drugs should consider their modulation of other channels such as TREK and TASK-2.