Effective activation of bk_ca channels by qo-40 (5-(chloromethyl)-3-(naphthalen-1-yl)-2-(trifluoromethyl)pyrazolo [1,5-a]pyrimidin-7(4h)-one), known to be an opener of kcnq2/q3 channels

QO-40 (5-(chloromethyl)-3-(naphthalene-1-yl)-2-(trifluoromethyl) pyrazolo[1,5-a]pyrimidin-7(4H)-one) is a novel and selective activator of KCNQ2/KCNQ3 K⁺ channels. However, it remains largely unknown whether this compound can modify any other type of plasmalemmal ionic channel. The effects of QO-40 on ion channels in pituitary GH₃ lactotrophs were investigated in this study. QO-40 stimulated Ca²⁺-activated K⁺ current (I_K(Ca) ) with an EC₅₀ value of 2.3 µM in these cells. QO-40-stimulated I_K(Ca) was attenuated by the further addition of GAL-021 or paxilline but not by linopirdine or TRAM-34. In inside-out mode, this compound added to the intracellular leaflet of the detached patches stimulated large-conductance Ca²⁺-activated K⁺ (BK_Ca ) channels with no change in single-channel conductance; however, there was a decrease in the slow component of the mean closed time of BK_Ca channels. The K_D value required for the QO-40-mediated decrease in the slow component at the mean closure time was 1.96 µM. This compound shifted the steady-state activation curve of BK_Ca channels to a less positive voltage and decreased the gating charge of the channel. The application of QO-40 also increased the hysteretic strength of BK_Ca channels elicited by a long-lasting isosceles-triangular ramp voltage. In HEK293T cells expressing α-hSlo, QO-40 stimulated BK_Ca channel activity. Overall, these findings demonstrate that QO-40 can interact directly with the BK_Ca channel to increase the amplitude of I_K(Ca) in GH₃ cells.