Pharmacological dissection of AHP currents

GH Go Eun Ha
JL Jaekwang Lee
HK Hankyul Kwak
KS Kiyeong Song
JK Jea Kwon
SJ Soon-Young Jung
JH Joohyeon Hong
GC Gyeong-Eon Chang
EH Eun Mi Hwang
HS Hee-Sup Shin
CL C. Justin Lee
EC Eunji Cheong
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For dissection of AHP currents, the intrapipette solution contained KCl, 60 mM; K-gluconate, 73 mM; MgSO4, 1 mM; HEPES, 10 mM; EGTA, 0.1 mM; Mg-ATP, 4 mM; and Na2-GTP, 0.3 mM (pH 7.35 and 285 mOsm). TTX (0.5 μM), apamin (0.1 μM) and/or NFA (100 μM) were applied after achieving the whole-cell configuration. The bath solution was treated with TTX for recordings of Ca2+-dependent AHP currents and was perfused with TTX and apamin in order to obtain apamin-sensitive K+ currents. For dissection of NFA-sensitive anion currents, recording aCSF was perfused with TTX, apamin and NFA. Apamin-sensitive K+ currents and NFA-sensitive anion currents were calculated by trace subtraction.

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