[1] Pankaj Sah. Ca(2+)-activated K+ currents in neurones: types, physiological roles and modulation[J]. Trends Neurosci, 1996, 19(4):150-154.[2] Nicholas P Poolos, Daniel Johnston. Calcium-activated potassium conductances contribute to action potential repolarization at the soma but not the dendrites of hippocampal CA1 pyramidal neurons[J]. J Neurosci, 1999, 19(13):5205-5212.[3] Juan Martinez-Pinna, Philip J Davies, Elspeth M McLachlan. Diversity of channels involved in Ca(2+) activation of K(+) channels during the prolonged AHP in guinea-pig sympathetic neurons[J]. J Neurophysiol, 2000, 84(3):1346-1354.[4] E S Louise Faber, Pankaj Sah. Ca2+-activated K+ (BK) channel inactivation contributes to spike broadening during repetitive firing in the rat lateral amygdala [J]. J Physiol, 2003, 552(Pt 2):483-497.[5] Womack MD, Hoang C, Khodakhah K. Large conductance calcium-activated potassium channels affect both spontaneous firing and intracellular calcium concentration in cerebellar Purkinje neurons[J]. Neuroscience, 2009, 162(4):989-1000.[6] Haghdoost-Yazdi H, Janahmadi M, Behzadi G. Iberiotoxin-sensitive large conductance Ca2+ -dependent K+ (BK) channels regulate the spike configuration in the burst firing of cerebellar Purkinje neurons[J]. Brain Res, 2008, 1212:1-8.[7] Lancaster B, Nicoll RA, Perkel DJ. Calcium activates two types of potassium channels in rat hippocampal neurons in culture[J]. J Neurosci, 1991, 11(1):23-30.[8] Lee BC, Lim HH, Kim S, et al. Localization of a site of action for benzofuroindole-induced potentiation of BKCa channels[J]. Mol Pharmacol, 2012, 82(2):143-155.[9] Shao Li-rong, Ragnhild Halvorsrud, Lyle Borg-Graham, et al. The role of BK-type Ca2+-dependent K+ channels in spike broadening during repetitive firing in rat hippocampal pyramidal cells[J]. J Physiol, 1999, 521 (Pt 1):135-146.[10] Marianne R Smith, Alexandra B Nelson, Sascha Du Lac. Regulation of firing response gain by calcium-dependent mechanisms in vestibular nucleus neurons[J]. J Neurophysiol, 2002, 87(4):2031-2042.[11] Sun Fang, Emiko Hayama, Yasuhiro Katsube, et al. The role of the large-conductance voltage-dependent and calcium-activated potassium (BK(Ca)) channels in the regulation of rat ductus arteriosus tone[J]. Heart Vessels, 2010, 25(6):556-564.[12] Alexandra B Nelson, Claudia M Krispel, Chris Sekirnjak, et al. Long-lasting increases in intrinsic excitability triggered by inhibition[J]. Neuron, 2003, 40(3):609-620.[13] Andrea L Meredith, Steven W Wiler, Brooke H Miller, et al. BK calcium-activated potassium channels regulate circadian behavioral rhythms and pacemaker output[J]. Nat Neurosci, 2006, 9(8):1041-1049.[14] Edwin Santini, Gregory J Quirk, James T Porter. Fear conditioning and extinction differentially modify the intrinsic excitability of infralimbic neurons[J]. J Neurosci, 2008, 28(15):4028-4036.[15] Elizabeth A Matthews, Aldis P Weible, Samit Shah, et al. The BK-mediated fAHP is modulated by learning a hippocampus-dependent task[J]. Proc Natl Acad Sci USA, 2008, 105(39):15154-15159.[16] Guo YY, Liu SB, Cui GB, et al. Acute stress induces down-regulation of large-conductance Ca2+-activated potassium channels in the lateral amygdala[J]. J Physiol, 2012, 590(Pt 4):875-886.[17] Bliss TV, Collingridge GL. A synaptic model of memory: long-term potentiation in the hippocampus[J]. Nature, 1993, 361(6407):31-39.[18] Stephen Maren. Long-term potentiation in the amygdala: a mechanism for emotional learning and memory[J]. Trends Neurosci, 1999, 22(12):561-567.[19] Zhao Ming-gao, Toyoda Hiroki, Lee Yong Seok, et al. Roles of NMDA NR2B subtype receptor in prefrontal long-term potentiation and contextual fear memory[J]. Neuron, 2005, 47(6):859-872.[20] Jeffry S Isaacson, Gabe J Murphy. Glutamate-mediated extrasynaptic inhibition: direct coupling of NMDA receptors to Ca(2+)-activated K+ channels[J]. Neuron, 2001, 31(6):1027-1034.[21] Wang Han-sen, Wu Long-jun, Susan S Kim, et al. FMRP acts as a key messenger for dopamine modulation in the forebrain[J]. Neuron, 2008, 59(4):634-647.[22] Brewer G J, Torricelli J R, Evege E K, et al. Optimized survival of hippocampal neurons in B27-supplemented Neurobasal, a new serum-free medium combination[J]. J Neurosci Res, 1993, 35(5):567-576.[23] Evgeny Tsvetkov, Ryong Moon Shin, Vadim Y Bolshakov. Glutamate uptake determines pathway specificity of long-term potentiation in the neural circuitry of fear conditioning[J]. Neuron, 2004, 41(1):139-151.[24] Evgeny Tsvetkov, William A Carlezon, Francine M Benes, et al. Fear conditioning occludes LTP-induced presynaptic enhancement of synaptic transmission in the cortical pathway to the lateral amygdala[J]. Neuron, 2002, 34(2):289-300.[25] Wu Long-jun, Shanelle W Ko, Hiroki Toyoda, et al. Increased anxiety-like behavior and enhanced synaptic efficacy in the amygdala of GluR5 knockout mice[J]. PLoS One, 2007, 2(1):e167.[26] Mala M Shah, Dennis G Haylett. K+ currents generated by NMDA receptor activation in rat hippocampal pyramidal neurons[J]. J Neurophysiol, 2002, 87(6):2983-2989.[27] Ko Shanelle, Zhao Ming-gao, Toyoda Hiroki, et al. Altered behavioral responses to noxious stimuli and fear in glutamate receptor 5 (GluR5)- or GluR6-deficient mice[J]. J Neurosci, 2005, 25(4):977-984.[28] Roger A Nicoll, Robert C Malenka. Contrasting properties of two forms of long-term potentiation in the hippocampus[J]. Nature, 1995, 377(6545):115-118.[29] Zalutsky R A, Nicoll R A. Comparison of two forms of long-term potentiation in single hippocampal neurons[J]. Science, 1990, 248(4963):1619-1624.[30] Bernd Fakler, John P Adelman. Control of K(Ca) channels by calcium nano/microdomains[J]. Neuron, 2008, 59(6):873-881.[31] Jeremy R Edgerton, Peter H Reinhart. Distinct contributions of small and large conductance Ca2+-activated K+ channels to rat Purkinje neuron function[J]. J Physiol, 2003, 548(Pt 1):53-69.[32] Murali Prakriya, Christopher J Lingle. BK channel activation by brief depolarizations requires Ca2+ influx through L- and Q-type Ca2+ channels in rat chromaffin cells[J]. J Neurophysiol, 1999, 81(5):2267-2278.[33] Andreas Muller, Maria Kukley, Mischa Uebachs, et al. Nanodomains of single Ca2+ channels contribute to action potential repolarization in cortical neurons[J]. J Neurosci, 2007, 27(3):483-495.[34] Thu Jennifer Ngo-Anh, Brenda L Bloodgood, Michael Lin, et al. SK channels and NMDA receptors form a Ca2+-mediated feedback loop in dendritic spines[J]. Nat Neurosci, 2005, 8(5):642-649.[35] Faber ES, Delaney AJ, Sah P. SK channels regulate excitatory synaptic transmission and plasticity in the lateral amygdala[J]. Nat Neurosci, 2005, 8(5):635-641.[36] Robert Pawlak, Ana Maria Magarinos, Jerry Melchor, et al. Tissue plasminogen activator in the amygdala is critical for stress-induced anxiety-like behavior[J]. Nat Neurosci, 2003, 6(2):168-174.[37] Ingrid Ehrlich, Yann Humeau, Francois Grenier, et al. Amygdala inhibitory circuits and the control of fear memory[J]. Neuron, 2009, 62(6):757-771.[38] Jonathan C Gewirtz, Michael Davis. Second-order fear conditioning prevented by blocking NMDA receptors in amygdala[J]. Nature, 1997, 388(6641):471-474.[39] Gregory J Quirk, Christopher Repa, Joseph E LeDoux. Fear conditioning enhances short-latency auditory responses of lateral amygdala neurons: parallel recordings in the freely behaving rat[J]. Neuron, 1995, 15(5):1029-1039. |