Background and tandem-pore potassium channels in magnocellular neurosecretory cells of the rat supraoptic nucleus

被引:66
作者
Han, J
Gnatenco, C
Sladek, CD
Kim, D
机构
[1] Finch Univ Hlth Sci, Chicago Med Sch, Dept Physiol & Biophys, N Chicago, IL 60064 USA
[2] Univ Colorado, Ctr Hlth Sci, Dept Physiol, Denver, CO USA
[3] Gyeongsang Natl Univ, Sch Med, Dept Physiol, Chinju, South Korea
来源
JOURNAL OF PHYSIOLOGY-LONDON | 2003年 / 546卷 / 03期
关键词
D O I
10.1113/jphysiol.2002.032094
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Magnocellular neurosecretory cells (MNCs) were isolated from the supraoptic nucleus of rat hypothalamus, and properties of K+ channels that may regulate the resting membrane potential and the excitability of MNCs were studied. MNCs showed large transient outward currents, typical of vasopressin- and oxytocin-releasing neurons. K+ channels in MNCs were identified by recording K+ channels that were open at rest in cell-attached and inside-out patches in symmetrical 150 mm KCL Eight different K+ channels were identified and could be distinguished unambiguously by their single-channel kinetics and voltage-dependent rectification. Two K+ channels could be considered functional correlates of TASK-1 and TASK-3, as judged by their single-channel kinetics and high sensitivity to pH(o). Three K+ channels showed properties similar to TREK-type tandem-pore K+ channels (TREK-1, TREK-2 and a novel TREK), as judged by their activation by membrane stretch, intracellular acidosis and arachidonic acid. One K+ channel was activated by application of pressure, arachidonic acid and alkaline pH(i), and showed single-channel kinetics indistinguishable from those of TRAAK. One K+ channel showed strong inward rectification and single-channel conductance similar to those of a classical inward rectifier, IRK3. Finally, a K+ channel whose cloned counterpart has not yet been identified was highly sensitive to extracellular pH near the physiological range similar to those of TASK channels, and was the most active among all K+ channels. Our results show that in MNCs at rest, eight different types of K+ channels can be found and six of them belong to the tandem-pore K+ channel family. Various physiological and pathophysiological conditions may modulate these K+ channels and regulate the excitability of MNCs.
引用
收藏
页码:625 / 639
页数:15
相关论文
共 57 条
[21]   Caesium blocks depolarizing after-potentials and phasic firing in rat supraoptic neurones [J].
Ghamari-Langroudi, M ;
Bourque, CW .
JOURNAL OF PHYSIOLOGY-LONDON, 1998, 510 (01) :165-175
[22]   Single cell reverse transcription-polymerase chain reaction analysis of rat supraoptic magnocellular neurons:: Neuropeptide phenotypes and high voltage-gated calcium channel subtypes [J].
Glasgow, E ;
Kusano, K ;
Chin, HM ;
Mezey, É ;
Young, WS ;
Gainer, H .
ENDOCRINOLOGY, 1999, 140 (11) :5391-5401
[23]   Potassium leak channels and the KCNK family of two-P-domain subunits [J].
Goldstein, SAN ;
Bockenhauer, D ;
O'Kelly, I ;
Zilberberg, N .
NATURE REVIEWS NEUROSCIENCE, 2001, 2 (03) :175-184
[24]   Characterization of four types of background potassium channels in rat cerebellar granule neurons [J].
Han, J ;
Truell, J ;
Gnatenco, C ;
Kim, D .
JOURNAL OF PHYSIOLOGY-LONDON, 2002, 542 (02) :431-444
[25]   Inwardly rectifying potassium channels: Their molecular heterogeneity and function [J].
Isomoto, S ;
Kondo, C ;
Kurachi, Y .
JAPANESE JOURNAL OF PHYSIOLOGY, 1997, 47 (01) :11-39
[26]  
Karschin C, 1996, J NEUROSCI, V16, P3559
[27]   ARACHIDONIC-ACID ACTIVATION OF A NEW FAMILY OF K+ CHANNELS IN CULTURED RAT NEURONAL CELLS [J].
KIM, DH ;
SLADEK, CD ;
AGUADOVELASCO, C ;
MATHIASEN, JR .
JOURNAL OF PHYSIOLOGY-LONDON, 1995, 484 (03) :643-660
[28]   Synergistic interaction and the rose of C-terminus in the activation of TRAAK K+ channels by pressure, free fatty acids and alkali [J].
Kim, Y ;
Bang, H ;
Gnatenco, C ;
Kim, D .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 2001, 442 (01) :64-72
[29]   TBAK-1 and TASK-1, two-pore K+ channel subunits:: kinetic properties and expression in rat heart [J].
Kim, Y ;
Bang, H ;
Kim, D .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1999, 277 (05) :H1669-H1678
[30]   TASK-3, a new member of the tandem pore K+ channel family [J].
Kim, Y ;
Bang, H ;
Kim, D .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (13) :9340-9347