Modulation of potassium channels via the α1B-adrenergic receptor in human osteoblasts

被引:7
作者
Kodama, Daisuke [1 ]
Togari, Akifumi [1 ]
机构
[1] Aichi Gakuin Univ, Sch Dent, Dept Pharmacol, Chikusa Ku, Nagoya, Aichi 4648650, Japan
关键词
Noradrenaline; Human osteoblast; Sympathetic nerve system; alpha(1B)-Adrenergic receptor; Potassium channel; SYMPATHETIC-NERVOUS-SYSTEM; BONE-RESORPTION; ACTIVATION; EXPRESSION; DIFFERENTIATION; PROLIFERATION; STIMULATION; CURRENTS; SUBTYPE; PROTEIN;
D O I
10.1016/j.neulet.2010.08.073
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Recent studies have demonstrated the involvement of the sympathetic nerve system in bone metabolism We have previously demonstrated the expression of adrenergic receptors in the human osteoblast SaM-1 cell line The aim of this study was to reveal the function of these receptors in osteoblasts using electrophysiological methods During whole-cell patch clamp recording, the application of noradrenaline reduced the currents Induced by a voltage ramp, and the effect was larger in the positive potential range Pretreatment with the selective alpha(1B)-adrenergic receptor antagonist chloroethylclonidine eliminated the inhibitory effect of noradrenaline Using Cs-based pipette solution to block potassium channels, the inhibitory effect of noradrenaline disappeared In contrast, the effect was unaffected in the presence of tetraethylammonium (TEA), a potassium channel blocker These results suggest that noradrenaline suppresses Cs-sensitive and TEA-insensitive potassium channels via the alpha(1B)-adrenergic receptor in human osteoblasts (C) 2010 Elsevier Ireland Ltd. All rights reserved
引用
收藏
页码:102 / 106
页数:5
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