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从双斑蟋(Gryllus bimaculatus)大脑蘑菇体分离出的肯扬细胞中钠激活钾通道的单胺能调节。

Monoaminergic modulation of the Na+-activated K+ channel in Kenyon cells isolated from the mushroom body of the cricket (Gryllus bimaculatus) brain.

作者信息

Aoki Kozue, Kosakai Kumiko, Yoshino Masami

机构信息

Department of Biology, Tokyo Gakugei University, Tokyo, Japan.

出版信息

J Neurophysiol. 2008 Sep;100(3):1211-22. doi: 10.1152/jn.90459.2008. Epub 2008 Jun 11.

Abstract

Recent studies have suggested that octopamine (OA) and dopamine (DA) play important roles in mediating the reward and punishment signals, respectively, in olfactory learning in insect. However, their target molecules and the signaling mechanisms are not fully understood. In this study, we showed for the first time that OA and DA modulate the Na+-activated K+ (KNa) channels in an opposite way in Kenyon cells isolated from the mushroom body of the cricket, Gryllus bimaculatus. Patch-clamp recordings showed that the single-channel conductance of the KNa channel was about 122 pS with high K+ in the patch pipettes. The channel was found to be activated by intracellular Na+ but less activated by Li+. K+ channel blockers TEA and quinidine reduced the open probability (Po) of this channel. Bath application of OA and DA respectively increased and decreased the Po of KNa channel currents. An increase and a decrease in Po of KNa channels were also observed by applying the membrane-permeable analogs 8-Br-cyclic-AMP and 8-Br-cGMP, respectively. Furthermore, it was revealed that cAMP-induced increase and cGMP-induced decrease in Po were attenuated by the specific protein kinase A (PKA) inhibitor H-89 and protein kinase G (PKG) inhibitor KT5823, respectively. These results indicate that the KNa channel is a target molecule for OA and DA and that cAMP/PKA and cGMP/PKG signaling pathways are also involved in the modulation of KNa channels.

摘要

最近的研究表明,章鱼胺(OA)和多巴胺(DA)分别在昆虫嗅觉学习中调节奖赏和惩罚信号方面发挥重要作用。然而,它们的靶分子和信号传导机制尚未完全了解。在本研究中,我们首次表明,OA和DA以相反的方式调节从双斑蟋蟀蘑菇体分离的肯扬细胞中的钠激活钾(KNa)通道。膜片钳记录显示,当膜片电极内为高钾时,KNa通道的单通道电导约为122 pS。发现该通道由细胞内钠离子激活,但对锂离子的激活作用较小。钾通道阻滞剂TEA和奎尼丁降低了该通道的开放概率(Po)。分别浴用OA和DA可增加和降低KNa通道电流的Po。分别应用膜通透性类似物8-溴环磷酸腺苷(8-Br-cyclic-AMP)和8-溴环磷酸鸟苷(8-Br-cGMP)也观察到KNa通道Po的增加和降低。此外,还发现cAMP诱导的Po增加和cGMP诱导的Po降低分别被特异性蛋白激酶A(PKA)抑制剂H-89和蛋白激酶G(PKG)抑制剂KT5823减弱。这些结果表明,KNa通道是OA和DA的靶分子,并且cAMP/PKA和cGMP/PKG信号通路也参与KNa通道的调节。

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