首页> 外文期刊>Journal of Veterinary Science >Korean red ginseng excitation of paraventricular nucleus neurons via non-N-methyl-D-aspartate glutamate receptor activation in mice
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Korean red ginseng excitation of paraventricular nucleus neurons via non-N-methyl-D-aspartate glutamate receptor activation in mice

机译:非红-甲基-D-天冬氨酸谷氨酸受体激活小鼠脑室旁核神经元的高丽红参激发

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It has been reported that Korean red ginseng (KRG), a valuable and important traditional medicine, has varied effects on the central nervous system, suggesting its activities are complicated. The paraventricular nucleus (PVN) neurons of the hypothalamus has a critical role in stress responses and hormone secretions. Although the action mechanisms of KRG on various cells and systems have been reported, the direct membrane effects of KRG on PVN neurons have not been fully described. In this study, the direct membrane effects of KRG on PVN neuronal activity were investigated by using a perforated patch-clamp in ICR mice. In gramicidin perforated patch-clamp mode, KRG extract (KRGE) induced repeatable depolarization followed by hyperpolarization of PVN neurons. The KRGE-induced responses were concentration- dependent and persisted in the presence of tetrodotoxin, a voltage sensitive Na+ channel blocker. The KRGE-induced responses were suppressed by 6-cyano-7-nitroquinoxaline-2,3-dione (10 μM), a non-N-methyl-D-aspartate (NMDA) glutamate receptor antagonist, but not by picrotoxin, a type A gamma-aminobutyric acid receptor antagonist. The results indicate that KRG activates non-NMDA glutamate receptors of PVN neurons in mice, suggesting that KRG may be a candidate for use in regulation of stress responses by controlling autonomic nervous system and hormone secretion.
机译:据报道,韩国人参(KRG)是一种宝贵而重要的传统药物,对中枢神经系统有多种作用,表明其活动很复杂。下丘脑的室旁核(PVN)神经元在应激反应和激素分泌中起关键作用。尽管已报道了KRG对各种细胞和系统的作用机制,但尚未完全描述KRG对PVN神经元的直接膜作用。在这项研究中,通过在ICR小鼠中使用穿孔的膜片钳研究了KRG对PVN神经元活性的直接膜作用。在以短杆菌肽穿孔的膜片钳模式下,KRG提取物(KRGE)引起可重复的去极化,然后PVN神经元超极化。 KRGE诱导的反应是浓度依赖性的,并在河豚毒素(一种电压敏感的Na + 通道阻滞剂)存在下持续存在。 KRGE诱导的反应被一种非N-甲基-D-天冬氨酸(NMDA)谷氨酸受体拮抗剂6-氰基-7-硝基喹喔啉-2,3-二酮(10μM)抑制,但未被一种类型的微毒素抑制γ-氨基丁酸受体拮抗剂。结果表明,KRG激活了小鼠PVN神经元的非NMDA谷氨酸受体,这表明KRG可能是通过控制自主神经系统和激素分泌来调节应激反应的候选药物。

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