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食欲素A和B可引起大鼠大脑皮质切片释放去甲肾上腺素。

Orexin A and B evoke noradrenaline release from rat cerebrocortical slices.

作者信息

Hirota K, Kushikata T, Kudo M, Kudo T, Lambert D G, Matsuki A

机构信息

Department of Anesthesiology, University of Hirosaki School of Medicine, Hirosaki 036-8563, Japan.

出版信息

Br J Pharmacol. 2001 Dec;134(7):1461-6. doi: 10.1038/sj.bjp.0704409.

Abstract
  1. Orexin A and B, recently identified in the rat hypothalamus are endogenous neuropeptide agonists for the G-protein coupled orexin-1 (OX1) and orexin-2 (OX2) receptors. 2. In the present study, we have examined the effects of orexin A, B and raised extracellular K(+) on noradrenaline release from the rat cerebrocortical slice. We have compared this with other sleep-wake-related (excitatory) neurotransmitters; dopamine, glutamate, serotonin and histamine. 3. Neurotransmitter release studies were performed in rat cerebrocortical slices incubated in modified Krebs buffer (with and without Ca(2+)+EGTA 1 mM) with various concentrations of orexin A, B and K(+) for various times. 4. Orexin A and B-evoked (10(-7) M) noradrenaline release was time-dependent reaching a maximum some 10 min after stimulation. K(+) (40 mM) evoked release was also time dependent but reached a maximum after 6 min. Orexin A, B and K(+) stimulation of release was concentration dependent with pEC(50) and E(max) (% of basal) values of 8.74+/-0.32 (1.8 nM) and 263+/-14% and 8.61+/-0.38 (2.4 nM) and 173+/-7% and 1.43+/-0.02 (37 mM) and 1430+/-70%, respectively. Orexin-evoked release was partially extracellular Ca(2+) dependent. 5. Of the other transmitters studied there was a weak orexin A and B stimulation of glutamate release. In contrast K(+) evoked dopamine, glutamate, histamine and serotonin release with pEC(50) and E(max) (% of basal) values of 1.47+/-0.05 (34 mM) and 3430+/-410%, 1.38+/-0.04 (42 mM) and 1240+/-50%, 1.47+/-0.02 (34 mM) and 480+/-10% and 1.40+/-0.05 (40 mM) and 560+/-60% respectively. 6. We conclude that the neuropeptides orexin A and B evoke noradrenaline release from rat cerebrocortical slices.
摘要
  1. 食欲素A和B最近在大鼠下丘脑被发现,是G蛋白偶联的食欲素-1(OX1)和食欲素-2(OX2)受体的内源性神经肽激动剂。2. 在本研究中,我们检测了食欲素A、B以及细胞外钾离子浓度升高对大鼠大脑皮质切片去甲肾上腺素释放的影响。我们将其与其他与睡眠-觉醒相关的(兴奋性)神经递质;多巴胺、谷氨酸、5-羟色胺和组胺进行了比较。3. 在含有不同浓度的食欲素A、B和钾离子的改良Krebs缓冲液(含和不含1 mM Ca2+ + EGTA)中孵育的大鼠大脑皮质切片上,进行了不同时间的神经递质释放研究。4. 食欲素A和B诱发(10-7 M)的去甲肾上腺素释放呈时间依赖性,刺激后约10分钟达到最大值。钾离子(40 mM)诱发的释放也呈时间依赖性,但在6分钟后达到最大值。食欲素A、B和钾离子对释放的刺激呈浓度依赖性,其pEC50和E(max)(基础值的百分比)分别为8.74±0.32(1.8 nM)和263±14%、8.61±0.38(2.4 nM)和173±7%、1.43±0.02(37 mM)和1430±70%。食欲素诱发的释放部分依赖于细胞外钙离子。5. 在研究的其他递质中,食欲素A和B对谷氨酸释放有微弱刺激作用。相比之下,钾离子诱发多巴胺、谷氨酸、组胺和5-羟色胺释放,其pEC50和E(max)(基础值的百分比)分别为1.47±0.05(34 mM)和3430±410%、1.38±0.04(42 mM)和1240±50%、1.47±0.02(34 mM)和480±10%以及1.

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