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首页> 外文期刊>Japanese Journal of Pharmacology >Carteolol Is a Useful Tool to Prove the Tonically Functioning Nature of Presynaptic β-Adrenoceptors on Peripheral Noradrenergic Neurons but Not on Central Catecholaminergic Neurons
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Carteolol Is a Useful Tool to Prove the Tonically Functioning Nature of Presynaptic β-Adrenoceptors on Peripheral Noradrenergic Neurons but Not on Central Catecholaminergic Neurons

机译:卡特洛尔是一种有用的工具,可证明周围的去甲肾上腺素能神经元具有突触前β-肾上腺素能的功能性,但不能证明中枢儿茶酚胺能神经元具有突触前的β-肾上腺素能

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References(15) Effects of carteolol on norepinephrine (NE) release were studied at 2 Hz mainly in rat hypothalamic slices. Isoproterenol at 1 and 10 nM concentrationdependently facilitated NE release. Isoproterenol (10 nM)-induced facilitation was antagonized by 1 and 10 nM dl-carteolol, but not antagonized by 1 nM d-carteolol. dl-Carteolol alone at 1 nM to 10 μM did not inhibit NE release. In brainstem slices, 10 nM isoproterenol also facilitated NE release, and this facilitation tended to be antagonized by 1 nM dl-carteolol. Nanomolar concentrations of carteolol stereoselectively antagonized isoproterenol-induced facilitation of NE release via presynaptic β-adrenoceptors in rat hypothalamic slices.
机译:参考文献(15)主要在大鼠下丘脑片中研究了在2 Hz下卡地洛尔对去甲肾上腺素(NE)释放的影响。 1和10 nM浓度的异丙肾上腺素依赖性地促进NE释放。异丙肾上腺素(10 nM)诱导的促进作用被1和10 nM dl-胡萝卜素拮抗,但没有被1 nM d-胡萝卜素拮抗。仅1 nM至10μM的dl-麦芽酚不会抑制NE的释放。在脑干切片中,10 nM异丙肾上腺素也促进了NE的释放,并且这种促进作用倾向于被1 nM dl-胡萝卜素所拮抗。纳摩尔浓度的卡特洛尔通过大鼠下丘脑片中的突触前β-肾上腺素受体立体选择性拮抗异丙肾上腺素诱导的NE释放。

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