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首页> 外文期刊>Japanese Journal of Pharmacology >L-Dopa Potentiates Presynaptic Inhibitory α2-Adrenoceptor but Not Facilitatory Angiotensin II Receptor-Mediated Modulation of Noradrenaline Release from Rat Hypothalamic Slices
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L-Dopa Potentiates Presynaptic Inhibitory α2-Adrenoceptor but Not Facilitatory Angiotensin II Receptor-Mediated Modulation of Noradrenaline Release from Rat Hypothalamic Slices

机译:L多巴增强大鼠突触前抑制α2肾上腺素受体,但不促进血管紧张素II受体介导的去甲肾上腺素从大鼠下丘脑片释放的调节。

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References(15) Cited-By(4) L-Dopa is a potentiator for presynaptic β-adrenoceptors. We studied whether L-dopa potentiates the activities of other presynaptic receptors to modulate the evoked noradrenaline (NA) release in rat hypothalamic slices. UK14304 (0.1-1 μM), a selective α2-agonist, concentration-dependently inhibited NA release. Noneffective 10 pM L-dopa potentiated the UK14304-induced inhibition. This potentiation was selectively antagonized by 1 nM L-dopa methyl ester, a competitive L-dopa antagonist, while yohimbine antagonized both the inhibition by UK14304 alone and its potentiation by L-dopa. However, 10 pM L-dopa produced no effect on angiotensin II (0.1-1 nM)-induced facilitation. L-Dopa potentiates activities of presynaptic β- and α2-adrenoceptors but not those of angiotensin II receptors on rat hypothalamic NA neurons.
机译:参考文献(15)Cited-By(4)L-Dopa是突触前β-肾上腺素能受体的增强剂。我们研究了左旋多巴是否增强了其他突触前受体的活性,以调节大鼠下丘脑片中诱发的去甲肾上腺素(NA)释放。 UK14304(0.1-1μM),一种选择性的α2-激动剂,浓度依赖性地抑制NA的释放。无效的10 pM L-多巴可增强UK14304诱导的抑制作用。 1nM L-多巴甲酯(一种竞争性L-多巴拮抗剂)可选择性拮抗这种增强作用,而育亨宾既可单独抑制UK14304的抑制作用,又可拮抗L-多巴的增强作用。然而,10 pM L-多巴对血管紧张素II(0.1-1 nM)诱导的促进作用没有作用。 L-Dopa增强大鼠下丘脑NA神经元上突触前β-和α2-肾上腺素受体的活性,但不增强血管紧张素II受体的活性。

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