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接头前α2肾上腺素能受体调节兔隐静脉中刺激诱发的去甲肾上腺素释放。

Prejunctional alpha 2-adrenoceptors modulate stimulation-evoked norepinephrine release in rabbit lateral saphenous vein.

作者信息

Levitt B, Hieble J P

出版信息

Eur J Pharmacol. 1986 Dec 16;132(2-3):197-205. doi: 10.1016/0014-2999(86)90605-9.

Abstract

Segments of rabbit lateral saphenous vein prelabelled with [3H]noradrenaline were perfused and superfused with physiological salt solution. Tritium overflow evoked by transmural nerve stimulation (3 Hz for 2 min) was abolished by tetrodotoxin (1 microM). The selective alpha 2-adrenoceptor agonist UK 14,304 inhibited stimulation-evoked 3H-overflow in a concentration-dependent manner, with an IC50 of 71 nM. In contrast, the alpha 2-adrenoceptor agonist B-HT 933 had no effect on 3H-overflow in concentrations up to 10 microM. The selective alpha 2-adrenoceptor antagonists idazoxan and SKF 86466, as well as the non-selective alpha-antagonist phentolamine, facilitated the nerve stimulation evoked 3H-overflow, with an order of potency of idazoxan greater than or equal to phentolamine greater than SK&F 86466. Prazosin (100 nM) had little effect on 3H-overflow. These findings suggest that stimulation-evoked neurotransmitter release is modulated via prejunctional alpha 2-adrenoceptors.

摘要

预先用[3H]去甲肾上腺素标记的兔隐外侧静脉段,用生理盐溶液进行灌注和 superfused(这个词有误,可能是superfused,意为“表面灌注”)。经壁神经刺激(3Hz,持续2分钟)诱发的氚溢出被河豚毒素(1 microM)消除。选择性α2 - 肾上腺素能受体激动剂UK 14,304以浓度依赖性方式抑制刺激诱发的3H - 溢出,IC50为71 nM。相比之下,α2 - 肾上腺素能受体激动剂B - HT 933在浓度高达10 microM时对3H - 溢出没有影响。选择性α2 - 肾上腺素能受体拮抗剂咪唑克生和SKF 86466,以及非选择性α - 拮抗剂酚妥拉明,促进神经刺激诱发的3H - 溢出,效力顺序为咪唑克生大于或等于酚妥拉明大于SK&F 86466。哌唑嗪(100 nM)对3H - 溢出影响很小。这些发现表明,刺激诱发的神经递质释放是通过突触前α2 - 肾上腺素能受体调节的。

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