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小鼠肛门尾骨肌中突触后α-肾上腺素能受体的药理学

Pharmacology of postsynaptic alpha-adrenoreceptors in the mouse anococcygeus muscle.

作者信息

Gibson A, Yu O

出版信息

J Auton Pharmacol. 1983 Mar;3(1):1-6. doi: 10.1111/j.1474-8673.1983.tb00490.x.

Abstract
  1. The alpha-adrenoreceptor agonists noradrenaline (NA), methoxamine, phenylephrine, naphazoline, oxymetazoline, and xylazine produced contractions of the mouse anococcygeus muscle. All were full agonists. 2. Cocaine (2 microM) increased the pD2 values of NA and phenylephrine. 6-hydroxydopamine pretreatment increased the pD2 values of NA, phenylephrine, and xylazine. After both procedures the order of potency of the agonists was oxymetazoline greater than naphazoline greater than NA greater than phenylephrine greater than methoxamine greater than xylazine. 3. The order of potency of antagonists against all six agonists was prazosin greater than phentolamine greater than yohimbine. However, from differences in the pA2 values and slopes of the Schild plots of the antagonists it was possible to distinguish three distinct groups of agonists: the phenylethylamines; the imidazolines; and the thiazine derivative xylazine. 4. The results suggest that the postsynaptic alpha-adrenoreceptor of the mouse anococcygeus muscle may be broadly classified as alpha 1. However, there may be at least three drug recognition sites on the receptor which interact with agonists of differing chemical structure.
摘要
  1. α-肾上腺素能受体激动剂去甲肾上腺素(NA)、甲氧明、去氧肾上腺素、萘甲唑啉、羟甲唑啉和赛拉嗪可使小鼠肛门尾骨肌收缩。它们均为完全激动剂。2. 可卡因(2微摩尔)提高了NA和去氧肾上腺素的pD2值。6-羟基多巴胺预处理提高了NA、去氧肾上腺素和赛拉嗪的pD2值。经过这两种处理后,激动剂的效价顺序为羟甲唑啉>萘甲唑啉>NA>去氧肾上腺素>甲氧明>赛拉嗪。3. 针对所有六种激动剂的拮抗剂效价顺序为哌唑嗪>酚妥拉明>育亨宾。然而,根据拮抗剂的pA2值和舒尔德图斜率的差异,可以区分出三种不同的激动剂组:苯乙胺类;咪唑啉类;以及噻嗪衍生物赛拉嗪。4. 结果表明,小鼠肛门尾骨肌的突触后α-肾上腺素能受体可大致归类为α1。然而,该受体上可能至少有三个药物识别位点,它们与化学结构不同的激动剂相互作用。

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