κ3：牛肾上腺髓质中κ阿片受体位点的一种新型亚型，对甲硫氨酸脑啡肽-精氨酸6-苯丙氨酸7具有高度选择性。 - Suppr | 超能文献

Kappa 3: a novel subtype of the kappa opioid site in bovine adrenal medulla, highly selective for Met-enkephalin-Arg6-Phe7.

作者信息

Castanas E, Giraud P, Bourhim N, Cantau P, Oliver C

出版信息

Neuropeptides. 1984 Dec;5(1-3):133-6. doi: 10.1016/0143-4179(84)90045-3.

DOI:10.1016/0143-4179(84)90045-3

Abstract

摘要

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Kappa 3: a novel subtype of the kappa opioid site in bovine adrenal medulla, highly selective for Met-enkephalin-Arg6-Phe7.κ3：牛肾上腺髓质中κ阿片受体位点的一种新型亚型，对甲硫氨酸脑啡肽-精氨酸6-苯丙氨酸7具有高度选择性。

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Interaction of opiates with opioid binding sites in the bovine adrenal medulla: II. Interaction with kappa sites.

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Interaction of opiates with opioid binding sites in the bovine adrenal medulla: I. Interaction with delta and mu sites.

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Opiate receptor-mediated inhibition of catecholamine release in primary cultures of bovine adrenal chromaffin cells.阿片受体介导的对牛肾上腺嗜铬细胞原代培养物中儿茶酚胺释放的抑制作用。

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Evidence for multiple "Kappa" binding sites by use of opioid peptides in the guinea-pig lumbo-sacral spinal cord.在豚鼠腰骶脊髓中使用阿片肽证明存在多个“κ”结合位点。

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The distribution of opioid binding subtypes in the bovine adrenal medulla.

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Mammalian neuronal actions of FMRFamide and the structurally related opioid Met-enkephalin-Arg6-Phe7.FMRF酰胺及结构相关的阿片样物质甲硫氨酸脑啡肽-精氨酸6-苯丙氨酸7对哺乳动物神经元的作用。

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引用本文的文献

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Dihydrocodeinone-hydrazone, dihydrocodeinone-oxime, naloxone-3-OMe-oxime, and clocinnamox fail to irreversibly inhibit opioid kappa receptor binding.二氢可待因酮腙、二氢可待因酮肟、纳洛酮-3-甲氧基肟和氯辛肟不能不可逆地抑制阿片κ受体结合。

Neurochem Res. 1994 Sep;19(9):1159-63. doi: 10.1007/BF00965150.