3H-N-正丙基去甲阿扑吗啡：一种新型的中枢多巴胺受体激动剂配体。 - Suppr

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3H-N-n-propylnorapomorphine: a novel agonist ligand for central dopamine receptors.

作者信息

Creese I, Padgett L, Fazzini E, Lopez F

出版信息

Eur J Pharmacol. 1979 Jul 1;56(4):411-2. doi: 10.1016/0014-2999(79)90274-7.

DOI:10.1016/0014-2999(79)90274-7

PMID:477735

Abstract

摘要

相似文献

3H-N-n-propylnorapomorphine: a novel agonist ligand for central dopamine receptors.3H-N-正丙基去甲阿扑吗啡：一种新型的中枢多巴胺受体激动剂配体。

Eur J Pharmacol. 1979 Jul 1;56(4):411-2. doi: 10.1016/0014-2999(79)90274-7.

Selective labelling of different dopamine receptors by a new agonist 3H-ligand: 3H-N-propylnorapomorphine.一种新型激动剂3H配体：3H-N-丙基去甲阿朴吗啡对不同多巴胺受体的选择性标记。

Eur J Pharmacol. 1979 Jun 15;56(3):291-2. doi: 10.1016/0014-2999(79)90187-0.

Dopamine receptors in subcellular fractions from bovine caudate: enrichment of [3H]spiperone binding in a postsynaptic membrane fraction.来自牛尾状核亚细胞组分中的多巴胺受体：[3H]螺哌隆结合在突触后膜组分中的富集。

J Neurochem. 1981 Mar;36(3):1142-51. doi: 10.1111/j.1471-4159.1981.tb01711.x.

Affinities of drugs for the agonist and antagonist states of the dopamine receptor.药物对多巴胺受体激动剂和拮抗剂状态的亲和力。

Eur J Pharmacol. 1978 Sep 15;51(2):187-8. doi: 10.1016/0014-2999(78)90344-8.

Autoradiographic localization and quantification of dopamine D2 receptors in normal human brain with [3H]N-n-propylnorapomorphine.用[³H]N-正丙基去甲阿扑吗啡对正常人脑多巴胺D2受体进行放射自显影定位与定量分析。

Brain Res. 1986 Jun 4;375(1):135-49. doi: 10.1016/0006-8993(86)90966-2.

Antiparkinsonian drug doses and neuroleptic receptors.抗帕金森病药物剂量与抗精神病药物受体

Experientia. 1978 Nov 15;34(11):1490-2. doi: 10.1007/BF01932371.

Phenoxybenzamine treatment differentiates dopaminergic 3H-ligand binding sites in bovine caudate membranes.酚苄明治疗可区分牛尾状核膜中多巴胺能3H-配体结合位点。

Mol Pharmacol. 1982 Jan;21(1):44-51.

3H-Apomorphine interactions with dopamine receptors in calf brain.3H-阿扑吗啡与小牛脑内多巴胺受体的相互作用。

Eur J Pharmacol. 1978 Jun 1;49(3):295-9. doi: 10.1016/0014-2999(78)90105-x.

Binding of [3H]apomorphine to an aporphine binding site as well as to dopamine sites in tissue from bovine caudate nucleus.[3H]阿扑吗啡与牛尾状核组织中的阿朴啡结合位点以及多巴胺位点的结合。

Neuropharmacology. 1984 Aug;23(8):885-92. doi: 10.1016/0028-3908(84)90001-7.

Pharmacology of [3H]apomorphine binding to bovine brain tissue.[3H]阿扑吗啡与牛脑组织结合的药理学

Biochem Pharmacol. 1981 Dec 1;30(23):3171-9. doi: 10.1016/0006-2952(81)90515-3.

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Agonist high- and low-affinity states of dopamine D₂ receptors: methods of detection and clinical implications.多巴胺 D₂ 受体的激动剂高亲和态和低亲和态：检测方法及临床意义。

Naunyn Schmiedebergs Arch Pharmacol. 2013 Feb;386(2):135-54. doi: 10.1007/s00210-012-0817-0. Epub 2012 Dec 9.

A review of the discovery, pharmacological characterization, and behavioral effects of the dopamine D2-like receptor antagonist eticlopride.多巴胺D2样受体拮抗剂依托必利的发现、药理学特性及行为效应综述。

CNS Neurosci Ther. 2008 Fall;14(3):248-62. doi: 10.1111/j.1755-5949.2008.00047.x.

Neurotensin peptides antagonistically regulate postsynaptic dopamine D2 receptors in rat nucleus accumbens: a receptor binding and microdialysis study.神经降压素肽对大鼠伏隔核中的突触后多巴胺D2受体具有拮抗调节作用：一项受体结合和微透析研究。

J Neural Transm Gen Sect. 1995;102(2):125-37. doi: 10.1007/BF01276508.

Characterization of normal and supersensitive dopamine receptors: effects of ergot drugs and neuropeptides.正常和超敏多巴胺受体的特性：麦角药物和神经肽的作用

J Neural Transm. 1981;51(1-2):3-37. doi: 10.1007/BF01664003.

Agonist-induced subsensitivity of adenylate cyclase coupled with a dopamine receptor in slices from rat corpus striatum.激动剂诱导的腺苷酸环化酶亚敏感性与大鼠纹状体切片中多巴胺受体的关系。

Proc Natl Acad Sci U S A. 1982 Jul;79(14):4456-60. doi: 10.1073/pnas.79.14.4456.

Multiple daily amphetamine administration decreases both [3H]agonist and [3H]antagonist dopamine receptor binding.每日多次给予苯丙胺会降低[³H]激动剂和[³H]拮抗剂多巴胺受体结合。

Experientia. 1982 Oct 15;38(10):1224-5. doi: 10.1007/BF01959753.

Dopamine receptor sensitivity after chronic dopamine agonists. Striatal 3H-spiroperidol binding in mice after chronic administration of high doses of apomorphine, N-n-propylnorapomorphine and dextroamphetamine.慢性多巴胺激动剂后的多巴胺受体敏感性。高剂量阿扑吗啡、N-正丙基去甲阿扑吗啡和右旋苯丙胺慢性给药后小鼠纹状体的3H-螺哌啶结合。

Psychopharmacology (Berl). 1982;77(2):146-9. doi: 10.1007/BF00431937.

Kinetic properties of the in vivo accumulation of 3H-(-)-N-n-propylnorapomorphine in mouse brain.3H-(-)-N-正丙基去甲阿朴吗啡在小鼠脑内的体内蓄积动力学特性。

Naunyn Schmiedebergs Arch Pharmacol. 1989 Jul;340(1):13-20. doi: 10.1007/BF00169200.

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