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。 - Suppr

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Selective labelling of different dopamine receptors by a new agonist 3H-ligand: 3H-N-propylnorapomorphine.

作者信息

Titeler M, Seeman P

出版信息

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

DOI:10.1016/0014-2999(79)90187-0

PMID:477726

Abstract

摘要

相似文献

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.

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 labeling of apomorphine receptors by 3H-LSD.用³H-LSD对阿扑吗啡受体进行选择性标记。

Eur J Pharmacol. 1979 Jun 15;56(3):269-71. doi: 10.1016/0014-2999(79)90182-1.

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.

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.

Differential labelling of dopamine receptors in rat brain in vivo: comparison of [3H]piribedil, [3H]S 3608 and [3H]N,n-propylnorapomorphine.大鼠脑内多巴胺受体的体内差异标记：[3H]哌立地尔、[3H]S 3608和[3H]N，N-丙基去甲阿扑吗啡的比较

Eur J Pharmacol. 1983 Jan 28;87(1):85-94. doi: 10.1016/0014-2999(83)90053-5.

Regional in vivo binding of [3H]N-propylnorapomorphine in the mouse brain. Evidence for labelling of central dopamine receptors.[3H]N-丙基去甲阿扑吗啡在小鼠脑内的区域活体结合。中枢多巴胺受体标记的证据。

Eur J Pharmacol. 1981 Jul 10;72(4):397-402. doi: 10.1016/0014-2999(81)90584-7.

Selective labeling of pre-synaptic receptors by 3H-dopamine, 3H-apomorphine and 3H-clonidine; labeling of post-synaptic sites by 3H-neuroleptics.用³H-多巴胺、³H-阿扑吗啡和³H-可乐定对突触前受体进行选择性标记；用³H-抗精神病药物对突触后位点进行标记。

Life Sci. 1978 Aug 14;23(6):587-91.

[3H]205-501, a non-catechol dopaminergic agonist, labels selectively and with high affinity dopamine D2 receptors.[3H]205 - 501，一种非儿茶酚胺多巴胺能激动剂，能选择性且高亲和力地标记多巴胺D2受体。

J Neural Transm. 1985;62(3-4):231-48. doi: 10.1007/BF01252239.

Eur J Pharmacol. 1979 Apr 15;55(2):137-42. doi: 10.1016/0014-2999(79)90385-6.

引用本文的文献

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.

Receptor-receptor interactions as an integrative mechanism in nerve cells.受体-受体相互作用作为神经细胞中的一种整合机制。

Mol Neurobiol. 1993 Fall-Winter;7(3-4):293-334. doi: 10.1007/BF02769180.

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.

Three classes of dopamine receptor (D-2, D-3, D-4) identified by binding studies with 3H-apomorphine and 3H-domperidone.通过用³H-阿扑吗啡和³H-多潘立酮进行结合研究鉴定出三类多巴胺受体（D-2、D-3、D-4）。

Naunyn Schmiedebergs Arch Pharmacol. 1980;315(2):89-102. doi: 10.1007/BF00499251.

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.

Calcium alters the sensitivity of intact horizontal cells to dopamine antagonists.钙会改变完整水平细胞对多巴胺拮抗剂的敏感性。

Proc Natl Acad Sci U S A. 1982 May;79(10):3350-4. doi: 10.1073/pnas.79.10.3350.

In vivo labeling of dopamine receptors: light microscopic localization at the cellular level by means of dipping autoradiography with the agonist (3H)N-n-propylnorapomorphine.多巴胺受体的体内标记：通过用激动剂（3H）N-正丙基去甲阿朴吗啡进行浸蘸放射自显影在细胞水平上进行光镜定位。

J Neural Transm. 1987;68(1-2):15-23. doi: 10.1007/BF01244636.

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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