大鼠下丘脑去甲肾上腺素转运载体的拓扑结构。三环摄取抑制剂的作用位点。 - Suppr | 超能文献

On the topology of the norepinephrine transport carrier in rat hypothalamus. The site of action of tricyclic uptake inhibitors.

作者信息

de Paulis T, Kelder D, Ross S B

出版信息

Mol Pharmacol. 1978 Jul;14(4):596-606.

Abstract

摘要

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

文档翻译

学术文献翻译模型，支持多种主流文档格式。

相似文献

1

On the topology of the norepinephrine transport carrier in rat hypothalamus. The site of action of tricyclic uptake inhibitors.大鼠下丘脑去甲肾上腺素转运载体的拓扑结构。三环摄取抑制剂的作用位点。

Mol Pharmacol. 1978 Jul;14(4):596-606.

2

A new inhibitor of norepinephrine uptake devoid of affinity for receptors in rat brain.一种对大鼠脑内受体无亲和力的去甲肾上腺素摄取新抑制剂。

J Pharmacol Exp Ther. 1982 Jul;222(1):61-5.

3

[Topography of the active site of the noradrenaline neuronal membrane carrier based on the theoretical conformation analysis of inhibitors of neuronal catecholamine uptake].基于去甲肾上腺素神经元膜载体活性位点的理论构象分析[神经元儿茶酚胺摄取抑制剂的研究]

Bioorg Khim. 1983 Feb;9(2):200-15.

4

A comparison of the inhibitory effects of new non-tricyclic amine uptake inhibitors on the uptake of norepinephrine and 5-hydroxytryptamine into synaptosomes of the rat brain.新型非三环胺摄取抑制剂对去甲肾上腺素和5-羟色胺摄取到大鼠脑突触体中的抑制作用比较。

Neuropharmacology. 1980 Apr;19(4):349-54. doi: 10.1016/0028-3908(80)90186-0.

5

Molecular features affecting the potency of tricyclic antidepressants and structurally related compounds as inhibitors of the uptake of tritiated norepinephrine by rabbit aortic strips.影响三环类抗抑郁药及结构相关化合物作为兔主动脉条摄取氚化去甲肾上腺素抑制剂效力的分子特征。

J Pharmacol Exp Ther. 1969 Apr;166(2):320-9.

6

Interaction between tricyclic and nontricyclic 5-hydroxytryptamine uptake inhibitors and the presynaptic 5-hydroxytryptamine inhibitory autoreceptors in the rat hypothalamus.三环类和非三环类5-羟色胺摄取抑制剂与大鼠下丘脑突触前5-羟色胺抑制性自身受体之间的相互作用。

J Pharmacol Exp Ther. 1985 Oct;235(1):200-11.

7

Inhibition of 5-hydroxytryptamine and noradrenaline uptake in platelets and synaptosomes incubated in plasma from human subjects treated with amitryptyline or nortriptyline: utilization of the principle for a bioassay method.阿米替林或去甲替林治疗的人类受试者血浆中孵育的血小板和突触体对5-羟色胺和去甲肾上腺素摄取的抑制作用：生物测定方法原理的应用

Psychopharmacology (Berl). 1980;69(2):137-42. doi: 10.1007/BF00427639.

8

A structure-activity study of the transport sites for the hypothalamic and striatal catecholamine uptake systems. Similarities and differences.

Mol Pharmacol. 1982 Mar;21(2):374-9.

9

The comparison of fluoxetine and nisoxetine with tricyclic antidepressants in blocking the neurotoxicity of p-chloroamphetamine and 6-hydroxydopamine in the rat brain.氟西汀和去甲替林与三环类抗抑郁药在阻断对氯苯丙胺和6-羟基多巴胺对大鼠脑的神经毒性方面的比较。

Res Commun Chem Pathol Pharmacol. 1976 Oct;15(2):221-31.

10

Conformation study of the inhibition of monoamine uptake in rat brain synaptosomes.大鼠脑突触体中单胺摄取抑制的构象研究。

Ann Med Exp Biol Fenn. 1973;51(2):51-8.

引用本文的文献

1

Chimeric dopamine-norepinephrine transporters delineate structural domains influencing selectivity for catecholamines and 1-methyl-4-phenylpyridinium.嵌合多巴胺-去甲肾上腺素转运体描绘了影响儿茶酚胺和1-甲基-4-苯基吡啶鎓选择性的结构域。

Proc Natl Acad Sci U S A. 1994 Dec 20;91(26):12584-8. doi: 10.1073/pnas.91.26.12584.

2

Effect of mianserin on noradrenergic transmission in the rat anococcygeus muscle.米安色林对大鼠肛尾肌去甲肾上腺素能传递的影响。

Br J Pharmacol. 1980 Feb;68(2):241-50. doi: 10.1111/j.1476-5381.1980.tb10413.x.

3

Binding of 3H-desipramine to the neuronal noradrenaline carrier of rat phaeochromocytoma cells (PC-12 cells).

Naunyn Schmiedebergs Arch Pharmacol. 1986 Dec;334(4):403-11. doi: 10.1007/BF00569378.