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[3H]GBR-12935: a specific high affinity ligand for labeling the dopamine transport complex.

作者信息

Berger P, Janowsky A, Vocci F, Skolnick P, Schweri M M, Paul S M

出版信息

Eur J Pharmacol. 1985 Jan 2;107(2):289-90. doi: 10.1016/0014-2999(85)90075-5.

DOI:10.1016/0014-2999(85)90075-5
PMID:3979428
Abstract
摘要

相似文献

1
[3H]GBR-12935: a specific high affinity ligand for labeling the dopamine transport complex.[3H]GBR - 12935：一种用于标记多巴胺转运复合物的特异性高亲和力配体。
Eur J Pharmacol. 1985 Jan 2;107(2):289-90. doi: 10.1016/0014-2999(85)90075-5.
2
Characterization of sodium-dependent [3H]GBR-12935 binding in brain: a radioligand for selective labelling of the dopamine transport complex.脑中钠依赖性[3H]GBR - 12935结合的表征：一种用于多巴胺转运复合物选择性标记的放射性配体。
J Neurochem. 1986 Apr;46(4):1272-6. doi: 10.1111/j.1471-4159.1986.tb00649.x.
3
High-affinity [3H]GBR 12783 binding to a specific site associated with the neuronal dopamine uptake complex in the central nervous system.高亲和力的[3H]GBR 12783与中枢神经系统中与神经元多巴胺摄取复合物相关的特定位点结合。
Eur J Pharmacol. 1986 Jul 31;126(3):211-22. doi: 10.1016/0014-2999(86)90050-6.
4
[3H]GBR-12935 binding to dopamine uptake sites in rat striatum.[3H]GBR - 12935与大鼠纹状体中多巴胺摄取位点的结合。
Neuropsychobiology. 1990;23(4):177-81. doi: 10.1159/000119449.
5
Quantitative autoradiography of the dopamine uptake complex in rat brain using [3H]GBR 12935: binding characteristics.使用[3H]GBR 12935对大鼠脑内多巴胺摄取复合物进行定量放射自显影：结合特性
Brain Res. 1991 Feb 1;540(1-2):1-13. doi: 10.1016/0006-8993(91)90486-f.
6
[3H]GBR 12935 binding to dopamine uptake sites: subcellular localization and reduction in Parkinson's disease and progressive supranuclear palsy.[3H]GBR 12935与多巴胺摄取位点的结合：亚细胞定位以及在帕金森病和进行性核上性麻痹中的减少
Eur J Pharmacol. 1988 Nov 8;156(3):331-40. doi: 10.1016/0014-2999(88)90278-6.
7
Correlation between (3H)dopamine specific uptake and (3H)GBR 12783 specific binding during the maturation of rat striatum.大鼠纹状体成熟过程中(3H)多巴胺特异性摄取与(3H)GBR 12783特异性结合之间的相关性。
Life Sci. 1989;44(23):1759-65. doi: 10.1016/0024-3205(89)90563-8.
8
Interaction of [3H]GBR 12935 and GBR 12909 with the dopamine uptake complex in nucleus accumbens.
Eur J Pharmacol. 1990 Feb 20;177(1-2):91-4. doi: 10.1016/0014-2999(90)90554-j.
9
In vivo labelling of the neuronal dopamine uptake complex in the mouse striatum by [3H]GBR 12783.利用[3H]GBR 12783对小鼠纹状体中神经元多巴胺摄取复合物进行体内标记。
Eur J Pharmacol. 1992 Jan 7;210(1):77-84. doi: 10.1016/0014-2999(92)90654-m.
10
Effect of CH3HgCl and several transition metals on the dopamine neuronal carrier; peculiar behaviour of Zn2+.
Eur J Pharmacol. 1994 Jan 1;266(1):87-97. doi: 10.1016/0922-4106(94)90213-5.

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Studies of the biogenic amine transporters. 1. Dopamine reuptake blockers inhibit [3H]mazindol binding to the dopamine transporter by a competitive mechanism: preliminary evidence for different binding domains.生物胺转运体的研究。1. 多巴胺再摄取阻滞剂通过竞争机制抑制[3H]麦角吲哚与多巴胺转运体的结合：不同结合结构域的初步证据。
Neurochem Res. 1994 Feb;19(2):201-8. doi: 10.1007/BF00966817.
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Preparation of a potential positron emission tomographic radioligand for the dopamine transporter.一种用于多巴胺转运体的潜在正电子发射断层显像放射性配体的制备。
Eur J Nucl Med. 1994 Feb;21(2):131-7. doi: 10.1007/BF00175760.
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Comparison of the subregional distributions of the monoamine vesicular transporter and dopamine uptake complex in the rat striatum and changes during aging.
J Neural Transm Gen Sect. 1994;97(2):93-106. doi: 10.1007/BF01277946.
7
Further in vitro and in vivo studies with the putative presynaptic dopamine agonist N,N-dipropyl-7-hydroxy-2-aminotetralin.使用假定的突触前多巴胺激动剂N，N-二丙基-7-羟基-2-氨基四氢萘进行的进一步体外和体内研究。
Naunyn Schmiedebergs Arch Pharmacol. 1987 Nov;336(5):494-501. doi: 10.1007/BF00169305.
8
Radiolabeling of dopamine uptake sites in mouse striatum: comparison of binding sites for cocaine, mazindol, and GBR 12935.小鼠纹状体中多巴胺摄取位点的放射性标记：可卡因、马吲哚和GBR 12935结合位点的比较。
Naunyn Schmiedebergs Arch Pharmacol. 1992 Mar;345(3):309-18. doi: 10.1007/BF00168692.
9
Autoradiographic localization of dopamine uptake sites in the rat brain with 3H-GBR 12935.用³H-GBR 12935对大鼠脑内多巴胺摄取位点进行放射自显影定位
J Neural Transm Gen Sect. 1992;87(1):1-14. doi: 10.1007/BF01253106.
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MPTP lesions of the nigrostriatal dopaminergic projection decrease [3H]1-[1-(2-thienyl)cyclohexyl]piperidine binding to PCP site 2: further evidence that PCP site 2 is associated with the biogenic amine reuptake complex.
Neurochem Res. 1992 Mar;17(3):261-4. doi: 10.1007/BF00966668.