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[3H]8-OH-DPAT labels the serotonin transporter in the rat striatum.

作者信息

Schoemaker H, Langer S Z

出版信息

Eur J Pharmacol. 1986 May 27;124(3):371-3. doi: 10.1016/0014-2999(86)90243-8.

DOI:10.1016/0014-2999(86)90243-8
PMID:2942413
Abstract
摘要

相似文献

1
[3H]8-OH-DPAT labels the serotonin transporter in the rat striatum.[3H]8-羟基二丙胺基四氢萘标记大鼠纹状体中的5-羟色胺转运体。
Eur J Pharmacol. 1986 May 27;124(3):371-3. doi: 10.1016/0014-2999(86)90243-8.
2
[3H]8-OH-DPAT labels the 5-hydroxytryptamine uptake recognition site and the 5-HT1A binding site in the rat striatum.[3H]8-羟基二丙胺标记大鼠纹状体中的5-羟色胺摄取识别位点和5-HT1A结合位点。
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Differentiation of pre- and post-synaptic high affinity serotonin receptor binding sites using physico-chemical parameters and modifying agents.利用物理化学参数和修饰剂区分突触前和突触后高亲和力5-羟色胺受体结合位点。
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Nucleotide interactions with 5-HT1A binding sites directly labeled by [3H]-8-hydroxy-2-(DI-n-propylamino)tetralin ([3H]-8-OH-DPAT).核苷酸与由[3H]-8-羟基-2-(二正丙基氨基)四氢萘([3H]-8-OH-DPAT)直接标记的5-HT1A结合位点的相互作用。
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[Multiple [3H]8-hydroxy-2-(di-n-propylamino)-tetralin binding sites in rat brain: modulation by GTP and cations].[大鼠脑中多个[3H]8-羟基-2-(二正丙基氨基)四氢萘结合位点:GTP和阳离子的调节作用]
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125I-Bolton-Hunter-8-methoxy-2-[N-propyl-N-propylamino]tetralin as a new selective radioligand of 5-HT1A sites in the rat brain. In vitro binding and autoradiographic studies.
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Possible in vivo 5-HT reuptake blocking properties of 8-OH-DPAT assessed by measuring hippocampal extracellular 5-HT using microdialysis in rats.通过在大鼠中使用微透析测量海马细胞外5-羟色胺来评估8-羟基二丙胺可能的体内5-羟色胺再摄取阻断特性。
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