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放射性碘化HEAT(一种α-1肾上腺素能受体配体)在大鼠脑内的体内结合及放射性药物制备

In vivo binding in rat brain and radiopharmaceutical preparation of radioiodinated HEAT, an alpha-1 adrenoceptor ligand.

作者信息

Couch M W, Greer D M, Thonoor C M, Williams C M

机构信息

Nuclear Medicine Service, Veterans Administration Medical Center, Gainesville, FL 32602.

出版信息

J Nucl Med. 1988 Mar;29(3):356-62.

PMID:2894417
Abstract

In vivo binding of [125I]-2-[beta-(3-iodo-4-hydroxyphenyl)ethylaminomethyl tetralone) ([125I]HEAT) to alpha-1 adrenoceptors in the rat brain was determined over 4 hr. Uptake in the thalamus and frontal cortex was approximately 0.1% injected dose per gram tissue. Thalamus/cerebellum ratios of 10:1 and frontal cortex/cerebellum ratios of 5:1 were found at 4 hr. Pretreatment with prazosin, an alpha-1 antagonist, completely inhibited the accumulation of [125I]HEAT in thalamus and frontal cortex; yet uptake of radioactivity was not significantly affected by antagonists and agonists for other receptors classes (propranolol, beta-1; apomorphine, D-1; spiperone, D-2). Binding of [125I]HEAT is saturable. At 4 hr, [125I]HEAT or [123I]HEAT was shown to be the only radioactive material in rat thalamus and frontal cortex. Iodine-123 HEAT and [125I]HEAT were synthesized as radiopharmaceuticals within 3 hr in 99% radiochemical purity.

摘要

在4小时内测定了[125I]-2-β-(3-碘-4-羟基苯基)乙氨基甲基四氢萘酮在大鼠脑内与α-1肾上腺素能受体的体内结合情况。丘脑和额叶皮质的摄取量约为每克组织注射剂量的0.1%。在4小时时,丘脑/小脑的比值为10:1,额叶皮质/小脑的比值为5:1。用α-1拮抗剂哌唑嗪预处理可完全抑制[125I]HEAT在丘脑和额叶皮质的蓄积;然而,放射性摄取并未受到其他受体类型拮抗剂和激动剂(普萘洛尔,β-1;阿扑吗啡,D-1;螺哌隆,D-2)的显著影响。[125I]HEAT的结合是可饱和的。在4小时时,[125I]HEAT或[123I]HEAT被证明是大鼠丘脑和额叶皮质中唯一的放射性物质。碘-123 HEAT和[125I]HEAT在3小时内被合成为放射性药物,放射化学纯度为99%。

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