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四氢罂粟碱抑制大鼠脑突触体中的多巴胺摄取。

Tetrahydropapaveroline inhibits dopamine uptake in rat brain synaptosomes.

作者信息

Shier W T, Rossier J, Koda L Y, Bloom F E

出版信息

Adv Exp Med Biol. 1980;132:807-12. doi: 10.1007/978-1-4757-1419-7_84.

Abstract

THP, which can be formed by the condensation of dopamine with dopaldehyde, has been proposed to be involved in mediating some of the effects of ethanol on the central nervous system. We have observed that THP induces small granular vesicles (SGVs), visible with the electron microscope, in central dopamine fibers (Koda et al., 1978). In order to investigate the mechanism of SGV induction by THP, we examined dopamine and THP uptake into synaptosomes. [3H]THP (1.25 Ci/mmole), prepared by catalytic exchange labeling, exhibited no active uptake into synaptosomes (kinetics consistent with simple diffusion). THP did exhibit competitive inhibition (Ki = 4.2 x 10(-5) M) of [3H] dopamine uptake (Km = 2.6 x 10(-7) M; Vmax = 8.5 nmoles/min/g pellet) in these preparations. It is unlikely that endogenous THP would accumulate to concentrations sufficiently high to inhibit dopamine uptake under physiological conditions.

摘要

四氢异喹啉(THP)可由多巴胺与多巴胺醛缩合而成,有人提出它参与介导乙醇对中枢神经系统的某些作用。我们观察到,THP能在中枢多巴胺纤维中诱导出用电子显微镜可见的小颗粒囊泡(SGV)(Koda等人,1978年)。为了研究THP诱导SGV的机制,我们检测了多巴胺和THP进入突触体的摄取情况。通过催化交换标记制备的[3H]THP(1.25 Ci/毫摩尔),在突触体中未表现出主动摄取(动力学与简单扩散一致)。在这些制剂中,THP确实对[3H]多巴胺摄取表现出竞争性抑制(Ki = 4.2×10⁻⁵ M)(Km = 2.6×10⁻⁷ M;Vmax = 8.5纳摩尔/分钟/克沉淀)。在生理条件下,内源性THP不太可能积累到足以抑制多巴胺摄取的浓度。

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