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Comparison of the monoamine transporters from human and mouse in their sensitivities to psychostimulant drugs

机译:人和小鼠单胺转运蛋白对精神刺激药物敏感性的比较

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摘要

BackgroundThe plasma membrane neurotransmitter transporters terminate neurotransmissions by the reuptake of the released neurotransmitters. The transporters for the monoamines dopamine, norepinephrine, and serotonin (DAT, NET, and SERT) are targets for several popular psychostimulant drugs of abuse. The potencies of the psychostimulant on the monoamine transporters have been studied by several laboratories. However, there are significant discrepancies in the reported data with differences up to 60-fold. In addition, the drug potencies of the 3 monoamine transporters from mouse have not been compared in the same experiments or along side the human transporters. Further studies and systematic comparisons are needed.
机译:背景质膜神经递质转运蛋白通过重新摄取释放的神经递质来终止神经传递。单胺多巴胺,去甲肾上腺素和血清素(DAT,NET和SERT)的转运蛋白是几种流行的精神刺激药物的靶标。几个实验室已经研究了精神刺激药对单胺转运蛋白的作用。但是,所报告的数据存在显着差异,差异最多可达到60倍。此外,在同一实验中或在人类转运蛋白旁边未对来自小鼠的3种单胺转运蛋白的药效进行比较。需要进一步研究和系统比较。

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