去甲肾上腺素神经元对多巴胺的再摄取:例外还是规律?

Ezio Carboni, Alessandra Silvagni
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引用次数: 83

摘要

去甲肾上腺素终端对多巴胺的再摄取可发生在前额皮质、伏隔核壳和终纹床核等脑区,这些脑区受多巴胺和去甲肾上腺素神经元的支配,尽管不均匀。因此,选择性结合去甲肾上腺素转运体的抗抑郁药可能通过提高除去甲肾上腺素外的细胞外多巴胺浓度来发挥其治疗作用。此外,即使在多巴胺转运蛋白被敲除的小鼠中,可卡因也能增强多巴胺转运蛋白的作用,因为它可能通过阻止去甲肾上腺素转运蛋白对突触多巴胺的吸收而提高伏隔核外壳中的突触多巴胺,这种效应甚至可能发生在野生动物身上。最近,也有研究表明,多巴胺可以通过去甲肾上腺素神经元与去甲肾上腺素共同释放,尽管尚不清楚这一特征是否与去甲肾上腺素转运体先前非特异性摄取多巴胺有关。在这篇综述中,我们讨论了去甲肾上腺素转运体对多巴胺的非特异性摄取在滥用药物、抗精神病药和抗抑郁药的作用机制中的潜在作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dopamine reuptake by norepinephrine neurons: exception or rule?

Dopamine reuptake by norepinephrine terminals can occur in brain areas such as the prefrontal cortex, the nucleus accumbens shell, and the bed nucleus of stria terminalis that are innervated, although unevenly, by both dopamine and norepinephrine neurons. Therefore the antidepressants that bind selectively the norepinephrine transporter might produce their therapeutic effect by raising the extracellular concentration of dopamine besides that of norepinephrine. Moreover, cocaine can be reinforcing even in knock-out mice for the dopamine transporter because it might raise synaptic dopamine in the nucleus accumbens shell by preventing its uptake by the norepinephrine transporter, an effect that could take place even in wild animals. Recently, it has also been suggested that dopamine can be co-released with norepinephrine by norepinephrine neurons, although it is not clear whether this feature might be related to a previous nonspecific uptake of dopamine by the norepinephrine transporter. In this review we discuss the potential role of the nonspecific uptake of dopamine by norepinephrine transporter in the mechanism of action of drugs of abuse, antipsychotics, and antidepressants.

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