Department of Endocrinology and Metabolism, Academic Medical Center, 1105 AZ Amsterdam, Netherlands.
Department of Psychiatry, Yale University School of Medicine, New Haven, CT 06519, USA.
Sci Transl Med. 2018 May 23;10(442). doi: 10.1126/scitranslmed.aar3752.
The brain is emerging as an important regulator of systemic glucose metabolism. Accumulating data from animal and observational human studies suggest that striatal dopamine signaling plays a role in glucose regulation, but direct evidence in humans is currently lacking. We present a series of experiments supporting the regulation of peripheral glucose metabolism by striatal dopamine signaling. First, we present the case of a diabetes patient who displayed strongly reduced insulin requirements after treatment with bilateral deep brain stimulation (DBS) targeting the anterior limb of the internal capsule. Next, we show that DBS in this striatal area, which induced dopamine release, increased hepatic and peripheral insulin sensitivity in 14 nondiabetic patients with obsessive-compulsive disorder. Conversely, systemic dopamine depletion reduced peripheral insulin sensitivity in healthy subjects. Supporting these human data, we demonstrate that optogenetic activation of dopamine D receptor-expressing neurons in the nucleus accumbens increased glucose tolerance and insulin sensitivity in mice. Together, these findings support the hypothesis that striatal neuronal activity regulates systemic glucose metabolism.
大脑正成为系统葡萄糖代谢的重要调节者。越来越多的动物和观察性人体研究数据表明,纹状体多巴胺信号在葡萄糖调节中发挥作用,但目前人类缺乏直接证据。我们提出了一系列支持纹状体多巴胺信号调节外周葡萄糖代谢的实验。首先,我们介绍了一位糖尿病患者的病例,该患者在接受双侧深部脑刺激(DBS)治疗后,其胰岛素需求明显降低,刺激靶点为内囊前肢。接下来,我们发现,DBS 刺激这一纹状体区域会导致多巴胺释放,从而增加 14 名非糖尿病强迫症患者的肝脏和外周胰岛素敏感性。相反,系统性多巴胺耗竭会降低健康受试者的外周胰岛素敏感性。这些人体数据得到了支持,我们证明,在伏隔核中表达多巴胺 D 受体的神经元的光遗传学激活会增加小鼠的葡萄糖耐量和胰岛素敏感性。综上所述,这些发现支持了纹状体神经元活动调节系统葡萄糖代谢的假说。