University of Utah, Salt Lake City, UT, 84108, USA.
University of Michigan, Ann Arbor, MI, 48109, USA.
Neuropsychopharmacology. 2019 Feb;44(3):495-502. doi: 10.1038/s41386-018-0230-6. Epub 2018 Oct 2.
Neuropeptide Y (NPY) produces anxiolytic effects in rodent models, and naturally occurring low NPY expression in humans has been associated with negative emotional phenotypes. Studies in rodent models have also demonstrated that NPY elicits reward behaviors through its action in the nucleus accumbens (NAc), but the impact of NPY on the human NAc is largely unexplored. We recruited 222 healthy young adults of either sex and genetically selected 53 of these subjects at the extremes of NPY expression (Low-NPY and High-NPY) to participate in functional magnetic resonance imaging. Responses of the NAc and surrounding ventral striatum were quantified during a monetary incentive delay task in which stimuli varied by salience (high versus low) and valence (win versus loss). We found that bilateral NAc responses to high-salience versus low-salience stimuli were greater for Low-NPY subjects relative to High-NPY subjects, regardless of stimulus valence. To our knowledge, these results provide the first evidence in humans linking NPY with salience sensitivity of the NAc, raising the possibility that individual differences in NPY expression moderate the risk for disorders of mesoaccumbal function such as addictions and mood disorders. Additionally, we found that head motion was greater among High-NPY subjects, consistent with previous reports linking NPY with hyperactivity. Future studies in animal models are warranted to elucidate the neural mechanisms through which NPY influences NAc function and related behaviors.
神经肽 Y(NPY)在啮齿动物模型中产生抗焦虑作用,而人类中自然存在的低 NPY 表达与负面情绪表型有关。啮齿动物模型中的研究还表明,NPY 通过其在伏隔核(NAc)中的作用引发奖励行为,但 NPY 对人类 NAc 的影响在很大程度上尚未得到探索。我们招募了 222 名健康的年轻成年人,无论性别如何,并从这些人中选择了 53 名表达 NPY 水平处于极端的个体(低 NPY 和高 NPY)参与功能磁共振成像研究。在一项货币奖励延迟任务中,对 NAc 和周围腹侧纹状体的反应进行了量化,在该任务中,刺激物的显著度(高与低)和效价(赢与输)不同。我们发现,无论刺激的效价如何,低 NPY 组的双侧 NAc 对高显著度刺激的反应大于高 NPY 组。据我们所知,这些结果首次在人类中提供了将 NPY 与 NAc 的显著敏感性联系起来的证据,这增加了 NPY 表达个体差异调节中脑腹侧功能障碍(如成瘾和情绪障碍)风险的可能性。此外,我们发现高 NPY 组的头部运动更大,这与之前将 NPY 与过度活跃联系起来的报告一致。需要在动物模型中进行进一步的研究,以阐明 NPY 影响 NAc 功能和相关行为的神经机制。