神经科学
羟考酮
类阿片
臂旁核
前额叶皮质
人口
心理学
药理学
医学
受体
核心
内科学
环境卫生
认知
作者
Alexander C.W. Smith,Soham Ghoshal,Samuel W. Centanni,Mary P. Heyer,Alberto Corona,Lauren Wills,Emma Andraka,Ye Lei,Richard M. O’Connor,Stephanie P. B. Caligiuri,Sohail Ahmed Khan,Kristin G. Beaumont,Robert Sebra,Brigitte L. Kieffer,Danny G. Winder,Masago Ishikawa,Paul J. Kenny
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2024-06-06
卷期号:384 (6700)
被引量:1
标识
DOI:10.1126/science.adn0886
摘要
In addition to their intrinsic rewarding properties, opioids can also evoke aversive reactions that protect against misuse. Cellular mechanisms that govern the interplay between opioid reward and aversion are poorly understood. We used whole-brain activity mapping in mice to show that neurons in the dorsal peduncular nucleus (DPn) are highly responsive to the opioid oxycodone. Connectomic profiling revealed that DPn neurons innervate the parabrachial nucleus (PBn). Spatial and single-nuclei transcriptomics resolved a population of PBn-projecting pyramidal neurons in the DPn that express μ-opioid receptors (μORs). Disrupting μOR signaling in the DPn switched oxycodone from rewarding to aversive and exacerbated the severity of opioid withdrawal. These findings identify the DPn as a key substrate for the abuse liability of opioids.
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