Department of Neurobiology, CNS Discovery, Teva Pharmaceuticals, West Chester, PA, USA.
Peter Boris Centre for Addiction Research, Department of Psychiatry and Behavioural Neurosciences, McMaster University, Hamilton, ON, Canada.
Pharmacol Ther. 2018 Feb;182:15-27. doi: 10.1016/j.pharmthera.2017.08.002. Epub 2017 Aug 19.
Binge-eating disorder (BED) is the most prevalent eating disorder with estimates of 2-5% of the general adult population. Nonetheless, its pathophysiology is poorly understood. Furthermore, there exist few therapeutic options for its effective treatment. Here we review the current state of binge-eating neurobiology and pharmacology, drawing from clinical therapeutic, neuroimaging, cognitive, human genetic and animal model studies. These studies, which are still in their infancy, indicate that while there are many gaps in our knowledge, several key neural substrates appear to underpin binge-eating and may be conserved between human and animals. This observation suggests that behavioral intermediate phenotypes or endophenotypes relevant to BED may be modeled in animals, facilitating the identification and testing of novel pharmacological targets. The development of novel, safe and effective pharmacological therapies for the treatment of BED will enhance the ability of clinicians to provide optimal care for people with BED.
暴食症(BED)是最常见的饮食失调症,估计有 2-5%的普通成年人口患有该病。尽管如此,其病理生理学仍未被充分理解。此外,针对其有效治疗的治疗方法也很少。在这里,我们从临床治疗、神经影像学、认知、人类遗传学和动物模型研究中回顾了暴食症的神经生物学和药理学现状。这些研究仍处于起步阶段,但表明尽管我们的知识仍存在许多空白,但几个关键的神经基质似乎是暴食的基础,并且在人类和动物之间可能是保守的。这一观察结果表明,与 BED 相关的行为中间表型或内表型可能在动物中得到模拟,从而有助于确定和测试新的药理学靶点。开发新的、安全有效的治疗暴食症的药理学疗法将增强临床医生为暴食症患者提供最佳护理的能力。