构建基于活动的厌食症小鼠模型

Maria Consolata Miletta, Tamas L Horvath
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摘要

神经性厌食症(AN)是一种精神疾病,主要表现为极度食欲低下、体重严重下降、多动和低体温。目前,神经性厌食症是死亡率最高的精神疾病。尽管经过数十年的研究,AN 仍无有效的治疗方法,对其病因也无明确的认识。由于遗传、环境、社会和文化因素之间复杂的相互作用是这种疾病的关键所在,因此迄今为止一直难以开发出合适的动物模型。在这里,我们介绍了将功能缺失小鼠模型与基于活动的厌食症模型(ABA)相结合的方案。我们深入了解了驱动厌食症患者生存的神经回路,与以往的方案不同的是,我们提出的模型模拟了主要促进人类厌食症的条件,如青春期发病率增加、发病前出现负能量平衡以及强迫性运动增加等。该方案将有助于未来的研究,以确定促进这种毁灭性进食障碍发病或长期维持的神经元群或大脑回路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Construction of Activity-based Anorexia Mouse Models.

Anorexia nervosa (AN) is a psychiatric disorder mainly characterized by extreme hypophagia, severe body weight loss, hyperactivity, and hypothermia. Currently, AN has the highest mortality rate among psychiatric illnesses. Despite decades of research, there is no effective cure for AN nor is there a clear understanding of its etiology. Since a complex interaction between genetic, environmental, social, and cultural factors underlines this disorder, the development of a suitable animal model has been difficult so far. Here, we present our protocol that couples a loss-of-function mouse model to the activity-based anorexia model (ABA), which involves self-imposed starvation in response to exposure to food restriction and exercise. We provide insights into a neural circuit that drives survival in AN and, in contrast to previous protocols, propose a model that mimics the conditions that mainly promote AN in humans, such as increased incidence during adolescence, onset preceded by negative energy balance, and increased compulsive exercise. This protocol will be useful for future studies that aim to identify neuronal populations or brain circuits that promote the onset or long-term maintenance of this devastating eating disorder.

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