Martín-García Elena, Domingo-Rodriguez Laura, Maldonado Rafael
Laboratory of Neuropharmacology-Neurophar, Department of Experimental and Health Sciences, Universitat Pompeu Fabra (U.P.F.), Barcelona, Spain.
Hospital del Mar Medical Research Institute (IMIM), Barcelona, Spain.
Bio Protoc. 2020 Oct 5;10(19):e3777. doi: 10.21769/BioProtoc.3777.
The study of food addiction comprises 3 hallmarks that include the persistence to response without an outcome, the strong motivation for palatable food, and the loss of inhibitory control over food intake that leads to compulsive behavior in addicted individuals. The complex multifactorial nature of this disorder and the unknown neurobiological mechanistic correlation explains the lack of effective treatments. Our operant conditioning model allows deciphering why some individuals are vulnerable and develop food addiction while others are resilient and do not. It is a translational approach since it is based on the Diagnostic and Statistical Manual of Mental Disorders 5th edition (DSM-5) and the Yale Food Addiction Scale (YFAS 2.0). This model allows to evaluate the addiction criteria in 2 time-points at an early and a late period by grouping them into 1) persistence to response during a period of non-availability of food, 2) motivation for food with a progressive ratio, and 3) compulsivity when the reward is associated with a punishment such as an electric foot-shock. The advantage of this model is that it allows us to measure 4 phenotypic traits suggested as predisposing factors related to vulnerability to addiction. Also, it is possible to evaluate the long food addiction mouse model with mice genetically modified. Importantly, the novelty of this protocol is the adaptation of this food addiction model to a short protocol to evaluate genetic manipulations targeting specific brain circuitries by using a chemogenetic approach that could promote the rapid development of this addictive behavior. These adaptations lead to a short food addiction mouse protocol, in which mice follow the same behavioral procedure of the early period in the long food addiction protocol with some variations due to the surgical viral vector injection. To our knowledge, there is no paradigm in mice allowing us to study the combination of such a robust behavioral approach that allows uncovering the neurobiology of food addiction at the brain circuit level. We can study using this protocol if modifying the excitability of a specific brain network confers resilience or vulnerability to developing food addiction. Understanding these neurobiological mechanisms is expected to help to find novel and efficient interventions to battle food addiction.
食物成瘾的研究包含三个特征,即无结果时反应的持续性、对美味食物的强烈动机,以及对食物摄入抑制控制的丧失,这会导致成瘾个体出现强迫行为。这种疾病复杂的多因素性质以及未知的神经生物学机制相关性解释了为何缺乏有效的治疗方法。我们的操作性条件反射模型能够解释为什么有些人容易患上食物成瘾,而另一些人则具有抵抗力而不会。这是一种转化方法,因为它基于《精神疾病诊断与统计手册》第5版(DSM-5)和耶鲁食物成瘾量表(YFAS 2.0)。该模型允许在早期和晚期两个时间点评估成瘾标准,将其分为:1)在食物不可得期间反应的持续性;2)食物动机与渐进比率;3)当奖励与惩罚(如电击足部)相关联时的强迫性。该模型的优点在于它使我们能够测量被认为是与成瘾易感性相关的4种表型特征。此外,还可以用基因改造小鼠来评估长期食物成瘾小鼠模型。重要的是,该方案的新颖之处在于将这种食物成瘾模型改编为一个简短方案,以通过使用化学遗传学方法来评估针对特定脑回路的基因操作,这种方法可以促进这种成瘾行为的快速发展。这些改编产生了一个简短的食物成瘾小鼠方案,其中小鼠遵循长期食物成瘾方案中早期的相同行为程序,但由于手术性病毒载体注射而存在一些差异。据我们所知,在小鼠中没有一种范式能让我们研究这种强大的行为方法的组合,这种方法能够在脑回路水平揭示食物成瘾的神经生物学机制。我们可以使用这个方案来研究改变特定脑网络的兴奋性是否会赋予对食物成瘾发展的抵抗力或易感性。了解这些神经生物学机制有望有助于找到对抗食物成瘾的新颖且有效的干预措施。