Department of Anatomy, Howard University College of Medicine, 520 W Street, NW, Washington D.C., 20059, United States; Developmental Neuropsychopharmacology Laboratory, Howard University College of Medicine, 520 W Street, NW, Washington D.C., 20059, United States.
Developmental Neuropsychopharmacology Laboratory, Howard University College of Medicine, 520 W Street, NW, Washington D.C., 20059, United States; Department of Science Education, Donald and Barbara Zucker School of Medicine at Hofstra/ Northwell, 500 Hofstra University, Hempstead, NY 11549, United States.
Neurosci Biobehav Rev. 2020 Aug;115:164-188. doi: 10.1016/j.neubiorev.2020.04.021. Epub 2020 Apr 28.
Individuals with mood disorders or with addiction, impulsivity and some personality disorders can share in common a dysfunction in how the brain perceives reward, where processing of natural endorphins or the response to exogenous dopamine stimulants is impaired. Reward Deficiency Syndrome (RDS) is a polygenic trait with implications that suggest cross-talk between different neurological systems that include the known reward pathway, neuroendocrine systems, and motivational systems. In this review we evaluate well-characterized animal models for their construct validity and as potential models for RDS. Animal models used to study substance use disorder, major depressive disorder (MDD), early life stress, immune dysregulation, attention deficit hyperactivity disorder (ADHD), post traumatic stress disorder (PTSD), compulsive gambling and compulsive eating disorders are discussed. These disorders recruit underlying reward deficiency mechanisms in multiple brain centers. Because of the widespread and remarkable array of associated/overlapping behavioral manifestations with a common root of hypodopaminergia, the basic endophenotype recognized as RDS is indeed likened to a behavioral octopus. We conclude this review with a look ahead on how these models can be used to investigate potential therapeutics that target the underlying common deficiency.
具有情绪障碍或成瘾、冲动和某些人格障碍的个体可能具有共同的大脑感知奖励的功能障碍,其中天然内啡肽的处理或对外源性多巴胺刺激物的反应受损。奖励缺陷综合征(RDS)是一种多基因特征,其意义表明不同神经系统之间存在交叉对话,包括已知的奖励途径、神经内分泌系统和动机系统。在这篇综述中,我们评估了经过充分特征描述的动物模型的构建有效性,并将其作为 RDS 的潜在模型。讨论了用于研究物质使用障碍、重度抑郁症(MDD)、早期生活压力、免疫失调、注意缺陷多动障碍(ADHD)、创伤后应激障碍(PTSD)、强迫性赌博和强迫性进食障碍的动物模型。这些疾病在多个大脑中心招募了潜在的奖励缺陷机制。由于与低多巴胺能症有共同根源的广泛而显著的相关/重叠行为表现,被认为是 RDS 的基本表型确实类似于行为章鱼。我们以展望这些模型如何用于研究针对潜在共同缺陷的潜在治疗方法结束了这篇综述。