Ubaldi Massimo, Cannella Nazzareno, Ciccocioppo Roberto
School of Pharmacy, Pharmacology Unit, University of Camerino, Camerino, Italy.
Institute of Psychopharmacology, Central Institute of Mental Health, Medical Faculty Mannheim/Heidelberg University, Mannheim, Germany.
Prog Brain Res. 2016;224:251-84. doi: 10.1016/bs.pbr.2015.07.018. Epub 2015 Nov 26.
Drug abuse represents a considerable burden of disease and has enormous economic impacts on societies. Over the years, few medications have been developed for clinical use. Their utilization is endowed with several limitations, including partial efficacy or significant side effects. On the other hand, the successful advancement of these compounds provides an important proof of concept for the feasibility of drug development programs in addiction. In recent years, a wealth of information has been generated on the psychological mechanisms, genetic or epigenetic predisposing factors, and neurobiological adaptations induced by drug consumption that interact with each other to contribute to disease progression. It is now clear that addiction develops through phases, from initial recreational use to excessive consumption and compulsive drug seeking, with a shift from positive to negative reinforcement driving motivated behaviors. A greater understanding of these mechanisms has opened new vistas in drug development programs. Researchers' attention has been shifted from investigation of classical targets associated with reward to biological substrates responsible for negative reinforcement, impulse loss of control, and maladaptive mechanisms resulting from protracted drug use. From this research, several new biological targets for the development of innovative therapies have started to emerge. This chapter offers an overview of targets currently under scrutiny for the development of new medications for addiction. This work is not exhaustive but rather it provides a few examples of how this research has advanced in recent years by virtue of studies carried out in our laboratory.
药物滥用给疾病带来了相当大的负担,并对社会产生了巨大的经济影响。多年来,用于临床的药物开发很少。它们的使用存在一些局限性,包括疗效不全面或副作用严重。另一方面,这些化合物的成功研发为成瘾药物开发项目的可行性提供了重要的概念验证。近年来,关于药物消费所引发的心理机制、遗传或表观遗传易感性因素以及神经生物学适应性的信息大量涌现,这些因素相互作用,共同推动疾病进展。现在很清楚,成瘾是分阶段发展的,从最初的娱乐性使用到过度消费以及强迫性觅药,从正性强化向负性强化的转变驱动着动机行为。对这些机制的更深入理解为药物开发项目开辟了新的前景。研究人员的注意力已从与奖赏相关的经典靶点研究转向负责负性强化、冲动失控以及长期药物使用导致的适应不良机制的生物学基质。通过这项研究,一些用于开发创新疗法的新生物学靶点开始出现。本章概述了目前正在研究的用于开发成瘾新药的靶点。这项工作并不详尽,而是通过我们实验室开展的研究,提供了一些近年来该研究进展情况的实例。