Division on Substance Use Disorders, New York State Psychiatric Institute and Columbia University Vagelos College of Physicians and Surgeons, 1051 Riverside Drive, New York, NY, 10032, USA.
CNS Drugs. 2020 Jul;34(7):697-722. doi: 10.1007/s40263-020-00721-9.
The pervasive and devastating nature of substance use disorders underlies the need for the continued development of novel pharmacotherapies. We now know that glia play a much greater role in neuronal processes than once believed. The various types of glial cells (e.g., astrocytes, microglial, oligodendrocytes) participate in numerous functions that are crucial to healthy central nervous system function. Drugs of abuse have been shown to interact with glia in ways that directly contribute to the pharmacodynamic effects responsible for their abuse potential. Through their effect upon glia, drugs of abuse also alter brain function resulting in behavioral changes associated with substance use disorders. Therefore, drug-induced changes in glia and inflammation within the central nervous system (neuroinflammation) have been investigated to treat various aspects of drug abuse and dependence. This article presents a brief overview of the effects of each of the major classes of addictive drugs on glia. Next, the paper reviews the pre-clinical and clinical studies assessing the effects that glial modulators have on abuse-related behavioral effects, such as pleasure, withdrawal, and motivation. There is a strong body of pre-clinical literature demonstrating the general effectiveness of several glia-modulating drugs in models of reward and relapse. Clinical studies have also yielded promising results, though not as robust. There is still much to disentangle regarding the integration between addictive drugs and glial cells. Improved understanding of the relationship between glia and the pathophysiology of drug abuse should allow for more precise exploration in the development and testing of glial-directed treatments for substance use disorders.
物质使用障碍的普遍和毁灭性性质是需要不断开发新的药物治疗的原因。我们现在知道,神经胶质细胞在神经元过程中发挥的作用比以前认为的要大得多。各种类型的神经胶质细胞(如星形胶质细胞、小胶质细胞、少突胶质细胞)参与了许多对中枢神经系统健康至关重要的功能。已经证明,滥用药物会以直接导致其滥用潜力的药效学作用与神经胶质细胞相互作用。通过对神经胶质细胞的作用,滥用药物还会改变大脑功能,导致与物质使用障碍相关的行为变化。因此,已经研究了药物引起的神经胶质细胞和中枢神经系统内炎症(神经炎症)的变化,以治疗药物滥用和依赖的各个方面。本文简要概述了每一大类成瘾药物对神经胶质细胞的影响。接下来,本文回顾了评估神经胶质调节剂对与滥用相关的行为效应(如快感、戒断和动机)的临床前和临床研究。有大量的临床前文献表明,几种神经胶质调节药物在奖励和复发模型中通常有效。临床研究也取得了有希望的结果,尽管不如前者那么可靠。关于成瘾药物和神经胶质细胞之间的整合仍有许多需要厘清。更好地理解神经胶质细胞与药物滥用的病理生理学之间的关系,应该可以更精确地探索针对物质使用障碍的神经胶质细胞导向治疗的开发和测试。