Heal David J, Smith Sharon Lesley, Gosden Jane, Rowlett James
DevelRx Ltd, BioCity, Nottingham, UK.
Department of Life Sciences, University of Bath, Bath, UK.
J Psychopharmacol. 2025 Jul;39(7):629-651. doi: 10.1177/02698811251330780. Epub 2025 Apr 17.
Nonclinical testing to predict the abuse potential of central nervous system (CNS) drug candidates is a mandatory part of the safety pharmacology assessment for medications seeking approval for human use. In the "standard model," the drug candidate is tested to determine whether its psychoactive effects generalize to the discriminative cue of an abused drug that animals have been trained to recognize. However, CNS drugs with novel pharmacological mechanisms are challenging, and in response, the regulatory agencies have recommended alternative experimental designs. Variant 1: test the drug candidate in a series of drug-discrimination experiments that exemplify the major classes of abused drugs. Variant 2: use the drug candidate as a training cue. Back-test examples from established classes of abused drugs to see if they generalize to the drug candidate's cue. We critically assessed the pharmacological and translational validity of these protocols. The standard model is underpinned by decades of research and refinement and has the highest degree of translational validity. Question marks exist over the validity of substitution results when the drug candidate has no affinity for known abuse-related targets. Published research does not support the use of either of the alternative models. On the contrary, these models have no pharmacological rationale and, consequently, no translational validity. The review contains a decision tree on the appropriate application of the standard drug-discrimination model, together with recommendations for adapting the test when characterizing the psychoactive properties of drug candidates acting on novel CNS targets.
预测中枢神经系统(CNS)候选药物滥用潜力的非临床测试是寻求人类使用批准的药物安全性药理学评估的强制性部分。在“标准模型”中,对候选药物进行测试,以确定其精神活性作用是否能推广到动物已被训练识别的滥用药物的辨别线索上。然而,具有新型药理机制的中枢神经系统药物具有挑战性,对此,监管机构推荐了替代实验设计。变体1:在一系列药物辨别实验中测试候选药物,这些实验代表了主要类别的滥用药物。变体2:将候选药物用作训练线索。对既定类别的滥用药物进行回测,看它们是否能推广到候选药物的线索上。我们严格评估了这些方案的药理学和转化有效性。标准模型有几十年的研究和完善作为支撑,具有最高程度的转化有效性。当候选药物对已知的与滥用相关的靶点没有亲和力时,替代结果的有效性存在疑问。已发表的研究不支持使用任何一种替代模型。相反,这些模型没有药理学依据,因此也没有转化有效性。该综述包含一个关于标准药物辨别模型适当应用的决策树,以及在表征作用于新型中枢神经系统靶点的候选药物的精神活性特性时调整测试的建议。