Sanofi, Exploratory Unit, Chilly-Mazarin 91385, France.
Nat Rev Drug Discov. 2013 Sep;12(9):667-87. doi: 10.1038/nrd4075.
Anxiety disorders are the most prevalent group of psychiatric diseases, and have high personal and societal costs. The search for novel pharmacological treatments for these conditions is driven by the growing medical need to improve on the effectiveness and the side effect profile of existing drugs. A huge volume of data has been generated by anxiolytic drug discovery studies, which has led to the progression of numerous new molecules into clinical trials. However, the clinical outcome of these efforts has been disappointing, as promising results with novel agents in rodent studies have very rarely translated into effectiveness in humans. Here, we analyse the major trends from preclinical studies over the past 50 years conducted in the search for new drugs beyond those that target the prototypical anxiety-associated GABA (γ-aminobutyric acid)-benzodiazepine system, which have focused most intensively on the serotonin, neuropeptide, glutamate and endocannabinoid systems. We highlight various key issues that may have hampered progress in the field, and offer recommendations for how anxiolytic drug discovery can be more effective in the future.
焦虑障碍是最常见的精神疾病群体,给个人和社会带来了高昂的代价。由于医疗上迫切需要提高现有药物的疗效和减少副作用,人们正在寻找治疗这些疾病的新型药理学疗法。大量的焦虑药物研发数据已经产生,这导致了许多新分子进入临床试验。然而,这些努力的临床结果令人失望,因为在啮齿动物研究中新型药物有前景的结果很少能转化为对人类的有效性。在这里,我们分析了过去 50 年来在寻找除了针对典型焦虑相关 GABA(γ-氨基丁酸)-苯二氮䓬系统的药物之外的新药的临床前研究中的主要趋势,这些研究主要集中在 5 个系统,包括 5-羟色胺、神经肽、谷氨酸和内源性大麻素系统。我们强调了可能阻碍该领域进展的各种关键问题,并就如何提高未来抗焦虑药物的发现提出了建议。