Chepke, MD, DFAPA, Excel Psychiatric Associates, Huntersville, NC; Atrium Health, Charlotte, NC.
Brunner, MD, Otsuka Pharmaceutical Development & Commercialization, Inc., Princeton, NJ.
Psychopharmacol Bull. 2024 Aug 19;54(4):45-80.
Serotonin has been implicated in the neurobiology of attention-deficit/hyperactivity disorder (ADHD) due to its association with impulsivity, attention, and emotional regulation. Many compounds with serotonergic properties have been evaluated in ADHD, but few have been approved by regulatory authorities. Utilizing a search of public databases, we identified interventions studied in ADHD. Prescribing information and peer-reviewed and gray literature helped us to determine which compounds had an underlying mechanism of action associated with changing serotonin levels. Of the 24 compounds that met the search criteria, 16 had either failed clinical studies in an ADHD population or had been discontinued from future development. The available evidence was assessed to identify the developmental history of drugs with serotonergic activity and the outlook for new ADHD drug candidates targeting serotonin. Several treatment candidates floundered due to an inability to balance effectiveness with safety, underscoring the potential importance of potency, and selectivity. Ongoing drug development includes compounds with multimodal mechanisms of action targeting neurotransmission across serotonin, norepinephrine, and dopamine pathways; it appears likely that treatment which balances competing and complementary monoamine effects may provide improved outcomes for patients. It is hoped that continuing research into ADHD treatment will produce new therapeutic options targeting the serotonergic system, which can positively impact a wide range of symptoms, including mood, anxiety, and sleep as well as attention and hyperactivity.
血清素与冲动、注意力和情绪调节有关,因此它与注意力缺陷多动障碍(ADHD)的神经生物学有关。许多具有血清素能特性的化合物已在 ADHD 中进行了评估,但很少有被监管机构批准。我们利用公共数据库的搜索,确定了在 ADHD 中研究的干预措施。处方信息以及同行评议和灰色文献帮助我们确定了哪些化合物具有与改变血清素水平相关的潜在作用机制。在符合搜索标准的 24 种化合物中,有 16 种在 ADHD 人群中的临床研究失败,或已停止未来开发。对现有证据进行了评估,以确定具有血清素活性的药物的发展历史,以及针对血清素的新 ADHD 候选药物的前景。由于无法平衡有效性与安全性,几种候选治疗药物失败,这突显了效力和选择性的潜在重要性。正在进行的药物开发包括针对血清素、去甲肾上腺素和多巴胺途径的神经传递的多模式作用机制的化合物;似乎平衡竞争和互补单胺作用的治疗方法可能为患者提供更好的结果。人们希望对 ADHD 治疗的持续研究将产生针对血清素系统的新治疗选择,这可以积极影响广泛的症状,包括情绪、焦虑和睡眠以及注意力和多动。