NeSMOS Department (Neurosciences, Mental Health, and Sensory Organs), School of Medicine and Psychology, Sapienza University, UOC Psychiatry, SantAndrea Hospital, Rome, Italy.
CNS Drugs. 2012 Aug 1;26(8):663-90. doi: 10.2165/11634390-000000000-00000.
Memantine, a non-competitive NMDA receptor antagonist approved for Alzheimer's disease with a good safety profile, is increasingly being studied in a variety of non-dementia psychiatric disorders. We aimed to critically review relevant literature on the use of the drug in such disorders. We performed a PubMed search of the effects of memantine in animal models of psychiatric disorders and its effects in human studies of specific psychiatric disorders. The bulk of the data relates to the effects of memantine in major depressive disorder and schizophrenia, although more recent studies have provided data on the use of the drug in bipolar disorder as an add-on. Despite interesting preclinical data, results in major depression are not encouraging. Animal studies investigating the possible usefulness of memantine in schizophrenia are controversial; however, interesting findings were obtained in open studies of schizophrenia, but negative placebo-controlled, double-blind studies cast doubt on their validity. The effects of memantine in anxiety disorders have been poorly investigated, but data indicate that the use of the drug in obsessive-compulsive disorder and post-traumatic stress disorder holds promise, while findings relating to generalized anxiety disorder are rather disappointing. Results in eating disorders, catatonia, impulse control disorders (pathological gambling), substance and alcohol abuse/dependence, and attention-deficit hyperactivity disorder are inconclusive. In most psychiatric non-Alzheimer's disease conditions, the clinical data fail to support the usefulness of memantine as monotherapy or add-on treatment However, recent preclinical and clinical findings suggest that add-on memantine may show antimanic and mood-stabilizing effects in treatment-resistant bipolar disorder.
美金刚是一种非竞争性 NMDA 受体拮抗剂,已被批准用于治疗阿尔茨海默病,具有良好的安全性,目前越来越多地被用于研究各种非痴呆性精神疾病。我们旨在对该药物在这些疾病中的应用的相关文献进行批判性回顾。我们在 PubMed 上搜索了美金刚在精神障碍动物模型中的作用及其在特定精神障碍人类研究中的作用。大量数据与美金刚在重性抑郁症和精神分裂症中的作用有关,尽管最近的研究提供了关于将该药作为附加药物用于双相情感障碍的使用数据。尽管有有趣的临床前数据,但重性抑郁症的结果并不令人鼓舞。研究美金刚在精神分裂症中可能有用性的动物研究存在争议;然而,在精神分裂症的开放性研究中获得了有趣的发现,但阴性安慰剂对照、双盲研究对其有效性提出了质疑。美金刚在焦虑障碍中的作用研究甚少,但数据表明该药在强迫症和创伤后应激障碍中的应用有希望,而与广泛性焦虑障碍相关的发现则令人失望。在饮食障碍、紧张症、冲动控制障碍(病理性赌博)、物质和酒精滥用/依赖以及注意缺陷多动障碍中的研究结果尚无定论。在大多数非阿尔茨海默病的精神疾病中,临床数据无法支持美金刚作为单一疗法或附加治疗的有效性。然而,最近的临床前和临床发现表明,附加美金刚可能对治疗抵抗性双相情感障碍具有抗躁狂和稳定情绪的作用。