Noetzel Meredith J, Jones Carrie K, Conn P Jeffrey
Department of Pharmacology and Vanderbilt Center for Neuroscience Drug Discovery, Vanderbilt University Medical Center, Nashville, Tennessee 37202, USA.
Discov Med. 2012 Nov;14(78):335-43.
Treatment options for schizophrenia that address all symptom categories (positive, negative, and cognitive) are lacking. Novel compounds that regulate signaling by the major excitatory neurotransmitter in the brain, glutamate, are emerging as a novel approach for the treatment of this disorder. Currently available medications ameliorate positive symptoms but do not have efficacy in reducing negative symptoms or cognitive disturbances. It is possible that agents that target glutamatergic signaling in the CNS could have efficacy in reducing all major symptom clusters, providing a more comprehensive treatment strategy, and also avoiding some of the adverse effects that are seen with currently available treatments. Three major approaches for targeting glutamate signaling are now advancing in preclinical and clinical development. First are inhibitors for a transporter for glycine termed GlyT1. Glycine is a co-agonist with glutamate for a specific subtype of glutamate receptor, termed the NMDA receptor, which is thought to be critically involved in brain circuits that are disrupted in schizophrenia patients. Inhibiting GlyT1 increases glycine levels and can selectively increase NMDA receptor signaling. Another promising approach is to increase activity of another family of glutamate receptors, termed metabotropic glutamate receptors (mGlus), which play important modulatory roles in brain circuits that are thought to be disrupted in schizophrenia patients. Activation of the group I (mGlu5) and the group II (mGlu2 and mGlu3) mGlus is hypothesized to normalize the disruption of aberrant signaling in these circuits. Novel drug-like molecules that increase activity of these receptors have robust efficacy in animal models that predict efficacy in treatment of schizophrenia. Early clinical studies provide some support for potential utility of these targets in reducing symptoms in schizophrenia patients. Clinical studies that are underway will provide further insights into the potential utility of these compounds in the treatment of multiple symptom domains in schizophrenia patients.
目前缺乏能解决精神分裂症所有症状类别(阳性、阴性和认知症状)的治疗方案。调节大脑中主要兴奋性神经递质谷氨酸信号传导的新型化合物正成为治疗这种疾病的一种新方法。目前可用的药物可改善阳性症状,但对减轻阴性症状或认知障碍无效。针对中枢神经系统中谷氨酸能信号传导的药物有可能有效减轻所有主要症状群,提供更全面的治疗策略,同时避免目前可用治疗方法所出现的一些不良反应。目前有三种针对谷氨酸信号传导的主要方法正在进行临床前和临床开发。第一种是针对一种名为甘氨酸转运体1(GlyT1)的抑制剂。甘氨酸是谷氨酸的协同激动剂,作用于一种特定的谷氨酸受体亚型,即N-甲基-D-天冬氨酸受体(NMDA受体),该受体被认为在精神分裂症患者中受到破坏的脑回路中起关键作用。抑制GlyT1可提高甘氨酸水平,并可选择性地增强NMDA受体信号传导。另一种有前景的方法是增强另一类谷氨酸受体的活性,这类受体称为代谢型谷氨酸受体(mGlu),它们在被认为在精神分裂症患者中受到破坏的脑回路中起重要的调节作用。据推测,激活I组(mGlu5)和II组(mGlu2和mGlu3)mGlu可使这些回路中异常信号传导的破坏恢复正常。能增强这些受体活性的新型类药物分子在预测精神分裂症治疗疗效的动物模型中具有强大的疗效。早期临床研究为这些靶点在减轻精神分裂症患者症状方面的潜在效用提供了一些支持。正在进行的临床研究将进一步深入了解这些化合物在治疗精神分裂症患者多种症状领域的潜在效用。