Swanson Chad J, Bures Mark, Johnson Michael P, Linden Anni-Maija, Monn James A, Schoepp Darryle D
Eli Lilly and Company, Neuroscience Division, Lilly Corporate Center DC 0510, Indianapolis, Indiana 46285, USA.
Nat Rev Drug Discov. 2005 Feb;4(2):131-44. doi: 10.1038/nrd1630.
Anxiety and stress disorders are the most commonly occurring of all mental illnesses, and current treatments are less than satisfactory. So, the discovery of novel approaches to treat anxiety disorders remains an important area of neuroscience research. Glutamate is the major excitatory neurotransmitter in the mammalian central nervous system, and G-protein-coupled metabotropic glutamate (mGlu) receptors function to regulate excitability via pre- and postsynaptic mechanisms. Various mGlu receptor subtypes, including group I (mGlu(1) and mGlu(5)), group II (mGlu(2) and mGlu(3)), and group III (mGlu(4), mGlu(7) and mGlu(8)) receptors, specifically modulate excitability within crucial brain structures involved in anxiety states. In addition, agonists for group II (mGlu(2/3)) receptors and antagonists for group I (in particular mGlu(5)) receptors have shown activity in animal and/or human conditions of fear, anxiety or stress. These studies indicate that metabotropic glutamate receptors are interesting new targets to treat anxiety disorders in humans.
焦虑症和应激障碍是所有精神疾病中最常见的,而目前的治疗方法并不令人满意。因此,发现治疗焦虑症的新方法仍然是神经科学研究的一个重要领域。谷氨酸是哺乳动物中枢神经系统中的主要兴奋性神经递质,G蛋白偶联代谢型谷氨酸(mGlu)受体通过突触前和突触后机制调节兴奋性。各种mGlu受体亚型,包括I组(mGlu(1)和mGlu(5))、II组(mGlu(2)和mGlu(3))和III组(mGlu(4)、mGlu(7)和mGlu(8))受体,特异性调节参与焦虑状态的关键脑结构内的兴奋性。此外,II组(mGlu(2/3))受体激动剂和I组(特别是mGlu(5))受体拮抗剂在动物和/或人类的恐惧、焦虑或应激状态下已显示出活性。这些研究表明,代谢型谷氨酸受体是治疗人类焦虑症的有趣新靶点。