Department of Anatomy and Neurosciences and Marine Biomedical Institute, University of Texas, Medical Branch, Galveston, TX 77555-1069, USA.
Expert Rev Neurother. 2001 Nov;1(2):207-24. doi: 10.1002/1615-9861(200102)1:2<207::AID-PROT207>3.0.CO;2-3.
Metabotropic glutamate receptors (mGluRs) are a relatively new family of G-protein coupled receptors that can be activated by the major excitatory neurotransmitter, L-glutamate. The eight known mGluR subtypes are classified into three groups based on their sequence homology, signal transduction mechanisms and receptor pharmacology. Extensive research has implicated mGluRs in neuroplasticity associated with normal brain functions, but also in various neurological and psychiatric disorders. Evidence is accumulating to suggest an important role of mGluRs in nociception and pain. With the availability in recent years of selective pharmacological tools, behavioral and electrophysiological studies have shown that mGluR subgroups and subtypes mediate and modulate nociceptive processing at different levels of the nervous system: periphery, spinal cord and brain. Thus, mGluRs may provide important novel therapeutic targets for the relief of pain associated with altered neurotransmission and neuronal excitability.
代谢型谷氨酸受体(mGluRs)是一种相对较新的 G 蛋白偶联受体家族,可被主要的兴奋性神经递质 L-谷氨酸激活。已知的 8 种 mGluR 亚型根据其序列同源性、信号转导机制和受体药理学分为三组。广泛的研究表明 mGluRs 与正常大脑功能相关的神经可塑性有关,但也与各种神经和精神疾病有关。有证据表明 mGluRs 在痛觉和疼痛中起重要作用。近年来,随着选择性药理学工具的出现,行为和电生理学研究表明,mGluR 亚群和亚型在神经系统的不同水平(外周、脊髓和大脑)介导和调节痛觉处理。因此,mGluRs 可能为缓解与神经递质改变和神经元兴奋性相关的疼痛提供重要的新的治疗靶点。