Department of CNS-Neuroscience, Research and Early Development, Johnson and Johnson Research and Development, Turnhoutseweg 30, 2340 Beerse, Belgium.
Eur J Pharmacol. 2010 Aug 10;639(1-3):2-16. doi: 10.1016/j.ejphar.2009.12.043. Epub 2010 Apr 2.
Metabotropic glutamate mGlu(1) receptors play a modulatory role in the nervous system. They enhance cell excitability, modulate synaptic neurotransmission and are involved in synaptic plasticity. During the last 10 years, several selective metabotropic glutamate mGlu(1) receptor competitive antagonists and potentiators have been discovered. These pharmacological tools, together with early and later work in metabotropic glutamate mGlu(1) receptor mutant mice have allowed studying the role of the receptor in various aspects of psychiatric illnesses such as anxiety, depression and schizophrenia. We here review the data on selective metabotropic glutamate mGlu(1) receptor antagonists in support of their potential as anxiolytic and antidepressant treatments. We propose a rationale for the development of metabotropic glutamate mGlu(1) receptor positive allosteric modulators for the treatment of schizophrenia. Potential side effects of blockade and activation of metabotropic glutamate mGlu(1) receptors are addressed, with special focus on the differential effects of metabotropic glutamate mGlu(1) receptor antagonists in cognition models with positive reinforcement versus those that use aversive learning procedures. Further development of negative allosteric modulators and more drug-like positive allosteric modulators will be required in order to decipher the therapeutic efficacy and safety margin of these compounds in the clinic.
代谢型谷氨酸 mGlu(1) 受体在神经系统中发挥调节作用。它们增强细胞兴奋性,调节突触神经传递,并参与突触可塑性。在过去的 10 年中,已经发现了几种选择性代谢型谷氨酸 mGlu(1) 受体竞争性拮抗剂和激动剂。这些药理学工具,以及代谢型谷氨酸 mGlu(1) 受体突变小鼠的早期和后期工作,使人们能够研究该受体在焦虑、抑郁和精神分裂症等精神疾病的各个方面的作用。我们在这里回顾了选择性代谢型谷氨酸 mGlu(1) 受体拮抗剂的数据,以支持它们作为抗焦虑和抗抑郁治疗的潜力。我们提出了开发代谢型谷氨酸 mGlu(1) 受体正变构调节剂治疗精神分裂症的原理。还讨论了代谢型谷氨酸 mGlu(1) 受体阻断和激活的潜在副作用,特别关注代谢型谷氨酸 mGlu(1) 受体拮抗剂在具有正强化的认知模型与使用厌恶学习程序的模型中的差异作用。为了解这些化合物在临床上的治疗效果和安全范围,需要进一步开发负变构调节剂和更具类药性的正变构调节剂。