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Pharmacology of Basimglurant (RO4917523, RG7090), a Unique Metabotropic Glutamate Receptor 5 Negative Allosteric Modulator in Clinical Development for Depression

药理学 代谢型谷氨酸受体 代谢型谷氨酸受体5 变构调节 代谢受体 萧条(经济学) 代谢型谷氨酸受体4 变构调节剂 代谢型谷氨酸受体3 谷氨酸受体 神经科学 受体 化学 心理学 医学 内科学 经济 宏观经济学
作者
Lothar Lindemann,Richard H. Porter,Sebastian H. Scharf,Basil Kuennecke,Andreas Bruns,Markus von Kienlin,Anthony Harrison,Axel Paehler,Christoph Funk,Andreas Gloge,Manfred Schneider,Neil Parrott,Liudmila Polonchuk,U Niederhäuser,Stephen R. Morairty,Thomas S. Kilduff,Eric Vieira,Sabine Kolczewski,Juergen Wichmann,Thomas Härtung
出处
期刊:Journal of Pharmacology and Experimental Therapeutics [American Society for Pharmacology and Experimental Therapeutics]
卷期号:353 (1): 213-233 被引量:98
标识
DOI:10.1124/jpet.114.222463
摘要

Major depressive disorder (MDD) is a serious public health burden and a leading cause of disability. Its pharmacotherapy is currently limited to modulators of monoamine neurotransmitters and second-generation antipsychotics. Recently, glutamatergic approaches for the treatment of MDD have increasingly received attention, and preclinical research suggests that metabotropic glutamate receptor 5 (mGlu5) inhibitors have antidepressant-like properties. Basimglurant (2-chloro-4-[1-(4-fluoro-phenyl)-2,5-dimethyl-1H-imidazol-4-ylethynyl]-pyridine) is a novel mGlu5 negative allosteric modulator currently in phase 2 clinical development for MDD and fragile X syndrome. Here, the comprehensive preclinical pharmacological profile of basimglurant is presented with a focus on its therapeutic potential for MDD and drug-like properties. Basimglurant is a potent, selective, and safe mGlu5 inhibitor with good oral bioavailability and long half-life supportive of once-daily administration, good brain penetration, and high in vivo potency. It has antidepressant properties that are corroborated by its functional magnetic imaging profile as well as anxiolytic-like and antinociceptive features. In electroencephalography recordings, basimglurant shows wake-promoting effects followed by increased delta power during subsequent non–rapid eye movement sleep. In microdialysis studies, basimglurant had no effect on monoamine transmitter levels in the frontal cortex or nucleus accumbens except for a moderate increase of accumbal dopamine, which is in line with its lack of pharmacological activity on monoamine reuptake transporters. These data taken together, basimglurant has favorable drug-like properties, a differentiated molecular mechanism of action, and antidepressant-like features that suggest the possibility of also addressing important comorbidities of MDD including anxiety and pain as well as daytime sleepiness and apathy or lethargy.
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