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

被引:85
作者
Lindemann, Lothar [1 ]
Porter, Richard H. [3 ]
Scharf, Sebastian H. [1 ]
Kuennecke, Basil [1 ]
Bruns, Andreas [1 ]
von Kienlin, Markus [1 ]
Harrison, Anthony C. [4 ]
Paehler, Axel [4 ]
Funk, Christoph [4 ]
Gloge, Andreas [4 ]
Schneider, Manfred [4 ]
Parrott, Neil J. [4 ]
Polonchuk, Liudmila [4 ]
Niederhauser, Urs [4 ]
Morairty, Stephen R. [6 ]
Kilduff, Thomas S. [6 ]
Vieira, Eric [2 ]
Kolczewski, Sabine [2 ]
Wichmann, Juergen [2 ]
Hartung, Thomas [5 ]
Honer, Michael [1 ]
Borroni, Edilio [1 ]
Moreau, Jean-Luc [3 ]
Prinssen, Eric [1 ]
Spooren, Will [1 ]
Wettstein, Joseph G. [1 ]
Jaeschke, Georg [2 ]
机构
[1] Roche Innovat Ctr Basel, Roche Pharmaceut Res & Early Dev, Discovery Neurosci, Neurosci Ophthalmol & Rare Dis, CH-4070 Basel, Switzerland
[2] Roche Innovat Ctr Basel, Discovery Chem, CH-4070 Basel, Switzerland
[3] Roche Innovat Ctr Basel, Operat Neurosci Ophthalmol & Rare Dis, CH-4070 Basel, Switzerland
[4] Roche Innovat Ctr Basel, Pharmaceut Sci, CH-4070 Basel, Switzerland
[5] Roche Innovat Ctr Basel, Small Mol Proc Res & Synth, CH-4070 Basel, Switzerland
[6] SRI Int, Ctr Neurosci, Biosci Div, Menlo Pk, CA 94025 USA
关键词
STRESS-INDUCED ANHEDONIA; FRAGILE-X-SYNDROME; ZERO DOSE CONTROL; MAJOR DEPRESSION; CHRONIC PAIN; SPINAL-CORD; ANTIDEPRESSANT TREATMENT; COGNITIVE PERFORMANCE; BLADDER NOCICEPTION; PARKINSONS-DISEASE;
D O I
10.1124/jpet.114.222463
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
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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收藏
页码:213 / 233
页数:21
相关论文
共 116 条
[1]
Ahmadi N., 2010, Sleep and Mental Illness, P165, DOI [10.1017/CBO9781139042734.017, DOI 10.1017/CBO9781139042734.017]
[2]
Negative versus positive allosteric modulation of metabotropic glutamate receptors (mGluR5): indices for potential pro-cognitive drug properties based on EEG network oscillations and sleep-wake organization in rats [J].
Ahnaou, A. ;
Langlois, X. ;
Steckler, T. ;
Bartolome-Nebreda, J. M. ;
Drinkenburg, W. H. I. M. .
PSYCHOPHARMACOLOGY, 2015, 232 (06) :1107-1122
[3]
PLASMID COPY NUMBER AND MUTANT FREQUENCIES IN S-TYPHIMURIUM TA102 [J].
ALBERTINI, S ;
GOCKE, E .
ENVIRONMENTAL AND MOLECULAR MUTAGENESIS, 1988, 12 (04) :353-363
[4]
Reduced transit-time sensitivity in noninvasive magnetic resonance imaging of human cerebral blood flow [J].
Alsop, DC ;
Detre, JA .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1996, 16 (06) :1236-1249
[5]
Ametamey SM, 2007, J NUCL MED, V48, P247
[6]
Ametamey SM, 2006, J NUCL MED, V47, P698
[7]
APA A.P. A., 2000, Diagnostic and statistical manual of mental disorders: DSM-IV, V4th
[8]
Expression and functional role of mGluR3 and mGluR5 in human astrocytes and glioma cells: opposite regulation of glutamate transporter proteins [J].
Aronica, E ;
Gorter, JA ;
Ijlst-Keizers, H ;
Rozemuller, AJ ;
Yankaya, B ;
Leenstra, S ;
Troost, D .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2003, 17 (10) :2106-2118
[9]
The effect of the mGlu5 receptor antagonist MPEP in rodent tests of anxiety and cognition: a comparison [J].
Ballard, TM ;
Woolley, ML ;
Prinssen, E ;
Huwyler, J ;
Porter, R ;
Spooren, W .
PSYCHOPHARMACOLOGY, 2005, 179 (01) :218-229
[10]
Characterization of the Antinociceptive actions of bicifadine in models of acute, persistent, and chronic pain [J].
Basile, Anthony S. ;
Janowsky, Aaron ;
Golembiowska, Krystyna ;
Kowalska, Magdalena ;
Tam, Eyal ;
Benveniste, Morris ;
Popik, Piotr ;
Nikiforuk, Agnieszka ;
Krawczyk, Martyna ;
Nowak, Gabriel ;
Krieter, Philip A. ;
Lippa, Arnold S. ;
Skolnick, Phil ;
Koustova, Elena .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2007, 321 (03) :1208-1225