Comparison of the mGlu5 receptor positive allosteric modulator ADX47273 and the mGlu2/3 receptor agonist LY354740 in tests for antipsychotic-like activity

被引:39
作者
Schlumberger, Chantal [1 ]
Pietraszek, Malgorzata [1 ]
Gravius, Andreas [1 ]
Klein, Kai-Uwe [2 ]
Greco, Sergio [3 ]
More, Lorenzo [1 ]
Danysz, Wojciech [1 ]
机构
[1] Merz Pharmaceut GmbH, Dept Vivo Pharmacol, D-60318 Frankfurt, Germany
[2] Merz Pharmaceut GmbH, Dept Nonclin DMPK, D-60318 Frankfurt, Germany
[3] Merz Pharmaceut GmbH, Dept Biol Analyt, D-60318 Frankfurt, Germany
关键词
Prepulse inhibition; Locomotor activity; mGlu(5) receptor positive allosteric modulator; mGlu(2/3) receptor agonist; ADX47273; LY354740; METABOTROPIC GLUTAMATE-RECEPTOR; SENSORIMOTOR GATING DEFICITS; METHYL-D-ASPARTATE; PREPULSE INHIBITION; IN-VIVO; D-AMPHETAMINE; DOPAMINE-D-2; RECEPTORS; LOCOMOTOR-ACTIVITY; ANIMAL-MODELS; MGLUR2/3; AGONIST;
D O I
10.1016/j.ejphar.2009.09.006
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Recently, it has been proposed that activation of either metabotropic glutamate receptors e.g. mGlu(5) by positive allosteric modulators or stimulation of mGluR(2/3) receptors by agonists may offer new strategy in schizophrenia treatment. The aim of the present Study Was to compare the effect of mGlu(5) receptor positive allosteric modulator, ADX47273 (30 mg/kg i.p). haloperidol (0.1 and 0.2 mg/kg i.p.) and mGluR(2/3) agonist, LY354740 ((1S,2S,5R,6S)-2-aminobicyclo[3.1.0]hexane-2,6-dicarboxylate monohydrate) and selected neuroleptics in animal models for positive schizophrenia symptoms. ADX47273 (3 and 10 mg/kg i.p.), the typical antipsychotic haloperidol (0.1 and 0.2 mg/kg i.p.), the atypical antipsychotics aripiprazole ( 1.25-5 mg/kg i.p.) and olanzapine (2.5 and 5 mg/kg i.p.) all reduced amphetamine-induced hyperlocomotion in Sprague-Dawley rats, unlike the mGlu(2/3) receptor agonist LY354740 (1-10 mg/kg i.p.). Interestingly, haloperidol (0.1 and 0.2 mg/kg i.p.), aripiprazole (4.25-5 mg/kg i.p.) and olanzapine ( 1.25-5 mg/kg i.p.), but not ADX47273 (1-10 mg/kg i.p.), all reduced spontaneous locomotion and rearings at doses effective against amphetamine-induced hyperlocomotion. This indicates that the effect of ADX47273 in combination with amphetamine may be specific, and also suggests a lack of sedative side effects. Moreover, ADX47273 (30 mg/kg i.p.), haloperidol (0.1 and 0.2 mg/kg i.p.) and aripiprazole (5 and 10 mg/kg i.p.) reversed apomorphine (0.5 mg/kg s.c.)-induced deficits of prepulse inhibition,whereas neither LY354740(1-10 mg/kg i.p.) nor olanzapine (1.25-5 mg/kg i.p.) produced this effect. Lack of effect of olanzapine Was unexpected and at present no convincing explanation call be provided. In conclusion, in selected rodent models for positive schizophrenia symptoms, ADX47273 showed better efficacy than LY354740. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:73 / 83
页数:11
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