Literature DB >> 19707745

Combined administration of an mGlu2/3 receptor agonist and a 5-HT 2A receptor antagonist markedly attenuate the psychomotor-activating and neurochemical effects of psychostimulants.

Jason M Uslaner1, Sean M Smith, Sarah L Huszar, Rashida Pachmerhiwala, Richard M Hinchliffe, Joshua D Vardigan, Pete H Hutson.   

Abstract

RATIONALE: It was recently reported that administration of the metabotropic glutamate 2 and 3 (mGlu2/3) receptor agonist prodrug LY2140023 to schizophrenic patients decreased positive symptoms. However, at the single, potentially suboptimal, dose that was tested, LY2140023 trended towards being inferior to olanzapine on several indices of efficacy within the Positive and Negative Syndrome Scale.
OBJECTIVES: In this study, we examined whether the antipsychotic potential of mGlu2/3 receptor agonism can be enhanced with 5-HT(2A) receptor antagonism.
MATERIALS AND METHODS: Specifically, we characterized the effects of co-administering submaximally effective doses of the 5-HT(2A) receptor antagonist M100907 (0.2 mg/kg) and the mGlu2/3 receptor agonist LY379268 (1 mg/kg) on amphetamine-induced and MK-801-induced psychomotor activity in rats, an assay sensitive to antipsychotics. We also determined the effects of co-administering these two compounds on MK-801-induced dopamine and norepinephrine efflux in the nucleus accumbens (NAc).
RESULTS: At the submaximally effective doses tested, the effects of M100907 and LY379268 on amphetamine-induced and MK-801-induced psychomotor activity were significantly greater when given together than when given separately. Furthermore, coadministration of these doses of M100907 and LY379268 reduced MK-801-induced dopamine efflux in the NAc. This effect on dopamine release was not observed with the administration of either compound alone, even at higher doses that attenuated MK-801-induced psychomotor activity.
CONCLUSIONS: Our results suggest that a single compound having both mGlu2/3 receptor agonist and 5-HT(2A) receptor antagonist activity, or coadministration of two compounds selective for these receptors, could be superior in terms of efficacy and/or reduced side-effect liability relative to an mGlu2/3 receptor agonist alone.

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Year:  2009        PMID: 19707745     DOI: 10.1007/s00213-009-1644-y

Source DB:  PubMed          Journal:  Psychopharmacology (Berl)        ISSN: 0033-3158            Impact factor:   4.530


  47 in total

1.  Tolerance to the motor impairment, but not to the reversal of PCP-induced motor activities by oral administration of the mGlu2/3 receptor agonist, LY379268.

Authors:  J Cartmell; J A Monn; D D Schoepp
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2000-01       Impact factor: 3.000

2.  Reversal of phencyclidine effects by a group II metabotropic glutamate receptor agonist in rats.

Authors:  B Moghaddam; B W Adams
Journal:  Science       Date:  1998-08-28       Impact factor: 47.728

3.  The ratios of serotonin2 and dopamine2 affinities differentiate atypical and typical antipsychotic drugs.

Authors:  H Y Meltzer; S Matsubara; J C Lee
Journal:  Psychopharmacol Bull       Date:  1989

4.  The group II metabotropic glutamate receptor agonist (-)-2-oxa-4-aminobicyclo[3.1.0.]hexane-4,6-dicarboxylate (LY379268) and clozapine reverse phencyclidine-induced behaviors in monoamine-depleted rats.

Authors:  Chad J Swanson; Darryle D Schoepp
Journal:  J Pharmacol Exp Ther       Date:  2002-12       Impact factor: 4.030

5.  Dopamine is not required for the hyperlocomotor response to NMDA receptor antagonists.

Authors:  Elena H Chartoff; Carrie L Heusner; Richard D Palmiter
Journal:  Neuropsychopharmacology       Date:  2005-07       Impact factor: 7.853

6.  Physiological antagonism between 5-hydroxytryptamine(2A) and group II metabotropic glutamate receptors in prefrontal cortex.

Authors:  G J Marek; R A Wright; D D Schoepp; J A Monn; G K Aghajanian
Journal:  J Pharmacol Exp Ther       Date:  2000-01       Impact factor: 4.030

7.  Effects of ritanserin on sleep disturbances of dysthymic patients.

Authors:  T Paiva; F Arriaga; A Wauquier; E Lara; R Largo; J N Leitao
Journal:  Psychopharmacology (Berl)       Date:  1988       Impact factor: 4.530

8.  Enhancement of antipsychoticlike properties of raclopride in rats using the selective serotonin2A receptor antagonist MDL 100,907.

Authors:  M L Wadenberg; P B Hicks; J T Richter; K A Young
Journal:  Biol Psychiatry       Date:  1998-09-15       Impact factor: 13.382

9.  Group II mGlu receptor activation suppresses norepinephrine release in the ventral hippocampus and locomotor responses to acute ketamine challenge.

Authors:  Daniel S Lorrain; Hervé Schaffhauser; Una C Campbell; Christopher S Baccei; Lucia D Correa; Blake Rowe; Dana E Rodriguez; Jeffery J Anderson; Mark A Varney; Anthony B Pinkerton; Jean-Michel Vernier; Linda J Bristow
Journal:  Neuropsychopharmacology       Date:  2003-06-25       Impact factor: 7.853

10.  Differential effects of classical and newer antipsychotics on the hypermotility induced by two dose levels of D-amphetamine.

Authors:  J Arnt
Journal:  Eur J Pharmacol       Date:  1995-09-05       Impact factor: 4.432

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  11 in total

1.  Activation of metabotropic glutamate 2/3 receptors attenuates methamphetamine-induced hyperlocomotion and increase in prefrontal serotonergic neurotransmission.

Authors:  Yukio Ago; Ryota Araki; Koji Yano; Naoki Hiramatsu; Toshiyuki Kawasaki; Shigeyuki Chaki; Atsuro Nakazato; Hirotaka Onoe; Hitoshi Hashimoto; Akemichi Baba; Kazuhiro Takuma; Toshio Matsuda
Journal:  Psychopharmacology (Berl)       Date:  2011-04-13       Impact factor: 4.530

2.  Decoding the signaling of a GPCR heteromeric complex reveals a unifying mechanism of action of antipsychotic drugs.

Authors:  Miguel Fribourg; José L Moreno; Terrell Holloway; Davide Provasi; Lia Baki; Rahul Mahajan; Gyu Park; Scott K Adney; Candice Hatcher; José M Eltit; Jeffrey D Ruta; Laura Albizu; Zheng Li; Adrienne Umali; Jihyun Shim; Alexandre Fabiato; Alexander D MacKerell; Vladimir Brezina; Stuart C Sealfon; Marta Filizola; Javier González-Maeso; Diomedes E Logothetis
Journal:  Cell       Date:  2011-11-23       Impact factor: 41.582

3.  Pre-treatment with the mGlu2/3 receptor agonist LY379268 attenuates DOI-induced impulsive responding and regional c-Fos protein expression.

Authors:  Lena Wischhof; Michael Koch
Journal:  Psychopharmacology (Berl)       Date:  2011-08-24       Impact factor: 4.530

4.  The metabotropic glutamate 2/3 receptor agonist LY379268 blocked nicotine-induced increases in nucleus accumbens shell dopamine only in the presence of a nicotine-associated context in rats.

Authors:  Manoranjan S D'Souza; Matthias E Liechti; Ana M Ramirez-Niño; Ronald Kuczenski; Athina Markou
Journal:  Neuropsychopharmacology       Date:  2011-06-08       Impact factor: 7.853

5.  Impact of metabotropic glutamate 2/3 receptor stimulation on activated dopamine release and locomotion.

Authors:  Alan L Pehrson; Bita Moghaddam
Journal:  Psychopharmacology (Berl)       Date:  2010-06-29       Impact factor: 4.530

Review 6.  Metabotropic glutamate receptors as therapeutic targets for schizophrenia.

Authors:  Paige N Vinson; P Jeffrey Conn
Journal:  Neuropharmacology       Date:  2011-05-19       Impact factor: 5.250

Review 7.  Preclinical models of antipsychotic drug action.

Authors:  José L Moreno; Javier González-Maeso
Journal:  Int J Neuropsychopharmacol       Date:  2013-06-10       Impact factor: 5.176

8.  Interaction of mGlu2/3 agonism with clozapine and lurasidone to restore novel object recognition in subchronic phencyclidine-treated rats.

Authors:  Masakuni Horiguchi; Mei Huang; Herbert Y Meltzer
Journal:  Psychopharmacology (Berl)       Date:  2011-03-25       Impact factor: 4.530

Review 9.  The Role of G Protein-Coupled Receptors (GPCRs) and Calcium Signaling in Schizophrenia. Focus on GPCRs Activated by Neurotransmitters and Chemokines.

Authors:  Tomasz Boczek; Joanna Mackiewicz; Marta Sobolczyk; Julia Wawrzyniak; Malwina Lisek; Bozena Ferenc; Feng Guo; Ludmila Zylinska
Journal:  Cells       Date:  2021-05-17       Impact factor: 6.600

10.  The antipsychotic-like effects of the mGlu group III orthosteric agonist, LSP1-2111, involves 5-HT₁A signalling.

Authors:  Joanna M Wierońska; Francine C Acher; Anna Sławińska; Piotr Gruca; Magdalena Lasoń-Tyburkiewicz; Mariusz Papp; Andrzej Pilc
Journal:  Psychopharmacology (Berl)       Date:  2013-03-10       Impact factor: 4.530

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