Negative modulation of GABAA α5 receptors by RO4938581 attenuates discrete sub-chronic and early postnatal phencyclidine (PCP)-induced cognitive deficits in rats

被引:54
作者
Redrobe, John P. [1 ]
Elster, Lisbeth [1 ]
Frederiksen, Kristen [1 ]
Bundgaard, Christoffer [1 ]
de Jong, Inge E. M. [1 ]
Smith, Garrick P. [1 ]
Bruun, Anne Techau [1 ]
Larsen, Peter H. [1 ]
Didriksen, Michael [1 ]
机构
[1] H Lundbeck & Co AS, Neurosci Res DK, Synapt Transmiss I, DK-2500 Valby, Denmark
关键词
GABA alpha5 receptors; Negative allosteric modulator; Sub-chronic PCP; Early postnatal PCP; Novel object recognition; Attentional set shifting; Cognition; Rat; PARVALBUMIN-IMMUNOREACTIVE NEURONS; OBJECT-RECOGNITION MEMORY; PCP-INDUCED DEFICITS; PREFRONTAL CORTEX; CHRONIC-SCHIZOPHRENIA; INVERSE AGONIST; ANTIPSYCHOTIC-DRUGS; ENHANCES COGNITION; GAMMA-OSCILLATIONS; FRONTAL-CORTEX;
D O I
10.1007/s00213-011-2593-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Rationale A growing body of evidence suggests that negative modulation of gamma-aminobutyric acid (GABA) GABA(A) alpha 5 receptors may be a promising strategy for the treatment of certain facets of cognitive impairment; however, selective modulators of GABA(A) alpha 5 receptors have not yet been tested in "schizophrenia-relevant" cognitive assay/model systems in animals. Objectives The objectives of this study were to investigate the potential of RO4938581, a negative modulator of GABA(A) alpha 5 receptors, and to attenuate cognitive impairments induced following sub-chronic (sub-PCP) and early postnatal PCP (neo-PCP) administration in the novel object recognition (NOR) and intra-extradimensional shift (ID/ED) paradigms in rats. Complementary in vitro, ex vivo and in vivo studies were performed to confirm negative modulatory activity of RO4938581 and to investigate animal model validity, concept validity and potential side effect issues, respectively. Results In vitro studies confirmed the reported negative modulatory activity of RO4938581, whilst immunohistochemical analyses revealed significantly reduced parvalbumin-positive cells in the prefrontal cortex of sub-PCP- and neo-PCP-treated rats. RO4938581 (1 mg/kg) ameliorated both sub-PCP- and neo-PCP-induced cognitive deficits in NOR and ID/ED performance, respectively. In contrast, QH-II-066 (1 and 3 mg/kg), a GABA(A) alpha 5 receptor positive modulator, impaired cognitive performance in the NOR task when administered to vehicle-treated animals. Additional studies revealed that both RO4938581 (1 mg/kg) and QH-II-066 (1 and 3 mg/kg) attenuated amphetamine-induced hyperactivity in rats. Conclusions Taken together, these novel findings suggest that negative modulation of GABA(A) alpha 5 receptors may represent an attractive treatment option for the cognitive impairments, and potentially positive symptoms, associated with schizophrenia.
引用
收藏
页码:451 / 468
页数:18
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