In vivo effectiveness of CGP7930, a positive allosteric modulator of the GABAB receptor
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作者:
Carai, MAM
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Univ Cagliari, Bernard B Brodie Dept Neurosci, I-09126 Cagliari, CA, ItalyUniv Cagliari, Bernard B Brodie Dept Neurosci, I-09126 Cagliari, CA, Italy
Carai, MAM
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Colombo, G
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机构:Univ Cagliari, Bernard B Brodie Dept Neurosci, I-09126 Cagliari, CA, Italy
Colombo, G
Froestl, W
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机构:Univ Cagliari, Bernard B Brodie Dept Neurosci, I-09126 Cagliari, CA, Italy
Froestl, W
Gessa, GL
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机构:Univ Cagliari, Bernard B Brodie Dept Neurosci, I-09126 Cagliari, CA, Italy
Gessa, GL
机构:
[1] Univ Cagliari, Bernard B Brodie Dept Neurosci, I-09126 Cagliari, CA, Italy
[2] CNR, Inst Neurosci, Sect Cagliari, I-09126 Cagliari, CA, Italy
[3] Novartis Pharma AG, Res Dept, CH-4002 Basel, Switzerland
The present study was aimed at assessing the in vivo effectiveness of the positive allosteric modulator of the gamma-aminobutyric acid(B) (GABA(B)) receptor, CGP7930 [2,6-di-tert-butyl-4-(3-hydroxy-2,2-dimethyl-propyl)-phenol]. The synergistic potentiation of GABA(B) receptor functioning, previously observed in different in vitro assays, has been confirmed in the present work, where pretreatment with CGP7930 (10-170 mg/kg, i.p.) resulted in a marked potentiation of the sedative/hypnotic effect of the GABAB receptor agonists, baclofen (40 mg/kg, i.p.) and gamma-hydroxybutyric acid (500 mg/kg, i.p.), in DBA mice. Pretreatment with the GABA(B) receptor antagonist, SCH 50911 [(S)-5,5-dimethyl-2-morpholine acetic acid; 100 mg/kg, i.p.], resulted in a complete blockade of the sedative/hypnotic effect of the combination of CGP7930 with either baclofen or gamma-hydroxybutyric acid. These results confirm that CGP7930 may constitute an interesting tool for pharmacological studies in the GABA(B) receptor field. (C) 2004 Elsevier B.V. All rights reserved.