In vivo effectiveness of CGP7930, a positive allosteric modulator of the GABAB receptor

被引:35
作者
Carai, MAM [1 ]
Colombo, G
Froestl, W
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
基金
美国国家航空航天局; 英国科学技术设施理事会;
关键词
CGP7930; positive allosteric modulation of GABA(B) receptor; baclofen gamma-hydroxybutyric acid (GHB); SCH; 50911; DBA; mouse;
D O I
10.1016/j.ejphar.2004.10.008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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.
引用
收藏
页码:213 / 216
页数:4
相关论文
共 8 条
  • [1] The heptahelical domain of GABAB2 is activated directly by CGP7930, a positive allosteric modulator of the GABAB receptor
    Binet, V
    Brajon, C
    Le Corre, L
    Acher, F
    Pin, JP
    Prézeau, L
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (28) : 29085 - 29091
  • [2] Substituted morpholine-2S-acetic acid derivatives: Sch 50911 and related compounds as novel GABA(B) antagonists
    Blythin, DJ
    Kuo, SC
    Shue, HJ
    McPhail, AT
    Chapman, RW
    Kreutner, W
    Rizzo, C
    She, HS
    West, R
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1996, 6 (13) : 1529 - 1534
  • [3] Suppression of GABAB receptor function in vivo by disulfide reducing agent, DL-dithiothreitol (DTT)
    Carai, MAM
    Vacca, G
    Serra, S
    Colombo, G
    Froestl, W
    Gessa, GL
    [J]. PSYCHOPHARMACOLOGY, 2004, 174 (02) : 283 - 290
  • [4] Role of GABAB receptors in the sedative/hypnotic effect of γ-hydroxybutyric acid
    Carai, MAM
    Colombo, G
    Brunetti, G
    Melis, S
    Serra, S
    Vacca, G
    Mastinu, S
    Pistuddi, AM
    Solinas, C
    Cignarella, G
    Minardi, G
    Gessa, GL
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 2001, 428 (03) : 315 - 321
  • [5] Maitre M, 2002, GAMMA-HYDROXYBUTYRATE: MOLECULAR, FUNCTIONAL, AND CLINICAL ASPECTS, P236, DOI 10.4324/9780203300992_chapter_14
  • [6] Positive regulation of GABAB receptors dually coupled to cyclic AMP by the allosteric agent CGP7930
    Onali, P
    Mascia, FM
    Olianas, MC
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 2003, 471 (02) : 77 - 84
  • [7] Effects of positive allosteric modulators of the GABAB receptor on cocaine self-administration in rats
    Smith, MA
    Yancey, DL
    Morgan, D
    Liu, Y
    Froestl, W
    Roberts, DCS
    [J]. PSYCHOPHARMACOLOGY, 2004, 173 (1-2) : 105 - 111
  • [8] Positive allosteric modulation of native and recombinant,γ-aminobutyric acidB receptors by 2,6-Di-tert-butyl-4-(3-hydroxy-2,2-dimethyl-propyl)-phenol (CGP7930) and its aldehyde analog CGP13501
    Urwyler, S
    Mosbacher, J
    Lingenhoehl, K
    Heid, J
    Hofstetter, K
    Froestl, W
    Bettler, B
    Kaupmann, K
    [J]. MOLECULAR PHARMACOLOGY, 2001, 60 (05) : 963 - 971