Comparison of the effects of the GABAB receptor positive modulator BHF177 and the GABAB receptor agonist baclofen on anxiety-like behavior, learning, and memory in mice

NEUROPHARMACOLOGY

卷:70

Article

Li, Xia¹  Risbrough, Victoria B.^1,4  Cates-Gatto, Chelsea²  Kaczanowska, Katarzyna³  Finn, M. G.³  Roberts, Amanda J.²  Markou, Athina¹ 

[1] Univ Calif San Diego, Sch Med, Dept Psychiat, La Jolla, CA 92093 USA

[2] Scripps Res Inst, Mol & Integrat Neurosci Dept, La Jolla, CA 92037 USA

[3] Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA

[4] Vet Affairs Ctr Excellence Stress & Mental Hlth, La Jolla, CA USA

关键词: GABA(B) receptor;    Positive allosteric modulator;    Anxiety;    Learning;    Memory;   

DOI  :  10.1016/j.neuropharm.2013.01.018

来源: Elsevier

【 摘 要 】

gamma-Arninobutyric acid B (GABA(B)) receptor activation is a potential therapeutic approach for the treatment of drug addiction, pain, anxiety, and depression. However, full agonists of this receptor induce side-effects, such as sedation, muscle relaxation, tolerance, and cognitive disruption. Positive allosteric modulators (PAMs) of the GABA(B) receptor may have similar therapeutic effects as agonists with superior side-effect profiles. The present study behaviorally characterized N-([1R,2R,4S]-bicyclo[2.2.1]hept-2-yl)-2-methyl-5-(4-[trifluoromethyl]phenyl)-4-pyrimidinamine (BHF177), a GABA(B) receptor PAM, in mouse models of anxiety-like behavior, learning and memory. In addition, the effects of BHF177 were compared with the agonist baclofen. Unlike the anxiolytic chlordiazepoxide, baclofen (0.5, 1.5, and 2.5 mg/kg, intraperitoneally) and BHF177 (10, 20, and 40 mg/kg, orally) had no effect on anxiety-like behavior in the elevated plus maze, light/dark box, or Vogel conflict test. Baclofen increased punished drinking in the Vogel conflict test, but this effect may be attributable to the analgesic actions of baclofen. At the highest dose tested (2.5 mg/kg), baclofen-treated mice exhibited sedation-like effects (i.e., reduced locomotor activity) across many of the tests, whereas BHF177-treated mice exhibited no sedation-like effects. BHF177 exhibited pro-convulsion properties only in mice, but not in rats, indicating that this effect may be species-specific. At doses that were not sedative or pro-convulsant, baclofen and BHF177 had no selective effects on fear memory retrieval in contextual and cued fear conditioning or spatial learning and memory in the Barnes maze. These data suggest that BHF177 has little sedative activity, no anxiolytic-like profile, and minimal impairment of learning and memory in mice. (C) 2013 Elsevier Ltd. All rights reserved.

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