MK-7128, a novel CB1 receptor inverse agonist, improves scopolamine-induced learning and memory deficits in mice

被引:10
作者
Dillon, Gregory M. [1 ]
Lubbers, Laura S. [2 ]
Ferguson, Mitchell T. [1 ]
Lao, Julie Z. [3 ]
Huang, Ruey-Ruey C. [3 ]
Xiao, Jing C. [3 ]
Fong, Tung M. [3 ]
Hale, Jeffrey J. [3 ]
Rupprecht, Kathleen [3 ]
Miao, Shouwu [3 ]
Rowe, Blake A. [2 ]
Kornecook, Thomas J. [1 ]
Dodart, Jean-Cosme [1 ]
机构
[1] Merck Res Labs, Boston, MA USA
[2] MRL, West Point, PA USA
[3] MRL, Rahway, NJ USA
来源
BEHAVIOURAL PHARMACOLOGY | 2011年 / 22卷 / 02期
关键词
cannabinoids; CB1; receptor; cognition; mouse; receptor occupancy; scopolamine; LONG-TERM POTENTIATION; MEDIAL-PREFRONTAL CORTEX; CANNABINOID RECEPTOR; SPONTANEOUS-ALTERNATION; RECOGNITION MEMORY; IN-VIVO; ENDOCANNABINOID SYSTEM; ACETYLCHOLINE-RELEASE; HIPPOCAMPAL DAMAGE; CYTOTOXIC LESIONS;
D O I
10.1097/FBP.0b013e3283423d7e
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Cannabinoid receptors (CBRs) play an important role in a variety of physiological functions and have been considered drug targets for obesity and psychiatric disorders. In particular, the CB1R is highly expressed in brain regions crucial to learning and memory processes, and several lines of evidence indicate that pharmacological blockade of this receptor could have therapeutic applications in the treatment of cognitive disorders. In this study, we investigated whether MK-7128 (0.1, 0.3, and 1 mg/kg, orally), a novel and selective CB1R inverse agonist, could improve learning and memory deficits induced by scopolamine (1mg/kg, subcutaneously) in mice. The investigators also assessed CB1R occupancy in the brain to ensure target engagement of MK-7128, and showed that MK-7128 significantly improved both Y-maze spontaneous alternation and object habituation performance in scopolamine-treated mice and inhibits the binding of radioiodinated AM251 in murine cortex and hippocampus. These data indicate that MK-7128 improves cognitive performance in a model of cholinergic hypofunction and suggest that efficacy is achieved at relatively low levels of CB1R occupancy in the brain. Our results extend earlier findings suggesting a role of CB1Rs in the modulation of memory processes and a potential therapeutic application for CB1R inverse agonists in cognitive disorders. Behavioural Pharmacology 22:91-100 (C) 2011 Wolters Kluwer Health | Lippincott Williams & Wilkins.
引用
收藏
页码:91 / 100
页数:10
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