5-HT6 receptor antagonists reverse delay-dependent deficits in novel object discrimination by enhancing consolidation - an effect sensitive to NMDA receptor antagonism

被引:181
作者
King, MV [1 ]
Sleight, AJ
Woolley, ML
Topham, IA
Marsden, CA
Fone, KCF
机构
[1] Univ Nottingham, Sch Biomed Sci, Queens Med Ctr, Inst Neurosci, Nottingham NG7 2UH, England
[2] Hoffmann La Roche Ag, PRBD N, CH-4070 Basel, Switzerland
关键词
5-HT6; receptor; Ro; 04-6790; SB-271046; cognition; object discrimination; glutamate;
D O I
10.1016/j.neuropharm.2004.03.012
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
5-HT6 receptors are expressed in brain regions associated with learning and memory, and blockade of their function increases central cholinergic and glutamatergic neurotransmission and enhances cognitive processes. This study examined the effects of acute systemic administration of two selective 5-HT6 receptor antagonists Ro 04-6790 and SB-271046(10 mg kg(-1) i.p.) on acquisition, consolidation, and retrieval in the novel object discrimination (NOD) task, a two-trial test of recognition memory in which rats exposed to two identical objects during a familiarisation trial can discriminate a novel from a familiar object during the subsequent choice trial, following inter-trial delays of up to 3 h. 5-HT6 receptor antagonist administration 20 min prior to or immediately after the familiarisation trial, but not 20 min prior to the choice trial reversed the deficit in object discrimination produced by a 4 h inter-trial interval. The nootropic effects of the 5-HT6 receptor antagonists in this task thus appear to involve enhanced consolidation. Pre-treatment with the non-competitive NMDA receptor antagonist MK-801 (0.05 mg kg(-1) i.p.) prevented the effect of Ro 04-6790 on delay-induced deficits in object discrimination. This suggests that the 5-HT6 receptor antagonist-induced enhancement of consolidation involves increased central glutamatergic neurotransmission. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:195 / 204
页数:10
相关论文
共 64 条
[41]  
ROGERS DC, 2000, SOC NEUR ABSTR, V26, P680
[42]   Characterization of SB-271046:: A potent, selective and orally active 5-HT6 receptor antagonist [J].
Routledge, C ;
Bromidge, SM ;
Moss, SF ;
Price, GW ;
Hirst, W ;
Newman, H ;
Riley, G ;
Gager, T ;
Stean, T ;
Upton, N ;
Clarke, SE ;
Brown, AM ;
Middlemiss, DN .
BRITISH JOURNAL OF PHARMACOLOGY, 2000, 130 (07) :1606-1612
[43]  
Routledge C., 1999, BR J PHARM S, V127, P21
[44]   A NOVEL RAT SEROTONIN (5-HT6) RECEPTOR - MOLECULAR-CLONING, LOCALIZATION AND STIMULATION OF CAMP ACCUMULATION [J].
RUAT, M ;
TRAIFFORT, E ;
ARRANG, JM ;
TARDIVELLACOMBE, J ;
DIAZ, J ;
LEURS, R ;
SCHWARTZ, JC .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1993, 193 (01) :268-276
[45]   NMDA receptor-dependent synaptic reinforcement as a crucial process for memory consolidation [J].
Shimizu, E ;
Tang, YP ;
Rampon, C ;
Tsien, JZ .
SCIENCE, 2000, 290 (5494) :1170-1174
[46]   Effects of typical and atypical antipsychotics and receptor selective compounds on acetylcholine efflux in the hippocampus of the rat [J].
Shirazi-Southall, S ;
Rodriguez, DE ;
Nomikos, GG .
NEUROPSYCHOPHARMACOLOGY, 2002, 26 (05) :583-594
[47]   Characterization of Ro 04-6790 and Ro 63-0563:: potent and selective antagonists at human and rat 5-HT6 receptors [J].
Sleight, AJ ;
Boess, FG ;
Bös, M ;
Levet-Trafit, B ;
Riemer, C ;
Bourson, A .
BRITISH JOURNAL OF PHARMACOLOGY, 1998, 124 (03) :556-562
[48]  
Sleight AJ, 1999, BEHAV PHARMACOL, V10, pS86
[49]   NMDA RECEPTOR CHANNEL ANTAGONISM BY DIZOCILPINE (MK-801) IMPAIRS PERFORMANCE OF RATS IN AVERSIVELY MOTIVATED COMPLEX MAZE TASKS [J].
SPANGLER, EL ;
BRESNAHAN, EL ;
GAROFALO, P ;
MUTH, NJ ;
HELLER, B ;
INGRAM, DK .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1991, 40 (04) :949-958
[50]   Pharmacological profile of SB-357134:: A potent, selective, brain penetrant, and orally active 5-HT6 receptor antagonist [J].
Stean, TO ;
Hirst, WD ;
Thomas, DR ;
Price, GW ;
Rogers, D ;
Riley, G ;
Bromidge, SM ;
Serafinowska, HT ;
Smith, DR ;
Bartlett, S ;
Deeks, N ;
Duxon, M ;
Upton, N .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2002, 71 (04) :645-654