Effects of the novel 5-HT6 receptor antagonist RO4368554 in rat models for cognition and sensorimotor gating

被引:70
作者
Schreiber, Rudy
Vivian, Jef
Hedley, Linda
Szczepanski, Krystine
Secchi, Rob L.
Zuzow, Marcus
van Laarhoven, Susanne
Moreau, Jean-Luc
Martin, James R.
Sik, Ayhan
Blokland, Arjan
机构
[1] Sepracor Inc, Discovery Grp, Marlborough, MA 01752 USA
[2] Roche Palo Alto LLC, CNS Neurobehav, Palo Alto, CA 94304 USA
[3] F Hoffmann La Roche Ltd, PRBD N, Neurosci Res, CH-4070 Basel, Switzerland
[4] Univ Limburg, EURON, Dept Psychol, Brain & Behav Inst, NL-6200 MD Maastricht, Netherlands
关键词
acetylcholine; learning; memory; prepulse inhibition; schizophrenia; serotonin;
D O I
10.1016/j.euroneuro.2006.06.009
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Serotonin(6) (5-HT6) receptors are almost exclusively located in the central nervous system. High expression in the hippocampus, nucleus accumbens and striatum is consistent with a potential role in cognition and psychosis. The availability of potent, selective and brain-penetrating 5-HT6 antagonists such as 804368554 allows further characterization of the role of the 5-HT6 receptor in these processes. Herein, we tested 804368554 in several cognition tasks, as well as sensorimotor gating tests. Using scopolamine-impaired and unimpaired adult male rats, 804368554 was given in novel object discrimination, social recognition, social discrimination, Morris water maze, passive avoidance and autoshaping procedures. 804368554 reversed the effects of scopolamine in novel object discrimination (active doses in mg/kg, i.p., 3, 10), social recognition (3, 10), social discrimination (1, 3, 10) and passive avoidance (10, 30 i.p. and 100 p.o.) tasks. In unimpaired rats, 804368554 enhanced object discrimination (3, 10; 4-h forgetting interval) and autoshaping learning (3), but was inactive in a water maze task (doses tested: 1-10 mg/kg, i.p.). In tests sensitive to antipsychotics, 804368554 did not reverse sensorimotor gating deficits induced by the psychostimulants dizocilpine and amphetamine (doses tested: 1-30 mg/kg, i.p.) or neonatal lesion of the ventral hippocampus (1-10 mg/kg, i.p.). In conclusion, 804368554 enhanced learning and memory processes in unimpaired and scopolamine-impaired rats, supporting the notion that the cognitive enhancing effects of 5-HT6 receptor antagonists involve modulation of cholinergic neurotransmission. (c) 2006 Elsevier B.V and ECNP All rights reserved.
引用
收藏
页码:277 / 288
页数:12
相关论文
共 43 条
[31]  
Rogers DC, 2001, PSYCHOPHARMACOLOGY, V158, P114
[32]   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
[33]  
Russell Michael G. N., 2002, Current Topics in Medicinal Chemistry, V2, P643, DOI 10.2174/1568026023393877
[34]   Neonatal lesions of the rat ventral hippocampus result in hyperlocomotion and deficits in social behaviour in adulthood [J].
SamsDodd, F ;
Lipska, BK ;
Weinberger, DR .
PSYCHOPHARMACOLOGY, 1997, 132 (03) :303-310
[35]  
Schreiber R, 2006, RECEPTORS, P495
[36]  
SLEIGHT AJ, 1999, BEHAV PHARMACOL, V10, P586
[37]   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
[38]  
SUTTON JE, 2004, SOC NEUR ABSTR, P30
[39]  
SZCZEPANSKI K, 2002, SOC NEUR ABSTR, V28, P290
[40]  
WOLFF MC, 2002, SOC NEUR ABSTR, V28