Evidence for improved performance in cognitive tasks following selective NR2B NMDA receptor antagonist pre-treatment in the rat

被引:66
作者
Higgins, GA [1 ]
Ballard, TM
Enderlin, M
Haman, M
Kemp, JA
机构
[1] F Hoffmann La Roche & Co Ltd, PRBN, Basel, Switzerland
[2] NPS Pharmaceut, Parsippany, NJ 07054 USA
[3] Evotec Neurosci GMBH, D-22525 Hamburg, Germany
关键词
traxoprodil; (CP101; 606); Ro; 63-1908; dizocilpine; five-choice serial reaction time task; impulsivity; cognition;
D O I
10.1007/s00213-005-2203-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Rationale: We previously reported that the NR2B subunit-selective N-methyl-D-aspartate (NMDA) antagonist Ro 63-1908 produced a marked deficit in response control in the five-choice serial reaction time task (5-CSRTT). Objectives: The present studies were designed to investigate this further by studying the NR2B NMDA antagonists, ifenprodil, traxoprodil (CP101,606), Ro 25-6981 as well as Ro 63-1908 in this test. Methods: Following training in the 5-CSRTT, separate groups of rats were either tested under (1) standard test conditions [5 s inter-trial interval (ITI), 0.5 s stimulus duration, 100 trials], (2) high (3 s ITI) and low (10 s ITI) event rate of stimulus presentation and (3) a 250-trial protocol in aged 2-year-old rats. In a final study, the effects of traxoprodil were investigated in an operant delayed match to position (DMTP) task, a test of working memory, and compared to dizocilpine and Ro 63-1908. Results: Similar to Ro 63-1908, both traxoprodil (1-10 mg/kg) and Ro 25-6981 (3-30 mg/kg) increased premature responding but also increased response speed with no error trade-off. Conversely, ifenprodil (1-10 mg/kg) slowed response speed and increased omissions with no effect on premature responding. Tested under a variable ITI, Ro 63-1908 (1 mg/kg) increased premature responding at all ITIs, but this change was proportional to controls. At short ITI (3 s), Ro 63-1908 reliably improved performance both in terms of response speed and accuracy (percent correct). In a 250-trial protocol in aged rats, both Ro 63-1908 (0.1-0.3 mg/kg) and, particularly, traxoprodil (1-3 mg/kg) improved performance-increasing response speed and increasing the number of rewards earned during test. Finally, traxoprodil (1-10 mg/kg) improved accuracy and increased response speed in the DMTP task. Conclusions: The present studies support the view that selective NR2B NMDA antagonists promote impulsive-type responding in the 5-CSRTT; however, under certain test conditions, drugs of this class-notably traxoprodil-may also improve task performance.
引用
收藏
页码:85 / 98
页数:14
相关论文
共 74 条
[1]  
Anson LC, 1998, J NEUROSCI, V18, P581
[2]   5-phosphonomethylquinoxalinediones as competitive NMDA receptor antagonists with a preference for the human 1A/2A, rather than 1A/2B receptor composition [J].
Auberson, YP ;
Allgeier, H ;
Bischoff, S ;
Lingenhoehl, K ;
Moretti, R ;
Schmutz, M .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2002, 12 (07) :1099-1102
[3]   Characterisation of the effects of nicotine in the five-choice serial reaction time task in rats: antagonist studies [J].
Blondel, A ;
Sanger, DJ ;
Moser, PC .
PSYCHOPHARMACOLOGY, 2000, 149 (03) :293-305
[4]   Selective NMDA NR2B antagonists induce antinociception without motor dysfunction: correlation with restricted localisation of NR2B subunit in dorsal horn [J].
Boyce, S ;
Wyatt, A ;
Webb, JK ;
O'Donnell, R ;
Mason, G ;
Rigby, M ;
Sirinathsinghji, D ;
Hill, RG ;
Rupniak, NMJ .
NEUROPHARMACOLOGY, 1999, 38 (05) :611-623
[5]  
Brimecombe JC, 1998, J PHARMACOL EXP THER, V286, P627
[6]   EFFECTS OF LESIONS TO ASCENDING NORADRENERGIC NEURONS ON PERFORMANCE OF A 5-CHOICE SERIAL REACTION TASK IN RATS - IMPLICATIONS FOR THEORIES OF DORSAL NORADRENERGIC BUNDLE FUNCTION BASED ON SELECTIVE ATTENTION AND AROUSAL [J].
CARLI, M ;
ROBBINS, TW ;
EVENDEN, JL ;
EVERITT, BJ .
BEHAVIOURAL BRAIN RESEARCH, 1983, 9 (03) :361-380
[7]   The serotonin 5-HT2A receptors antagonist M100907 prevents impairment in attentional performance by NMDA receptor blockade in the rat prefrontal cortex (vol 29, pg 1637, 2004) [J].
Carli, M ;
Baviera, M ;
Invernizzi, RW ;
Balducci, C .
NEUROPSYCHOPHARMACOLOGY, 2004, 29 (12) :2300-2300
[8]   IFENPRODIL AND SL-82.0715 ARE ANTAGONISTS AT THE POLYAMINE SITE OF THE N-METHYL-D-ASPARTATE (NMDA) RECEPTOR [J].
CARTER, C ;
RIVY, JP ;
SCATTON, B .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1989, 164 (03) :611-612
[9]   Substitution for PCP, disruption of prepulse inhibition and hyperactivity induced by N-methyl-D-aspartate receptor antagonists:: preferential involvement of the NR2B rather than NR2A subunit [J].
Chaperon, F ;
Müller, W ;
Auberson, YP ;
Tricklebank, MD ;
Neijt, HC .
BEHAVIOURAL PHARMACOLOGY, 2003, 14 (5-6) :477-487
[10]   Studies on the subtype selectivity of CP-101,606: evidence for two classes of NR2B-selective NMDA receptor antagonists [J].
Chazot, PL ;
Lawrence, S ;
Thompson, CL .
NEUROPHARMACOLOGY, 2002, 42 (03) :319-324