Modulatory influence of dopamine receptors on consolidation of object recognition memory

被引:89
作者
Martins de Lima, Maria Noemia [1 ,2 ,3 ]
Presti-Torres, Juliana [1 ,2 ]
Dornelles, Arethuza [1 ,2 ]
Scalco, Felipe Siciliani [1 ,2 ]
Roesler, Rafael [2 ,4 ,5 ]
Garcia, Vanessa Athaide [1 ,2 ]
Schroeder, Nadja [1 ,2 ]
机构
[1] Pontifical Catholic Univ, Fac Biosci, Neurobiol & Dev Biol Lab, BR-90619900 Porto Alegre, RS, Brazil
[2] Natl Inst Translat Med INCT TM, Porto Alegre, RS, Brazil
[3] NeuroAssay Ltd, Porto Alegre, RS, Brazil
[4] Univ Fed Rio Grande do Sul, Inst Basic Hlth Sci, Dept Pharmacol, Lab Mol Neuropharmacol, Porto Alegre, RS, Brazil
[5] Univ Fed Rio Grande do Sul, Univ Hosp Res Ctr CPE HCPA, Canc Res Lab, Porto Alegre, RS, Brazil
关键词
D1; receptor; D2; Dopamine receptor; Recognition memory; Memory modulation; Memory consolidation; MEDIAL PREFRONTAL CORTEX; SPATIAL WORKING-MEMORY; PERIRHINAL CORTEX; NUCLEUS-ACCUMBENS; VENTRAL HIPPOCAMPUS; COGNITIVE FUNCTION; ANGIOTENSIN-IV; D-1; RECEPTOR; D1; RATS;
D O I
10.1016/j.nlm.2010.12.007
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
The role of dopamine receptors in regulating the formation of recognition memory remains poorly understood. Here we show the effects of systemic administration of dopamine receptor agonists and antagonists on the formation of memory for novel object recognition in rats. In Experiment I, rats received an intraperitoneal (i.p.) injection of vehicle, the selective D1 receptor agonist SKF38393 (1.0 and 5.0 mg/kg), or the D2 receptor agonist quinpirole (1.0 and 5.0 mg/kg) immediately after training. In Experiment II, rats received an injection of vehicle, the dopamine receptor antagonist SCH23390 (0.1 and 0.05 mg/kg), or the D2 receptor antagonist raclopride (0.5 and 0.1 mg/kg) before training, followed by an injection of vehicle or the nonselective dopamine receptor agonist apomorphine (0.05 mg/kg) immediately after training. SKF38393 at 5 mg/kg produced an enhancement of novel object recognition memory measured at both 24 and 72 h after training, whereas the dose of 10 mg/kg impaired 24-h retention. Posttraining administration of quinpirole did not affect 24-h retention. Apomorphine enhanced memory in rats given pretraining raclopride, suggesting that the effect was mediated by selective activation of D1 receptors. The results indicate that activation of D1 receptors can enhance recognition memory consolidation. Importantly, pharmacological activation of D1 receptors enhanced novel object recognition memory even under conditions in which control rats showed significant retention. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:305 / 310
页数:6
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