首页 | 本学科首页   官方微博 | 高级检索  
检索        


Adenosine and memory storage:
Authors:Silvia R Kopf  Alessia Melani  Felicita Pedata  G Pepeu
Institution:Pharmakologisches Institut, Universit?t Mainz, Obere Zahlbacher Strasse 67, D-5501 Mainz, Deutschland, DE
Department of Pharmacology, University of Florence, Viale Pieraccini 6, I-50139 Florence, Italy e-mail: pepeu@server1.pharm.unifi.it Fax: +39-055-4271-280, IT
Abstract:Rationale: Caffeine is a non-selective A1/A2 adenosine receptor antagonist which is known to improve cognitive performance in humans. This effect of caffeine has been attributed to its antagonism of adenosine receptors. Objective: The present study was devised to identify the role of A1 and A2A adenosine receptors in the facilitation of memory consolidation in mice performing a passive avoidance task. Methods: Adult albino Swiss male mice were used. The mice were trained in a step-through inhibitory avoidance task in which they were punished by a foot-shock (0.4 mA, 5 Hz, for 3 s) delivered through the grid floor. Caffeine (0.1, 0.3, 1.0 and 3.0 mg/kg), SCH 58261 (0.1, 0.3, 1.0 and 3.0 mg/kg) and DPCPX (0.1, 0.3, 1.0 and 3.0 mg/kg) were injected IP immediately or 180 min after training. The retention test was performed 24 h after training. Results: Caffeine and the selective A2A adenosine receptor antagonist SCH 58261 facilitated retention when administered immediately after training, but not when administered 180 min later. The dose response was a bell-shaped curve. Conversely, post-training administration of the selective A1 adenosine receptor antagonist DPCPX did not affect retention. Caffeine and SCH 58261 had no effect in mice not given the foot-shock on the training trial, a finding indicating that the drug’s effect on retention was specific. Conclusions: These results suggest that A2A but not A1 adenosine receptors are involved in memory retention and consolidation. Received: 14 February 1999 / Final version: 23 April 1999
Keywords:  Adenosine  Memory  Passive avoidance  Caffeine  DPCPX  SCH 58261
本文献已被 SpringerLink 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号