Post training administration of anandamide (1.5, 3, 6 mg/kg) dose-dependently impaired retention of an inhibitory avoidance response in DBA/2 mice, while improving it in C57BW6 mice. The effects on retention performance induced by the drug appear to be due to an effect on memory consolidation. They were observed when drug was given at short, but not long, periods of time after training, i.e. when the memory trace was susceptible to modulation. These effects of anandamide parallel those of opioid agonists, as previously reported. Moreover, the opioid antagonist naltrexone improved retention in DBA/2 mice, while impairing it in C57BL/6 mice. Pre-treatment with the opioid antagonist at a non-effective dose (0.1 mg/kg) antagonized the effects of anandamide on memory consolidation in both strains. These results strongly suggest that endogenous cannabinoids affect memory processes through opioid systems. The possible involvement of other neurotransmitter systems, such as dopamine, in strain-dependent effects of anandamide in memory consolidation is discussed. (C) 1999 Lippincott Williams & Wilkins.
Strain-dependent effects of anandamide on memory consolidation in mice are antagonized by naltrexone / C., Castellano; Ventura, Rossella; Cabib, Simona; PUGLISI ALLEGRA, Stefano. - In: BEHAVIOURAL PHARMACOLOGY. - ISSN 0955-8810. - 10:5(1999), pp. 453-457. [10.1097/00008877-199909000-00003]
Strain-dependent effects of anandamide on memory consolidation in mice are antagonized by naltrexone
VENTURA, Rossella;CABIB, Simona;PUGLISI ALLEGRA, Stefano
1999
Abstract
Post training administration of anandamide (1.5, 3, 6 mg/kg) dose-dependently impaired retention of an inhibitory avoidance response in DBA/2 mice, while improving it in C57BW6 mice. The effects on retention performance induced by the drug appear to be due to an effect on memory consolidation. They were observed when drug was given at short, but not long, periods of time after training, i.e. when the memory trace was susceptible to modulation. These effects of anandamide parallel those of opioid agonists, as previously reported. Moreover, the opioid antagonist naltrexone improved retention in DBA/2 mice, while impairing it in C57BL/6 mice. Pre-treatment with the opioid antagonist at a non-effective dose (0.1 mg/kg) antagonized the effects of anandamide on memory consolidation in both strains. These results strongly suggest that endogenous cannabinoids affect memory processes through opioid systems. The possible involvement of other neurotransmitter systems, such as dopamine, in strain-dependent effects of anandamide in memory consolidation is discussed. (C) 1999 Lippincott Williams & Wilkins.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.