Sildenafil, a selective phosphodiesterase type 5 inhibitor, enhances memory reconsolidation of an inhibitory avoidance task in mice

• Published in: Behavioural brain research 2011-07, Vol.220 (2), p.319-324
• Main Authors: Boccia, M.M., Blake, M.G., Krawczyk, M.C., Baratti, C.M.
• Format: Article
• Language: English
• Subjects: Age Factors; Animals; Avoidance Learning - drug effects; Behavior, Animal - drug effects; Behavioral psychophysiology; Biological and medical sciences; Dose-Response Relationship, Drug; Electroshock - adverse effects; Female; Fundamental and applied biological sciences. Psychology; Inhibitory avoidance; Male; Memory; Memory - drug effects; Mice; NO/cGMP/PKG pathway; Phosphodiesterase 5 Inhibitors - pharmacology; Piperazines - pharmacology; Psychology. Psychoanalysis. Psychiatry; Psychology. Psychophysiology; Purines - pharmacology; Reconsolidation; Retention (Psychology) - drug effects; Sildenafil; Sildenafil Citrate; Statistics, Nonparametric; Sulfones - pharmacology; Time Factors
• ISSN: 0166-4328; 1872-7549
• DOI: 10.1016/j.bbr.2011.02.016

[Display omitted] ► The injection of sildenafil immediately after the first retention test enhanced retention performance of an inhibitory avoidance task in mice. ► Sildenafil effects were dose- and time-dependent and also were long lasting. ► The enhancing effect of sildenafil was dependent on the age of the original memory. ► Sildenafil enhances memory reconsolidation. Intracellular levels of the second messengers cAMP and cGMP are maintained through a balance between production, carried out by adenyl cyclase (AC) and guanylyl cyclase (GC), and degradation, carried out by phosphodiesterases (PDEs). Recently, PDEs have gained increased attention as potential new targets for cognition enhancement, with particular reference to phosphodiesterase type 5 (PDE5A). It is accepted that once consolidation is completed memory becomes permanent, but it has also been suggested that reactivation (memory retrieval) of the original memory makes it sensitive to the same treatments that affect memory consolidation when given after training. This new period of sensitivity coined the term reconsolidation. Sildenafil (1, 3, and 10 mg/kg, ip), a cGMP-PDE5 inhibitor, facilitated retention performance of a one-trial step-through inhibitory avoidance task, when administered to CF-1 male mice immediately after retrieval. The effects of sildenafil (1 mg/kg, ip) were time-dependent, long-lasting and inversely correlated with memory age. The administration of sildenafil (1 mg/kg, ip) 30 min prior to the 2nd retention test did not affect retention of mice given post-retrieval injections of either vehicle or sildenafil (1 mg/kg, ip). Finally, an enhancement of retention was also observed in CF-1 female mice receiving sildenafil (1 mg/kg, ip) immediately, but not 180 min after retrieval. In the present paper we reported for the first time that systemic administration of sildenafil after memory reactivation enhances retention performance of the original learning. Our results indirectly point out cGMP, a component of the NO/cGMP/PKG pathway, as a necessary factor for memory reconsolidation.