کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
4312847 | 1612992 | 2013 | 10 صفحه PDF | دانلود رایگان |

Aging is characterized by a progressive cognitive decline that leads to memory impairment. Because the cyclic nucleotide cascade is essential for the integrity of synaptic function and memory, and it is down-regulated during aging and in neurodegenerative disorders, we investigated whether an increase in cGMP levels might rescue age-related synaptic and memory deficits in mice. We demonstrated that acute perfusion with the phosphodiesterase-5 inhibitor sildenafil (50 nM) ameliorated long-term potentiation in hippocampal slices from 26–30-month-old mice. Moreover, chronic intraperitoneal injection of sildenafil (3 mg/kg for 3 weeks) improved age-related spatial learning and reference memory as tested by the Morris Water Maze, and recognition memory as tested by the Object Recognition Test. Finally, sildenafil restored central cAMP responsive element-binding protein (CREB) phosphorylation, which is crucial for synaptic plasticity and memory. Our data suggest that inhibition of phosphodiesterase-5 may be beneficial to treat age-related cognitive dysfunction in a physiological mouse model of aging.
► We used 26–30 months-old wild type mice as a physiological model of aging.
► We analyzed hippocampal basal synaptic transmission and long-term potentiation.
► We analyzed spatial learning, reference and recognition memory.
► Sildenafil improved synaptic function and memory in aged mice.
► Sildenafil restored central CREB phosphorylation in old mice.
Journal: Behavioural Brain Research - Volume 240, 1 March 2013, Pages 11–20