Objectives: Some authors have advocated the daily use of sildenafil for prophylaxis against, or treatment of, erectile dysfunction. However, no information has been published to support such a dosage regimen. The safety profile of uninterrupted use of sildenafil has not been evaluated as it pertains to alteration of PDE type 6 in the retina. In the present study we investigated whether short- or long-term exposure to a variety of sildenafil doses affect the expression of an enzyme important in the normal phototransduction cascade. Methods: Sustained-release sildenafil pellets were implanted in 120-day-old male rats with concentrations from 1-200 mg. Rat retinal tissue was harvested 7, 14, and 29 days after implantation. Quantitative reverse transcriptase-polymerase chain reaction (RT-PCR) using GAPDH as an endogenous internal standard was used to quantitate PDE type 6 gene expression. Results: Expression of PDE type 6 was upregulated after 7 days with dosages ≤ 5 mg (P < 0.02). Significant downregulation of PDE type 6 expression was first noted with high dose sildenafil 14 days after implantation (P < 0.02). Expression of PDE type 6 was significantly and profoundly downregulated 29 days after implantation for all pellet formulations ≥ 10 mg (P < 0.01). Conclusions: Sildenafil downregulates PDE type 6 expression in a dose- and time-dependent fashion. These findings support the explanation that PDE type 6 inhibition causes the dose-dependent clinical effects of visual disturbance in men taking sildenafil. Implications for long-term, daily use of sildenafil in men are not clear.
|Original language||English (US)|
|Journal||International Journal of Impotence Research|
|Issue number||SUPPL. 1|
|State||Published - Sep 1999|
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