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KMID : 1037120190370020240
The World Journal of Men¡Çs Health
2019 Volume.37 No. 2 p.240 ~ p.248
Persistent Erectile Dysfunction after Discontinuation of 5-Alpha Reductase Inhibitor Therapy in Rats Depending on the Duration of Treatment
Sung Hyun-Hwan

Yu Ji-Woong
Kang Su-Jeong
Chae Mee-Ree
So In-Suk
Park Jong-Kwan
Lee Sung-Won
Abstract
Purpose: The current study is aimed to assess whether a longer duration of 5¥á-reductase inhibitor (5¥á-RI) exposure was associated with higher rate of permanent erectile dysfunction (ED) in a rat model.

Materials and Methods: Male Sprague-Dawley rats (n=76) were assigned to five groups: (i) normal control group; (ii) dutasteride (0.5 mg/rat/d) for 4-weeks group; (iii) dutasteride for 4-weeks plus 2-weeks of resting group; (iv) dutasteride for 8-weeks group; and (v) dutasteride for 8-weeks plus 2-weeks of resting group. In vivo erectile responses to electrical stimulation, and changes of fibrotic factors and smooth muscle/collagen contents in the corpus cavernosum were evaluated in each group.

Results: Dutasteride administration for 4 and 8 weeks significantly decreased erectile parameters compared with the control group. Reduced erectile responses were recovered during 2 weeks of drug-free time in the 4-week treatment group, but were not in the 8-week group. Protein levels of fibrosis-related factors transforming growth factor (TGF)-¥â1, TGF-¥â2, and p-Smad/Smad (Smad 2/3) in the corpus cavernosum showed no significant change after 4 weeks of dutasteride oral administration, but were enhanced after 8 weeks. Dutasteride markedly decreased smooth muscle content and increased collagen after 4 and 8 weeks of use, but no nuclear size changes; however, neither group showed significant improvement in the smooth muscle to collagen ratio after the rest period.

Conclusions: Our study showed that recovery from ED depended on the duration of medication, and administration of dutasteride for more than 8-weeks in rats could result in irreversible ED even after discontinuation of medication.
KEYWORD
5-alpha reductase inhibitors, Dutasteride, Erectile dysfunction, Finasteride
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