The pathogenesis of nonbacterial prostatitis (NBP) is not understood mainly
due to the lack of appropriate experimental models. We developed a new exp
erimental model of NBP by inducing a partial obstruction of the urethra (PU
O) in the rat. Male Wistar rats aged 12 weeks were used. PUO was produced b
y a nylon ligature on the urethra over a rubber tube, The tube was slipped
out after the ligature had been tied. Two rats were examined histologically
6 h, 1 day, 3 days and 7 days after PUO. In another group, two rats were k
illed at 1, 3 and 7 days after the release of the PUO that had been left in
place for 3 days. On day 3, another eight rats with PUO and eight control
rats had 2 ml of urine in the bladder replaced by the same volume of lucife
r yellow (LY; 10 mu g/ml, MW 500), microperoxidase (MP; 20 mu g/ml, MW 1900
), horseradish peroxidase (HRP; 10 mu g/ml, MW 40 000), or saline as contro
l, respectively. Lymphocytic infiltration and interstitial edema were noted
in the prostate following PUO, being most prominent on day 3. After the re
lease of the PUO, these inflammatory changes gradually disappeared. Only LU
was noted within the prostatic stroma of the rats 2 h after bladder instil
lation. Intraprostatic urinary reflux may be an etiologic factor in NBP. Th
e present study showed that lower urinary tract obstruction caused NBP in t
he rat. Penetration of prostatic tissue by low-molecular-weight substances
in the urine may trigger NBP.