Stereological Comparison of the Effects of Pentoxifylline, Captopril, Simvastatin, and Tamoxifen on Kidney and Bladder Structure After Partial Urethral Obstruction in Rats.
10.4111/kju.2014.55.11.756
- Author:
Mehdi SHIRAZI
1
;
Mohammad Reza SOLTANI
;
Zahra JAHANABADI
;
Mohammad Amin ABDOLLAHIFAR
;
Nader TANIDEH
;
Ali NOORAFSHAN
Author Information
1. Histomorphometry and Stereology Research Centre, Shiraz University of Medical Sciences, Shiraz Iran. noora@sums.ac.ir
- Publication Type:Original Article ; Comparative Study ; Research Support, Non-U.S. Gov't
- Keywords:
Captopril;
Pentoxifylline;
Simvastatin;
Tamoxifen;
Urethral obstruction
- MeSH:
Angiotensin-Converting Enzyme Inhibitors/pharmacology;
Animals;
Captopril/*pharmacology;
Disease Models, Animal;
Estrogen Antagonists/pharmacology;
Free Radical Scavengers/pharmacology;
Hydroxymethylglutaryl-CoA Reductase Inhibitors/pharmacology;
Kidney/*drug effects/pathology;
Male;
Pentoxifylline/*pharmacology;
Rats;
Simvastatin/*pharmacology;
Tamoxifen/*pharmacology;
Urethral Obstruction/*drug therapy;
Urinary Bladder Neck Obstruction/*drug therapy
- From:Korean Journal of Urology
2014;55(11):756-763
- CountryRepublic of Korea
- Language:English
-
Abstract:
PURPOSE: Limited studies have shown antifibrotic effects of pentoxifylline, captopril, simvastatin, and tamoxifen. No comparisons are available of the effects of these drugs on prevention of renal and bladder changes in partial urethral obstruction (PUO). MATERIALS AND METHODS: The rats were divided into six groups (n=7). The sham-operated rats (group I) only underwent laparotomy and did not receive any treatments. The PUO groups (group II-VI) received normal saline (PUO+NS), pentoxifylline (100 mg/kg/d; PUO+PEN), captopril (35 mg/kg/d; PUO+CAP), simvastatin (15 mg/kg/d; PUO+SIM), or tamoxifen (10 mg/kg/d; PUO+TAM) by gavage for 28 days. Then, the volume and/or length of the kidney components (tubules, vessels, and fibrous tissue) and the bladder components (epithelial and muscular layers, fibrous tissue, fibroblast and fibrocyte number) were quantitatively evaluated on the microscopic sections by use of stereological techniques. RESULTS: The volume of renal and bladder fibrosis was significantly ameliorated in the PUO+PEN group, followed by the PUO+CAP, PUO+SIM, and PUO+TAM groups. Also, the volume and length of the renal tubules and vessels and bladder layers were more significantly protected in the PUO+PEN group, followed by the PUO+CAP, PUO+SIM, and PUO+TAM groups. CONCLUSIONS: Treatment of PUO with PEN was more effective in the prevention of renal and bladder fibrosis and in the preservation of renal and bladder structures.
