Structural modifications of the prostate in hypoxia, oxidative stress, and chronic ischemia.
10.4111/kju.2015.56.3.187
- Author:
Portia THURMOND
1
;
Jing Hua YANG
;
Yedan LI
;
Lori B LERNER
;
Kazem M AZADZOI
Author Information
1. Department of Urology, VA Boston Healthcare System and Boston University School of Medicine, Boston, MA, USA.
- Publication Type:Brief Communication ; Research Support, U.S. Gov't, Non-P.H.S.
- Keywords:
Fibrosis;
Ischemia;
Oxidative stress;
Prostate
- MeSH:
Animals;
Anoxia/*complications;
Atherosclerosis/complications;
Biomarkers;
Cells, Cultured;
DNA Damage;
Disease Models, Animal;
Epithelial Cells/ultrastructure;
Fibrosis;
Humans;
Ischemia/*complications;
Lipid Peroxidation;
Male;
Myocytes, Smooth Muscle/ultrastructure;
Nerve Degeneration;
*Oxidative Stress;
Prostate/*anatomy & histology/*cytology;
Rabbits;
Stromal Cells/ultrastructure;
Urinary Bladder Neck Obstruction/complications
- From:Korean Journal of Urology
2015;56(3):187-196
- CountryRepublic of Korea
- Language:English
-
Abstract:
PURPOSE: Clinical studies have reported a correlation between pelvic ischemia and voiding dysfunction in elderly men. The aim of this study was to identify and compare prostate structural modifications in cultured cells and in a rabbit model after exposure to hypoxia, oxidative stress, and chronic ischemia. MATERIALS AND METHODS: Cultured human prostate smooth muscle cells (SMCs), epithelial cells (ECs), and stromal cells (SCs) were incubated under normoxia, hypoxia, and oxidative stress conditions by use of a computerized oxycycler system. We developed a rabbit model of chronic prostate ischemia by creating aorto-iliac arterial atherosclerosis. Markers of oxidative stress were examined by using fluorometric analysis and enzyme immunoassay. Prostate structure was examined by using Masson's trichrome staining and transmission electron microscopy (TEM). RESULTS: Lipid peroxidation was found in SMCs exposed to hypoxia and in all cell types exposed to oxidative stress. We identified protein oxidation in ECs exposed to hypoxia and in all cell types exposed to oxidative stress. Markers indicating oxidative damage were present in chronically ischemic rabbit prostate tissue. These reactions were associated with DNA damage. Prostate ischemia resulted in epithelial atrophy, loss of smooth muscle, and diffuse fibrosis. TEM showed swollen mitochondria with degraded cristae, loss of membrane, loss of Golgi bodies, degenerated nerves, and disrupted cell-to-cell junctions. CONCLUSIONS: Human prostate cells exhibited differential reactions to hypoxia and oxidative stress with widespread DNA damage. Structural modifications in ischemic prostate tissue were similar to those in cells exposed to oxidative stress. Structural changes due to ischemia and oxidative stress may contribute to prostatic noncompliance in aging men.
