The Effect of Anthocyanin on the Prostate in an Andropause Animal Model: Rapid Prostatic Cell Death by Apoptosis Is Partially Prevented by Anthocyanin Supplementation.
10.5534/wjmh.2013.31.3.239
- Author:
Hoon JANG
1
;
Woong Jin BAE
;
Su Jin KIM
;
Seoung Mo YUK
;
Dong Seok HAN
;
U Syn HA
;
Sung Yeoun HWANG
;
Shin Hee YOON
;
Zhiping WANG
;
Sae Woong KIM
Author Information
1. Department of Urology, The Catholic University of Korea College of Medicine, Seoul, Korea. ksw1227@catholic.ac.kr
- Publication Type:Original Article
- Keywords:
Andropause;
Anthocyanins;
Antioxidants;
Apoptosis
- MeSH:
Andropause*;
Animals*;
Anthocyanins*;
Antioxidants;
Apoptosis*;
Cell Death*;
Male;
Models, Animal*;
Orchiectomy;
Oxidative Stress;
Prostate*;
Rats;
Rats, Sprague-Dawley;
Superoxide Dismutase;
Testosterone
- From:The World Journal of Men's Health
2013;31(3):239-246
- CountryRepublic of Korea
- Language:English
-
Abstract:
PURPOSE: To evaluate the anti-apoptotic effect of the antioxidant reaction of anthocyanin on the prostate in an andropause animal model. MATERIALS AND METHODS: Sprague-Dawley rats were divided into three groups (n=12 in each): control (Group I), andropause (Group II), andropause treated with anthocyanin (Group III). For induction of andropause, Group II and III underwent bilateral orchiectomy. Group III was treated with daily oral anthocyanin (160 mg/kg) for 8 weeks. After 8 weeks, the rats were sacrificed and their blood and prostates were examined pathohistologically and evaluated for oxidative stress and apoptosis. Oxidative stress was assessed by the activity of superoxide dismutase (SOD) and apoptosis in the prostate was identified by terminal deoxyribonucleotidyl transferase-mediated dUTP-digoxigenin nick end-labelling assay. RESULTS: Group II showed markedly increased activity of SOD in serum over that observed in Group I, whereas the rats in Group III showed reduced oxidative stress compared to Group II. Despite no significant differences in prostate weight between Group II and III (p=0.078), the apoptotic index was significantly greater in Group II than Group I, and was significantly lesser in Group III than Group II. CONCLUSIONS: We suggest that the oxidative stress caused by low testosterone may be another inducer of apoptosis, and this apoptosis may partly contribute to the overall apoptosis of the prostate in the andropause animal model. Therefore, anthocyanin supplementation may contribute to preventing excessively rapid cell death by apoptosis in the prostate in an animal model of andropause.
