PMID- 20687229 OWN - NLM STAT- MEDLINE DCOM- 20100923 LR - 20131121 IS - 1097-0045 (Electronic) IS - 0270-4137 (Linking) VI - 70 IP - 14 DP - 2010 Oct 1 TI - The effect of estrogen supplementation on cell proliferation and expression of c-kit positive cells in the rat prostate. PG - 1555-62 LID - 10.1002/pros.21191 [doi] AB - BACKGROUND: Benign prostatic hyperplasia (BPH) is associated with the proliferation of prostate tissue and an increase in smooth muscle tone. However, the way in which the hormonal environment affects cell proliferation and prostatic interstitial cells (PIC) responsible for the maintenance of the smooth muscle tone is not clear. The present study investigated the effect of estrogen supplementation on cell proliferation, androgen/estrogen ratio, and expression and/or distribution of PIC. METHODS: Male Sprague-Dawley rats were anesthetized with isoflurane/oxygen breathing mixture and subcutaneously implanted with silastic capsules. These capsules were either empty or filled with a 10 or 20 mg of crystalline estrogen. RESULTS: Estrogen exerted a potent effect on ventral prostate weight, which was manifested as a significant decrease between controls and the E(10)- and E(20)-treated rats. Active cell proliferation detected as Ki67-positive nuclei was observed in the stromal and epithelial cells of the ventral prostatic lobes from estrogen-treated rats and controls. Estrogen supplementation caused a significant and dose-dependent increase in prostatic estradiol and 5alpha-dihydrotestosterone (DHT) concentration but the ratios of either DHT/E(2) or E(2)/DHT were not significantly affected. PIC were observed in the region between the fibromuscular stroma and the glandular epithelium in all three experimental groups. E(20)-treated rats showed a higher expression of PIC than controls and E(10)-treated rats. CONCLUSIONS: The present study provides novel information regarding the synergistic role of estrogens and androgens in the prostate: estrogen may prevent prostatic hyperplasia via mechanisms other than affecting cell proliferation or DHT/estrogen ratio. CI - (c) 2010 Wiley-Liss, Inc. FAU - Kusljic, Snezana AU - Kusljic S AD - Department of Nursing, University of Melbourne, Carlton, Victoria, Australia. FAU - Exintaris, Betty AU - Exintaris B LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - United States TA - Prostate JT - The Prostate JID - 8101368 RN - 0 (Androgens) RN - 0 (Estrogens) RN - 0 (Ki-67 Antigen) RN - 08J2K08A3Y (Dihydrotestosterone) RN - 3XMK78S47O (Testosterone) RN - 4TI98Z838E (Estradiol) RN - EC 2.7.10.1 (Proto-Oncogene Proteins c-kit) SB - IM MH - Androgens/metabolism/physiology MH - Animals MH - Body Weight/drug effects MH - Cell Division/drug effects MH - Dietary Supplements MH - Dihydrotestosterone/metabolism MH - Estradiol/metabolism MH - Estrogens/administration & dosage/metabolism/*pharmacology/physiology MH - Ki-67 Antigen/drug effects/metabolism MH - Leydig Cells/drug effects/physiology MH - Male MH - Organ Size/drug effects MH - Prostate/anatomy & histology/*cytology/drug effects/*physiology MH - Prostatic Hyperplasia/pathology MH - Proto-Oncogene Proteins c-kit/drug effects/*genetics/metabolism MH - Rats MH - Rats, Sprague-Dawley MH - Testosterone/metabolism EDAT- 2010/08/06 06:00 MHDA- 2010/09/24 06:00 CRDT- 2010/08/06 06:00 PHST- 2010/08/06 06:00 [entrez] PHST- 2010/08/06 06:00 [pubmed] PHST- 2010/09/24 06:00 [medline] AID - 10.1002/pros.21191 [doi] PST - ppublish SO - Prostate. 2010 Oct 1;70(14):1555-62. doi: 10.1002/pros.21191.