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The potential of hormones and selective oestrogen receptor modulators in preventing voiding dysfunction in rats
Author(s) -
Tantiwongse Kavirach,
Fandel Thomas M.,
Wang Guifang,
Breyer Benjamin N.,
Walsh Thomas J.,
Bella Anthony J.,
Lue Tom F.
Publication year - 2008
Publication title -
bju international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.773
H-Index - 148
eISSN - 1464-410X
pISSN - 1464-4096
DOI - 10.1111/j.1464-410x.2008.07582.x
Subject(s) - medicine , cystometry , raloxifene , endocrinology , urology , saline , overactive bladder , hypoestrogenism , hormone , urinary system , tamoxifen , alternative medicine , pathology , cancer , breast cancer
OBJECTIVE To investigate whether oestrogen, selective oestrogen receptor modulators (SERMs), and growth hormone (GH) can prevent the development of voiding dysfunction in a postpartum postmenopausal rat model of voiding dysfunction. MATERIALS AND METHODS Immediately after spontaneous delivery, nine primiparous Sprague‐Dawley rats served as uninjured controls (sham group) and 54 underwent intravaginal balloon dilation. On day 7, the 54 subject rats underwent bilateral ovariectomy. A week later, six treatment groups of nine rats were randomized to receive: normal saline (injured control group), 17β‐oestradiol (E 2 ), raloxifene, levormeloxifene, GH, or GH + E 2 . The treatment groups received daily subcutaneous injections for 3 weeks. The effects of hormone treatment were examined by conscious cystometry at the end of the study. Voiding dysfunction was defined to include overactive bladder and sphincter deficiency. RESULTS The sham rats had a mean ( sd ) voiding frequency of 3 (0.87) times in 10 min and a bladder capacity of 0.43 (0.13) mL with smooth cystometry curves. The number of rats in each treatment group (each group contained nine rats) that had voiding dysfunction was as follows: E 2 , three; raloxifene, six; levormeloxifene, four; and controls, four ( P > 0.05 among the groups). Only one rat in the GH‐treated group and no rats in the GH + E 2 ‐treated group had voiding dysfunction, which was significantly less in the GH + E 2 ‐treated group than in the controls ( P = 0.041). CONCLUSION This functional data suggest that the development of voiding dysfunction can be prevented by short‐term administration of GH and GH + E 2 in our rat model. SERMs and E 2 alone seem to have no therapeutic effect.