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Effects of combined growth hormone and testosterone treatments in a rat model of micropenis

Authors
Oh, Jin KyuIm, Young JaePark, KwanjinPaick, Jae-Seung
Issue Date
Nov-2018
Publisher
BIOSCIENTIFICA LTD
Keywords
micropenis; testosterone; growth hormone; combination treatment
Citation
ENDOCRINE CONNECTIONS, v.7, no.11, pp.1150 - 1157
Journal Title
ENDOCRINE CONNECTIONS
Volume
7
Number
11
Start Page
1150
End Page
1157
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/3184
DOI
10.1530/EC-18-0200
ISSN
2049-3614
Abstract
Although it is well known that penile growth is dependent on androgens, few clinical studies have reported successful treatment of micropenis with testosterone, likely due to concerns regarding the efficacy and safety of prolonged testosterone use. Thus, we assessed the synergenic effects of growth hormone (GH) treatments with and without testosterone on phallic growth in a rat model of micropenis. Fifty Sprague-Dawley rats were assigned to control (C), microphallus (MP), testosterone, GH (G) and GH plus testosterone (GT) treatment groups, and microphallus was induced by secondary hypogonadism. Pre-pubertal treatments with testosterone, GH or the combination were initiated from 7 days after birth and were maintained until 12 weeks of age. To assess the efficacy of treatments, phallic dimensions were determined and histological markers of cavernosal integrity were evaluated. Skeletal and gonadal safety profiles of the treatments were then assessed according to right tibial lengths and testicular weights, respectively. No monotreatments normalised penile dimensions, whereas combination treatments led to complete restoration. The combination treatment also prevented decreases in histological indicators of cavernosal integrity, including smooth muscle actin and collagen Ill expression levels and fat globule accumulation and sinusoidal density. These synergenic effects of GH treatments on penile growth may follow changes in androgen receptor expression levels and were accompanied by decreased testicular volume losses. Although the physiological conditions of phallic growth differ between humans and rats, this proof-of-concept study provides a strategy for circumventing the problems of testosterone monotherapy for human micropenis.
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