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An animal study to compare the degree of the suppressive effects on the afferent pathways of micturition between tamsulosin and sildenafil

Authors
Kim, Sung-EunKo, Il-GyuHwang, LakkyongChoi, In-YoungShin, Mal-SoonKim, Chang-JuKim, Khae-Hawn
Issue Date
25-Oct-2013
Publisher
BIOMED CENTRAL LTD
Keywords
Overactive bladder syndrome; Tamsulosin; Sildenafil; Neuronal activity; Afferent pathways of micturition
Citation
JOURNAL OF BIOMEDICAL SCIENCE, v.20
Journal Title
JOURNAL OF BIOMEDICAL SCIENCE
Volume
20
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/14207
DOI
10.1186/1423-0127-20-81
ISSN
1021-7770
Abstract
Background: Tamsulosin, an alpha 1-adrenoceptor antagonist, and sildenafil, a phosphodiesterase (PDE) inhibitor, are reported to improve lower urinary tract symptoms including overactive bladder (OAB). This study is aimed at investing the effects of tamsulosin and sildenafil and comparing the degree of the suppressive effects on the afferent pathways of micturition between them using an animal model of OAB, the spontaneously hypertensive rat (SHR). Results: The cystometric parameters, the basal pressure and duration of bladder contraction, were significantly increased in the SHR group as compared with the Wistar-Kyoto (WKY) group. The intercontraction interval also significantly decreased in the SHR group. In the SHR-Tam 0.01 mg/kg group and the SHR-Sil 1 mg/kg group, however, the basal pressure and duration were significantly reduced and the intercontraction interval was significantly prolonged. Moreover, the degree of the expression of c-Fos and NGF was significantly higher in the SHR group as compared with the WKY group. But it was significantly reduced in the SHR-Tam 0.01 mg/kg group and the SHR-Sil 1 mg/kg group. Furthermore, tamsulosin had a higher degree of effect as compared with sildenafil. Conclusions: In conclusion, alpha 1-adrenergic receptor antagonists and PDE-5 inhibitors may have an effect in improving the voiding functions through an inhibition of the neuronal activity in the afferent pathways of micturition.
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