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A comparison of the relaxation responses of isolated cavernosal smooth muscles by endothelium-independent and endothelium-dependent vasodilators in diabetic men with impotenceopen access

Authors
Kim, Sae-ChulAhn, Seung-YongPark, Sung-HoLee, Moo-YeolUhm, Dae-Yong
Issue Date
Feb-1995
Keywords
Diabetes mellitus; Impotence; Cavernosal smooth muscle; Endothelium-dependent vasodilator
Citation
Journal of Korean medical science, v.10, no.1, pp 1 - 6
Pages
6
Journal Title
Journal of Korean medical science
Volume
10
Number
1
Start Page
1
End Page
6
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/66600
DOI
10.3346/jkms.1995.10.1.1
ISSN
1011-8934
1598-6357
Abstract
This study was intended to explore the effects of endothelium-independent, direct smooth muscle relaxants(papaverine, verapamil) and endothelium-dependent vasodilators(acetylcholine, bradykinin, adenosine) on the isolated cavernosal smooth muscle strips taken from diabetic men with impotence. When smooth muscle contraction was evoked with norepinephrine for the study of relaxation to these vasodilators, the tension induced was similar in diabetic and non-diabetic men with importance. Papaverine showed the strongest relaxation response followed by verapamil, acetylcholine, bradykinin and adenosine both in non-diabetic and in diabetic men. Relaxation of the cavernosal tissues to endothelium-independent vasodilators was similar in non-diabetic and diabetic men. However, the relaxation response of the tissues to endothelium-dependent vasodilators was significantly reduced in the diabetic group compared with that in the non-diabetic group (p < 0.05). In conclusion, the impairment of endothelium-mediated relaxation of cavernosal smooth muscle seems to play a more important role in the pathogenesis of diabetogenic impotence rather than the problem of smooth muscle itself. This finding forms a rational basis for the use of intracavernosal injections of vasodilators to induce endothelium-independent relaxation of the cavernosal smooth muscle in the patients with diabetogenic impotence.
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