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Pancreatic kininogenase improves erectile function in streptozotocin-induced type 2 diabetic rats with erectile dysfunction

Erectile dysfunction (ED) associated with type 2 diabetes is a severe problem that requires effective treatment. Pancreatic kininogenase (PK) has the potential to improve the erectile function of ED patients. This study aims to investigate the effect of PK on erectile function in streptozotocin-indu...

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Autores principales: Chen, Guo-Tao, Yang, Bai-Bing, Chen, Jian-Huai, Zhang, Zheng, Zhu, Lei-Lei, Jiang, He-Song, Yu, Wen, Chen, Yun, Dai, Yu-Tian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6116675/
https://www.ncbi.nlm.nih.gov/pubmed/29676291
http://dx.doi.org/10.4103/aja.aja_23_18
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author Chen, Guo-Tao
Yang, Bai-Bing
Chen, Jian-Huai
Zhang, Zheng
Zhu, Lei-Lei
Jiang, He-Song
Yu, Wen
Chen, Yun
Dai, Yu-Tian
author_facet Chen, Guo-Tao
Yang, Bai-Bing
Chen, Jian-Huai
Zhang, Zheng
Zhu, Lei-Lei
Jiang, He-Song
Yu, Wen
Chen, Yun
Dai, Yu-Tian
author_sort Chen, Guo-Tao
collection PubMed
description Erectile dysfunction (ED) associated with type 2 diabetes is a severe problem that requires effective treatment. Pancreatic kininogenase (PK) has the potential to improve the erectile function of ED patients. This study aims to investigate the effect of PK on erectile function in streptozotocin-induced type 2 diabetic ED rats. To achieve this goal, we divided male Sprague–Dawley rats into five groups. One group was not treated, and the other four groups were treated with saline, sildenafil, PK or sildenafil, and PK, respectively, for 4 weeks after the induction of type 2 diabetic ED. Then, intracavernous pressure under cavernous nerve stimulation was measured, and penile tissue was collected for further study. Endothelial nitric oxide synthase levels, smooth muscle content, endothelium content, cyclic guanosine monophosphate (cGMP) levels in the corpus cavernosum, and neuronal nitric oxide synthase levels in the dorsal penile nerve were measured. Improved erectile function and endothelium and smooth muscle content in the corpus cavernosum were observed in diabetic ED rats. When treating diabetic ED rats with PK and sildenafil at the same time, a better therapeutic effect was achieved. These data demonstrate that intraperitoneal injection of PK can improve erectile function in a rat model of type 2 diabetic ED. With further research on specific mechanisms of erectile function improvement, PK may become a novel treatment for diabetic ED.
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spelling pubmed-61166752018-09-05 Pancreatic kininogenase improves erectile function in streptozotocin-induced type 2 diabetic rats with erectile dysfunction Chen, Guo-Tao Yang, Bai-Bing Chen, Jian-Huai Zhang, Zheng Zhu, Lei-Lei Jiang, He-Song Yu, Wen Chen, Yun Dai, Yu-Tian Asian J Androl Original Article Erectile dysfunction (ED) associated with type 2 diabetes is a severe problem that requires effective treatment. Pancreatic kininogenase (PK) has the potential to improve the erectile function of ED patients. This study aims to investigate the effect of PK on erectile function in streptozotocin-induced type 2 diabetic ED rats. To achieve this goal, we divided male Sprague–Dawley rats into five groups. One group was not treated, and the other four groups were treated with saline, sildenafil, PK or sildenafil, and PK, respectively, for 4 weeks after the induction of type 2 diabetic ED. Then, intracavernous pressure under cavernous nerve stimulation was measured, and penile tissue was collected for further study. Endothelial nitric oxide synthase levels, smooth muscle content, endothelium content, cyclic guanosine monophosphate (cGMP) levels in the corpus cavernosum, and neuronal nitric oxide synthase levels in the dorsal penile nerve were measured. Improved erectile function and endothelium and smooth muscle content in the corpus cavernosum were observed in diabetic ED rats. When treating diabetic ED rats with PK and sildenafil at the same time, a better therapeutic effect was achieved. These data demonstrate that intraperitoneal injection of PK can improve erectile function in a rat model of type 2 diabetic ED. With further research on specific mechanisms of erectile function improvement, PK may become a novel treatment for diabetic ED. Medknow Publications & Media Pvt Ltd 2018 2018-04-20 /pmc/articles/PMC6116675/ /pubmed/29676291 http://dx.doi.org/10.4103/aja.aja_23_18 Text en Copyright: © The Author(s)(2018) http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Chen, Guo-Tao
Yang, Bai-Bing
Chen, Jian-Huai
Zhang, Zheng
Zhu, Lei-Lei
Jiang, He-Song
Yu, Wen
Chen, Yun
Dai, Yu-Tian
Pancreatic kininogenase improves erectile function in streptozotocin-induced type 2 diabetic rats with erectile dysfunction
title Pancreatic kininogenase improves erectile function in streptozotocin-induced type 2 diabetic rats with erectile dysfunction
title_full Pancreatic kininogenase improves erectile function in streptozotocin-induced type 2 diabetic rats with erectile dysfunction
title_fullStr Pancreatic kininogenase improves erectile function in streptozotocin-induced type 2 diabetic rats with erectile dysfunction
title_full_unstemmed Pancreatic kininogenase improves erectile function in streptozotocin-induced type 2 diabetic rats with erectile dysfunction
title_short Pancreatic kininogenase improves erectile function in streptozotocin-induced type 2 diabetic rats with erectile dysfunction
title_sort pancreatic kininogenase improves erectile function in streptozotocin-induced type 2 diabetic rats with erectile dysfunction
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6116675/
https://www.ncbi.nlm.nih.gov/pubmed/29676291
http://dx.doi.org/10.4103/aja.aja_23_18
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