Cargando…

Islet transplantation improved penile tissue fibrosis in a rat model of type 1 diabetes

BACKGROUND: Glycaemic control is one of the most effective strategies for the treatment of diabetes-related erectile dysfunction (DMED). Compared to conventional anti-diabetic drugs and insulin, islet transplantation is more effective in the treatment of diabetic complications. The aim of this study...

Descripción completa

Detalles Bibliográficos
Autores principales: Wu, Zhigang, Wang, Hongwei, Ni, Fubiao, Jiang, Xuan, Xu, Ziqiang, Liu, Chengyang, Cai, Yong, Fu, Hongxing, Luo, Jiao, Chen, Wenwei, Chen, Bicheng, Yu, Zhixian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6064149/
https://www.ncbi.nlm.nih.gov/pubmed/30053902
http://dx.doi.org/10.1186/s12902-018-0276-9
_version_ 1783342675904167936
author Wu, Zhigang
Wang, Hongwei
Ni, Fubiao
Jiang, Xuan
Xu, Ziqiang
Liu, Chengyang
Cai, Yong
Fu, Hongxing
Luo, Jiao
Chen, Wenwei
Chen, Bicheng
Yu, Zhixian
author_facet Wu, Zhigang
Wang, Hongwei
Ni, Fubiao
Jiang, Xuan
Xu, Ziqiang
Liu, Chengyang
Cai, Yong
Fu, Hongxing
Luo, Jiao
Chen, Wenwei
Chen, Bicheng
Yu, Zhixian
author_sort Wu, Zhigang
collection PubMed
description BACKGROUND: Glycaemic control is one of the most effective strategies for the treatment of diabetes-related erectile dysfunction (DMED). Compared to conventional anti-diabetic drugs and insulin, islet transplantation is more effective in the treatment of diabetic complications. The aim of this study was to investigate the efficacy of islet transplantation for reversing advanced-stage DMED in rats and to observe its influence on corpus cavernosum fibrosis. METHODS: Wistar rats were intraperitoneally injected with streptozotocin to establish a diabetes model. After 12 weeks, the rats were divided into 4 groups: diabetic, insulin, islet transplantation, and normal control. Following supplementation, the changes in blood glucose and weight were determined sequentially. Penile erectile function was evaluated by apomorphine experiments in the fourth week, and the penile corpus cavernosum was also collected for assessment by Masson staining, immunohistochemistry and Western blot to observe the spongy tissue and the related cellular changes at the molecular level. RESULTS: Islet transplantation significantly ameliorated penile erectile function in advanced-stage diabetic rats. The ratio of corpus cavernosum smooth muscle cells to fibroblasts and the expression level of α-SMA in the islet transplantation group were significantly higher than those in the diabetic and insulin groups. In addition, the expression levels of TGF-β1, p-Samd2, and connective tissue growth factor (CTGF) in the islet transplantation and insulin groups were much lower than those in the diabetic group, while those in the islet transplantation group were significantly lower than those in the insulin group. CONCLUSIONS: Our findings strongly suggest that islet transplantation can promote the regeneration of smooth muscle cells and ameliorate corpus cavernosum fibrosis to restore its normal structure in advanced-stage diabetic rats. The possible mechanism of ameliorating corpus cavernosum fibrosis by islet transplantation may be associated with improvement of the hyperglycaemic status in diabetic rats, thereby inhibiting the TGF-β1/Samd2/CTGF pathway.
format Online
Article
Text
id pubmed-6064149
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-60641492018-08-01 Islet transplantation improved penile tissue fibrosis in a rat model of type 1 diabetes Wu, Zhigang Wang, Hongwei Ni, Fubiao Jiang, Xuan Xu, Ziqiang Liu, Chengyang Cai, Yong Fu, Hongxing Luo, Jiao Chen, Wenwei Chen, Bicheng Yu, Zhixian BMC Endocr Disord Research Article BACKGROUND: Glycaemic control is one of the most effective strategies for the treatment of diabetes-related erectile dysfunction (DMED). Compared to conventional anti-diabetic drugs and insulin, islet transplantation is more effective in the treatment of diabetic complications. The aim of this study was to investigate the efficacy of islet transplantation for reversing advanced-stage DMED in rats and to observe its influence on corpus cavernosum fibrosis. METHODS: Wistar rats were intraperitoneally injected with streptozotocin to establish a diabetes model. After 12 weeks, the rats were divided into 4 groups: diabetic, insulin, islet transplantation, and normal control. Following supplementation, the changes in blood glucose and weight were determined sequentially. Penile erectile function was evaluated by apomorphine experiments in the fourth week, and the penile corpus cavernosum was also collected for assessment by Masson staining, immunohistochemistry and Western blot to observe the spongy tissue and the related cellular changes at the molecular level. RESULTS: Islet transplantation significantly ameliorated penile erectile function in advanced-stage diabetic rats. The ratio of corpus cavernosum smooth muscle cells to fibroblasts and the expression level of α-SMA in the islet transplantation group were significantly higher than those in the diabetic and insulin groups. In addition, the expression levels of TGF-β1, p-Samd2, and connective tissue growth factor (CTGF) in the islet transplantation and insulin groups were much lower than those in the diabetic group, while those in the islet transplantation group were significantly lower than those in the insulin group. CONCLUSIONS: Our findings strongly suggest that islet transplantation can promote the regeneration of smooth muscle cells and ameliorate corpus cavernosum fibrosis to restore its normal structure in advanced-stage diabetic rats. The possible mechanism of ameliorating corpus cavernosum fibrosis by islet transplantation may be associated with improvement of the hyperglycaemic status in diabetic rats, thereby inhibiting the TGF-β1/Samd2/CTGF pathway. BioMed Central 2018-07-27 /pmc/articles/PMC6064149/ /pubmed/30053902 http://dx.doi.org/10.1186/s12902-018-0276-9 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Wu, Zhigang
Wang, Hongwei
Ni, Fubiao
Jiang, Xuan
Xu, Ziqiang
Liu, Chengyang
Cai, Yong
Fu, Hongxing
Luo, Jiao
Chen, Wenwei
Chen, Bicheng
Yu, Zhixian
Islet transplantation improved penile tissue fibrosis in a rat model of type 1 diabetes
title Islet transplantation improved penile tissue fibrosis in a rat model of type 1 diabetes
title_full Islet transplantation improved penile tissue fibrosis in a rat model of type 1 diabetes
title_fullStr Islet transplantation improved penile tissue fibrosis in a rat model of type 1 diabetes
title_full_unstemmed Islet transplantation improved penile tissue fibrosis in a rat model of type 1 diabetes
title_short Islet transplantation improved penile tissue fibrosis in a rat model of type 1 diabetes
title_sort islet transplantation improved penile tissue fibrosis in a rat model of type 1 diabetes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6064149/
https://www.ncbi.nlm.nih.gov/pubmed/30053902
http://dx.doi.org/10.1186/s12902-018-0276-9
work_keys_str_mv AT wuzhigang islettransplantationimprovedpeniletissuefibrosisinaratmodeloftype1diabetes
AT wanghongwei islettransplantationimprovedpeniletissuefibrosisinaratmodeloftype1diabetes
AT nifubiao islettransplantationimprovedpeniletissuefibrosisinaratmodeloftype1diabetes
AT jiangxuan islettransplantationimprovedpeniletissuefibrosisinaratmodeloftype1diabetes
AT xuziqiang islettransplantationimprovedpeniletissuefibrosisinaratmodeloftype1diabetes
AT liuchengyang islettransplantationimprovedpeniletissuefibrosisinaratmodeloftype1diabetes
AT caiyong islettransplantationimprovedpeniletissuefibrosisinaratmodeloftype1diabetes
AT fuhongxing islettransplantationimprovedpeniletissuefibrosisinaratmodeloftype1diabetes
AT luojiao islettransplantationimprovedpeniletissuefibrosisinaratmodeloftype1diabetes
AT chenwenwei islettransplantationimprovedpeniletissuefibrosisinaratmodeloftype1diabetes
AT chenbicheng islettransplantationimprovedpeniletissuefibrosisinaratmodeloftype1diabetes
AT yuzhixian islettransplantationimprovedpeniletissuefibrosisinaratmodeloftype1diabetes