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Combination of stromal vascular fraction and Ad-COMP-Ang1 gene therapy improves long-term therapeutic efficacy for diabetes-induced erectile dysfunction.

Authors :
Guo-Nan Yin
Lin Wang
Xiang-Nan Lin
Lei Shi
Zhen-Lin Gao
Feng-Chan Han
Ping Li
Yin-Chuan Jin
Jun-Kyu Suh
Ji-Kan Ryu
Xiong Wang
Hai-Rong Jin
Source :
Asian Journal of Andrology; Sep/Oct2018, Vol. 20 Issue 5, p465-472, 8p
Publication Year :
2018

Abstract

Men with diabetic erectile dysfunction (ED) respond poorly to the currently available oral phosphodiesterase-5 inhibitors. Therefore, functional therapies for diabetic ED are needed. Stromal vascular fraction (SVF) and the adenovirus-mediated cartilage oligomeric matrix angiopoietin-1 (Ad-COMP-Ang1) gene are known to play critical roles in penile erection. We previously reported that SVF and Ad-COMP-Ang1 have only a short-term effect in restoring erectile function. Further improvements to ED therapy are needed for long-lasting effects. In the present study, we aimed to test if the combination of SVF and Ad-COMP-Ang1 could extend the erection effect in diabetic ED. We found that the combination therapy showed a long-term effect in restoring erectile function through enhanced penile endothelial and neural cell regeneration. Combination therapy with SVF and Ad-COMP-Ang1 notably restored cavernous endothelial cell numbers, pericyte numbers, endothelial cell-cell junctions, decreased cavernous endothelial cell permeability, and promoted neural regeneration for at least 4 weeks in diabetic mice. In summary, this is an initial description of the long-term effect of combination therapy with SVF and Ad-COMP-Ang1 in restoring erectile function through a dual effect on endothelial and neural cell regeneration. Such combination therapy may have therapeutic potential for the treatment of diabetic ED. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1008682X
Volume :
20
Issue :
5
Database :
Complementary Index
Journal :
Asian Journal of Andrology
Publication Type :
Academic Journal
Accession number :
131379041
Full Text :
https://doi.org/10.4103/aja.aja_16_18