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Asian Journal of Andrology ; (6): 465-472, 2018.
Artículo en Inglés | WPRIM | ID: wpr-1009603

RESUMEN

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.


Asunto(s)
Animales , Masculino , Ratones , Angiopoyetina 1/genética , Diabetes Mellitus Experimental/metabolismo , Endotelio Vascular/metabolismo , Disfunción Eréctil/terapia , Terapia Genética/métodos , Uniones Intercelulares/metabolismo , Trasplante de Células Madre Mesenquimatosas , Erección Peniana/fisiología , Permeabilidad
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