Urine-Derived Stem Cells Versus Their Lysate in Ameliorating Erectile Dysfunction in a Rat Model of Type 2 Diabetes

• Published in: Frontiers in physiology Vol. 13; p. 854949
• Main Authors: Galhom, Rania A, Korayem, Horeya Erfan, Ibrahim, Mahrous A, Abd-Eltawab Tammam, Ahmed, Khalifa, Mohamed Mansour, Rashwan, Eman K, Al Badawi, Manal H
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Media S.A 10-05-2022
• Subjects: diabetes mellitus; erectile dysfunction; lysate; Physiology; rats; urine-derived stem cells (UDSCs); diabetes mellitus; rats; lysate; erectile dysfunction; urine-derived stem cells (UDSCs)
• ISSN: 1664-042X; 1664-042X
• DOI: 10.3389/fphys.2022.854949

Diabetic erectile dysfunction (DED) is a significant consequence of diabetes mellitus, and it is a multifactorial phenomenon that has no definitive treatment until now. Many therapeutic options provide symptomatic improvement rather than addressing the underlying etiology or restoring normal function. Stem cell (SC) therapy represents a potential hope in DED management. It is well established that the regenerative effect of stem cells can be attained by their paracrine action and their ability to differentiate into many cell lineages, including endothelial and smooth muscle cells. Hence, we tried to compare the effects of transplantation of urine-derived stem cells (USCs) or their lysate (USC-L) into the corpora cavernosa (CCs) of rats with DED.
A total of 55 adult male Wistar rats were included in this study. USCs were obtained from ten healthy rats. Another ten rats did not subject to any intervention and served as a control (group I). Type 2 DM and DED were induced in the remaining 35 rats, but DED was tested and proved in only 24 rats, which were randomly divided into three groups (
= 8 in each). The DED group (group II) and either USCs (2 × 10
cells) or their lysate (200 μl) were transplanted into the CCs of each rat in the other two groups (groups III and IV), respectively.
Although the DED rats exhibited deterioration in all copulatory functions as compared to the control group, our histopathological, immunohistochemical, and morphometric results revealed that both USCs and USC-L have significantly restored the cavernous spaces, the ultrastructures of the endothelium that line the cavernous spaces, collagen/smooth muscle ratio, and the mean area percentage of α-SMA in the CCs as compared to DED rats. A respectable number of USCs was detected in the CCs of group III at the 4th week after transplantation, but this number significantly declined by the 8th week.
Both USCs and USC-L can repair the structure and ultrastructure of CCs and improve the copulatory functions in the DED rat model. However, USC-L could be better used in DED to guard against the strange behavior of USCs after transplantation and their decreased survivability with time.