A study of diabetes-induced erectile dysfunction treated with human umbilical cord mesenchymal stem cells.
Shangren WangAiqiao ZhangKang LiuYang PanJia-Qi KangShuai NiuYu-Xuan SongZhexin ZhangYuezheng LiLi LiuXiao-Qiang LiuPublished in: Andrologia (2022)
The present study aimed to assess the value of human umbilical cord mesenchymal stem cells (hUC-MSCs) for the treatment of diabetes-induced erectile dysfunction (DMED). We established a type 1 diabetes model through intra-abdominal streptozotocin injection. After 10 weeks, an apomorphine test was performed to screen the rats for erectile dysfunction (ED). The rats were divided into three groups: normal control group (n = 10), DMED group (n = 9) and DMED+hUC-MSC group (n = 9). After 4 weeks of hUC-MSC therapy, erectile function was evaluated by intracavernous pressure measurements, and penile tissue collagen and smooth muscle were examined by haematoxylin-eosin and Masson's trichrome staining. In addition, western blotting, immunohistochemistry and RT-PCR analysis of TLR4, VEGF and eNOS were performed. The results showed that hUC-MSC treatment restored erectile function (p < .05) and reversed the smooth muscle/collagen ratio changes of DMED rats (p < .05). Furthermore, hUC-MSC treatment inhibited the expression of TLR4 (p < .05) and enhanced VEGF and eNOS expression (p < .05). In conclusion, hUC-MSC treatment restored the erectile function of diabetic rats by inhibiting TLR4, improving corpora cavernosa fibrosis, and increasing VEGF and eNOS expression.
Keyphrases
- mesenchymal stem cells
- umbilical cord
- endothelial cells
- diabetic rats
- type diabetes
- smooth muscle
- poor prognosis
- high glucose
- oxidative stress
- cardiovascular disease
- immune response
- inflammatory response
- bone marrow
- vascular endothelial growth factor
- toll like receptor
- prostate cancer
- stem cells
- emergency department
- signaling pathway
- glycemic control
- metabolic syndrome
- nitric oxide synthase
- nitric oxide
- high throughput
- cell therapy
- insulin resistance
- south africa
- pi k akt
- long non coding rna
- replacement therapy
- drug induced
- skeletal muscle
- smoking cessation
- single cell
- liver fibrosis