Medicine for treating erectile dysfunction and application thereof
A technology of erectile dysfunction and drugs, applied in the field of biomedicine, to achieve the effect of inhibiting the fibrosis of the cavernous body of the human penis
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Embodiment 1
[0035] In this embodiment, human cavernous body fibroblasts are isolated and cultured in vitro, including:
[0036] Separation of human corpus cavernosum tissue, the corpus cavernosum tissue obtained by surgery, rinsed with PBS three times to remove blood, and then cut into 2mm×2mm size block tissue, using digestive enzymes (including 4mg / mL type IV collagenase, 4mg / mL collagenase Type I collagenase, 3mg / mL hyaluronidase and 1.5mg / mL trypsin) digest for 30min, then use a tissue strainer to remove the bulk tissue, centrifuge to retain the cell components, use DMEM medium with 10% fetal bovine serum Culture after resuspension.
Embodiment 2
[0038] In this embodiment, the human cavernous tissue is isolated and cultured in vitro, including:
[0039] The fresh cavernous body tissue obtained by surgery was cut into about 2mm×2mm in size, and the low-sugar DMEM medium with 10% FBS was used, and an oscillating shaker was placed in a 37°C incubator, and the tissue was placed on the shaker for culture.
Embodiment 3
[0041] In this example, the human cavernous fibroblasts cultured in Example 1 are used to test the effect of inhibitors of the Wnt signaling pathway on human cavernous fibroblasts.
[0042] The human cavernous body fibroblasts cultured in Example 1 were taken for cultivation, the culture medium was a high-glucose DMED medium containing 2% fetal bovine serum, and the culture conditions were 37° C., 5% concentration of CO 2 , when the cell growth density was 50%, ICG-001 was used for treatment at a concentration of 10 μM, and an equal amount of dimethyl sulfoxide (DMSO) was used as a control. After 14 days of treatment, the cell morphology was observed, as shown in figure 1As shown in , it can be seen that the cells changed from long spindles to thin strips, the internal refractive index was significantly increased, and the cell volume was significantly decreased ( figure 2 ), indicating that the cells gradually transitioned to non-fibrotic morphology, and the transcriptome seq...
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