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Intracavernous Delivery of Freshly Isolated Stromal Vascular Fraction Rescues Erectile Function by Enhancing Endothelial Regeneration in the Streptozotocin‐Induced Diabetic Mouse
Authors:Ji‐Kan Ryu  Munkhbayar Tumurbaatar  Hai‐Rong Jin  Woo Jean Kim  Mi‐Hye Kwon  Shuguang Piao  Min Ji Choi  Guo Nan Yin  Kang‐Moon Song  Yong‐Jin Kang  Young Jun Koh  Gou Young Koh  Jun‐Kyu Suh
Institution:2. Department of Urology, Yuhuangding Hospital, Yantai, Shandong Province, China;3. Department of Biological Sciences and Laboratory for Vascular Biology, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, Korea;2. Endocrinology Unit, Maggiore‐Bellaria Hospital, Bologna, Italy;3. Epidemiological Unit, Azienda Sanitaria Locale, Florence, Italy;4. Diabetes Section, Geriatric Unit, Department of Critical Care University of Florence, Florence, Italy;3. Department of Urology, Sestri Levante Hospital, Sestri Levante (Genoa), Italy;2. 1st Cardiology Clinic Onassis Cardiosurgery Center, Athens, Greece;2. INSERM, U955, Créteil, France;3. Faculté de Médecine, Université Paris Est, Créteil, France
Abstract:IntroductionMen with diabetic erectile dysfunction (ED) often have severe endothelial dysfunction and respond poorly to oral phosphodiesterase‐5 inhibitors.AimTo examine whether and how freshly isolated stromal vascular fraction (SVF) promotes cavernous endothelial regeneration and restores erectile function in diabetic animals.MethodsEight‐week‐old C57BL/6J mice were used. Diabetes was induced by intraperitoneal injection of streptozotocin. SVF was isolated from epididymal adipose tissues of green fluorescence protein transgenic mice. At 8 weeks after the induction of diabetes, the animals were divided into six groups: controls, diabetic mice, and diabetic mice treated with a single intracavernous injection of phosphate‐buffered saline (PBS) or SVF (1 × 104 cells, 1 × 105 cells, or 2 × 105 cells/20 µL, respectively).Main Outcome MeasuresTwo weeks later, erectile function was measured by cavernous nerve stimulation. The penis was stained with antibodies to CD31, CD34, phosphohistone H3, phospho‐endothelial nitric oxide synthase (eNOS), and vascular endothelial growth factor‐A (VEGF‐A). We also performed Western blot for phospho‐eNOS and eNOS, and determined cyclic guanosine monophosphate (cGMP) concentration in the corpus cavernosum tissue.ResultsSignificant improvement in erectile function was noted in diabetic mice treated with SVF at concentrations of 1 × 105 and 2 × 105 cells, which reached up to 82% of the control values. Local delivery of SVF significantly increased cavernous endothelial cell proliferation, eNOS phosphorylation, and cGMP expression compared with that in the untreated group and the PBS‐treated diabetic group. Intracavernous injection of SVF increased cavernous VEGF‐A expression and induced recruitment of CD34(+)CD31(?) progenitor cells. Some SVF underwent differentiation into cavernous endothelial cells. SVF‐induced promotion of cavernous angiogenesis and erectile function was abolished in the presence of VEGF‐Trap, a soluble VEGF‐A neutralizing antibody.ConclusionThe results support the concept of cavernous endothelial regeneration by use of SVF as a curative therapy for diabetic ED. Ryu J‐K, Tumurbaatar M, Jin H‐R, Kim WJ, Kwon M‐H, Piao S, Choi MJ, Yin GN, Song K‐M, Kang Y‐J, Koh YJ, Koh GY, and Suh J‐K. Intracavernous delivery of freshly isolated stromal vascular fraction rescues erectile function by enhancing endothelial regeneration in the streptozotocin‐induced diabetic mouse. J Sex Med 2012;9:3051–3065.
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