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首页> 外文期刊>Regenerative Therapy >Exosomes from adipose-derived stem cells protect against high glucose-induced erectile dysfunction by delivery of corin in a streptozotocin-induced diabetic rat model
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Exosomes from adipose-derived stem cells protect against high glucose-induced erectile dysfunction by delivery of corin in a streptozotocin-induced diabetic rat model

机译:来自脂肪衍生的干细胞的外泌体通过在链脲佐菌素诱导的糖尿病大鼠模型中递送Corin来保护抗高葡萄糖诱导的勃起功能障碍

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Introduction Increasing study have found that stem cell transplantation have a therapeutical effect to diabetes mellitus (DM)-induced erectile dysfunction (ED). So, the aim of this study was to evaluate the beneficial effect of corin from adipose-derived stem cells (ADSCs) on DM-induced ED. Methods Exosomes were isolated from ADSCs (ADSC-EXOs) or from ADSCs in which corin gene expression was silenced by siRNA (siCorin). For in?vivo studies, rats with streptozotocin-induced DM were intravenously injected with ADSC-EXOs or siCorin-ADSC-EXOs. Two weeks later, intracavernosal pressure (ICP) and mean arterial pressure (MAP) were measured to assess erectile function, and penile tissues were harvested for further evaluation of levels of inflammatory factors and expression of atrial natriuretic peptide (ANP), brain natriuretic peptide (BNP) and neuronal nitric oxide synthase (nNOS). We also evaluated the recovery of neurovascular function in penile tissues by immunofluorescence analysis. Results The results showed that ADSC-EXOs restored erectile function in diabetic rats, as determined by the ICP/MAP ratio. Exosomes from ADSCs also promoted neurovascular function and suppressed expression of inflammatory factors. In contrast, the decreased content of corin in exosomes after silencing corin in ADSCs reduced the therapeutic effect of exosomes on ED. Conclusion These findings demonstrated the therapeutic mechanism underlying the use of ADSC-EXOs for treating ED and the beneficial effect of corin.
机译:引言增加的研究发现,干细胞移植对糖尿病(DM)诱导的勃起功能障碍(ED)具有治疗效果。因此,本研究的目的是评估对脂肪衍生的干细胞(ADSC)对DM诱导的ED的有益效果。方法从ADSCs(ADSC-EXOS)中分离出外泌体或来自SiRNA(Sicorin)沉默的ADSC。对于体内的研究,用adsc-exos或sicorin-Adsc-exos静脉内注射串联诱导的链霉菌诱导的DM的大鼠。两周后,测量胞内压力(ICP)和平均动脉压(MAP)评估勃起功能,收获阴茎组织以进一步评估炎症因子水平和心房钠肽(ANP)的表达,脑钠尿肽( BNP)和神经元一氧化氮合酶(NNOS)。我们还通过免疫荧光分析评估了阴茎组织中神经血管功能的回收率。结果结果表明,通过ICP / MAP比例确定的糖尿病大鼠ADSC-EXOS恢复勃起功能。来自ADSCs的外泌体还促进了神经血管功能并抑制了炎症因素的表达。相比之下,在ADSC中沉默的沉默后,外泌体在外泌体中的含量降低降低了外来体对ED的治疗效果。结论这些研究结果证明了使用ADSC-EXOS的治疗机制,用于治疗Corin的受益作用。

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