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首页> 外文期刊>Asian journal of andrology >Therapeutic effects of adipose-derived stem cells-based microtissues on erectile dysfunction in streptozotocin-induced diabetic rats
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Therapeutic effects of adipose-derived stem cells-based microtissues on erectile dysfunction in streptozotocin-induced diabetic rats

机译:脂肪干细胞基微组织对链脲佐菌素诱发的糖尿病大鼠勃起功能障碍的治疗作用

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摘要

This study aimed to explore the therapeutic effects of adipose-derived stem cells (ADSCs)-based microtissues (MTs) on erectile dysfunction (ED) in streptozotocin (STZ)-induced diabetic rats. Fifty-six 8-week-old Sprague-Dawley rats received intraperitoneal injection of STZ (60 mg kg?1 ), and 8 weeks later, the determined diabetic rats randomly received intracavernous (IC) injection of phosphate buffer solution (PBS), ADSCs, or MTs. Another eight normal rats equally got IC injection of PBS. MTs were generated with a hanging drop method, and the injected cells were tracked in ADSC- and MT-injected rats. Four weeks after the treatments, intracavernous pressure (ICP), histopathological changes in corpus cavernosum (CC), and functional proteins were measured. Rat cytokine antibody array was used to detect ADSCs or MTs lysate. The results showed that MTs expressed vascular endothelial growth factor (VEGF), nerve growth factor (NGF), and tumor necrosis factor-stimulated gene-6 (TSG-6). MTs injection had a higher retention than ADSCs injection and MTs treatment improved ICP, neuronal nitric oxide synthase (nNOS) expression, smooth muscle, and endothelial contents in diabetic rats, ameliorated local inflammation in CC better. Thus, our findings demonstrate that IC injection of MTs improves erectile function and histopathological changes in STZ-induced diabetic rats and appears to be more promising than traditional ADSCs. The underlying mechanisms involve increased cell retention accompanied with neuroprotection and anti-inflammatory behaviors of the paracrine factors.
机译:这项研究旨在探讨基于脂肪的干细胞(ADSCs)的微组织(MTs)对链脲佐菌素(STZ)诱导的糖尿病大鼠勃起功能障碍(ED)的治疗作用。接受腹腔注射STZ(60 mg kg ?1 )的56只8周大的Sprague-Dawley大鼠,在8周后,确定的糖尿病大鼠随机接受了海绵体(IC)注射磷酸盐缓冲液(PBS),ADSC或MT。另外八只正常大鼠同样接受了PBS的IC注射。用悬滴法产生MT,并在注射ADSC和MT的大鼠中追踪注射的细胞。治疗后四周,测量海绵内压(ICP),海绵体(CC)的组织病理学变化和功能蛋白。大鼠细胞因子抗体阵列用于检测ADSC或MTs裂解物。结果表明,MTs表达了血管内皮生长因子(VEGF),神经生长因子(NGF)和肿瘤坏死因子刺激基因6(TSG-6)。 MTs注射比ADSCs注射保留更高,MTs治疗改善了糖尿病大鼠的ICP,一氧化氮合酶(nNOS)表达,平滑肌和内皮含量,改善了CC的局部炎症。因此,我们的发现表明IC注射MTs可以改善STZ诱导的糖尿病大鼠的勃起功能和组织病理学变化,并且比传统的ADSCs更有前景。潜在的机制涉及增加的细胞滞留以及旁分泌因子的神经保护和抗炎行为。

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