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肾上腺髓质素介导脂肪组织源性干细胞诱导糖尿病大鼠勃起功能恢复。

Adrenomedullin mediates adipose tissue-derived stem cell-induced restoration of erectile function in diabetic rats.

机构信息

The Department of Urology, Faculty of Medicine, University of Tokyo, Bunkyo-ku, Tokyo, Japan.

出版信息

J Sex Med. 2012 Feb;9(2):482-93. doi: 10.1111/j.1743-6109.2011.02469.x. Epub 2011 Sep 23.

Abstract

INTRODUCTION

Erectile dysfunction (ED) is a major health problem. It is known that diabetic patients are more refractory to common treatments for ED.

AIM

To explore the better treatment for ED, we examined the effects of adipose-derived stem cells (ASC) on ED using a diabetic rat model. We also analyzed the cytokines produced by ASC and implicated in ASC-induced restoration of erectile function.

METHODS

Male Wistar rats were injected with streptozotocin (STZ) to induce diabetes. ASC or adenoviruses were injected into the penis 6 weeks after STZ administration. Erectile function, penile histology and protein expression were analyzed 4 weeks after the injection of ASC or adenoviruses.

MAIN OUTCOME MEASURES

Intracavernous pressure and mean arterial pressure were measured to evaluate erectile function. The morphology of the penis was analyzed by Elastica van Gieson stain and immunohistochemistry. The expression of proteins specific for vascular endothelial cells (VEC) was assessed by Western blot analysis.

RESULTS

ASC restored erectile function especially when they were cultured in medium containing growth factors for VEC. This restoration was associated with improvement in the histology of the cavernous body, and increased expression of VEC markers such as VE-cadherin and endothelial nitric oxide synthase (eNOS). When the expression of adrenomedullin (AM), a vasoactive peptide originally isolated from human pheochromocytoma tissue, was knocked down, the effect of ASC on ED was significantly diminished. Knockdown of AM was associated with decreased expressions of VE-cadherin and eNOS. Furthermore, overexpression of AM induced by adenovirus infection significantly improved erectile function in these diabetic rats. Overexpression of AM was associated with increased expressions of VE-cadherin and eNOS.

CONCLUSIONS

These results suggested that ASC have the potentials to restore erectile function and that AM produced by ASC plays a major role in the restoration of erectile function.

摘要

简介

勃起功能障碍(ED)是一个主要的健康问题。已知糖尿病患者对 ED 的常见治疗方法更具抗性。

目的

为了探索更好的 ED 治疗方法,我们使用糖尿病大鼠模型研究了脂肪源性干细胞(ASC)对 ED 的影响。我们还分析了 ASC 产生的细胞因子,并探讨了其在 ASC 诱导的勃起功能恢复中的作用。

方法

雄性 Wistar 大鼠注射链脲佐菌素(STZ)以诱导糖尿病。在 STZ 给药后 6 周,将 ASC 或腺病毒注射到阴茎中。在注射 ASC 或腺病毒 4 周后,分析勃起功能、阴茎组织学和蛋白质表达。

主要观察指标

测量海绵体内压和平均动脉压以评估勃起功能。用弹性 Van Gieson 染色和免疫组织化学分析阴茎的形态。通过 Western blot 分析评估血管内皮细胞(VEC)特异性蛋白的表达。

结果

ASC 恢复了勃起功能,尤其是在含有 VEC 生长因子的培养基中培养时。这种恢复与海绵体组织学的改善以及 VEC 标志物如 VE-钙黏蛋白和内皮型一氧化氮合酶(eNOS)的表达增加有关。当血管活性肽肾上腺髓质素(AM)的表达被敲低时,ASC 对 ED 的作用明显减弱。AM 的敲低与 VE-钙黏蛋白和 eNOS 的表达减少有关。此外,腺病毒感染引起的 AM 过表达显著改善了这些糖尿病大鼠的勃起功能。AM 的过表达与 VE-钙黏蛋白和 eNOS 的表达增加有关。

结论

这些结果表明 ASC 具有恢复勃起功能的潜力,并且 ASC 产生的 AM 在勃起功能恢复中起主要作用。

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