首页> 外文期刊>The Journal of Urology >Small intestinal submucosa as a tunica albuginea graft material.
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Small intestinal submucosa as a tunica albuginea graft material.

机译:小肠粘膜下层作为白膜移植物。

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PURPOSE: We evaluated the morphological, immunological and functional response to small intestinal submucosa grafting of the tunica albuginea to determine its potential as a grafting material for penile surgery. MATERIALS AND METHODS: Male New Zealand White rabbits underwent a sham procedure (6) or tunical excision and grafting with small intestinal submucosa (6). The erectile response to the intracavernous vasoactive agents sodium nitroprusside plus a papaverine, phentolamine and prostaglandin E1 combination (Sigma Chemical Co., St. Louis, Missouri) was evaluated 45-day postoperatively. The area under the graft was evaluated for stromal collagen and smooth muscle content by Masson's trichrome stain. Protein expression of smooth muscle specific alpha-actin and the inflammatory markers inducible nitric oxide synthase (NOS) and transforming growth factor-beta1 (TGF-beta1) was evaluated by immunohistochemical methods. Total RNA was extracted from the corpora cavernosum underlying the small intestinal submucosa graft and reverse transcriptase-polymerase chain reaction (RT-PCR) was done using an Access system (Promega, Madison, Wisconsin) with gene specific primers for inducible NOS, TGF-beta1 and vascular endothelial growth factor (VEGF). RESULTS: Grafting of the tunica albuginea with small intestinal submucosa had no significant effect on the magnitude or duration of the erectile response to intracavernous vasoactive agents. Histological examination demonstrated no inflammatory changes in the tunica albuginea or corporeal tissue underlying the area of the small intestinal submucosa graft and there was no appreciable alteration in smooth muscle or collagen content. The 2 groups showed intense positive immunostaining to alpha-actin. Weak expression of TGF-beta1 predominantly associated with smooth muscle fibers was identified in the 2 groups of rabbits by immunostaining and RT-PCR. No significant inducible NOS was detected by immunostaining or RT-PCR in either group. Strong VEGF expression was observed in grafted rabbits. The most noticeable (3-fold) increase in expression was detected in splice variant 165. CONCLUSIONS: Small intestinal submucosa grafting of the tunica albuginea preserves the duration and magnitude of the erectile response to vasoactive agents. This type of tunical grafting does not stimulate a significant inflammatory response, or cause corporeal fibrosis or loss of cavernous smooth muscle content. Stimulating VEGF may facilitate wound healing and the maintenance of normal erectile function.
机译:目的:我们评估了对白膜小肠粘膜下移植的形态,免疫和功能反应,以确定其作为阴茎手术移植材料的潜力。材料和方法:雄性新西兰白兔进行假手术(6)或局部切除并移植小肠粘膜下层(6)。术后45天评估了对海绵体内血管活性剂硝普钠加罂粟碱,苯妥拉明和前列腺素E1组合(西格玛化学公司,圣路易斯,密苏里州)的勃起反应。通过Masson氏三色染色法评估移植物下方区域的基质胶原和平滑肌含量。通过免疫组织化学方法评估了平滑肌特异性α-肌动蛋白和炎症标志物诱导型一氧化氮合酶(NOS)和转化生长因子-β1(TGF-β1)的蛋白质表达。从小肠粘膜下移植物下面的海绵体中提取总RNA,并使用Access系统(Promega,Madison,Wisconsin)使用可诱导NOS,TGF-beta1的基因特异性引物进行逆转录酶-聚合酶链反应(RT-PCR)和血管内皮生长因子(VEGF)。结果:小肠黏膜下白膜的嫁接对海绵体血管活性药物的勃起反应的幅度或持续时间没有显着影响。组织学检查表明小肠粘膜下移植物区域下方的白膜或有孔组织无炎性变化,平滑肌或胶原蛋白含量无明显变化。两组显示出对α-肌动蛋白的强烈阳性免疫染色。通过免疫染色和RT-PCR在两组兔子中鉴定出主要与平滑肌纤维相关的TGF-β1弱表达。两组均未通过免疫染色或RT-PCR检测到明显的诱导型NOS。在移植兔中观察到强VEGF表达。在剪接变体165中检测到最明显的表达增加(3倍)。结论:白膜的小肠粘膜下移植物保留了对血管活性剂的勃起反应的持续时间和强度。这种类型的管膜移植术不会刺激明显的炎症反应,也不会引起海绵状纤维化或海绵状平滑肌含量的损失。刺激VEGF可以促进伤口愈合和维持正常的勃起功能。

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