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The protective effect of dexpanthenol on testicular atrophy at 60th day following experimental testicular torsion

机译:实验性睾丸扭转后第60天,右泛醇对睾丸萎缩的保护作用

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Despite the prompt diagnosis and treatment of testicular torsion (TT), there are problems with fertility and atrophy after testicular salvage. Dexpanthenol (Dxp) is the biologically active alcohol of pantothenic acid (PA). Dxp is converted to PA in tissues. PA increases the content of reduced glutathione (GSH), Coenzyme A and ATP synthesis in cells. GSH and glutathione-dependent peroxidases (GPX) are the major defense systems against oxidative stress. GPX-4 is the major antioxidant in testicular tissue. However, the activity of GPX-4 appeared and increased only after puberty. We investigated the effect of Dxp on testicular atrophy after TT at the 60th day. Rats were separated randomly into four groups. Group C: control group, group Td: torsion + detorsion, group Sal: torsion + saline + detorsion, group Dxp: torsion + Dxp + detorsion. The left testis was rotated 720° for 2 h. In group Sal, normal saline and in group Dxp, Dexpanthenol were injected intraperitonally, 30 min before detorsion. After 60 days, the testicular weights and volumes were measured. Histopathology of the left testis was evaluated with mean seminiferous tubular diameter (MSTD) and mean testicular biopsy score (MTBS). The left (torsed) testicular weight and volume of groups Td and Sal were significantly lower compared to group Dxp. The MSTD and MTBS of group Td and Sal were significantly lower than group Dxp. Contralateral testicular weight and volume of groups Td, Sal and Dxp had no significant difference compared to the control group. Dxp significantly prevented testicular atrophy after 60 days of TT. Dxp has FDA approval, is safe, cost effective and readily available. Its relevance for clinical trials may especially be for the problem of testicular atrophy catastrophe, seen very frequently following testicular salvage.
机译:尽管对睾丸扭转(TT)进行了迅速的诊断和治疗,但保留睾丸后仍存在生育力和萎缩的问题。 Dexpanthenol(Dxp)是泛酸(PA)的生物活性醇。 Dxp在组织中转化为PA。 PA增加了细胞中还原型谷胱甘肽(GSH),辅酶A和ATP合成的含量。 GSH和谷胱甘肽依赖性过氧化物酶(GPX)是抵抗氧化应激的主要防御系统。 GPX-4是睾丸组织中的主要抗氧化剂。但是,GPX-4的活性仅在青春期后才出现并增加。我们在第60天调查了Dxp对TT后睾丸萎缩的影响。将大鼠随机分为四组。 C组:对照组,Td组:扭转+扭转,Sal组:扭转+盐水+扭转,Dxp组:扭转+ Dxp +扭转。将左睾丸旋转720°2小时。 Sal组,在扭曲前30分钟腹膜内注射生理盐水,Dxp组,Dexpanthenol。 60天后,测量睾丸的重量和体积。左睾丸的组织病理学用平均生精小管直径(MSTD)和平均睾丸活检评分(MTBS)进行评估。与Dxp组相比,Td和Sal组的左(扭曲)睾丸重量和体积显着降低。 Td和Sal组的MSTD和MTBS显着低于Dxp组。 Td,Sal和Dxp组的对侧睾丸重量和体积与对照组相比无显着差异。 TT 60天后,Dxp显着预防了睾丸萎缩。 Dxp已获得FDA批准,安全,具有成本效益且易于获得。它与临床试验的相关性尤其可能在于睾丸挽救后经常出现的睾丸萎缩灾难问题。

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