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首页> 外文期刊>BMC Urology >Little effects of Insulin-like Growth Factor-I on testicular atrophy induced by hypoxia
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Little effects of Insulin-like Growth Factor-I on testicular atrophy induced by hypoxia

机译:胰岛素样生长因子-I对缺氧所致睾丸萎缩的影响很小

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Background Insulin-like Growth Factor-I (IGF-I) supplementation restores testicular atrophy associated with advanced liver cirrhosis that is a condition of IGF-I deficiency. The aim of this work was to evaluate the effect of IGF-I in rats with ischemia-induced testicular atrophy (AT) without liver disease and consequently with normal serum level of IGF-I. Methods Testicular atrophy was induced by epinephrine (1, 2 mg/Kg intra-scrotal injection five times per week) during 11 weeks. Then, rats with testicular atrophy (AT) were divided into two groups (n = 10 each): untreated rats (AT) receiving saline sc, and AT+IGF, which were treated with IGF-I (2 μg.100 g b.w.-1.day-1, sc.) for 28d. Healthy controls (CO, n = 10) were studied in parallel. Animals were sacrificed on day 29th. Hypophyso-gonadal axis, IGF-I and IGFBPs levels, testicular morphometry and histopathology, immuno-histochemical studies and antioxidant enzyme activity phospholipid hydroperoxide glutathione peroxidase (PHGPx) were assessed. Results Compared to controls, AT rats displayed a reduction in testicular size and weight, with histological testicular atrophy, decreased cellular proliferation and transferrin expression, and all of these alterations were slightly improved by IGF-I at low doses. IGF-I therapy increased signifincantly steroidogenesis and PHGPx activity (p Conclusion In testicular atrophy by hypoxia, condition without IGF-I deficiency, IGF-treatment induces only partial effects. These findings suggest that IGF-I therapy appears as an appropriate treatment in hypogonadism only when this is associated to conditions of IGF-I deficiency (such as Laron Syndrom or liver cirrhosis).
机译:背景技术胰岛素样生长因子-I(IGF-I)补充剂可恢复与晚期肝硬化相关的睾丸萎缩,后者是IGF-I缺乏症。这项工作的目的是评估IGF-I在缺血性诱导的睾丸萎缩(AT)大鼠中无肝病,因此血清IGF-I正常的大鼠中的作用。方法在11周内,肾上腺素(每周两次,每次5次,每次1次,每次2mg / Kg阴囊内阴囊注射)诱发睾丸萎缩。然后,将睾丸萎缩(AT)的大鼠分为两组(每组n = 10):接受盐水皮下注射的未经治疗的大鼠(AT)和经IGF-I(2μg。100 g bw < sup> -1 .day -1 ,sc。),持续28天。平行研究健康对照(CO,n = 10)。在第29天 处死动物。评估了垂体下性腺轴,IGF-I和IGFBPs水平,睾丸形态和组织病理学,免疫组织化学研究以及抗氧化酶活性磷脂氢过氧化物谷胱甘肽过氧化物酶(PHGPx)。结果与对照组相比,AT大鼠的睾丸尺寸和重量减少,组织学性睾丸萎缩,细胞增殖和转铁蛋白表达降低,低剂量的IGF-1改善了所有这些改变。 IGF-I治疗显着增加了类固醇生成和PHGPx活性(p结论在缺氧引起的睾丸萎缩,无IGF-I缺乏症的情况下,IGF-治疗仅引起部分作用。这些发现表明,IGF-I治疗仅作为性腺功能减退症的适当治疗方法。与IGF-I缺乏症(例如Laron Syndrom或肝硬化)相关时。

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