首页> 外文期刊>The Journal of Urology >Restoring erectile function by antioxidant therapy in diabetic rats.
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Restoring erectile function by antioxidant therapy in diabetic rats.

机译:通过抗氧化剂治疗糖尿病大鼠恢复勃起功能。

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PURPOSE: Diabetes mediates an increase in reactive oxygen species that can lead to impaired endothelial function, decreased smooth muscle in the diabetic corpus cavernosum and increased apoptosis. We hypothesized that antioxidant therapy may restore erectile function by inhibiting apoptosis in diabetic rat crura. MATERIALS AND METHODS: A total of 40 male Sprague-Dawley rats were randomized to 5 groups of 8 each, including healthy controls, rats with diabetes, and rats with diabetes with the antioxidant tempol (4-hydroxytetramethyl-piperidine-1-oxyl) (Sigma-Aldrich), with insulin, and with tempol and insulin. Intracavernous pressure was measured for functional analysis. Smooth muscle and collagen fiber levels in the rat penile corpus cavernosum were assessed by hematoxylin and eosin, and Masson's trichrome staining. Endothelial cells were assessed by CD31 staining. Reactive oxygen species related genes were analyzed by cDNA microarray. We confirmed mRNA and protein expression profiles for these genes in diabetic and treated rats using real-time reverse transcriptase-polymerase chain reaction and immunohistochemistry. TUNEL assay was done to analyze apoptosis status. RESULTS: Intracavernous pressure in diabetic rats was significantly decreased vs controls. After treatment with tempol or insulin alone intracavernous pressure was significantly increased compared to that in untreated diabetic rats. In the diabetic group mean smooth muscle area significantly decreased but was restored after combined tempol and insulin. Endothelial cell area in diabetic rats significantly decreased and was not restored by any treatments. However, apoptosis was restored to normal by combined insulin and tempol. Of 84 reactive oxidative stress and antioxidant genes 32 were identified specific to diabetic rats compared to healthy controls. UCP3 expression was significantly increased in diabetic rats and normal levels were restored by all treatments. CONCLUSIONS: To our knowledge this is the first report that tempol and insulin can restore erectile function in diabetic rats by inhibiting apoptosis.
机译:目的:糖尿病介导的活性氧增加,可导致内皮功能受损,糖尿病海绵体平滑肌减少和细胞凋亡增加。我们假设抗氧化剂治疗可以通过抑制糖尿病大鼠小腿的细胞凋亡来恢复勃起功能。材料与方法:将40只雄性Sprague-Dawley大鼠随机分为5组,每组8只,包括健康对照组,糖尿病大鼠和使用抗氧化剂tempol(4-羟基四甲基-哌啶-1-氧基)的糖尿病大鼠( Sigma-Aldrich),胰岛素,tempol和胰岛素。测量海绵体内压力以进行功能分析。用苏木精和曙红,以及马森三色染色评估大鼠阴茎海绵体中的平滑肌和胶原纤维水平。通过CD31染色评估内皮细胞。通过cDNA微阵列分析与活性氧相关的基因。我们使用实时逆转录酶-聚合酶链反应和免疫组化方法在糖尿病和治疗大鼠中证实了这些基因的mRNA和蛋白质表达谱。进行TUNEL分析以分析细胞凋亡状态。结果:与对照组相比,糖尿病大鼠的海绵体内压明显降低。与未治疗的糖尿病大鼠相比,单独用tempol或胰岛素治疗后,海绵体内压力显着增加。糖尿病组的平均平滑肌面积显着减少,但在tempol和胰岛素联合使用后恢复。糖尿病大鼠的内皮细胞面积显着减少,且未通过任何治疗恢复。然而,通过胰岛素和tempol的联合,细​​胞凋亡恢复了正常。与健康对照组相比,在84种反应性氧化应激和抗氧化剂基因中,鉴定出32种对糖尿病大鼠具有特异性。在所有大鼠中,UCP3表达均在糖尿病大鼠中显着增加,并且正常水平得以恢复。结论:据我们所知,这是第一份有关tempol和胰岛素可通过抑制细胞凋亡恢复糖尿病大鼠勃起功能的报道。

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