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Effects of coenzyme Q10 on bladder dysfunction induced by chronic bladder ischemia in a rat model

机译:辅酶Q10对慢性膀胱缺血所致大鼠膀胱功能障碍的影响。

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Purpose: We investigated the protective effects of coenzyme Q10 on bladder dysfunction in a rat model of atherosclerosis induced chronic bladder ischemia. Materials and Methods: A total of 24 male Sprague-Dawley? rats at age 16 weeks were divided into 4 groups of 6 each, including group 1 - untreated, sham operated rats, group 2 - coenzyme Q10 treated, sham operated rats, group 3 - untreated rats with chronic bladder ischemia and group 4 - coenzyme Q10 treated rats with chronic bladder ischemia. Groups 3 and 4 received an endothelial injury to the iliac arteries and were fed a 2% cholesterol diet for 8 weeks. Groups 2 and 4 were treated with coenzyme Q10 and the others were treated with vehicle for 4 weeks. Eight weeks postoperatively we performed continuous in vivo cystometry, an in vitro detrusor muscle strip study and a malondialdehyde assay. Histological examination of the bladder walls and iliac arteries was also done. Results: In vivo cystometry revealed that coenzyme Q10 administration after the induction of chronic bladder ischemia prolonged micturition frequency and the intercontraction interval, and increased bladder capacity compared to those in untreated rats with chronic bladder ischemia. In the detrusor muscle strip study coenzyme Q10 administration after the induction of chronic bladder ischemia increased contractile responses compared to those in untreated rats with chronic bladder ischemia. Rats with chronic bladder ischemia also showed higher malondialdehyde in bladder tissue and serum than the other groups. Chronic bladder ischemia induced submucosal fibrosis of the bladder walls and a degenerative change in the blood vessel tunical media, as shown on histological examination. Conclusions: Our study suggests that coenzyme Q10 acts as an antioxidant to protect bladder function in this chronic bladder ischemia model.
机译:目的:我们研究了辅酶Q10对动脉粥样硬化诱发的慢性膀胱缺血大鼠模型中膀胱功能障碍的保护作用。材料和方法:共有24例男性Sprague-Dawley?将16周龄的大鼠分为4组,每组6组,包括第1组-未经治疗的假手术大鼠,第2组-辅酶Q10处理,假手术大鼠,第3组-未经治疗的慢性膀胱缺血大鼠和第4组-辅酶Q10治疗患有慢性膀胱缺血的大鼠。第3组和第4组受到the动脉内皮损伤,并以2%胆固醇饮食喂养8周。第2组和第4组用辅酶Q10治疗,其他组用赋形剂治疗4周。术后八周,我们进行了连续的体内膀胱测压,体外逼尿肌剥离研究和丙二醛测定。还对膀胱壁和动脉进行了组织学检查。结果:体内膀胱测量法显示,与未经治疗的慢性膀胱缺血大鼠相比,诱导慢性膀胱缺血后给予辅酶Q10可以延长排尿频率和收缩间隔,并增加膀胱容量。在逼尿肌剥离研究中,与未治疗的慢性膀胱缺血大鼠相比,诱导慢性膀胱缺血后辅酶Q10的给药增加了收缩反应。患有慢性膀胱缺血的大鼠在膀胱组织和血清中的丙二醛含量也高于其他两组。如组织学检查所示,慢性膀胱缺血可引起膀胱壁粘膜下纤维化,血管的中膜变性。结论:我们的研究表明,在这种慢性膀胱缺血模型中,辅酶Q10作为抗氧化剂来保护膀胱功能。

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