Department of Urology, Korea University College of Medicine, Seoul, Republic of Korea.
J Urol. 2013 Jun;189(6):2371-6. doi: 10.1016/j.juro.2012.12.101. Epub 2013 Jan 8.
We investigated the protective effects of coenzyme Q10 on bladder dysfunction in a rat model of atherosclerosis induced chronic bladder ischemia.
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.
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.
Our study suggests that coenzyme Q10 acts as an antioxidant to protect bladder function in this chronic bladder ischemia model.
我们研究了辅酶 Q10 在动脉粥样硬化诱导的慢性膀胱缺血大鼠模型中对膀胱功能障碍的保护作用。
16 周龄雄性 Sprague-Dawley®大鼠 24 只,随机分为 4 组,每组 6 只,分别为:1 组-未处理、假手术对照大鼠;2 组-辅酶 Q10 处理、假手术对照大鼠;3 组-慢性膀胱缺血未处理大鼠;4 组-慢性膀胱缺血辅酶 Q10 处理大鼠。3 组和 4 组大鼠接受髂动脉内皮损伤,并给予 2%胆固醇饮食 8 周。2 组和 4 组给予辅酶 Q10 治疗,其余各组给予载体治疗 4 周。术后 8 周,行连续体内膀胱测压、离体逼尿肌肌条研究和丙二醛测定。还对膀胱壁和髂动脉进行了组织学检查。
体内膀胱测压显示,慢性膀胱缺血诱导后给予辅酶 Q10 治疗可延长逼尿肌频率和两次收缩之间的间隔,并增加膀胱容量,与未处理的慢性膀胱缺血大鼠相比。在逼尿肌肌条研究中,慢性膀胱缺血诱导后给予辅酶 Q10 治疗可增加收缩反应,与未处理的慢性膀胱缺血大鼠相比。慢性膀胱缺血大鼠的膀胱组织和血清中的丙二醛水平也高于其他组。慢性膀胱缺血引起膀胱壁黏膜下纤维化和血管中膜退行性改变,组织学检查可见。
我们的研究表明,辅酶 Q10 作为一种抗氧化剂,可在这种慢性膀胱缺血模型中保护膀胱功能。