首页> 外文期刊>BMC Urology >Changes of neuregulin-1(NRG-1) expression in a rat model of overactive bladder induced by partial urethral obstruction: is NRG-1 a new biomarker of overactive bladder?
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Changes of neuregulin-1(NRG-1) expression in a rat model of overactive bladder induced by partial urethral obstruction: is NRG-1 a new biomarker of overactive bladder?

机译:大鼠部分尿道梗阻所致膀胱过度活动模型中神经调节蛋白1(NRG-1)表达的变化:NRG-1是膀胱过度活动症的新生物标志物吗?

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Background To determine whether neuregulin-1(NRG-1) is a potential new biomarker of overactive bladder (OAB) induced by partial urethral obstruction in a rat model of OAB and to evaluate the urothelium as a therapeutic target of OAB. Methods Female Sprague–Dawley rats were separated into three 20-animal groups: normal, OAB, and 5-hydroxymethyl tolterodine (5-HMT)-treated OAB. In the OAB and OAB?+?5-HMT groups, the urethra of each animal was partially obstructed; the OAB?+?5-HMT group received intravenous 5-HMT for 3?weeks. At the conclusion of the 5-HMT dosing, the rats in each group underwent cystometrography, and the bladders were histologically evaluated. The expression of brain derived-neurotrophic factor (BDNF) and NRG-1 were evaluated in the urothelium. Results Compared with the control group, the OAB group showed a markedly increased bladder weight and a significant decrease in the micturition interval and volume; rats in the OAB?+?5-HMT group showed decreased bladder weights and an improved micturition interval and volume. BDNF and NRG-1 were expressed at significantly higher levels in the OAB group, and were significantly reduced in the OAB?+?5-HMT group compared with the control group. Conclusions The study suggests that NRG-1 is a potential new biomarker of OAB; the urothelium might be a therapeutic target for OAB treatment.
机译:背景技术为了确定神经调节蛋白1(NRG-1)是否是OAB大鼠模型中部分尿道梗阻诱导的过度活动性膀胱(OAB)的潜在新生物标记,并评估尿路上皮作为OAB的治疗靶标。方法将雌性Sprague–Dawley大鼠分为20只动物,分为三组:正常,OAB和5-羟甲基托特罗定(5-HMT)处理的OAB。在OAB和OAB + + 5-5-HMT组中,每只动物的尿道被部分阻塞。 OAB + + 5-HMT组接受静脉内5-HMT治疗3周。在5-HMT给药结束时,对每组大鼠进行膀胱造影,并对膀胱进行组织学评价。在尿路上皮中评估了脑源性神经营养因子(BDNF)和NRG-1的表达。结果与对照组相比,OAB组膀胱重量明显增加,排尿间隔和排尿量明显减少。 OABβ+β5-HMT组的大鼠膀胱重量减少,排尿间隔和容量增加。与对照组相比,在OAB组中BDNF和NRG-1的表达明显升高,而在OABα+β5-HMT组中则明显降低。结论该研究表明NRG-1是OAB的潜在新生物标志物。尿路上皮可能是OAB治疗的治疗靶标。

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