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In the Human Urothelium and Suburothelium, Intradetrusor Botulinum Neurotoxin Type A Does Not Induce Apoptosis: Preliminary Results

机译:在人类的尿路上皮和尿路上皮下,Intrutrusor A型肉毒杆菌神经毒素不会诱导细胞凋亡:初步结果

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Background: Intradetrusor injections of botulinum neurotoxin type A (BoNTA) are emerging as the preferred second-line treatment for neurogenic and idiopathic overactive bladder (OAB). In animal experiments, intradetrusor BoNTA injections have been shown to cause apoptosis in the bladder urothelium and suburothelium but not the detrusor. Objective: To investigate BoNTA-induced apoptosis in patients with refractory neurogenic OAB. Design, setting, and participants: Twelve refractory OAB patients with neurogenic detrusor overactivity resulting from multiple sclerosis (MS) and seven controls were included prospectively. Measurements: The number of apoptotic cells before and 4 wk after first intradetrusor BoNTA (300 U of BOTOX [Allergan, Irvine, CA, USA]) injections were estimated using terminal deoxynucleotidyl transferase-mediated dUTP nick-end labelling (TUNEL) staining. Results and limitations: Comparison of TUNEL-positive cells (yes vs no) in the bladder urothelium and suburothelium revealed no significant differences in OAB patients before (4 of 12,33%) versus after (3 of 12,25%) BoNTA treatment (p = 0.99). In addition, no significant differences (p = 0.99) were found in OAB patients versus controls. Because our findings are based on first intradetrusor BoNTA injections only, it is unclear whether the results could be extrapolated to repeat injections. Conclusions: In contrast to preliminary animal experiments, first intradetrusor BoNTA injections for treating refractory neurogenic OAB-a highly effective treatment-did not induce apoptosis in the bladder urothelium and suburothelium.
机译:背景:A型肉毒杆菌神经毒素(BoNTA)的Intrutrusor注射剂正成为神经性和特发性膀胱过度活动症(OAB)的首选二线治疗方法。在动物实验中,注射Intradetrusor的BoNTA会导致膀胱尿路上皮和尿路上皮下的细胞凋亡,但不会引起逼尿肌的凋亡。目的:研究BoNTA诱导的难治性神经源性OAB患者的细胞凋亡。设计,地点和参与者:前瞻性纳入了12例难治性OAB患者,其中多发性硬化症(MS)导致神经源性逼尿肌过度活跃,其中有7名对照。测量:使用终末脱氧核苷酸转移酶介导的dUTP缺口末端标记(TUNEL)染色,估计首次注射InNT注射BoNTA(300U BOTOX [Allergan,Irvine,CA,美国])之前和之后4周的凋亡细胞数量。结果与局限性:比较膀胱尿路上皮和尿路上皮下TUNEL阳性细胞(是与否),发现OAB患者在BoNTA治疗之前(占12,33%的4个)与术后(占12.25%的3个)无显着差异( p = 0.99)。此外,在OAB患者与对照组之间没有发现显着差异(p = 0.99)。由于我们的发现仅基于Intrutrusor BoNTA的首次注射,因此尚不清楚是否可以将结果外推至重复注射。结论:与初步的动物实验相反,用于治疗难治性神经源性OAB的首例Intrutrusor BoNTA注射剂并未诱导膀胱尿路上皮和尿路上皮下的细胞凋亡。

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