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用于治疗下尿路症状的树脂毒素和A型肉毒杆菌毒素。

Resiniferatoxin and botulinum toxin type A for treatment of lower urinary tract symptoms.

作者信息

Cruz Francisco, Dinis Paulo

机构信息

Department of Urology, Hospital de S. João, Faculty of Medicine/IBMC of Porto, Porto, Portugal. cruzfjmr@med,up.pt

出版信息

Neurourol Urodyn. 2007 Oct;26(6 Suppl):920-7. doi: 10.1002/nau.20479.

DOI:10.1002/nau.20479
PMID:17705161
Abstract

Resiniferatoxin (RTX) and botulinum toxin subtype A (BTX-A) are increasingly viewed as potential treatments for lower urinary tract symptoms (LUTS) refractory to conventional therapy. RTX, a capsaicin analogue devoid of severe pungent properties, acts by desensitizing the transient receptor potential vanilloid type 1 (TRPV1) receptor and inactivating C-fibers. BTX-A cleaves soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) proteins in afferent and efferent nerve endings, therefore impeding the fusion of synaptic vesicles with the neuronal membrane necessary for the release of neurotransmitters. In patients with neurogenic and idiopathic detrusor overactivity, RTX and BTX-A have been shown to increase the volume to first detrusor contraction, increase bladder capacity, and improve urinary incontinence and quality of life. Recent data also suggest a role for these neurotoxins in treating urgency, the primary symptom in overactive bladder (OAB) syndrome. Furthermore, experimental data strongly support the use of both neurotoxins in the treatment of pain and frequency in patients with interstitial cystitis/painful bladder syndrome (IC/PBS), although the results from available clinical trials for this use are still inconclusive. In spite of promising results overall, it should be made clear that the administration of these neurotoxins is still considered an experimental procedure and that more clinical studies are necessary before a license for their use will be issued by health authorities.

摘要

树脂毒素(RTX)和A型肉毒杆菌毒素(BTX-A)越来越被视为治疗对传统疗法难治的下尿路症状(LUTS)的潜在方法。RTX是一种没有严重刺激性的辣椒素类似物,其作用是使瞬时受体电位香草酸亚型1(TRPV1)受体脱敏并使C纤维失活。BTX-A可切割传入和传出神经末梢中的可溶性N-乙基马来酰亚胺敏感因子附着蛋白受体(SNARE)蛋白,从而阻碍神经递质释放所需的突触小泡与神经元膜的融合。在神经源性和特发性逼尿肌过度活动的患者中,RTX和BTX-A已被证明可增加首次逼尿肌收缩的容量、增加膀胱容量,并改善尿失禁和生活质量。最近的数据还表明这些神经毒素在治疗尿急(膀胱过度活动症(OAB)综合征的主要症状)方面也有作用。此外,实验数据有力地支持了这两种神经毒素用于治疗间质性膀胱炎/疼痛性膀胱综合征(IC/PBS)患者的疼痛和尿频,尽管目前关于此用途的临床试验结果仍无定论。尽管总体结果很有前景,但应该明确的是,这些神经毒素的给药仍被视为一种实验性程序,在卫生当局发放其使用许可之前,还需要更多的临床研究。

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