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本文引用的文献

1
Changes in the oxidative stress factors and inflammatory proteins following the treatment of BPH-induced dogs with an anti-proliferative agent called tadalafil.用一种名为他达拉非的抗增殖剂治疗前列腺增生诱导犬后氧化应激因子和炎症蛋白的变化。
J Vet Pharmacol Ther. 2019 Nov;42(6):665-672. doi: 10.1111/jvp.12805. Epub 2019 Aug 13.
2
Bladder overactivity and afferent hyperexcitability induced by prostate-to-bladder cross-sensitization in rats with prostatic inflammation.前列腺炎大鼠前列腺至膀胱交叉致敏引起的膀胱过度活动和传入性高反应性。
J Physiol. 2019 Apr;597(7):2063-2078. doi: 10.1113/JP277452. Epub 2019 Feb 12.
3
Botulinum toxin blocks mast cells and prevents rosacea like inflammation.肉毒杆菌毒素可阻断肥大细胞并预防类酒渣鼻炎症。
J Dermatol Sci. 2019 Jan;93(1):58-64. doi: 10.1016/j.jdermsci.2018.12.004. Epub 2018 Dec 28.
4
Synthetic nickel-containing superoxide dismutase attenuates para-phenylenediamine-induced bladder dysfunction in rats.合成含镍超氧化物歧化酶减轻对苯二胺诱导的大鼠膀胱功能障碍。
Oncotarget. 2017 Nov 11;8(62):105735-105748. doi: 10.18632/oncotarget.22395. eCollection 2017 Dec 1.
5
Serotonin regulates prostate growth through androgen receptor modulation.血清素通过调节雄激素受体来调控前列腺的生长。
Sci Rep. 2017 Nov 13;7(1):15428. doi: 10.1038/s41598-017-15832-5.
6
Infiltrating mast cells enhance benign prostatic hyperplasia through IL-6/STAT3/Cyclin D1 signals.浸润性肥大细胞通过IL-6/STAT3/细胞周期蛋白D1信号通路促进良性前列腺增生。
Oncotarget. 2017 Jul 22;8(35):59156-59164. doi: 10.18632/oncotarget.19465. eCollection 2017 Aug 29.
7
Prevalence of Lower Urinary Tract Symptoms in China, Taiwan, and South Korea: Results from a Cross-Sectional, Population-Based Study.中国、台湾地区和韩国下尿路症状的患病率:一项基于人群的横断面研究结果。
Adv Ther. 2017 Aug;34(8):1953-1965. doi: 10.1007/s12325-017-0577-9. Epub 2017 Jul 7.
8
Elevated insulin and reduced insulin like growth factor binding protein-3/prostate specific antigen ratio with increase in prostate size in Benign Prostatic Hyperplasia.良性前列腺增生症中前列腺体积增大与胰岛素升高和胰岛素样生长因子结合蛋白-3/前列腺特异性抗原比值降低有关。
Clin Chim Acta. 2017 Jun;469:37-41. doi: 10.1016/j.cca.2017.03.012. Epub 2017 Mar 11.
9
Efficacy and safety of botulinum toxin injection for benign prostatic hyperplasia: a systematic review and meta-analysis.肉毒杆菌毒素注射治疗良性前列腺增生的疗效与安全性:一项系统评价和荟萃分析。
Int Urol Nephrol. 2016 Jan;48(1):19-30. doi: 10.1007/s11255-015-1153-3. Epub 2015 Nov 11.
10
Metformin Attenuates Testosterone-Induced Prostatic Hyperplasia in Rats: A Pharmacological Perspective.二甲双胍减轻睾酮诱导的大鼠前列腺增生:药理学视角
Sci Rep. 2015 Oct 23;5:15639. doi: 10.1038/srep15639.

A型肉毒杆菌毒素能否通过抑制慢性前列腺炎仍在治疗下尿路症状/良性前列腺增生中发挥作用?

Can Botulinum Toxin A Still Have a Role in Treatment of Lower Urinary Tract Symptoms/Benign Prostatic Hyperplasia Through Inhibition of Chronic Prostatic Inflammation?

作者信息

Chiang Bing-Juin, Kuo Hann-Chorng, Liao Chun-Hou

机构信息

College of Medicine, Fu-Jen Catholic University, New Taipei City 24205, Taiwan.

Department of Urology, Cardinal Tien Hospital, New Taipei City 23148, Taiwan.

出版信息

Toxins (Basel). 2019 Sep 19;11(9):547. doi: 10.3390/toxins11090547.

DOI:10.3390/toxins11090547
PMID:31546892
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6784075/
Abstract

Patients with benign prostatic hyperplasia (BPH) can exhibit various lower urinary tract symptoms (LUTS) owing to bladder outlet obstruction (BOO), prostatic inflammation, and bladder response to BOO. The pathogenesis of BPH involves an imbalance of internal hormones and chronic prostatic inflammation, possibly triggered by prostatic infection, autoimmune responses, neurogenic inflammation, oxidative stress, and autonomic dysfunction. Botulinum toxin A (BoNT-A) is well recognized for its ability to block acetylcholine release at the neuromuscular junction by cleaving synaptosomal-associated proteins. Although current large clinical trials have shown no clinical benefits of BoNT-A for the management of LUTS due to BPH, BoNT-A has demonstrated beneficial effects in certain subsets of BPH patients with LUTS, especially in males with concomitant chronic prostatitis/chronic pelvic pain syndrome and smaller prostate. We conducted a review of published literature in Pubmed, using Botulinum toxin, BPH, BOO, inflammation, LUTS, and prostatitis as the key words. This article reviewed the mechanisms of BPH pathogenesis and anti-inflammatory effects of BoNT-A. The results suggested that to achieve effectiveness, the treatment of BPH with BoNT-A should be tailored according to more detailed clinical information and reliable biomarkers.

摘要

良性前列腺增生(BPH)患者由于膀胱出口梗阻(BOO)、前列腺炎症以及膀胱对BOO的反应,可表现出各种下尿路症状(LUTS)。BPH的发病机制涉及体内激素失衡和慢性前列腺炎症,可能由前列腺感染、自身免疫反应、神经源性炎症、氧化应激和自主神经功能障碍引发。肉毒杆菌毒素A(BoNT-A)因其能够通过裂解突触体相关蛋白来阻断神经肌肉接头处乙酰胆碱的释放而广为人知。尽管目前的大型临床试验表明BoNT-A对治疗BPH所致LUTS无临床益处,但BoNT-A已在某些患有LUTS的BPH患者亚组中显示出有益效果,尤其是伴有慢性前列腺炎/慢性盆腔疼痛综合征且前列腺较小的男性患者。我们在Pubmed上对已发表的文献进行了综述,使用肉毒杆菌毒素、BPH、BOO、炎症、LUTS和前列腺炎作为关键词。本文综述了BPH的发病机制及BoNT-A的抗炎作用。结果表明,为达到疗效,使用BoNT-A治疗BPH应根据更详细的临床信息和可靠的生物标志物进行个体化治疗。