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本文引用的文献

1
Achalasia: a systematic review.贲门失弛缓症:系统评价。
JAMA. 2015 May 12;313(18):1841-52. doi: 10.1001/jama.2015.2996.
2
Ethanolamine oleate versus botulinum toxin in the treatment of idiopathic achalasia.油酸乙醇胺与肉毒杆菌毒素治疗特发性贲门失弛缓症的比较
Ann Gastroenterol. 2015 Apr-Jun;28(2):229-235.
3
Peroral esophageal myotomy versus laparoscopic Heller's myotomy for achalasia: a meta-analysis.经口食管肌层切开术与腹腔镜下Heller肌层切开术治疗贲门失弛缓症的Meta分析
J Laparoendosc Adv Surg Tech A. 2015 Feb;25(2):123-9. doi: 10.1089/lap.2014.0454.
4
Pharmaceutical, biological, and clinical properties of botulinum neurotoxin type A products.A型肉毒杆菌神经毒素产品的药学、生物学及临床特性
Drugs R D. 2015 Mar;15(1):1-9. doi: 10.1007/s40268-014-0077-1.
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Acrylamide inhibits nerve sprouting induced by botulinum toxin type A.丙烯酰胺抑制肉毒毒素 A 诱导的神经发芽。
Neural Regen Res. 2014 Aug 15;9(16):1525-31. doi: 10.4103/1673-5374.139479.
6
Establishment of alternative potency test for botulinum toxin type A using compound muscle action potential (CMAP) in rats.利用大鼠复合肌肉动作电位(CMAP)建立A型肉毒杆菌毒素替代效价试验。
Toxicon. 2014 Nov;90:97-105. doi: 10.1016/j.toxicon.2014.07.013. Epub 2014 Aug 7.
7
Incorrect reconstitution of incobotulinumtoxinA leads to loss of neurotoxin.因卡泊肉毒素A复溶不当会导致神经毒素丧失。
J Drugs Dermatol. 2014 Jun;13(6):735-8.
8
Persistence of botulinum neurotoxin a subtypes 1-5 in primary rat spinal cord cells.肉毒杆菌神经毒素A亚型1-5在原代大鼠脊髓细胞中的持久性。
PLoS One. 2014 Feb 27;9(2):e90252. doi: 10.1371/journal.pone.0090252. eCollection 2014.
9
Type A botulinum neurotoxin complex proteins differentially modulate host response of neuronal cells.A型肉毒杆菌神经毒素复合蛋白对神经元细胞的宿主反应有不同的调节作用。
Toxicon. 2014 May;82:52-60. doi: 10.1016/j.toxicon.2014.02.004. Epub 2014 Feb 21.
10
Impact of genetic polymorphisms on the pathogenesis of idiopathic achalasia: Association with IL33 gene variant.基因多态性对特发性贲门失弛缓症发病机制的影响:与IL33基因变异的关联。
Hum Immunol. 2014 Apr;75(4):364-9. doi: 10.1016/j.humimm.2014.01.004. Epub 2014 Jan 24.

贲门失弛缓症治疗的药物疗法:现状、挑战与未来方向

Pharmacotherapy for the management of achalasia: Current status, challenges and future directions.

作者信息

Nassri Ammar, Ramzan Zeeshan

机构信息

Ammar Nassri, Department of Internal Medicine, University of Texas at Austin Dell Medical School, Austin, TX 78701, United States.

出版信息

World J Gastrointest Pharmacol Ther. 2015 Nov 6;6(4):145-55. doi: 10.4292/wjgpt.v6.i4.145.

DOI:10.4292/wjgpt.v6.i4.145
PMID:26558149
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4635155/
Abstract

This article reviews currently available pharmacological options available for the treatment of achalasia, with a special focus on the role of botulinum toxin (BT) injection due to its superior therapeutic effect and side effect profile. The discussion on BT includes the role of different BT serotypes, better pharmacological formulations, improved BT injection techniques, the use of sprouting inhibitors, designer recombinant BT formulations and alternative substances used in endoscopic injections. The large body of ongoing research into achalasia and BT may provide a stronger role for BT injection as a form of minimally invasive, cost effective and efficacious form of therapy for patients with achalasia. The article also explores current issues and future research avenues that may prove beneficial in improving the efficacy of pharmacological treatment approaches in patients with achalasia.

摘要

本文综述了目前可用于治疗贲门失弛缓症的药物选择,特别关注肉毒杆菌毒素(BT)注射的作用,因为其具有卓越的治疗效果和副作用特征。关于BT的讨论包括不同BT血清型的作用、更好的药物制剂、改进的BT注射技术、发芽抑制剂的使用、定制重组BT制剂以及内镜注射中使用的替代物质。目前对贲门失弛缓症和BT的大量研究可能会使BT注射作为一种微创、经济有效且高效的治疗方式在贲门失弛缓症患者中发挥更重要的作用。本文还探讨了当前的问题以及未来的研究途径,这些可能有助于提高贲门失弛缓症患者药物治疗方法的疗效。