Botulinum toxin type A is a potential therapeutic drug for chronic orofacial pain

IF 2.6 Q1 DENTISTRY, ORAL SURGERY & MEDICINE Journal of Oral Biosciences Pub Date : 2024-06-21 DOI:10.1016/j.job.2024.06.004
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Abstract

Background

Botulinum toxin type A (BTX-A), produced by the gram-positive anaerobic bacterium Clostridium botulinum, acts by cleaving synaptosome-associated protein-25 (SNAP-25), an essential component of the presynaptic neuronal membrane that is necessary for fusion with the membrane proteins of neurotransmitter-containing vesicles. Recent studies have highlighted the efficacy of BTX-A in treating chronic pain conditions, including lower back pain, chronic neck pain, neuropathic pain, and trigeminal neuralgia, particularly when patients are unresponsive to traditional painkillers. This review focuses on the analgesic effects of BTX-A in various chronic pain conditions, with a particular emphasis on the orofacial region.

Highlight

This review focuses on the mechanisms by which BTX-A induces analgesia in patients with inflammatory and temporomandibular joint pain. This review also highlights the fact that BTX-A can effectively manage neuropathic pain and trigeminal neuralgia, which are difficult-to-treat chronic pain conditions. Herein, we present a comprehensive assessment of the central analgesic effects of BTX-A and a discussion of its various applications in clinical dental practice.

Conclusion

BTX-A is an approved treatment option for various chronic pain conditions. Although there is evidence of axonal transport of BTX-A from peripheral to central endings in motor neurons, the precise mechanism underlying its pain-modulating effects remains unclear. This review discusses the evidence supporting the effectiveness of BTX-A in controlling chronic pain conditions in the orofacial region. BTX-A is a promising therapeutic agent for treating pain conditions that do not respond to conventional analgesics.

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A 型肉毒杆菌毒素是一种治疗慢性口面部疼痛的潜在药物。
背景:A 型肉毒杆菌毒素(BTX-A)由革兰氏阳性厌氧菌肉毒梭菌产生,通过裂解突触体相关蛋白-25(SNAP-25)发挥作用,SNAP-25 是突触前神经元膜的重要组成部分,是与含神经递质囊泡的膜蛋白融合所必需的。最近的研究强调了 BTX-A 在治疗慢性疼痛(包括下背痛、慢性颈痛、神经性疼痛和三叉神经痛)方面的疗效,尤其是在患者对传统止痛药无反应的情况下。本综述重点关注 BTX-A 在各种慢性疼痛病症中的镇痛效果,尤其侧重于口面部区域:本综述重点探讨了 BTX-A 在炎症性疼痛和颞下颌关节疼痛患者中的镇痛机制。本综述还强调了 BTX-A 可有效控制神经性疼痛和三叉神经痛这些难以治疗的慢性疼痛。在此,我们对 BTX-A 的中枢镇痛作用进行了全面评估,并讨论了其在牙科临床实践中的各种应用:结论:BTX-A 是一种已获批准的治疗各种慢性疼痛的药物。虽然有证据表明 BTX-A 可以从运动神经元的外周末梢轴突运输到中枢末梢,但其疼痛调节作用的确切机制仍不清楚。本综述讨论了支持 BTX-A 有效控制口面部慢性疼痛的证据。BTX-A 是一种很有前景的治疗药物,可用于治疗对常规镇痛药无效的疼痛病症。
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来源期刊
Journal of Oral Biosciences
Journal of Oral Biosciences DENTISTRY, ORAL SURGERY & MEDICINE-
CiteScore
4.40
自引率
12.50%
发文量
57
审稿时长
37 days
期刊最新文献
Editorial Board Oral microbiome profiles of gingivitis and periodontitis by next-generation sequencing among a group of hospital patients in Korea: A cross-sectional study. Exploring the Mechanism of tiRNA-Val-CAC-002 in the Pathogenesis of Oral Submucous Fibrosis. Impact of organic, conventional, and stingless bee honeys on the antibacterial activity of gummy candies against oral bacteria. CCN2: a potential contributor to gingival overgrowth.
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