Casale Roberto, Tugnoli Valeria
Department of Clinical Neurophysiology and Pain Rehabilitation Unit, Foundation Salvatore Maugeri, IRCCS, Scientific Institute of Montescano, Montescano (PV), Italy.
Drugs R D. 2008;9(1):11-27. doi: 10.2165/00126839-200809010-00002.
Botulinum toxin (BTX) injection is being increasingly used 'off label' in the management of chronic pain. Data support the hypothesis of a direct analgesic effect of BTX, different to that exerted on muscle. Although the pain-reducing effect of BTX is mainly due to its ability to block acetylcholine release at the synapse, other effects on the nervous system are also thought to be involved. BTX affects cholinergic transmission in both the somatic and the autonomic nervous systems. Proposed mechanisms of action of BTX for pain relief of trigger points, muscular spasms, fibromyalgia and myofascial pain include direct action on muscle and indirect effects via action at the neuromuscular junction. Invitro and invivo data have shown that BTX has specific antinociceptive activity relating to its effects on inflammation, axonal transport, ganglion inhibition, and spinal and suprasegmental level inhibition. Our review of the mechanisms of action, efficacy, administration techniques and therapeutic dosage of BTX for the management of chronic pain in a variety of conditions shows that although muscular tone and movement disorders remain the most important therapeutic applications for BTX, research suggests that BTX can also provide benefits related to effects on cholinergic control of the vascular system, autonomic function, and cholinergic control of nociceptive and antinociceptive systems. Furthermore, it appears that BTX may influence the peripheral and central nervous systems. The therapeutic potential of BTX depends mainly on the ability to deliver the toxin to the target structures, cholinergic or otherwise. Evidence suggests that BTX can be administered at standard dosages in pain disorders, where the objective is alteration of muscle tone. For conditions requiring an analgesic effect, the optimal therapeutic dosage of BTX remains to be defined.
肉毒杆菌毒素(BTX)注射在慢性疼痛管理中越来越多地被“超适应证”使用。数据支持BTX具有直接镇痛作用的假说,这种作用不同于其对肌肉的作用。尽管BTX的止痛效果主要归因于其阻断突触处乙酰胆碱释放的能力,但人们也认为它对神经系统的其他作用也参与其中。BTX会影响躯体和自主神经系统中的胆碱能传递。BTX用于缓解触发点疼痛、肌肉痉挛、纤维肌痛和肌筋膜疼痛的作用机制包括对肌肉的直接作用以及通过在神经肌肉接头处的作用产生的间接效应。体外和体内数据表明,BTX具有与炎症、轴突运输、神经节抑制以及脊髓和节段上水平抑制相关的特定抗伤害感受活性。我们对BTX在多种情况下治疗慢性疼痛的作用机制、疗效、给药技术和治疗剂量的综述表明,尽管肌张力和运动障碍仍然是BTX最重要的治疗应用,但研究表明,BTX还可因对血管系统的胆碱能控制、自主功能以及伤害感受和抗伤害感受系统的胆碱能控制产生影响而带来益处。此外,BTX似乎可能会影响外周和中枢神经系统。BTX的治疗潜力主要取决于将毒素输送到靶结构(胆碱能或其他结构)的能力。有证据表明,在以改变肌张力为目标的疼痛性疾病中,可按标准剂量给予BTX。对于需要镇痛效果的病症,BTX的最佳治疗剂量仍有待确定。