Arezzo Joseph C
Department of Neuroscience, Albert Einstein College of Medicine, Bronx, New York, 10461, USA.
Clin J Pain. 2002 Nov-Dec;18(6 Suppl):S125-32. doi: 10.1097/00002508-200211001-00003.
The therapeutic effects of botulinum toxin are principally, if not exclusively, derived from an alteration in the release of acetylcholine (ACh) at pre-synaptic neurons. The rationale for how these effects could be beneficial in conditions characterized by excessive muscle contraction is clear, but the hypotheses regarding botulinum toxin-induced effects on pain are highly speculative. We explore five possible mechanisms by which botulinum toxin could directly or indirectly alter pain, including: 1) changes in the sensitivity and response patterns of group III and IV muscle nociceptors, 2) diminished activity in the gamma-motor neurons and consequent changes in muscle spindle afferents, 3) alterations in cholinergic control of vascular and autonomic functions, including neurogenic inflammation, 4) induced neuroplastic changes in the processing of afferent somatosensory activity at multiple levels of the neuroaxis, and 5) direct non-cholinergic effects on pain afferents.
肉毒杆菌毒素的治疗效果主要(即便不是唯一)源自突触前神经元乙酰胆碱(ACh)释放的改变。这些效果在以肌肉过度收缩为特征的病症中如何有益是明确的,但关于肉毒杆菌毒素对疼痛影响的假说极具推测性。我们探究了肉毒杆菌毒素可直接或间接改变疼痛的五种可能机制,包括:1)III类和IV类肌肉伤害感受器的敏感性和反应模式的变化;2)γ运动神经元活性降低及随之而来的肌梭传入纤维的变化;3)血管和自主功能的胆碱能控制的改变,包括神经源性炎症;4)在神经轴的多个层面上,传入体感活动处理过程中诱导的神经可塑性变化;5)对疼痛传入纤维的直接非胆碱能作用。