阿片类药物治疗头痛:从板凳的角度看

Michael H. Ossipov Ph.D.
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引用次数: 4

摘要

我们很清楚,在治疗严重头痛时过度使用药物可能会导致头痛强度和频率的矛盾增加,同时头痛本身的主观质量也会发生变化。一个平行的发展发现,越来越多的观察到,发展的矛盾异常疼痛可能发生在反应长时间暴露于阿片类药物。在这两种情况下,尚未建立明确的机制。在过去二十年中,阿片类药物用于慢性、非恶性疼痛(包括复发性头痛综合征)的临床管理的增加,导致对这一现象的研究兴趣增加。最近的研究表明,长时间的阿片类药物暴露会导致几种神经可塑性改变,最终导致RVM和脊髓致敏引起的下行促进。这些变化与RVM中CCK活性的增加有关,这可能导致脊髓运动啡的表达增加,而脊髓运动啡本身促进传入输入的增加。下行疼痛促进系统的激活以及脊髓啡肽的增加促进了初级传入神经元的兴奋性神经递质的释放。与脊髓神经元PGE2释放增加一起,初级传入纤维的神经递质流出增加使投射神经元敏感,进而激活下行疼痛促进系统。最终,对阿片类药物可能的有害作用机制的了解可能会使开发新的化学方法来防止这些影响。重要的是,越来越多的证据表明,药物引起的增强疼痛并非阿片类药物所独有,而可能通过g蛋白偶联受体系统作用于其他镇痛类药物。了解这些机制将有助于改善长期疼痛状况的治疗管理,包括复发性头痛。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Opioids in the Treatment of Headache: Perspective from the Bench

It is well appreciated that excessive use of medication in the treatment of severe headaches may result in a paradoxical increase in intensity and frequency of the headaches, along with changes in the subjective qualities of the headaches themselves. A parallel development is found in the increasing appreciation for the observations that development of paradoxic abnormal pain can occur in response to prolonged exposure to opioids. In both of these situations, no clear mechanisms have yet been established. The increase in opioid use for clinical management of chronic, nonmalignant pain, including recurrent headache syndromes, over the past two decades has resulted in increased interest in the study of this phenomenon. Recent studies have indicated that prolonged opioid exposure results in several neuroplastic changes that ultimately lead to the establishment of descending facilitation arising from the RVM and in spinal sensitization. These changes have been associated with increased activity of CCK in the RVM that likely results in increased expression of spinal dynorphin, which itself promotes increased afferent inputs. Activation of a descending pain facilitatory system along with increased spinal dynorphin promote the release of excitatory neurotransmitters from primary afferent neurons. Together with increased release of PGE2 from spinal neurons, the increased outflow of neurotransmitters from the primary afferent fibers sensitizes projection neurons that in turn activate descending pain facilitatory systems. Ultimately, knowledge of the mechanisms of possible deleterious actions of opiates may allow the development of new chemical approaches that can prevent these effects. Importantly, evidence is emerging that medication-induced enhanced pain is not unique to opioids, but may be generalized to other analgesic classes acting through G-protein coupled receptor systems. An understanding of these mechanisms would lead to improved therapeutic management of long-term painful conditions, including recurrent headache.

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