Bannister Kirsty, Kucharczyk Mateusz, Dickenson Anthony H
Department of Neuroscience, Physiology and Pharmacology, University College London, London, UK.
Pain Ther. 2017 Dec;6(2):117-128. doi: 10.1007/s40122-017-0073-6. Epub 2017 May 23.
Here we aim to present an accessible review of the pharmacological targets for pain management, and succinctly discuss the newest trends in pain therapy. A key task for current pain pharmacotherapy is the identification of receptors and channels orchestrating nociception. Notwithstanding peripheral alterations in the receptors and channels following pathophysiological events, the modulatory mechanisms in the central nervous system are also fundamental to the regulation of pain perception. Bridging preclinical and clinical studies of peripheral and central components of pain modulation, we present the different types of pain and relate these to pharmacological interventions. We firstly highlight the roles of several peripheral nociceptors, such as NGF, CGRP, sodium channels, and TRP-family channels that may become novel targets for therapies. In the central nervous system, the roles of calcium channels and gabapentinoids as well as NMDA receptors in generating excitability are covered including ideas on central sensitization. We then turn to central modulatory systems and discuss opioids and monoamines. We aim to explain the importance of central sensitization and the dialogue of the spinal circuits with the brain descending modulatory controls before discussing a mechanism-based effectiveness of antidepressants in pain therapy and their potential to modulate the descending controls. Emphasizing the roles of conditioned pain modulation and its animal's equivalent, diffuse noxious inhibitory controls, we discuss these unique descending modulations as a potential tool for understanding mechanisms in patients suffering from pain. Mechanism-based therapy is the key to picking the correct treatments and recent clinical studies using sensory symptoms of patients as surrogates for underlying mechanisms can be used to subgroup patients and reveal actions of drugs that may be lost when studying heterogenous groups of patients. Key advances in the understanding of basic pain principles will impact our thinking about therapy targets. The complexity of pain syndromes will require tailored pharmacological drugs, often in combination or through drugs with more than one action, and often psychotherapy, to fully control pain.
在此,我们旨在提供一篇关于疼痛管理药理学靶点的易懂综述,并简要讨论疼痛治疗的最新趋势。当前疼痛药物治疗的一项关键任务是识别参与伤害感受的受体和通道。尽管病理生理事件后受体和通道会发生外周改变,但中枢神经系统中的调节机制对于疼痛感知的调节也至关重要。通过衔接疼痛调制外周和中枢成分的临床前和临床研究,我们介绍了不同类型的疼痛,并将其与药物干预联系起来。我们首先强调几种外周伤害感受器的作用,如神经生长因子(NGF)、降钙素基因相关肽(CGRP)、钠通道和瞬时受体电位(TRP)家族通道,它们可能成为新的治疗靶点。在中枢神经系统中,涵盖了钙通道、加巴喷丁类药物以及N-甲基-D-天冬氨酸(NMDA)受体在产生兴奋性方面的作用,包括关于中枢敏化的观点。然后我们转向中枢调节系统,讨论阿片类药物和单胺类药物。在讨论抗抑郁药在疼痛治疗中的基于机制的有效性及其调节下行控制的潜力之前,我们旨在解释中枢敏化的重要性以及脊髓回路与大脑下行调节控制之间的相互作用。强调条件性疼痛调制及其在动物中的等效物——弥漫性有害抑制控制的作用,我们将这些独特的下行调制作为理解疼痛患者机制的潜在工具进行讨论。基于机制的治疗是选择正确治疗方法的关键,最近利用患者感觉症状作为潜在机制替代指标的临床研究可用于对患者进行亚组分析,并揭示在研究异质性患者群体时可能被忽视的药物作用。对基本疼痛原理理解的关键进展将影响我们对治疗靶点的思考。疼痛综合征的复杂性将需要定制的药物,通常是联合用药或使用具有多种作用的药物,并且常常需要心理治疗,以充分控制疼痛。