Schmidt Brian L
Department of Oral Maxillofacial Surgery, New York University College of Dentistry, New York, NY, USA Department of Neuroscience & Physiology, New York University School of Medicine, New York, NY, USA Bluestone Center for Clinical Research, New York University, NY, USA
Neuroscientist. 2014 Oct;20(5):546-62. doi: 10.1177/1073858414525828. Epub 2014 Mar 24.
The global burden of cancer pain is enormous and opioids, despite their side effects, remain the primary therapeutic approach. The cause of cancer pain is unknown. Mechanisms driving cancer pain differ from those mechanisms responsible for inflammatory and neuropathic pain. The prevailing hypothesis put forward to explain cancer pain posits that cancers generate and secrete mediators which sensitize and activate primary afferent nociceptors in the cancer microenvironment. Moreover, cancers induce neurochemical reorganization of the spinal cord, which contributes to spontaneous activity and enhanced responsiveness. The purpose of this review, which covers clinical and preclinical studies, is to highlight those peripheral and central mechanisms responsible for cancer pain. The challenges facing neuroscientists and clinicians studying and ultimately treating cancer pain are discussed.
癌症疼痛的全球负担巨大,尽管存在副作用,但阿片类药物仍然是主要的治疗方法。癌症疼痛的病因尚不清楚。导致癌症疼痛的机制与引起炎症性疼痛和神经性疼痛的机制不同。为解释癌症疼痛而提出的主流假说是,癌症产生并分泌介质,这些介质使癌症微环境中的初级传入伤害感受器敏感化并激活它们。此外,癌症会诱导脊髓的神经化学重组,这会导致自发活动并增强反应性。这篇涵盖临床和临床前研究的综述的目的是突出那些导致癌症疼痛的外周和中枢机制。文中还讨论了研究并最终治疗癌症疼痛的神经科学家和临床医生所面临的挑战。