From the Department of Anesthesiology, Perioperative, and Pain Medicine, Stanford University School of Medicine, Stanford, California.
University of Colorado School of Medicine, Denver, Colorado.
Anesth Analg. 2019 Apr;128(4):737-746. doi: 10.1213/ANE.0000000000004033.
With a widespread opioid epidemic and profound biopsychosocial implications, chronic pain is a multifaceted public health issue requiring urgent attention. The treatment of chronic pain is particularly important to anesthesiologists given our unique role as perioperative physicians and pain medicine specialists. The present review details the recent shift from a neuronal theory of chronic pain to one that includes complex neuron-glia interactions. In particular, we highlight microglia, the myeloid-lineage cells of the central nervous system, as initiators of a postinjury neuroimmune response that contributes to the acute to chronic pain transition. We discuss ever-advancing preclinical studies, wherein significant success has been made through pharmacologic and genetic modulation of microglia, and we emphasize where these approaches have made the transition to the clinical realm. Furthermore, we highlight the most current, novel efforts to visualize glial activation in vivo using positron emission tomography and improve the diagnosis of chronic pain through radiotracer binding of specific targets, like the 18 kDa translocator protein in microglia and myeloid-lineage cells. Our rapidly advancing knowledge about microglia and their involvement in pain suggests that the era of glial-targeted therapeutics is just beginning so long as we refocus our attention on optimizing preclinical studies using a clinically informed approach, before translation.
慢性疼痛是一个多方面的公共卫生问题,具有广泛的阿片类药物流行和深远的生物心理社会影响,需要紧急关注。鉴于我们作为围手术期医生和疼痛医学专家的独特角色,慢性疼痛的治疗对麻醉师尤为重要。本综述详细介绍了从慢性疼痛的神经元理论向包括复杂的神经元-胶质相互作用理论的转变。特别是,我们强调小胶质细胞,即中枢神经系统的髓系细胞,作为损伤后神经免疫反应的启动者,导致急性到慢性疼痛的转变。我们讨论了不断发展的临床前研究,其中通过小胶质细胞的药理学和遗传学调节取得了重大成功,并强调了这些方法在向临床领域过渡的情况。此外,我们还强调了使用正电子发射断层扫描术(PET)在体内可视化胶质细胞激活的最新、新颖的努力,并通过放射性示踪剂与特定靶点(如小胶质细胞和髓系细胞中的 18 kDa 转位蛋白)的结合来改善慢性疼痛的诊断。我们对小胶质细胞及其在疼痛中的作用的快速发展的认识表明,只要我们重新关注使用基于临床的方法优化临床前研究,在转化之前,靶向神经胶质的治疗时代才刚刚开始。