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以背根神经节和初级感觉神经元为靶点治疗慢性疼痛。

Targeting dorsal root ganglia and primary sensory neurons for the treatment of chronic pain.

作者信息

Berta Temugin, Qadri Yawar, Tan Ping-Heng, Ji Ru-Rong

机构信息

a Pain Research Center, Department of Anesthesiology , University of Cincinnati Medical Center , Cincinnati , OH , USA.

b Department of Anesthesiology , Duke University Medical Center , Durham , NC , USA.

出版信息

Expert Opin Ther Targets. 2017 Jul;21(7):695-703. doi: 10.1080/14728222.2017.1328057. Epub 2017 May 16.

Abstract

Currently the treatment of chronic pain is inadequate and compromised by debilitating central nervous system side effects. Here we discuss new therapeutic strategies that target dorsal root ganglia (DRGs) in the peripheral nervous system for a better and safer treatment of chronic pain. Areas covered: The DRGs contain the cell bodies of primary sensory neurons including nociceptive neurons. After painful injuries, primary sensory neurons demonstrate maladaptive molecular changes in DRG cell bodies and in their axons. These changes result in hypersensitivity and hyperexcitability of sensory neurons (peripheral sensitization) and are crucial for the onset and maintenance of chronic pain. We discuss the following new strategies to target DRGs and primary sensory neurons as a means of alleviating chronic pain and minimizing side effects: inhibition of sensory neuron-expressing ion channels such as TRPA1, TRPV1, and Nav1.7, selective blockade of C- and Aβ-afferent fibers, gene therapy, and implantation of bone marrow stem cells. Expert opinion: These peripheral pharmacological treatments, as well as gene and cell therapies, aimed at DRG tissues and primary sensory neurons can offer better and safer treatments for inflammatory, neuropathic, cancer, and other chronic pain states.

摘要

目前,慢性疼痛的治疗并不充分,且受到中枢神经系统副作用的影响而大打折扣。在此,我们讨论针对外周神经系统背根神经节(DRG)的新治疗策略,以期更有效、更安全地治疗慢性疼痛。涵盖领域:DRG包含初级感觉神经元(包括伤害性神经元)的细胞体。疼痛性损伤后,初级感觉神经元在DRG细胞体及其轴突中表现出适应性不良的分子变化。这些变化导致感觉神经元超敏和兴奋性过高(外周敏化),对慢性疼痛的发生和维持至关重要。我们讨论以下针对DRG和初级感觉神经元的新策略,作为减轻慢性疼痛并将副作用降至最低的手段:抑制表达感觉神经元的离子通道,如TRPA1、TRPV1和Nav1.7;选择性阻断C和Aβ传入纤维;基因治疗;以及植入骨髓干细胞。专家观点:这些针对DRG组织和初级感觉神经元的外周药物治疗以及基因和细胞疗法,可为炎症性、神经性、癌性和其他慢性疼痛状态提供更好、更安全的治疗方法。

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