Center for Translational Pain Medicine, Department of Anesthesiology, Duke University School of Medicine, Durham, North Carolina; Department of Pharmacology and Cancer Biology, Duke University School of Medicine, Durham, North Carolina; EydisBio Inc., Department of Research and Development Durham, North Carolina.
Center for Translational Pain Medicine, Department of Anesthesiology, Duke University School of Medicine, Durham, North Carolina; Department of Anesthesiology, Nanjing Medical University Affiliated Wuxi People's Hospital, Wuxi, Jiangsu, China.
J Pain. 2023 Sep;24(9):1633-1644. doi: 10.1016/j.jpain.2023.04.011. Epub 2023 Apr 29.
The origin of chronic pain is linked to inflammation, characterized by increased levels of proinflammatory cytokines in local tissues and systemic circulation. Transforming growth factor beta-activated kinase 1 (TAK1) is a key regulator of proinflammatory cytokine signaling that has been well characterized in the context of cancer and autoimmune disorders, yet its role in chronic pain is less clear. Here, we evaluated the ability of our TAK1 small-molecule inhibitor, takinib, to attenuate pain and inflammation in preclinical models of inflammatory, neuropathic, and primary pain. Inflammatory, neuropathic, and primary pain was modeled using intraplantar complete Freund's adjuvant (CFA), chronic constriction injury (CCI), and systemic delivery of the catechol-O-methyltransferase (COMT) inhibitor OR486, respectively. Behavioral responses evoked by mechanical and thermal stimuli were evaluated in separate groups of mice receiving takinib or vehicle prior to pain induction (baseline) and over 12 days following CFA injection, 4 weeks following CCI surgery, and 6 hours following OR486 delivery. Hindpaw edema was also measured prior to and 3 days following CFA injection. Upon termination of behavioral experiments, dorsal root ganglia (DRG) were collected to measure cytokines. We also evaluated the ability of takinib to modulate nociceptor activity via in vitro calcium imaging of neurons isolated from the DRG of Gcamp3 mice. In all 3 models, TAK1 inhibition significantly reduced hypersensitivity to mechanical and thermal stimuli and expression of proinflammatory cytokines in DRG. Furthermore, TAK1 inhibition significantly reduced the activity of tumor necrosis factor (TNF)-primed/capsaicin-evoked DRG nociceptive neurons. Overall, our results support the therapeutic potential of TAK1 as a novel drug target for the treatment of chronic pain syndromes with different etiologies. PERSPECTIVE: This article reports the therapeutic potential of TAK1 inhibitors for the treatment of chronic pain. This new treatment has the potential to provide a greater therapeutic offering to physicians and patients suffering from chronic pain as well as reduce the dependency on opioid-based pain treatments.
慢性疼痛的起源与炎症有关,其特征是局部组织和全身循环中促炎细胞因子水平升高。转化生长因子β激活激酶 1(TAK1)是促炎细胞因子信号的关键调节剂,在癌症和自身免疫性疾病的背景下已得到很好的描述,但在慢性疼痛中的作用尚不清楚。在这里,我们评估了我们的 TAK1 小分子抑制剂 takinib 减弱炎症、神经病理性和原发性疼痛的临床前模型中疼痛和炎症的能力。使用足底内完全弗氏佐剂(CFA)、慢性缩窄性损伤(CCI)和系统给予儿茶酚-O-甲基转移酶(COMT)抑制剂 OR486 分别模拟炎症、神经病理性和原发性疼痛。在 CFA 注射前(基线)和 CFA 注射后 12 天、CCI 手术后 4 周和 OR486 给药后 6 小时,分别在接受 takinib 或载体的单独组小鼠中评估机械和热刺激引起的行为反应。在 CFA 注射前和 3 天后还测量了后爪水肿。在行为实验结束时,收集背根神经节(DRG)以测量细胞因子。我们还通过对来自 Gcamp3 小鼠 DRG 的神经元进行体外钙成像来评估 takinib 调节伤害感受器活性的能力。在所有 3 种模型中,TAK1 抑制均显著减轻机械和热刺激的敏感性以及 DRG 中促炎细胞因子的表达。此外,TAK1 抑制显著降低了肿瘤坏死因子(TNF)引发/辣椒素诱发的 DRG 伤害感受神经元的活性。总体而言,我们的结果支持 TAK1 作为一种新型药物靶点治疗具有不同病因的慢性疼痛综合征的治疗潜力。观点:本文报道了 TAK1 抑制剂治疗慢性疼痛的治疗潜力。这种新的治疗方法有可能为患有慢性疼痛的医生和患者提供更大的治疗选择,并减少对阿片类药物为基础的疼痛治疗的依赖。