Gong Wei-Yi, Abdelhamid Ramy E, Carvalho Carolina S, Sluka Kathleen A
Department of Pain Management, Xuanwu Hospital, Capital Medical University, Beijing, China; Department of Physical Therapy and Rehabilitation Science, University of Iowa, Carver College of Medicine, Iowa City, Iowa.
Department of Physical Therapy and Rehabilitation Science, University of Iowa, Carver College of Medicine, Iowa City, Iowa.
J Pain. 2016 Oct;17(10):1081-1094. doi: 10.1016/j.jpain.2016.06.010. Epub 2016 Jul 1.
Macrophages play a role in innate immunity within the body, are located in muscle tissue, and can release inflammatory cytokines that sensitize local nociceptors. In this study we investigate the role of resident macrophages in the noninflammatory muscle pain model induced by 2 pH 4.0 preservative-free sterile saline (pH 4.0) injections 5 days apart in the gastrocnemius muscle. We showed that injecting 2 pH 4.0 injections into the gastrocnemius muscle increased the number of local muscle macrophages, and depleting muscle macrophages with clodronate liposomes before acid injections attenuated the hyperalgesia produced by this model. To further examine the contribution of local macrophages to this hyperalgesia, we injected mice intramuscularly with C34, a toll-like receptor 4 (TLR4) antagonist. When given before the first pH 4.0 injection, C34 attenuated the muscle and tactile hyperalgesia produced by the model. However, when given before the second injection C34 had no effect on the development of hyperalgesia. Then to test whether activation of local macrophages sensitizes nociceptors to normally non-nociceptive stimuli we replaced either the first or second acid injection with the immune cell activator lipopolysaccharide, or the inflammatory cytokine interleukin (IL)-6. Injecting LPS or IL-6 instead of the either the first or second pH 4.0 injection resulted in a dose-dependent increase in paw withdrawal responses and decrease in muscle withdrawal thresholds. The highest doses of LPS and IL-6 resulted in development of hyperalgesia bilaterally. The present study showed that resident macrophages in muscle are key to development of chronic muscle pain.
This article presents evidence for the role of macrophages in the development of chronic muscle pain using a mouse model. These data suggest that macrophages could be a potential therapeutic target to prevent transition of acute to chronic muscle pain particularly in tissue acidosis conditions.
巨噬细胞在体内固有免疫中发挥作用,存在于肌肉组织中,并可释放使局部伤害感受器敏感的炎性细胞因子。在本研究中,我们探究了驻留巨噬细胞在腓肠肌每隔5天注射2次pH 4.0无防腐剂无菌生理盐水(pH 4.0)所诱导的非炎性肌肉疼痛模型中的作用。我们发现,向腓肠肌注射2次pH 4.0会增加局部肌肉巨噬细胞的数量,并且在酸注射前用氯膦酸脂质体清除肌肉巨噬细胞可减轻该模型产生的痛觉过敏。为了进一步研究局部巨噬细胞对这种痛觉过敏的作用,我们给小鼠肌肉注射C34(一种Toll样受体4(TLR4)拮抗剂)。在第一次pH 4.0注射前给予C34可减轻该模型产生的肌肉和触觉痛觉过敏。然而,在第二次注射前给予C34对痛觉过敏的发展没有影响。然后,为了测试局部巨噬细胞的激活是否会使伤害感受器对正常的非伤害性刺激敏感,我们用免疫细胞激活剂脂多糖或炎性细胞因子白细胞介素(IL)-6替代第一次或第二次酸注射。注射脂多糖或IL-6而非第一次或第二次pH 4.0注射导致爪部退缩反应呈剂量依赖性增加,肌肉退缩阈值降低。脂多糖和IL-6的最高剂量导致双侧痛觉过敏的发生。本研究表明,肌肉中的驻留巨噬细胞是慢性肌肉疼痛发展的关键。
本文使用小鼠模型提供了巨噬细胞在慢性肌肉疼痛发展中作用的证据。这些数据表明,巨噬细胞可能是预防急性肌肉疼痛转变为慢性肌肉疼痛的潜在治疗靶点,尤其是在组织酸中毒的情况下。