Department of Neuroscience and Cell Biology, University of Texas Medical Branch, Galveston, TX 77555-1069, USA Department of Anesthesiology, Columbia University, New York, NY, USA.
Pain. 2013 Nov;154(11):2297-2309. doi: 10.1016/j.pain.2013.05.033. Epub 2013 May 24.
Patients receiving opioids for pain may experience decreased effectiveness of the drug and even abnormal pain sensitivity-hyperalgesia and/or allodynia. We hypothesized that peripheral nociceptor hyperexcitability contributes to opioid-induced hyperalgesia and tested this using an in vitro mouse glabrous skin-nerve preparation. Mice were injected intraperitoneally with escalating doses of morphine (5, 8, 10, 15 mg/kg) or saline every 12 hours for 48 hours and killed approximately 12 hours after the last injection. Receptive fields of nociceptors were tested for mechanical, heat, and cold sensitivity. Activity was also measured during an initial 2-minute period and during 5-minute periods between stimuli. Aberrant activity was common in fibers from morphine-treated mice but rare in saline-treated mice. Resting background activity was elevated in C-fibers from morphine-treated mice. Both C- and Aδ-fibers had afterdischarge in response to mechanical, heat, and/or cold stimulation of the skin as well as spontaneous, unevoked activity. Compared to saline, morphine treatment increased the proportion of fibers displaying polymodal rather than mechanical-only responses. A significant increase in Aδ-mechanoreceptive fibers responding to cold accounted for most of this change. In agreement with this, morphine-treated mice showed increased sensitivity in the cold tail flick test. In morphine-treated mice, aberrant activity and hyperexcitability of nociceptors could contribute to increased pain sensitivity. Importantly, this activity is likely driving central sensitization, a phenomenon contributing to abnormal sensory processing and chronic pain. If similar changes occur in human patients, aberrant nociceptor activity is likely to be interpreted as pain and could contribute to opioid-induced hyperalgesia.
接受阿片类药物治疗疼痛的患者可能会经历药物疗效降低,甚至出现异常疼痛敏感性——痛觉过敏和/或感觉异常。我们假设外周伤害感受器的过度兴奋有助于阿片类药物引起的痛觉过敏,并使用体外小鼠无毛皮肤-神经制备物对此进行了测试。小鼠每隔 12 小时腹膜内注射递增剂量的吗啡(5、8、10、15mg/kg)或生理盐水,共 48 小时,最后一次注射后约 12 小时处死。测试伤害感受器的机械、热和冷敏感性的感受野。在初始的 2 分钟期间和刺激之间的 5 分钟期间还测量了活性。在接受吗啡治疗的小鼠中,异常活动在纤维中很常见,但在接受生理盐水治疗的小鼠中很少见。来自吗啡处理小鼠的 C 纤维的静息背景活动升高。C 和 Aδ纤维在机械、热和/或皮肤冷刺激以及自发、无诱发活动时都会产生后放电。与生理盐水相比,吗啡处理增加了显示多模态而非仅机械反应的纤维的比例。对冷刺激有反应的 Aδ机械感觉纤维的比例显著增加,这在很大程度上解释了这种变化。与这一结果一致,接受吗啡治疗的小鼠在冷尾缩试验中表现出更高的敏感性。在接受吗啡治疗的小鼠中,伤害感受器的异常活动和过度兴奋可能导致疼痛敏感性增加。重要的是,这种活动很可能导致中枢敏化,这是一种导致异常感觉处理和慢性疼痛的现象。如果在人类患者中发生类似的变化,异常伤害感受器活动很可能被解释为疼痛,并可能导致阿片类药物引起的痛觉过敏。