Division of Neurobiology 2, Centre de Recherche Pierre Fabre, 17, avenue Jean Moulin, 81106 Castres, France.
Behav Brain Res. 2009 Dec 28;205(2):360-6. doi: 10.1016/j.bbr.2009.07.005. Epub 2009 Jul 16.
Whereas acute stress often results in analgesia, chronic stress can trigger hyperalgesia/allodynia. This influence of long-term stress on nociception is relevant to numerous painful pathologies, such as fibromyalgia (FM), characterized by diffuse muscular pain (hyperalgesia) and/or tenderness (allodynia). Hence, there is a need for pre-clinical models integrating a chronic-stress dimension to the study of pain. Here, we assessed the effects of protracted/intermittent stress produced by daily, 1h restraint periods in cylinders, 4 days/week over 5 weeks, on eight models of hyperalgesia and allodynia in rats. This type of stress potentiated chemical hyperalgesia in the formalin model (160 and 76% increase of pain score above controls, during the early and late phases, respectively). It also produced thermal allodynia in response to cold (paw acetone test: 200% increase of allodynia score during week 3-5) and heat (42 degrees C tail immersion test: 15% decrease of withdrawal threshold, from week 2 onward). This stress also resulted in mechanical allodynia in the von Frey filaments model (60% decrease in threshold during week 2-5). However, such a stress regimen had no influence in the Randall-Selitto test of mechanical hyperalgesia, and in the tail immersion models of cold (4 degrees C) or hot (48 degrees C) thermal hyperalgesia, as well as cold (15 degrees C) allodynia. This model of prolonged/intermittent restraint stress may be useful in investigating the mechanisms linking stress and pain, and provide an assay to assess the potential therapeutic efficacy of drugs targeted against painful pathologies with a strong stress component, including but not restricted to FM.
急性应激通常会导致镇痛,而慢性应激则会引发痛觉过敏/感觉异常。这种长期应激对伤害感受的影响与许多疼痛性病理有关,如纤维肌痛(FM),其特征为弥漫性肌肉疼痛(痛觉过敏)和/或压痛(感觉异常)。因此,需要将慢性应激维度纳入疼痛研究的临床前模型中。在这里,我们评估了每天 1 小时的圆柱体限制期,每周 4 天,持续 5 周的慢性/间歇性应激对大鼠 8 种痛觉过敏和感觉异常模型的影响。这种类型的应激会增强福尔马林模型中的化学痛觉过敏(疼痛评分分别在早期和晚期比对照组增加 160%和 76%)。它还会导致冷(爪子丙酮测试)和热(42 度尾巴浸入测试)引起的感觉异常,在第 3-5 周期间感觉异常评分增加 200%和 15%。这种应激还会导致 von Frey 细丝模型中的机械感觉异常(在第 2-5 周期间阈值降低 60%)。然而,这种应激方案对 Randall-Selitto 机械痛觉过敏测试、冷(4 度)或热(48 度)热痛觉过敏模型以及冷(15 度)感觉异常没有影响。这种长期/间歇性束缚应激模型可能有助于研究应激和疼痛之间的联系机制,并提供一种评估针对具有强烈应激成分的疼痛性病理的药物潜在治疗效果的方法,包括但不限于 FM。