Rehabilitation Medicine, Department of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden ; Pain and Rehabilitation Centre, County Council of Östergötland, Linköping, Sweden.
Rehabilitation Medicine, Department of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden ; Rehabilitation Medicine, Department of Medicine and Health Sciences, Linköping University, Linköping, Sweden.
J Pain Res. 2014 Jun 12;7:313-26. doi: 10.2147/JPR.S59144. eCollection 2014.
Chronic musculoskeletal pain conditions are multifaceted, and approximately 20% of the adult population lives with severe chronic pain, with a higher prevalence in women and in lower income groups. Chronic pain is influenced by and interacts with physical, emotional, psychological, and social factors, and a biopsychosocial framework is increasingly applied in clinical practice. However, there is still a lack of assessment procedures based on the activated neurobiological pain mechanisms (ie, the biological part of the biopsychosocial model of pain), which may be a necessary step for further optimizing outcomes after treatments for patients with chronic pain. It has been suggested that chronic pain conditions are mainly driven by alterations in the central nervous system with little or no peripheral stimuli or nociception. In contrast, other authors argue that such central alterations are driven by peripheral alterations and nociceptive input. Microdialysis is an in vivo method for studying local tissue alterations and allows for sampling of substances in the interstitium of the muscle, where nociceptor free nerve endings are found close to the muscle fibers. The extracellular matrix plays a key role in physiologic functions of cells, including the primary afferent nociceptor. The present review mainly concerns the results of microdialysis studies and how they can contribute to the understanding of activated peripheral nociceptive and pain mechanisms in humans with chronic pain. The primary aim was to review molecular studies using microdialysis for the investigation of human chronic muscle pain, ie, chronic masticatory muscle pain, chronic trapezius myalgia, chronic whiplash-associated disorders, and chronic widespread pain/fibromyalgia syndrome. Several studies clearly showed elevated levels of serotonin, glutamate, lactate, and pyruvate in localized chronic myalgias and may be potential biomarkers. These results indicate that peripheral muscle alterations are parts of the activated pain mechanisms in common chronic pain conditions. Muscle alterations have been reported in fibromyalgia syndrome and chronic widespread pain, but more studies are needed before definite conclusions can be drawn. For other substances, results are inconclusive across studies and patient groups.
慢性肌肉骨骼疼痛状况具有多面性,大约 20%的成年人口患有严重的慢性疼痛,女性和低收入群体的患病率更高。慢性疼痛受身体、情感、心理和社会因素的影响并与之相互作用,生物心理社会框架越来越多地应用于临床实践。然而,仍然缺乏基于激活的神经生物学疼痛机制(即疼痛的生物心理社会模型的生物学部分)的评估程序,这可能是进一步优化慢性疼痛患者治疗后结果的必要步骤。有人认为,慢性疼痛状况主要是由中枢神经系统的改变驱动的,而外周刺激或伤害感受很少或没有。相比之下,其他作者则认为,这种中枢改变是由外周改变和伤害感受输入驱动的。微透析是一种用于研究局部组织改变的体内方法,允许对肌肉间质中的物质进行采样,其中无伤害感受器的游离神经末梢靠近肌肉纤维。细胞外基质在细胞的生理功能中起着关键作用,包括初级传入伤害感受器。本综述主要涉及微透析研究的结果,以及它们如何有助于理解慢性疼痛患者中激活的外周伤害感受和疼痛机制。主要目的是综述使用微透析研究人类慢性肌肉疼痛的分子研究,即慢性咀嚼肌疼痛、慢性斜方肌肌痛、慢性挥鞭样损伤相关疾病和慢性广泛性疼痛/纤维肌痛综合征。几项研究清楚地表明,在局部慢性肌痛中,血清素、谷氨酸、乳酸和丙酮酸的水平升高,可能是潜在的生物标志物。这些结果表明,外周肌肉改变是常见慢性疼痛状况中激活的疼痛机制的一部分。纤维肌痛综合征和慢性广泛性疼痛中已经报道了肌肉改变,但在得出明确结论之前,还需要更多的研究。对于其他物质,不同的研究和患者群体的结果不一致。