From the Departments of Anesthesiology, Perioperative Care and Pain Medicine (Urien, Wang) and Neuroscience and Physiology (Wang), New York University School of Medicine, New York, New York.
Psychosom Med. 2019 Nov/Dec;81(9):851-858. doi: 10.1097/PSY.0000000000000744.
Acute pain has an evolutionary role in the detection of physical harm and the response to it. In some cases, however, acute pain can impair function and lead to other morbidities. Chronic pain, meanwhile, can present as a psychopathological condition that significantly interferes with daily living. Most basic and translational pain research has focused on the molecular and cellular mechanisms in the spinal and peripheral nervous systems. In contrast, the brain plays a key role in the affective manifestation and cognitive control of pain. In particular, several cortical regions, such as the somatosensory cortex, prefrontal cortex, insular, and anterior cingulate cortex, are well known to be activated by acute pain signals, and neurons in these regions have been demonstrated to undergo changes in response to chronic pain. Furthermore, these cortical regions can project to a number of forebrain and limbic structures to exert powerful top-down control of not only sensory pain transmission but also affective pain expression, and such cortical regulatory mechanisms are particularly relevant in chronic pain states. Newer techniques have emerged that allow for detailed studies of central pain circuits in animal models, as well as how such circuits are modified by the presence of chronic pain and other predisposing psychosomatic factors. These mechanistic approaches can complement imaging in human studies. At the therapeutic level, a number of pharmacological and nonpharmacological interventions have recently been shown to engage these top-down control systems to provide analgesia. In this review, we will discuss how pain signals reach important cortical regions and how these regions in turn project to subcortical areas of the brain to exert profound modulation of the pain experience. In addition, we will discuss the clinical relevance of such top-down pain regulation mechanisms.
急性疼痛在检测身体伤害和对伤害的反应方面具有进化作用。然而,在某些情况下,急性疼痛会损害功能并导致其他病态。与此同时,慢性疼痛可能表现为一种明显干扰日常生活的心理病理状况。大多数基础和转化疼痛研究都集中在脊髓和周围神经系统的分子和细胞机制上。相比之下,大脑在疼痛的情感表现和认知控制中起着关键作用。特别是,几个皮质区域,如躯体感觉皮质、前额叶皮质、岛叶和前扣带皮质,已知会被急性疼痛信号激活,并且这些区域的神经元已经被证明会对慢性疼痛产生变化。此外,这些皮质区域可以投射到许多前脑和边缘结构,对不仅是感觉疼痛传递,而且对情感疼痛表达施加强大的自上而下的控制,这种皮质调节机制在慢性疼痛状态下尤其相关。新技术的出现使得能够在动物模型中对中央疼痛回路进行详细研究,以及这些回路如何被慢性疼痛和其他潜在的身心因素所改变。这些机制方法可以补充人类研究中的成像。在治疗水平上,最近已经有一些药物和非药物干预措施被证明可以利用这些自上而下的控制系统来提供镇痛。在这篇综述中,我们将讨论疼痛信号如何到达重要的皮质区域,以及这些区域如何反过来投射到大脑的皮质下区域,从而对疼痛体验进行深刻的调节。此外,我们还将讨论这种自上而下的疼痛调节机制的临床相关性。