Laboratory of Neuroimmunology and Developmental Origins of Disease, University Medical Center Utrecht, Utrecht, The Netherlands.
Brain Behav Immun. 2011 Aug;25(6):1055-60. doi: 10.1016/j.bbi.2011.03.019. Epub 2011 Apr 5.
Pain is a hallmark of tissue damage and inflammation promoting tissue protection and thereby contributing to repair. Therefore, transient acute pain is an important feature of the adaptive response to damage. However, in a significant number of cases, pain persists for months to years after the problem that originally caused the pain has resolved. Such chronic pain is maladaptive as it no longer serves a protective aim. Chronic pain is debilitating, both physiologically and psychologically, and treatments to provide relief from chronic pain are often ineffective. The neurobiological mechanisms underlying the transition from adaptive acute pain to maladaptive chronic pain are only partially understood. In this review, we will summarize recent evidence that a kinase known as G protein-coupled receptor kinase (GRK2) is a key regulator of the transition from acute to chronic inflammatory pain. Our recent studies have shown that mice with a reduction in the cellular level of GRK2 develop chronic hyperalgesia in response to inflammatory mediators that induce only transient hyperalgesia in WT mice. This finding is clinically relevant because rodent models of chronic pain are associated with reduced cellular levels of GRK2. We propose that GRK2 is a newly discovered major player in the regulation of chronic pain. The pathways regulated by this kinase may open up new avenues for development of treatment strategies that target the cause, and not the symptoms of chronic pain.
疼痛是组织损伤和炎症的标志,促进组织保护,从而有助于修复。因此,短暂的急性疼痛是对损伤适应性反应的一个重要特征。然而,在相当多的情况下,在最初引起疼痛的问题解决后,疼痛会持续数月甚至数年。这种慢性疼痛是适应不良的,因为它不再起到保护作用。慢性疼痛在生理和心理上都使人衰弱,而缓解慢性疼痛的治疗方法往往效果不佳。从适应性急性疼痛到适应性慢性疼痛的转变的神经生物学机制仅部分被理解。在这篇综述中,我们将总结最近的证据,即一种被称为 G 蛋白偶联受体激酶(GRK2)的激酶是从急性到慢性炎症性疼痛转变的关键调节因子。我们最近的研究表明,细胞内 GRK2 水平降低的小鼠对仅在 WT 小鼠中引起短暂痛觉过敏的炎症介质会产生慢性痛觉过敏。这一发现具有临床相关性,因为慢性疼痛的啮齿动物模型与细胞内 GRK2 水平降低有关。我们提出,GRK2 是调节慢性疼痛的一个新发现的主要参与者。该激酶调节的途径可能为开发针对慢性疼痛的病因而非症状的治疗策略开辟新途径。