Griffett Kristine
College of Veterinary Medicine, Department of Anatomy, Physiology & Pharmacology, Auburn University, Auburn, Alabama 36849, United States.
ACS Pharmacol Transl Sci. 2022 May 19;5(6):440-444. doi: 10.1021/acsptsci.2c00063. eCollection 2022 Jun 10.
Pain is the unpleasant consequence of detrimental neuronal activity that can be triggered by chronic inflammation, noxious stimuli, and nerve damage. In the case of chronic inflammatory pain, the establishment and maintenance of pain states often depend on the chronic activation and immune response occurring at the site of the peripheral nerve injury. Many current analgesic drugs lack efficacy in long-term pain management. Targeting the nuclear receptor family of transcription factors may provide a novel avenue for the treatment of chronic inflammatory pain. Peroxisome proliferator-activated receptor (PPAR) ligands have demonstrated efficacy in several diabetic-related neuropathic pain models, while the REV-ERB receptors play a key role in the regulation of both P2X7 receptor expression and NLRP3 inflammasome expression and activation. As such, activating the REV-ERB receptor may provide an anti-inflammatory and analgesic option for chronic inflammatory pain sufferers.
疼痛是有害神经元活动的不良后果,可由慢性炎症、有害刺激和神经损伤引发。在慢性炎症性疼痛的情况下,疼痛状态的建立和维持通常取决于外周神经损伤部位发生的慢性激活和免疫反应。许多目前的镇痛药在长期疼痛管理中缺乏疗效。靶向转录因子的核受体家族可能为慢性炎症性疼痛的治疗提供一条新途径。过氧化物酶体增殖物激活受体(PPAR)配体在几种糖尿病相关的神经性疼痛模型中已显示出疗效,而REV-ERB受体在P2X7受体表达以及NLRP3炎性小体的表达和激活的调节中起关键作用。因此,激活REV-ERB受体可能为慢性炎症性疼痛患者提供一种抗炎和镇痛的选择。