Aghelan Zahra, Pashaee Somayeh, Abtahi Seyed Hosein, Karima Saeed, Khazaie Habibolah, Ezati Mohammad, Khodarahmi Reza
Department of Clinical Biochemistry, Faculty of Medicine, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Department of Laboratory Hematology and Blood Banking, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.
J Neuroimmune Pharmacol. 2023 Sep;18(3):294-309. doi: 10.1007/s11481-023-10078-7. Epub 2023 Aug 8.
Chronic insomnia is an inflammatory-related disease with an important pathological basis for various diseases which is a serious threat to a person's physical and mental health. So far, many hypotheses have been proposed to explain the pathogenesis of insomnia, among which inflammatory mechanisms have become the focus of scientific attention. In this regard, the aim of the present scooping review is to evaluate the potential benefits of natural compounds in treatment of chronic insomnia targeting nucleotide-binding oligomerization domain (NOD)-like receptor-pyrin-containing protein 3 (NLRP3)/caspase-1/IL-1β axis as one of the most important activators of inflammatory cascades. The data show that compounds that have the potential to cause inflammation induce sleep disorders, and that inflammatory mediators are key molecules in regulating the sleep-related activity of neurons. In the inflammatory process of insomnia, the role of NLRP3 in the pathogenesis of insomnia has been gradually considered by researchers. NLRP3 is an intracellular sensor that recognizes the widest range of pathogen-associated molecular patterns (PAMPs) and danger-associated molecular patterns (DAMPs). After identification and binding to damage factors, NLRP3 inflammasome is assembled to activate the caspase-1 and IL-1β. Increased production and secretion of IL-1β may be involved in central nervous system dysregulation of physiological sleep. The current scooping review reports the potential benefits of natural compounds that target NLRP3 inflammasome pathway activity and highlights the hypothesis which NLRP3 /caspase-1/IL-1β may serve as a potential therapeutic target for managing inflammation and improving symptoms in chronic insomnia.
慢性失眠是一种与炎症相关的疾病,是多种疾病的重要病理基础,严重威胁着人的身心健康。到目前为止,已经提出了许多假说来解释失眠的发病机制,其中炎症机制已成为科学关注的焦点。在这方面,本综述的目的是评估天然化合物在治疗慢性失眠中的潜在益处,其靶向核苷酸结合寡聚化结构域(NOD)样受体含吡啉蛋白3(NLRP3)/半胱天冬酶-1/白细胞介素-1β轴,这是炎症级联反应最重要的激活剂之一。数据表明,有可能引发炎症的化合物会导致睡眠障碍,并且炎症介质是调节神经元睡眠相关活动的关键分子。在失眠的炎症过程中,NLRP3在失眠发病机制中的作用已逐渐被研究人员所重视。NLRP3是一种细胞内传感器,可识别范围最广的病原体相关分子模式(PAMP)和危险相关分子模式(DAMP)。在识别并结合损伤因子后,NLRP3炎性小体组装以激活半胱天冬酶-1和白细胞介素-1β。白细胞介素-1β产生和分泌的增加可能参与了生理性睡眠的中枢神经系统失调。当前的综述报道了靶向NLRP3炎性小体途径活性的天然化合物的潜在益处,并强调了NLRP3/半胱天冬酶-1/白细胞介素-1β可能作为治疗慢性失眠炎症和改善症状的潜在治疗靶点的假说。