Natural Immunosuppressants as a Treatment for Chronic Insomnia Targeting the Inflammatory Response Induced by NLRP3/caspase-1/IL-1β Axis Activation: A Scooping Review.

Zahra Aghelan, Somayeh Pashaee, Seyed Hosein Abtahi, Saeed Karima, Habibolah Khazaie, Mohammad Ezati, Reza Khodarahmi
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Abstract

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.

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天然免疫抑制剂治疗慢性失眠靶向NLRP3/胱天蛋白酶1/IL-1β轴激活诱导的炎症反应:综述。
慢性失眠是一种炎症性疾病,是各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,人们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界关注的焦点。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结构域(NOD)样受体pyrin含蛋白3(NLRP3)/胱天蛋白酶1/IL-1β轴,作为炎症级联反应的最重要激活剂之一。数据显示,有可能引起炎症的化合物会导致睡眠障碍,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逐渐被研究人员所考虑。NLRP3是一种细胞内传感器,可识别最广泛的病原体相关分子模式(PAMP)和危险相关分子模式。在鉴定并与损伤因子结合后,NLRP3炎症小体被组装以激活胱天蛋白酶-1和IL-1β。IL-1β的产生和分泌增加可能与中枢神经系统生理性睡眠失调有关。目前的独家综述报道了靶向NLRP3炎症小体途径活性的天然化合物的潜在益处,并强调了NLRP3/胱天蛋白酶1/IL-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设。
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