School of Clinical Medicine, Shandong First Medical University & Shandong Academy of Medical Sciences, Jinan, Shandong Province, China.
Hospital of Shandong First Medical University, Jinan, Shandong Province, China.
Am J Drug Alcohol Abuse. 2024 Mar 3;50(2):139-149. doi: 10.1080/00952990.2023.2297349. Epub 2024 Jan 18.
Ethanol exposure has been suggested to be implicated in the initiation and progression of several non-communicable diseases (NCD), including neurological disorders, diabetes mellitus, alcoholic liver disease, gastric injury, pancreatitis, and atherosclerosis. Recent findings show that the NACHT, LRR, and PYD domains-containing protein 3 (NLRP3) inflammasome is involved in the progression of ethanol-induced NCDs. The aim of this review was to summarize the research progress on NCDs associated with the action of the NLRP3 inflammasome by ethanol and potential interventions, with a specific focus on preclinical literature. A literature search was conducted on PubMed using the keywords "[ethanol] and [NLRP3]" up until January 2023. Articles describing cases of NCDs caused by ethanol and associated with the NLRP3 inflammasome were included. After removing duplicates, 35 articles were included in this review. These studies, mostly conducted in animals or in vitro, provide evidence that ethanol can contribute to the development of NCDs, such as neurological disorders, alcoholic liver disease, gastric injury, pancreatitis, and atherosclerosis, by activating the NLRP3 inflammasome. Ethanol exposure primarily triggers NLRP3 inflammasome activation by influencing the TRL/NF-κB, ROS-TXNIP-NLRP3 and P2X7 receptor (P2X7R) signaling pathways. Several natural extracts and compounds have been found to alleviate NCDs caused by ethanol consumption by inhibiting the activation of the NLRP3 inflammasome. Preclinical research supports a role for ethanol-induced NLRP3 inflammasome in the development of NCDs. However, the clinical relevance remains uncertain in the relative absence of clinical studies.
乙醇暴露被认为与几种非传染性疾病(NCD)的发生和发展有关,包括神经紊乱、糖尿病、酒精性肝病、胃损伤、胰腺炎和动脉粥样硬化。最近的研究结果表明,NACHT、LRR 和 PYD 结构域包含蛋白 3(NLRP3)炎症小体参与了乙醇诱导的 NCD 的进展。本综述的目的是总结乙醇作用下与 NLRP3 炎症小体相关的 NCD 研究进展及其潜在干预措施,重点关注临床前文献。在 PubMed 上使用关键词“[乙醇]和[NLRP3]”进行文献检索,检索时间截至 2023 年 1 月。纳入描述由乙醇引起的与 NLRP3 炎症小体相关的 NCD 病例的文章。在去除重复项后,共有 35 篇文章纳入本综述。这些研究主要在动物或体外进行,提供了证据表明,乙醇通过激活 NLRP3 炎症小体,有助于 NCD 的发展,如神经紊乱、酒精性肝病、胃损伤、胰腺炎和动脉粥样硬化。乙醇暴露主要通过影响 TLR/NF-κB、ROS-TXNIP-NLRP3 和 P2X7 受体(P2X7R)信号通路来触发 NLRP3 炎症小体的激活。已发现几种天然提取物和化合物通过抑制 NLRP3 炎症小体的激活来缓解由乙醇消耗引起的 NCD。临床前研究支持乙醇诱导的 NLRP3 炎症小体在 NCD 发展中的作用。然而,由于缺乏临床研究,相对来说,其在临床中的相关性尚不确定。