NLRP3 inflammasome: a key player in neonatal brain injury

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Bibliographic Details
Title: NLRP3 inflammasome: a key player in neonatal brain injury
Authors: Cagla Kiser, Ilkcan Ercan, Defne Engur, Sermin Genc
Source: Clin Exp Pediatr
Clinical and Experimental Pediatrics, Vol 68, Iss 7, Pp 475-485 (2025)
Publisher Information: Korean Pediatric Society, 2025.
Publication Year: 2025
Subject Terms: neonatal, nlrp3 inflammasome, hypoxia, Review Article, brain injury, Pediatrics, RJ1-570
Description: Among neonates, hypoxic-ischemic encephalopathy is the most significant cause of mortality and hypoxia-ischemia is among the leading causes of brain damage. The microglia are primary mediators of neuroinflammation. NOD-like receptor family pyrin domain containing 3 (NLRP3) inflammasome activation is the first line of defense in the central nervous system. Numerous studies have shown that the NLRP3 inflammasome is activated and proinflammatory cytokines are upregulated upon hypoxia-ischemia–induced brain damage. However, aberrant activation of the NLRP3 inflammasome results in cell death and brain tissue damage. Given that neonates are particularly vulnerable to neuroinflammation, which may cause lifelong disabilities, it is important to target the pathways involved in its complex nature to improve their prognosis. The potential use of compounds or drugs that target inflammasome activation to relieve hypoxia-induced brain damage has become significant. This review describes the NLRP3 inflammasome in neonates to contribute to the development of therapeutic approaches.
Document Type: Article
Other literature type
Language: English
ISSN: 2713-4148
DOI: 10.3345/cep.2024.01935
Access URL: https://pubmed.ncbi.nlm.nih.gov/40211861
https://doaj.org/article/1c3a3831508e40b283ee6b7e59230aab
Rights: CC BY NC
Accession Number: edsair.doi.dedup.....7c74fb04807702997f091bafc66a773f
Database: OpenAIRE
Description
Abstract:Among neonates, hypoxic-ischemic encephalopathy is the most significant cause of mortality and hypoxia-ischemia is among the leading causes of brain damage. The microglia are primary mediators of neuroinflammation. NOD-like receptor family pyrin domain containing 3 (NLRP3) inflammasome activation is the first line of defense in the central nervous system. Numerous studies have shown that the NLRP3 inflammasome is activated and proinflammatory cytokines are upregulated upon hypoxia-ischemia–induced brain damage. However, aberrant activation of the NLRP3 inflammasome results in cell death and brain tissue damage. Given that neonates are particularly vulnerable to neuroinflammation, which may cause lifelong disabilities, it is important to target the pathways involved in its complex nature to improve their prognosis. The potential use of compounds or drugs that target inflammasome activation to relieve hypoxia-induced brain damage has become significant. This review describes the NLRP3 inflammasome in neonates to contribute to the development of therapeutic approaches.
ISSN:27134148
DOI:10.3345/cep.2024.01935