Molecular events in brain bilirubin toxicity revisited

被引:3
作者
Gazzin, Silvia [1 ]
Bellarosa, Cristina [1 ]
Tiribelli, Claudio [1 ]
机构
[1] Fdn Italiana Fegato Onlus, Liver Brain Unit Rita Moretti, Bldg Q,AREA Sci Pk,ss14,Km 163-5, I-34149 Trieste, Italy
关键词
DEVELOPING RAT-BRAIN; UNCONJUGATED BILIRUBIN; CEREBELLAR HYPOPLASIA; OXIDATIVE STRESS; GUNN RAT; CELL-DEATH; INFLAMMATORY RESPONSE; GLUTAMATE RELEASE; APOPTOSIS; NEURONS;
D O I
10.1038/s41390-024-03084-9
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
The mechanisms involved in bilirubin neurotoxicity are still far from being fully elucidated. Several different events concur to damage mainly the neurons among which inflammation and alteration of the redox state play a major role. An imbalance of cellular calcium homeostasis has been recently described to be associated with toxic concentrations of bilirubin, and this disequilibrium may in turn elicit an inflammatory reaction. The different and age-dependent sensitivity to bilirubin damage must also be considered in describing the dramatic clinical picture of bilirubin-induced neurological damage (BIND) formerly known as kernicterus spectrum disorder (KSD). This review aims to critically address what is known and what is not in the molecular events of bilirubin neurotoxicity to provide hints for a better diagnosis and more successful treatments. Part of these concepts have been presented at the 38th Annual Audrey K. Brown Kernicterus Symposium of Pediatric American Society, Washington DC, May 1, 2023.
引用
收藏
页码:1734 / 1740
页数:7
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