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重新审视脑胆红素毒性中的分子事件。

Molecular events in brain bilirubin toxicity revisited.

机构信息

Liver-Brain Unit "Rita Moretti", Fondazione Italiana Fegato-Onlus, Bldg. Q, AREA Science Park, ss14, Km 163.5, Basovizza, 34149, Trieste, Italy.

出版信息

Pediatr Res. 2024 Jun;95(7):1734-1740. doi: 10.1038/s41390-024-03084-9. Epub 2024 Feb 20.

Abstract

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.

摘要

胆红素神经毒性的机制仍远未完全阐明。几种不同的事件共同导致主要神经元损伤,其中炎症和氧化还原状态的改变起着主要作用。最近有研究表明,细胞内钙稳态失衡与胆红素的毒性浓度有关,这种失衡可能反过来引发炎症反应。在描述胆红素诱导的神经损伤(BIND)的显著临床特征时,即以前所知的核黄疸谱障碍(KSD),还必须考虑到不同的、与年龄相关的对胆红素损伤的敏感性。本综述旨在批判性地探讨胆红素神经毒性的分子事件中已知和未知的内容,为更好的诊断和更成功的治疗提供线索。这些概念的一部分已在 2023 年 5 月 1 日于华盛顿特区举行的第 38 届儿科美国社会奥黛丽·K·布朗核黄疸研讨会(38th Annual Audrey K. Brown Kernicterus Symposium of Pediatric American Society)上提出。

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