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一名患有核黄疸的早产儿的小脑轴突/髓鞘丢失、血管生成芽生以及血管内皮生长因子的神经元增加。

Cerebellar axon/myelin loss, angiogenic sprouting, and neuronal increase of vascular endothelial growth factor in a preterm infant with kernicterus.

作者信息

Brito Maria A, Zurolo Emanuele, Pereira Pedro, Barroso Cândida, Aronica Eleonora, Brites Dora

机构信息

Research Institute for Medicines and Pharmaceutical Sciences (iMed.UL) and Department of Biochemistry and Human Biology, Faculty of Pharmacy, University of Lisbon, Lisbon, Portugal.

出版信息

J Child Neurol. 2012 May;27(5):615-24. doi: 10.1177/0883073811423975. Epub 2011 Dec 21.

Abstract

We performed histologic and immunohistochemical analysis of cerebellar sections from a preterm infant (32 weeks 5 days) dead on the 4th day of life with the diagnosis of kernicterus and compared the results with 1 age-matched nonicteric patient. Poorer Luxol fast blue-periodic acid Schiff and Bodian-Luxol fast blue stainings as well as neurofilament expression were observed in the kernicterus case, indicating loss of axon neurites and myelin fibers. Elevated claudin-5 and cluster of differentiation 34 expression associated with increased blood vessel density suggests bilirubin-induced angiogenic sprouting. Upregulation of vascular endothelial growth factor and its receptor 2 was observed in nucleus dentatus and Purkinje neurons. Although upregulation of multidrug resistance-associated protein 1 was increased in cerebellar neurons, it was not able to prevent bilirubin-induced neurotoxicity. These data add new insights into the pathophysiology of kernicterus, revealing vascular endothelial growth factor and its receptor 2, as well as angiogenic sprouting, as new players in neurologic damage by unconjugated bilirubin.

摘要

我们对一名出生32周零5天、出生后第4天死亡且诊断为核黄疸的早产儿的小脑切片进行了组织学和免疫组织化学分析,并将结果与1名年龄匹配的非黄疸患儿进行了比较。在核黄疸病例中观察到卢戈氏碘液-过碘酸希夫染色和博迪安-卢戈氏碘液染色较差,以及神经丝表达减少,表明轴突神经突和髓鞘纤维丢失。紧密连接蛋白-5和分化簇34表达升高并伴有血管密度增加,提示胆红素诱导血管生成芽生。在齿状核和浦肯野神经元中观察到血管内皮生长因子及其受体2上调。虽然小脑神经元中多药耐药相关蛋白1上调,但它无法预防胆红素诱导的神经毒性。这些数据为核黄疸的病理生理学提供了新的见解,揭示了血管内皮生长因子及其受体2以及血管生成芽生是未结合胆红素神经损伤的新因素。

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