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新生儿胆汁淤积症胆汁酸转运体和转录调控的研究进展

Research progress of bile acid transporters and transcriptional regulation in neonatal cholestasis

来源期刊: 广州医药 | 104-109 发布时间:2023-05-18 收稿时间:2025/11/13 18:36:12 阅读量:18
作者:
关键词:
胆汁淤积转运体生物机制转录调控
cholestasistransporterbiological mechanismtranscriptional regulation
DOI:
10.3969/j.issn.1000-8535.2023.04.019
收稿时间:
2022-10-09 
修订日期:
 
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引用总数:
1  
新生儿引起肝内胆汁淤积是由感染、遗传代谢性疾病、胃肠外营养、基因突变等各种不同病因导致胆汁形成、分泌和排泄障碍。胆汁在体内淤积会影响新生儿的生长发育,严重者出现肝纤维化、肝功能衰竭等不可逆的改变,其发病的机制涉及参与肝脏胆汁酸分泌的各种转运体、肝细胞膜转运蛋白转录和和转录后的调控等。本文归纳总结近年来国内外关于胆汁酸转运体及其转录和转录后的调控,从而为此疾病的防治提供理论依据,为将来降低其发生率和改善预后。
Neonatal intrahepatic cholestasis is caused by infection,genetic metabolic diseases,parenteral nutrition,gene mutation and other different causes leading to bile formation,secretion and excretion disorders.Bile stasis in the body will affect the growth and development of the newborn,and in severe cases,irreversible changes such as liver fibrosis and liver failure will occur.The pathogenesis of bile stasis involves various transporters involved in the secretion of bile acids in the liver,transcription and post transcription regulation of liver cell membrane transporters.In this paper,we summarized the recent studies on bile acid transporters and their transcriptional and post transcriptional regulation at home and abroad,so as to provide a theoretical basis for the prevention and treatment of this disease,and to reduce its incidence and improve its prognosis in the future.
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