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本文引用的文献

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Failure to predict hemolysis and hyperbilirubinemia by IgG subclass in blood group A or B infants born to group O mothers.无法通过O型血母亲所生的A型或B型血婴儿的IgG亚类来预测溶血和高胆红素血症。
Pediatrics. 2009 Jan;123(1):e132-7. doi: 10.1542/peds.2008-2617. Epub 2008 Dec 29.
2
Aggressive vs. conservative phototherapy for infants with extremely low birth weight.极低出生体重儿积极与保守光疗的比较
N Engl J Med. 2008 Oct 30;359(18):1885-96. doi: 10.1056/NEJMoa0803024.
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Inhibition of heme oxygenase activity in newborn mice by azalanstat.
Can J Physiol Pharmacol. 2008 Oct;86(10):651-9. doi: 10.1139/y08-069.
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Heme oxygenase-1 and the vascular bed: from molecular mechanisms to therapeutic opportunities.血红素加氧酶-1与血管床:从分子机制到治疗机遇
Antioxid Redox Signal. 2008 Oct;10(10):1767-812. doi: 10.1089/ars.2008.2043.
5
Coexpression of gene polymorphisms involved in bilirubin production and metabolism.参与胆红素生成和代谢的基因多态性的共表达。
Pediatrics. 2008 Jul;122(1):e156-62. doi: 10.1542/peds.2007-3249. Epub 2008 Jun 16.
6
Negative regulation of soluble Flt-1 and soluble endoglin release by heme oxygenase-1.血红素加氧酶-1对可溶性Flt-1和可溶性内皮糖蛋白释放的负调控
Circulation. 2007 Apr 3;115(13):1789-97. doi: 10.1161/CIRCULATIONAHA.106.660134. Epub 2007 Mar 26.
7
Kernicterus and the molecular mechanisms of bilirubin-induced CNS injury in newborns.核黄疸与新生儿胆红素诱导的中枢神经系统损伤的分子机制
Neuromolecular Med. 2006;8(4):513-29. doi: 10.1385/NMM:8:4:513.
8
Imidazole-dioxolane compounds as isozyme-selective heme oxygenase inhibitors.作为同工酶选择性血红素加氧酶抑制剂的咪唑二氧戊环化合物
J Med Chem. 2006 Jul 13;49(14):4437-41. doi: 10.1021/jm0511435.
9
Selectivity of imidazole-dioxolane compounds for in vitro inhibition of microsomal haem oxygenase isoforms.咪唑二氧戊环化合物对微粒体血红素加氧酶同工型体外抑制的选择性。
Br J Pharmacol. 2006 Feb;147(3):307-15. doi: 10.1038/sj.bjp.0706555.
10
Generation of bile pigments by haem oxygenase: a refined cellular strategy in response to stressful insults.血红素加氧酶生成胆色素:应对应激损伤的一种精细细胞策略。
Biochem Soc Symp. 2004(71):177-92. doi: 10.1042/bss0710177.

金属卟啉在新生儿高胆红素血症治疗中的应用。

Metalloporphyrins in the management of neonatal hyperbilirubinemia.

机构信息

Department of Pediatrics, Stanford University School of Medicine, Palo Alto, CA 94304, USA.

出版信息

Semin Fetal Neonatal Med. 2010 Jun;15(3):164-8. doi: 10.1016/j.siny.2009.11.004. Epub 2009 Dec 16.

DOI:10.1016/j.siny.2009.11.004
PMID:20006567
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2859976/
Abstract

Neonatal jaundice in the first week of life is a common problem in newborns. It is due to an imbalance of bilirubin production and its elimination, which can lead to significantly elevated levels of circulating bilirubin or hyperbilirubinemia. Use of phototherapy and/or exchange transfusion are the current modes for treating neonatal hyperbilirubinemia and preventing any neurologic damage. These strategies, however, only remove bilirubin that has already been formed. Preventing the production of excess bilirubin may be a more logical approach. Synthetic heme analogs, metalloporphyrins, are competitive inhibitors of heme oxygenase, the rate-limiting enzyme in bilirubin production, and their use has been proposed as an attractive alternative strategy for preventing or treating severe hyperbilirubinemia.

摘要

新生儿在出生后的第一周内出现黄疸是一种常见的现象。这是由于胆红素的产生和排泄失衡所导致的,可能会导致循环胆红素水平显著升高或高胆红素血症。目前,光疗和/或换血是治疗新生儿高胆红素血症和预防任何神经损伤的主要手段。然而,这些策略只能去除已经形成的胆红素。预防过多胆红素的产生可能是一种更合理的方法。人工合成血红素类似物,金属卟啉,是血红素加氧酶的竞争性抑制剂,血红素加氧酶是胆红素生成的限速酶,因此,它们的使用被提议作为一种有吸引力的替代策略,用于预防或治疗严重的高胆红素血症。