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精氨酸代谢的最新进展:精氨酸酶的作用和调节。

Recent advances in arginine metabolism: roles and regulation of the arginases.

机构信息

Department of Microbiology and Molecular Genetics, University of Pittsburgh, Pittsburgh, PA 15261, USA.

出版信息

Br J Pharmacol. 2009 Jul;157(6):922-30. doi: 10.1111/j.1476-5381.2009.00278.x. Epub 2009 Jun 5.

DOI:10.1111/j.1476-5381.2009.00278.x
PMID:19508396
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2737650/
Abstract

As arginine can serve as precursor to a wide range of compounds, including nitric oxide, creatine, urea, polyamines, proline, glutamate and agmatine, there is considerable interest in elucidating mechanisms underlying regulation of its metabolism. It is now becoming apparent that the two isoforms of arginase in mammals play key roles in regulation of most aspects of arginine metabolism in health and disease. In particular, work over the past several years has focused on the roles and regulation of the arginases in vascular disease, pulmonary disease, infectious disease, immune cell function and cancer. As most of these topics have been considered in recent review articles, this review will focus more closely on results of recent studies on expression of the arginases in endothelial and vascular smooth muscle cells, post-translational modulation of arginase activity and applications of arginase inhibitors in vivo.

摘要

由于精氨酸可以作为多种化合物的前体,包括一氧化氮、肌酸、尿素、多胺、脯氨酸、谷氨酸和胍丁胺,因此人们对阐明其代谢调节的机制非常感兴趣。现在,人们越来越清楚地认识到哺乳动物中两种精氨酸酶同工酶在调节健康和疾病中精氨酸代谢的大多数方面起着关键作用。特别是,过去几年的工作集中在精氨酸酶在血管疾病、肺部疾病、传染病、免疫细胞功能和癌症中的作用和调节上。由于这些主题中的大多数都在最近的评论文章中进行了考虑,因此本次综述将更密切地关注最近关于内皮细胞和血管平滑肌细胞中精氨酸酶表达、精氨酸酶活性的翻译后调节以及精氨酸酶抑制剂在体内应用的研究结果。

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本文引用的文献

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The vascular effects of different arginase inhibitors in rat isolated aorta and mesenteric arteries.不同精氨酸酶抑制剂对大鼠离体主动脉和肠系膜动脉的血管效应。
Br J Pharmacol. 2009 Jan;156(1):84-93. doi: 10.1111/j.1476-5381.2008.00036.x.
2
Arginase enzymes in isolated airways from normal and nitric oxide synthase 2-knockout mice exposed to ovalbumin.来自暴露于卵清蛋白的正常小鼠和一氧化氮合酶2基因敲除小鼠的分离气道中的精氨酸酶。
Toxicol Appl Pharmacol. 2009 Feb 1;234(3):273-80. doi: 10.1016/j.taap.2008.10.007. Epub 2008 Nov 5.
3
Toll-like receptor-induced arginase 1 in macrophages thwarts effective immunity against intracellular pathogens.Toll样受体诱导巨噬细胞中的精氨酸酶1会阻碍针对细胞内病原体的有效免疫。
Nat Immunol. 2008 Dec;9(12):1399-406. doi: 10.1038/ni.1671. Epub 2008 Nov 2.
4
Uric acid decreases NO production and increases arginase activity in cultured pulmonary artery endothelial cells.尿酸可降低培养的肺动脉内皮细胞中一氧化氮的生成,并增加精氨酸酶活性。
Am J Physiol Cell Physiol. 2008 Nov;295(5):C1183-90. doi: 10.1152/ajpcell.00075.2008. Epub 2008 Sep 10.
5
Inhibition of arginase activity enhances inflammation in mice with allergic airway disease, in association with increases in protein S-nitrosylation and tyrosine nitration.精氨酸酶活性的抑制会增强变应性气道疾病小鼠的炎症反应,这与蛋白质S-亚硝基化和酪氨酸硝化作用的增加有关。
J Immunol. 2008 Sep 15;181(6):4255-64. doi: 10.4049/jimmunol.181.6.4255.
6
Cysteine-iron promotes arginase activity by driving the Fenton reaction.半胱氨酸铁通过驱动芬顿反应促进精氨酸酶活性。
Biochem Biophys Res Commun. 2008 Nov 7;376(1):116-20. doi: 10.1016/j.bbrc.2008.08.102. Epub 2008 Aug 30.
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J Appl Physiol (1985). 2008 Nov;105(5):1632-42. doi: 10.1152/japplphysiol.90627.2008. Epub 2008 Aug 21.
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Prostate. 2008 Oct 1;68(14):1561-9. doi: 10.1002/pros.20816.
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Arginase inhibition protects against allergen-induced airway obstruction, hyperresponsiveness, and inflammation.精氨酸酶抑制可预防变应原诱导的气道阻塞、高反应性和炎症。
Am J Respir Crit Care Med. 2008 Sep 15;178(6):565-73. doi: 10.1164/rccm.200710-1588OC. Epub 2008 Jun 26.
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Reprod Sci. 2008 Jul;15(6):591-7. doi: 10.1177/1933719108316908. Epub 2008 May 20.