Zimmermann Nives, Rothenberg Marc E
Division of Allergy and Immunology, Cincinnati Children's Hospital Medical Center and Department of Pediatrics, University of Cincinnati College of Medicine, OH 45229, USA.
Eur J Pharmacol. 2006 Mar 8;533(1-3):253-62. doi: 10.1016/j.ejphar.2005.12.047. Epub 2006 Feb 3.
Asthma, a complex chronic inflammatory pulmonary disorder, is on the rise despite intense ongoing research underscoring the need for new scientific inquiry. Using global microarray analysis, we have recently uncovered that asthmatic responses involve metabolism of arginine by arginase. We found that the cationic amino acid transporter (CAT)2, arginase I, and arginase II were particularly prominent among the allergen-induced gene transcripts. These genes are key regulators of critical processes associated with asthma including airway tone, cell hyperplasia and collagen deposition, respectively. Furthermore, systemic arginine levels and arginine metabolism via nitric oxide synthase (NOS) can have profound effect on lung inflammation. This review focuses on the current body of knowledge on l-arginine metabolism in asthma and lung inflammation.
哮喘是一种复杂的慢性炎症性肺部疾病,尽管正在进行的深入研究强调了新的科学探究的必要性,但哮喘的发病率仍在上升。通过全球微阵列分析,我们最近发现哮喘反应涉及精氨酸酶对精氨酸的代谢。我们发现阳离子氨基酸转运体(CAT)2、精氨酸酶I和精氨酸酶II在变应原诱导的基因转录物中尤为突出。这些基因分别是与哮喘相关的关键过程的关键调节因子,包括气道张力、细胞增生和胶原蛋白沉积。此外,全身精氨酸水平和通过一氧化氮合酶(NOS)的精氨酸代谢可对肺部炎症产生深远影响。本综述重点关注目前关于哮喘和肺部炎症中L-精氨酸代谢的知识体系。