期刊文献+

精氨酸和一氧化氮合成的关系及其在免疫调节中的作用 被引量:13

Relationship between Arginine and Nitric Oxide Synthesis and Its Role in Immune Regulation
下载PDF
导出
摘要 精氨酸 (Arginine,Arg)因其具有广泛的生物学作用而在所有氨基酸中占有重要地位。一定剂量的Arg可促进创伤愈合和胶原生成 ,刺激若干内分泌腺分泌激素 ,调节某些类型肿瘤生长 ,并增强细胞介导的免疫应答。因而常将Arg作为免疫增强膳食的一部分来对抗应激及严重疾病病人中常见的免疫抑制。Arg是高活性基团一氧化氮 (nitricoxide ,NO)的唯一供氮前体 ,已认定NO对越来越多的细胞过程有影响并存在于全身的许多组织。它可影响多种类型的免疫细胞。Arg自身或通过生成的NO参与了许多免疫调节过程 ,因此 ,对Arg体内合成。 Arginine occupies an important place in all of the amino acid because of its biological activities. Certain doses of arginine have shown to enhance wound healing and collagen production,stimulate hormonal secretion from several endocrine glands,regulate the growth of certain tumour types,and potentiate cell-mediated immune response. So arginine supplementation has been used as part of immunity-enhancing diet to combat the immune suppression seen in the stress and critical illness. Arginine has been identified as the sole nitrogen-providing precursor of the highly reactive radical nitric oxide(NO). NO is rapidly being identified to have significant effects on an ever-increasing number of cellular processes and in many tissues throughout the body. NO can affect most immune cell types. So,it will be very important for its reasonable use to know the role of arginine synthesis in vivo,metabolism and foreign arginine transport in NO synthesis.
出处 《氨基酸和生物资源》 CAS 2002年第1期46-49,共4页 Amino Acids & Biotic Resources
关键词 精氨酸 一氧化氮合成 免疫调节 arginine NO production immunity
  • 相关文献

参考文献29

  • 1[1]Geissler A et al. Real-time study of the urea cycle using[15]Nn. m. r. in the isolated perfused rat liver[J]. Biochem J,1992,287:813~820.
  • 2[2]Back K J et al. Macrophage nitric oxide subunits. Purification,characterization,and role of prosthetic groups and substrate in regulating their association into a dimeric enzyme[J]. J Biol Chem,1993,268:21120~21129.
  • 3[3]Wu J ,Brosnan JT. Macrophages can oonvert citrulline into arginine[J].Bicochem J ,1992,281:45~48.
  • 4[4]Wu J,Flynn NE.The activation of the argining-citrulline cycle in macrophages from the spontaneously diabetic BB rat[J].Biochem J,1993,294:113~118.
  • 5[5]billiar TR et al. Coinduction of argininosuccinate synthetase and nitric oxide synthaes by LPS and interferon-gamma in murine macrophages[J].J Leuko Biol,1992,52:18~23.
  • 6[6]Pastor CM et al. Sources of arginine for induced nitric oxide synthesis in the isolated perfused liver[J].Am J Physiol,1995,269:G861~G866.
  • 7[7]Morris SM Jr et al. Human type Ⅱ arginase:sequence analysis and tissue-specific expression[J]. Gene,1997,193:157~161.
  • 8[8]Modollel M et al. Reciprocal regulation of the nitric oxide synthase arginase balance in mouse bone marrow-derived macrophages by TH1 and TH2 cytokines[J].Eur J Immunol,1995,25:1101~1104.
  • 9[9]Griffith OW,Stuehr DJ. Nitric oxide synthases:properties and catalytic mechanism[J].Annu Rev Physiol,1995,57:707~736.
  • 10[10]Hey C et al. Inhibition of arginase in rat and rabbit alveolar macrophages by NW-hydroxy-L-indospicine,effects on L-arginine utilization by nitric oxide synthase[J].Br J Pharmacol,1997,121:395~400.

同被引文献137

引证文献13

二级引证文献136

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部