期刊文献+

猪苓多糖对小鼠腹腔巨噬细胞一氧化氮生成、iNOS活性和细胞内还原型谷胱甘肽含量的影响 被引量:12

Effect of polyporus polysaccharide on NO production,iNOS activity and intracellular reduced glutathione level from peritoneal macrophages of mice
下载PDF
导出
摘要 目的 :观察猪苓多糖 (PPS)对小鼠腹腔巨噬细胞一氧化氮 (NO)生成及其免疫调节作用和抗肿瘤作用机制。方法 :采用Griess反应、荧光法和DTNB比色法分别测定不同剂量的PPS作用小鼠腹腔巨噬细胞的NO生成量、诱导型一氧化氮合酶 (iNOS)活性及细胞内还原性谷胱甘肽 (GSH)含量的变化。结果 :PPS能使小鼠腹腔巨噬细胞NO生成增加 ,i NOS活性增高 ,并呈作用剂量依赖关系 ;PPS在刺激小鼠腹腔巨噬细胞NO合成同时 ,伴有细胞内GSH水平的降低 ,呈负相关 (P <0 .0 5 )。结论 :PPS能提高小鼠腹腔巨噬细胞iNOS活性 ,增加NO合成 ,消耗细胞内的GSH。 Objective:To investigate the effect of polyporus polysaccharide (PPS) on nitric oxide (NO)production from peritoneal macrophages of mice and its immunoregulatory and antineoplastic mechanism.Methods:NO output,iNOS(inducible nitric oxide synthase)activity and reduced glutathione(GSH)level were determined by Griess reaction,fluorimetry and DTNB colorimetry respectively.Results:PPS treatment resulted in a dose dependent increase of NO production and iNOS activity.There was a negative correlation between the increase of NO output and decrease of GSH concentration( P< 0.05).Conclusion:PPS is able to induce iNOS activity and to stimulate NO synthesis,which is associated with the consumption of intracellular GSH.Intracellular GSH could regulate NO synthesis of macrophages and protect host cells from NO mediated cytotoxicity.
出处 《广东医学院学报》 2003年第4期319-320,323,共3页 Journal of Guangdong Medical College
基金 广东省重点学科基金资助课题 (980 8)
关键词 猪苓多糖 一氧化氮 诱导型一氧化氮合酶 脱甘肽 巨噬细胞 polyporus polysaccharide nitric oxide inducible nitric oxide synthase glutathione macrophage.
  • 相关文献

参考文献10

  • 1Ding AH,Nathan CF,Stuehr DJ. Release of reactive nitrogen intermediates and reactive oxygen intermediates from mouse peritoneal macrophages: comparison of activatingcytokines and evidence for independent production [J]. J Immunol, 1988,141 (7) : 2407-2412.
  • 2Wang W ,Inoue N,Nakayama T,et al. An assay method for nitric oxide syrtthase in crude samples by determining product NADP[J]. Anal Biochem, 1995,227 (2) : 274-280.
  • 3Ghigo D,Alessio P,Foeo A,et al. Nitrie oxide synthesis is impaired in glutathione-depleted human umbilieal vein endothelial cells [J]. Am J physiol, 1993,265 (3 Ptl ) : C728-732.
  • 4Li Y,Ito N,Suzuki T,et al. Dexamathasone inhibits nitric oxide-mediated cytotoxicity via effects on both macrophages and target cells[J]. Immunopharmacology, 1995,30(2): 177-186.
  • 5Barnes PJ,Liew FY. NO and asthmatic inflammation[J].Immunol Today, 1995,16 (3) : 128-130.
  • 6Liu WK,Activation of peritoneal macrophages by polysaccharopeptide from the mushroom,coriolus versicolor[J].Immunopharmacology, 1993,26 (2) : 139-146.
  • 7Lorsbach RB,Russell SW. A specific sequence of stimulation is required to induce synthesis of the antimicrobial molecule nitric oxide by mouse macrophages[J]. Infect Immunol, 1992,60(5) : 2133-2135.
  • 8Coren KD. Evidence for antiviral effect of nitric oxide:inhibition of herpes simplex virus type-1 replication[J]. J Clin Invest, 1993,91 (6) : 2446-2448.
  • 9Chanq Cl,Liao JC,Kuo L. Macrophage arginase promotes tumor cell growth and suppresses nitrie oxide-mediated tumor cytotoxicity[J]. Cancer Res, 2001,61(3) : 1100-1106.
  • 10Soini Y, Kalhos K, Puhakka A, et al. Expression of inducible nitric oxide synthase in healthy pleura and in malignant mesothelioma [J]. Br J Cancer, 2000,83 (7) : 880-886.

同被引文献123

引证文献12

二级引证文献130

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