中国寄生虫学与寄生虫病杂志 ›› 1998, Vol. 16 ›› Issue (5): 326-330.

• 论著 • 上一篇    下一篇

L-精氨酸和L-瓜氨酸在体外活化巨噬细胞抗弓形虫感染中的作用

郑春福; 林建银   

  1. 福建医科大学寄生虫学教研室
  • 收稿日期:1900-01-01 修回日期:1900-01-01 出版日期:1998-10-31 发布日期:1998-10-31

THE ROLE OF L ARGININE AND L CITRULLINE IN ACTIVATED MACROPHAGE AGAINST TOXOPLASMA GONDII INFECTION IN VITRO

Zheng Chunfu; Lin Jianyin   

  1. epartment of Parasitology; Fujian Medical University; Fuzhou 350004
  • Received:1900-01-01 Revised:1900-01-01 Online:1998-10-31 Published:1998-10-31

摘要: 目的:探讨增加细胞外L-精氨酸(一氧化氮生物合成的底物)或L-瓜氨酸(通过再循环生成L-精氨酸)浓度是否可提高活化巨噬细胞(macrophage,M)诱生一氧化氮(NO)的产量及其对细胞内抑制或杀伤弓形虫速殖子的能力。方法:用RH株刚地弓形虫(Toxoplasmagondi)速殖子感染活化M后,观察活化M在含不同浓度L-精氨酸和L-瓜氨酸培养基中培养18h后的NO产量、感染率以及纳虫泡内弓形虫速殖子数。结果:(1)活化M在生理水平的L-精氨酸浓度(80μmol/L)下可明显抑制细胞内弓形虫速殖子的增殖,并依赖于NO的产量;(2)增加细胞外源的L-精氨酸或L-瓜氨酸可明显提高M诱生的NO产量,进而降低M的感染率,并抑制细胞内弓形虫速殖子的增殖;(3)L-瓜氨酸可完全替代L-精氨酸提高M诱生的NO产量及其抑制或杀伤弓形虫速殖子的能力。结论:活化M胞浆内生理水平的L-精氨酸诱生的内源性NO产量足以抑制细胞内弓形虫速殖子的繁殖,但不能防止细胞感染,增加细胞外生物合成NO的底物浓度可提高M抑制或杀伤细胞内弓形虫速殖子的能力。

关键词: 刚地弓形虫, 巨噬细胞, L-精氨酸, L-瓜氨酸, 感染, 增殖

Abstract:

AIM: To determine whether both the production of NO and the toxoplasmastatic or toxoplasmacidal activity of activated macrophages cultured in physiologic levels of arginine can be enhanced by increasing the availability of arginine, or citrulline. METHODS: After the activated Mφ were infected with the RH strain of T.gondii ,the levels of NO production, the infection rate of Mφ and the number of tachyzoites in parasitophorous vacuoles were determined after the Mφ were cultured in medium added with various concentrations of L-arginine or L-citrulline for 18 h. RESULTS: (1) The multiplication of intracelluar toxoplasmic tachyzoites could be inhibited by activated macrophages, depending on the production of NO in the presence of physiologic levels of arginine. (2) Increased exogenous arginine or citrulline resulted in a significant elevation of NO producion induced by activated macrophages and further reduction of infection rate of macrophages as well as inhibition of multiplication of intracelluar tachyzoites. (3) Citrulline could fully substitute for arginine in enhancing NO production and toxoplasmastatic or toxopasmacidal activity. CONCLUSION: The physiological levels of arginine were able to induce sufficient intrinsic NO production to inhibit intracellular
multiplication of toxoplasmatic tachyzoite but unable to protect cell from infection and that
increasing the substrate levels for NO biosynthesis may enhance in vitro toxoplasmastatic or
toxoplasmacidal activity of activated macrophages.

Key words: Toxoplasma gondii, macrophages, L-arginine, L-citrulline, infection, multiplication