Norris K A, Schrimpf J E, Flynn J L, Morris S M
Department of Molecular Genetics and Biochemistry, University of Pittsburgh School of Medicine, Pennsylvania 15261, USA.
Infect Immun. 1995 Jul;63(7):2793-6. doi: 10.1128/iai.63.7.2793-2796.1995.
The generation of nitric oxide (NO) is largely responsible for the intracellular killing of Trypanosoma cruzi by activated macrophages. The present study was carried out to determine whether the production of NO by activated murine macrophages cultured in physiologic levels of arginine can be augmented by increasing the availability of arginine, the substrate for NO biosynthesis. Increased exogenous arginine or citrulline resulted in a significant increase in NO production and complete clearance of the parasites by activated macrophages. As citrulline fully substituted for arginine in supporting NO production and trypanocidal activity, these results demonstrate the expression of a highly active citrulline-NO cycle in activated macrophages and that levels of arginine in plasma are limiting with respect to both NO production and trypanocidal activity in these cells. The results indicate that increasing plasma substrate levels for both arginine and NO biosynthesis may represent a means of enhancing microbicidal activity in vivo.
一氧化氮(NO)的产生在很大程度上负责活化巨噬细胞对克氏锥虫的细胞内杀伤作用。本研究旨在确定在生理水平精氨酸培养的活化小鼠巨噬细胞中,通过增加精氨酸(NO生物合成的底物)的可利用性,是否可以增强NO的产生。增加外源性精氨酸或瓜氨酸会导致活化巨噬细胞产生的NO显著增加,并使寄生虫被完全清除。由于瓜氨酸在支持NO产生和杀锥虫活性方面可完全替代精氨酸,这些结果证明活化巨噬细胞中存在高度活跃的瓜氨酸-NO循环,并且血浆中精氨酸水平对于这些细胞中的NO产生和杀锥虫活性而言是有限的。结果表明,提高精氨酸和NO生物合成的血浆底物水平可能是增强体内杀菌活性的一种手段。