Direct EPR Detection of Nitric Oxide in Mice Infected with the Pathogenic Mycobacterium Mycobacterium tuberculosis

被引:0
作者
Vanin, Anatoly F. [1 ]
Selitskaya, Raisa P. [2 ]
Serezhenkov, Vladimir A. [1 ]
Mozhokina, Galina N. [2 ]
机构
[1] Russian Acad Sci, NN Semenov Chem Phys Inst, Moscow, Russia
[2] IM Sechenov Moscow Med Acad, Res Inst Phthisiopulmonol, Moscow, Russia
基金
俄罗斯基础研究基金会;
关键词
IN-VIVO DETECTION; REACTIVE OXYGEN; SYNTHASE; MACROPHAGES; DEFENSE; DITHIOCARBAMATE; GENERATION; RESISTANCE; PHAGOSOMES; STRAINS;
D O I
10.1007/s00723-009-0038-y
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
It has been shown that treatment of mice preinfected with Mycobacterium tuberculosis with spin NO traps (iron complexes with diethyldithiocarbamate) enables detection of large amounts of NO in internal organs 2 and 4 weeks after infection (up to 55-57 mu mol/kg of wet lung tissue accumulated with spin NO traps during 30 min). The animals were infected with the drug-sensitive laboratory strain H37Rv and a clinical isolate nonrespondent to antituberculous drugs (the multidrug-resistant strain of M. tuberculosis) obtained from a patient with an active form of tuberculosis. Two weeks after infection with the multidrug-resistant strain, the NO level in the lungs, spleen, liver and kidney increased sharply concurrently with slight lesions of lung tissue. A reverse correlation, i.e., low level of NO in the lungs and other internal organs and extensive injury of lung tissue, was established for H37Rv-infected mice. Four weeks after infection, NO production in the lungs increased dramatically for both M. tuberculosis strains resulting in 80-84% damage of lung tissue. The lesion is suggested to be due to the development of defense mechanisms in M. tuberculosis counteracting NO effects.
引用
收藏
页码:95 / 104
页数:10
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