Kaminskaia G O, Abdullaev R Iu, Gedymin L E
Probl Tuberk. 1998(3):71-5.
An experiment was conducted on noninbred albino rats intraperitoneally inoculated with Mycobacteria tuberculosis (MBT) in a dose of 0.025 mg. Alveolar macrophages (AM), non fractionated cell sediments (NFCS) and circulating leukocytes were studied 1 day, 1, 2, and 6 weeks after inoculation. Spontaneous and killed BCG culture-stimulated killed HCT-test, the activity of superoxide dismutase (SOD) and catalase, the level of malonic dialdehyde (MDA) and platelet activation factor (PAF) were determined. Morphological changes were histologically controlled. The rats administered the MBT dose sufficient to initiate generalized tuberculosis in guinea pigs were found to develop nonspecific changes which became reversible by the end of the experiment. Throughout the process, there was no splash of basal oxidative metabolism in all phagocytic types and their functional decompensation did not develop. Following 1.5 months, all the types of phagocytes showed an increased oxygen burst during specific stimulation. The level of MDA did not exceed the control values in all periods. The activity of anti-oxidative enzymes changed heterodirectionally. At the final stage, the activity of catalase repeatedly increased with normal or reduced SOD values. In early infection, the concentration of PAF rose in the pulmonary phagocytes. When resistance was formed, in all cell types it fell below the control values.
对非近交系白化大鼠进行实验,以0.025毫克的剂量腹腔接种结核分枝杆菌(MBT)。在接种后1天、1周、2周和6周研究肺泡巨噬细胞(AM)、未分级细胞沉淀物(NFCS)和循环白细胞。测定自发和经卡介苗培养刺激的杀死的HCT试验、超氧化物歧化酶(SOD)和过氧化氢酶的活性、丙二醛(MDA)和血小板活化因子(PAF)的水平。通过组织学控制形态学变化。发现给予足以在豚鼠中引发全身性结核病的MBT剂量的大鼠出现非特异性变化,这些变化在实验结束时变得可逆。在整个过程中,所有吞噬细胞类型的基础氧化代谢均未出现激增,且其功能也未出现失代偿。1.5个月后,所有类型的吞噬细胞在特异性刺激期间均表现出氧爆发增加。在所有时期,MDA水平均未超过对照值。抗氧化酶的活性呈异向变化。在最后阶段,过氧化氢酶的活性反复增加,而SOD值正常或降低。在早期感染时,肺吞噬细胞中PAF的浓度升高。当形成抵抗力时,所有细胞类型中的PAF浓度均降至对照值以下。