Experiments on rats show a positive effect of prodigiosan phagocyte stimulation on humoral-cell interaction in the phagocytosis system in traumatic and burn shock accompanied by improvement of organism's resistance to extreme factors. Prodigiosan stimulation in the torpid phase against the background of altered phagocyte reactivity produced less pronounced and ambiguous effects.Key Words: shock; macrophages; neutrophils; fibronectin; phagocyte stimulation Our previous studies of the humoral and cellular components of phagocytosis at the early stages of traumatic and burn disease revealed complex structural and functional changes in stellate reticuloendotheliocytes (SRE), alveolar macrophages (AM), and neutrophils accompanied by shifts in the content of the nonspecific plasma opsonin fibronectin. It has been shown that macro-and microphage suppression against the background of hypofibronectinemia reflects the severity of postaggressive states and usually disappears in natural relieve of the shock [4][5][6]. These findings agree with the published data that organism's resistance to extreme factors strongly depends on the functional state of the phagocytosis system and plasma opsonizing activity [2,9,10,12,15]. In light of this, the search for new drugs that modulate phagocytic activity and improve nonspecific organism's resistance in shock is an important medical problem [4,8,11,13,14].
MATERIALS AND METHODSExperiments were carried out on albino rats. To stimulate phagocytes, 0.005% prodigiosan (bacterial polysaccharide) was injected intraperitoneally in a dose of 25 gg/100g body weight 24 h before mechanical or thermal trauma or at the peak of the torpid Department of Forensic Medicine, Kazan' State Medical University phase of traumatic or burn shock. Phagocytic capacity of the hepatic reticuloendothelial system was assessed by the clearance of gelatinized casein ink [3]. To this end, elimination half-time and elimination rate constant were calculated and SRE containing ink particles were counted a histological preparations. Total cytosis and cytogram of the bronchoalveolar lavage were determined, and dead cells were counted using the methylene blue exclusion test [3]. Functional state of AM and peripheral blood neutrophils was assessed using 24-h E. coil 065 culture. The parameters of phagocytosis, phagocytic index, and phagocytic number were determined with allowance for changes in total AM and neutrophil counts and shift in differential leukocyte count [7]. Oxygen-dependent metabolism was assessed by tetrazolium nitroblue (TNB) reduction in spontaneous (sTNB) and induced (iTNB) tests, coefficient of stimulation was also calculated. Plasma fibronectin was measured by enzyme-linked immunosorbent assay [1]. Samples for electron microscopy were prepared using routine techniques. The data were processed statistically using parametric ANOVA tests.