Після імунізації тварин міастогенними сироватками різного ступеня цитотоксичності виявили сенсибілізацію деяких показників вродженого імунітету − активності кисеньнезалежного і кисеньзалежного фагоцитозу, концентрації С3 і С4 компонентів комплементу.
Treatment of inflammatory and septic conditions is a serious problem due to the existing antibiotic resistance. It is necessary to find new
treatments using biological and physical factors that affect the course of inflammatory reactions in chronic processes. It is important to understand the mechanisms of interaction of light photons with cellular acceptors, which provide reactivity and resistance.
The aim – is to evaluate the low-intensity light effect of the red range spectrum (λ =630-660 nm) on the course of the inflammatory process in
experimental animals with LPS-induced peritonitis. Animals were divided into 3 groups: A – intact animals; B – animals with peritonitis induced by
intraperitoneal administration of LPS; C – animals with LPS-induced peritonitis after repeated exposure to red light. Irradiation of the abdominal wall was performed with LED matrices Korobov A. – Korobov V. "Barva-Flex/24FM", which emit in the red region of the spectrum. Methods of light microscopy (study of the barrier function in oxygen-independent phagocytosis of neutrophils, estimation of the lymphocytotoxicity degree in the Terasaki test) and spectrophotometry (determination of the concentration of circulating immune complexes) were used.
In animals after induction of peritonitis (group B) was observed inhibition of phagocytosis, which manifested itself in reduced adhesion and
endocytosis of antigens by neutrophils compared with intact animals. The use of light exposure of the red range spectrum (group C) significantly activated phagocytic cells and reduced the degree of lymphocytotoxicity and the concentration of circulating immune complexes at different stages of the inflammatory process. Thus, the action of red light contributed to the normalization of immunoresistance in animals, thereby reducing antigenic load by activating infiltration and exudation stages of the inflammatory process and induction of regenerative processes after repeated irradiation at the end of the experiment.
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