Abstract
We studied the capacity of 9 new muramyl dipeptide glycosides to stimulate mouse resistance to experimental sepsis induced by intraperitoneal injection of salmonella typhimurium culture. Preventive intraperitoneal injections of muramyl dipeptide β-glycosides better improved survival of infected animals compared to the original (unmodified) muramyl dipeptide and muramyl dipeptide α-glycosides. The most effective drug muramyl dipeptide β-heptylglycoside injected during sepsis development also reduced animal mortality, decreased bacterial contamination of the viscera, and increased phagocytic activity of peritoneal macrophages in infected animals.
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Kalyuzhin, O.V., Kalina, N.G., Bashtanenko, A.F. et al. Stimulation of Mouse Resistance to Bacterial Infection with Muramyl Dipeptide Glycoside. Bulletin of Experimental Biology and Medicine 135, 452–455 (2003). https://doi.org/10.1023/A:1024963325117
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DOI: https://doi.org/10.1023/A:1024963325117