Volume 9
Issue 2
Veterinary Medicine
JOURNAL OF
POLISH
AGRICULTURAL
UNIVERSITIES
Available Online: http://www.ejpau.media.pl/volume9/issue2/abs-12.html
GLYCOMACROPEPTIDE PROTECTS AGAINST EXPERIMENTAL ENDOTOXEMIA AND BACTEREMIA IN MICE
Michał Zimecki1, Jolanta Artym2, Grzegorz Chodaczek2, Maja Kocięba1, Jacek Rybka2, Anna Skórska2, Marian Kruzel3
1 Institute of Immunology and Experimental Therapy
of Polish Academy of Sciences, Wrocław, Poland
2 Laboratory of Immunobiology,
The Institute of Immunology and Experimental Therapy, Wrocław, Poland
3 University of Texas, Health Science Center, Houston, TX, USA
ABSTRACT
The aim of this study was to evaluate protective effects of glycomacropeptide (GMP), a kappa casein-derived peptide, in experimentally induced endotoxemia or bacteremia in mice. The results showed that BALB/c mice, given intraperitoneally (i.p.) GMP, 24h before intravenous (i.v.) injection of a high dose of lipopolysaccharide (LPS) from Escherichia coli, strongly inhibited serum levels of tumor necrosis factor alpha (TNF alpha) and interleukin 6 (IL-6), measured 2h later by bioassays. In addition, GMP, administered 24h before infection of CBA mice with a sublethal dose of E. coli, significantly lowered the number of bacterial cells in the spleen. The analysis of main blood cell types in mice pretreated 24h prior to infection with GMP revealed significant increase in the content of granulocytes and immature neutrophils. We, therefore, postulate, that induction of myelopoiesis by GMP may be a primary cause of the increased clearance of bacteria during the development of bacteremia in mice.
Key words: glycomacropeptide, endotoxemia, bacteremia, granulocytes.
Michał Zimecki
Institute of Immunology and Experimental Therapy
of Polish Academy of Sciences, Wrocław, Poland
R. Weigla 12, 53-114 Wrocław, Poland
email: zimecki@immuno.iitd.pan.wroc.pl
Jolanta Artym
Laboratory of Immunobiology,
The Institute of Immunology and Experimental Therapy, Wrocław, Poland
Grzegorz Chodaczek
Laboratory of Immunobiology,
The Institute of Immunology and Experimental Therapy, Wrocław, Poland
Maja Kocięba
Institute of Immunology and Experimental Therapy
of Polish Academy of Sciences, Wrocław, Poland
R. Weigla 12, 53-114 Wrocław, Poland
Jacek Rybka
Laboratory of Immunobiology,
The Institute of Immunology and Experimental Therapy, Wrocław, Poland
Anna Skórska
Laboratory of Immunobiology,
The Institute of Immunology and Experimental Therapy, Wrocław, Poland
Marian Kruzel
University of Texas, Health Science Center, Houston, TX, USA
Responses to this article, comments are invited and should be submitted within three months of the publication of the article. If accepted for publication, they will be published in the chapter headed 'Discussions' and hyperlinked to the article.