Pterins as sensors of response to the application of Fe3+ -dextran in piglets
Jazyk angličtina Země Švýcarsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
22315574
PubMed Central
PMC3270875
DOI
10.3390/s100100890
PII: s100100890
Knihovny.cz E-zdroje
- Klíčová slova
- biopterin, cortisol, iron, leukogram, neopterin,
- MeSH
- biologické markery krev MeSH
- fyziologický stres účinky léků imunologie MeSH
- hydrokortison krev MeSH
- prasata MeSH
- přirozená imunita účinky léků imunologie MeSH
- pteriny krev imunologie MeSH
- železo farmakologie MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- biologické markery MeSH
- hydrokortison MeSH
- pteriny MeSH
- železo MeSH
The aim of the presented study was to assess the effect of a single administration of Fe(3+)-dextran on immune cell counts and pterin biomolecule production as novel sensors of the piglets' immune system activation, and to determine concentrations of cortisol, a traditional hormonal biosensor of the stress response. Pterins (neopterin and biopterin) in the piglets' blood serum were analyzed by separation using reversed-phase HPLC. A single dose of Fe(3+)-dextran produced a special stress situation in the piglets' organism which manifested itself by an increased production of neopterin (p < 0.05) and biopterin (p < 0.01) in the experimental piglets. Changes in cortisol concentrations and leukocyte counts were influenced by handling stress and were not specifically correlated to iron dextran application. Iron concentrations in the internal environment of the experimental piglets' group were higher by an order of magnitude compared with the controls, and the highest serum concentrations of iron (p < 0.01) were reached 24 h following Fe(3+)-dextran administration. The data presented offer a new perspective on the evaluation of stress situations in the animal organism and, not least importantly, extends the rather modest current list of references on the role of pterins in livestock animals.
Zobrazit více v PubMed
Berdovska A., Zwirska-Korczala K. Neopterin measurement in clinical diagnosis. J. Clin. Pharm. Ther. 2001;26:319–329. PubMed
Brown G.M. The biosynthesis of pteridines. Adv. Enzymol. 1971;35:5–77. PubMed
Zimmerman A.W., Jyonouchi H., Comi A.M., Connors S.L., Milstien S., Varsou A. Cerebrospinal fluid and serum markers of inflammation in autism. Pediatr. Neurol. 2005;33:195–201. PubMed
Ziegler I., Fink M., Wilmanns W. Biopterin level in peripheral blood cells as marker for hemopoietic cell proliferation during leukemia and polycythemia vera. Blut. 1982;44:231–240. PubMed
Hashimoto R., Nagatsu T., Ohta T., Mizutani M., Omura I. Changes in the concentrations of tetrahydrobiopterin, the cofactor of tyrosine hydroxylase, in blood under physical stress and depression. Ann. N.Y. Acad. Sci. 2004;1018:378–386. PubMed
Murr C., Fuith L.C., Winder B., Wirleitner B., Baier-Bitterlich G., Fuchs D. Increased neopterin concentrations in patients with cancer: indicator of oxidative stress? Anticancer Res. 1999;19:1721–1728. PubMed
Forrest C.M., Youd P., Kennedy A., Gould S.R., Darlington L.G., Stone T.W. Purine, kynurenine, neopterin and lipid peroxidation levels in inflammatory bowel disease. J. Biomed. Sci. 2002;9:436–442. PubMed
Murr C., Winder B., Wirleitner B., Fuchs D. Neopterin as a marker for immune system activation. Curr. Drug Metab. 2002;3:175–187. PubMed
Fuchs D., Wachter H. International Clinical Laboratory Diagnostics. 1st ed. TH Books Verlagsgesellschaft mbH; Frankfurt, Germany: 1998. Neopterin.
Jerin A., Pozar-Lukanovic N., Sojar V., Stanisavljevic D., Pavern-Erzen V., Osredkar J. Neopterin: an early marker of surgical stress and hypoxic reperfusion damage during liver surgery. Clin. Chem. Lab. Med. 2002;40:663–666. PubMed
Svoboda M. Metabolické poruchy u prasat (Metabolic disorders in pigs) Farmář. 2004;12:35–36.
Guo D., Jaber B.L., Lee S., Perianaygam M.C., King A.J., Periba B.J.G., Balakrishnan V.S. Impact of iron dextran on polymorphonuclear cell function among hemodialysis patients. Clin. Nephrol. 2002;58:134–142. PubMed
Brohee D., Vanhaeverbeek M., Kennes B., Neve P. Leukocyte and lymphocyte subsets after a short pharmacological stress by intravenous epinephrine and hydrocortisone in healthy humans. Int. J. Neurosci. 1990;53:53–62. PubMed
Brock J.H. Iron and immunity. J. Nutr. Immunol. 1993;2:47–106.
Toman M. ‘Veterinární Imunologie (Veterinary Immunology) 1st ed. Grada Publishing; Prague, Czech Republic: 2000. p. 350.
Walker E.M., Jr., Walker S.M. Effects of iron overload on the immune system. Ann. Clin. Lab. Sci. 2000;30:354–365. PubMed
Cardier J.E., Romano E., Soyano A. T lymphocytes subsets in experimental iron overload. Immunopharmacol. Immunotoxicol. 1997;19:75–87. PubMed
Spear A.T., Sherman A.B. Iron deficiency alters DMBA-induced tumor burden and natural killer cell cytotoxicity rats. J. Nutr. 1992;122:46–55. PubMed
Kuvibidila S.R., Kitchens D., Baliga B.S. In vivo and in vitro iron deficiency reduces protein kinase C activity and translocation in murine splenic and purified T cells. J. Cell. Biochem. 1999;74:468–478. PubMed
Werner-Felmayer G., Golderer G., Werner E.R. Tetrahydrobiopterin biosynthesis, utilization and pharmacological effects. Curr. Drug Metab. 2002;3:159–173. PubMed
Razumovitch J.A., Semenkova G.N., Fuchs D., Cherenkevich S.N. Influence of neopterin on the generation of reactive oxygen species in human neutrophils. FEBS Lett. 2003;549:83–86. PubMed
Baier-Bitterlich G., Fuchs D., Murr C.H., Reibnegger G., Werner-Felmayer G., Sgonc R., Bőck G., Dierich M.P., Wachter H. Effect of neopterin and 7,8-dihydroneopterin on tumor necrosis factor-α induced programmed cell death. FEBS Lett. 1995;364:234–238. PubMed
Oettl K., Wirleitner B., Baier-Bitterlich G., Grammer T., Fuchs D., Reibnegger G. Formation of oxygen radicals in solutions of 7,8-dihydroneopterin. Biochem. Biophys. Res. Commun. 1999;264:262–267. PubMed
Schrodl W., Kunze R., Kruger M. Determination of C-reactive protein and neopterin in serum diseased and bacterially infected swine. Berl. Műnch. Tierärzth. Wschr. 1998;111:321–325. PubMed
Amann A., Winder B., Rieder J., Antretter H., Hoffmann G., Mayr V., Strohmenger H.U., Fuchs D. Monitoring of immune activation using biochemical changes in a porcine model of cardiac arrest. Mediat. Inflamm. 2001;10:343–346. PubMed PMC
Fujioka H., Shintaku H., Nakanishi H., Kim T.J., Kusuda S., Yamano T. Biopterin in the acute phase of hypoxia-ischemia in a neonatal pig model. Brain Develop. 2008;30:1–6. PubMed
Carru C., Zinellu A., Sotgia S., Serra R., Usai M.F., Pintus G.F., Pes G.M., Deiana L. A new HPLC methods for serum neopterin measurement and relationship with plasma thiols in healthy subjects. Biomed. Chromatogr. 2004;18:360–366. PubMed