Microcytic anemia and changes in ferrokinetics as late after-effects of glucan administration in murine hepatitis virus-infected C57BL/10ScSnPh mice
Jazyk angličtina Země Anglie, Velká Británie Médium print
Typ dokumentu časopisecké články
PubMed
8150555
DOI
10.1016/0192-0561(94)90118-x
PII: 0192-0561(94)90118-X
Knihovny.cz E-zdroje
- MeSH
- adjuvancia imunologická toxicita MeSH
- anemie etiologie imunologie metabolismus MeSH
- glukany toxicita MeSH
- hem metabolismus MeSH
- hematopoéza MeSH
- kinetika MeSH
- koronavirové infekce komplikace imunologie metabolismus MeSH
- myši inbrední C57BL MeSH
- myši MeSH
- virová hepatitida u zvířat komplikace imunologie metabolismus MeSH
- virus myší hepatitidy MeSH
- železo metabolismus MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- adjuvancia imunologická MeSH
- glukany MeSH
- hem MeSH
- železo MeSH
Mild microcytic anemia (without changes in mean corpuscular hemoglobin concentration, MCHC) was discovered 6-14 weeks after a single s.c. administration of 4 mg of particulate glucan to C57BL/10ScSnPh mice serologically positive for murine hepatitis (MHV). The anemia was associated with granulocytosis, decreased body weight and spleen hypertrophy. The overall intensity of erythropoiesis was measured by 59Fe-incorporation into the heme of erythropoietic organs. The localization of erythropoiesis became markedly redistributed--heme production was suppressed in the bone marrow while a several-fold increase was recorded for the spleen. A new steady state was also discovered in ferrokinetics: an iron pool localized away from the blood, erythropoietic organs and the liver was significantly elevated, and hypoferremia was detected. Anemia and wasting of mice were not observed in the same mouse strain free of MHV. A single administration of particulate glucan resulted in late impairment of red blood cell formation in the C57BL/10ScSnPh mouse strain infected with the mouse hepatitis virus. The anemia shares a number of features with those observed for the anemia of chronic diseases.
Citace poskytuje Crossref.org
Modulation of animal and human hematopoiesis by β-glucans: a review