Influence of the joint treatment with granulocyte colony-stimulating factor and drugs elevating extracellular adenosine on erythropoietic recovery following 5-fluorouracil-induced haematotoxicity in mice
Jazyk angličtina Země Velká Británie, Anglie Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
- MeSH
- adenosin metabolismus farmakologie MeSH
- adenosinmonofosfát farmakologie terapeutické užití MeSH
- antimetabolity toxicita MeSH
- časové faktory MeSH
- dipyridamol farmakologie terapeutické užití MeSH
- erytrocyty cytologie účinky léků MeSH
- erytroidní prekurzorové buňky cytologie účinky léků MeSH
- erytropoéza účinky léků MeSH
- faktor stimulující kolonie granulocytů farmakologie terapeutické užití MeSH
- fluoruracil toxicita MeSH
- hemoglobiny účinky léků metabolismus MeSH
- inhibitory fosfodiesteras farmakologie terapeutické užití MeSH
- kombinovaná farmakoterapie MeSH
- myši inbrední C57BL MeSH
- myši inbrední CBA MeSH
- myši MeSH
- počet erytrocytů MeSH
- retikulocyty cytologie účinky léků MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- adenosin MeSH
- adenosinmonofosfát MeSH
- antimetabolity MeSH
- dipyridamol MeSH
- faktor stimulující kolonie granulocytů MeSH
- fluoruracil MeSH
- hemoglobiny MeSH
- inhibitory fosfodiesteras MeSH
The presented data address the problem of pleiotropic effects of granulocyte colony-stimulating factor (G-CSF) and suggest the ability of drugs increasing the level of extracellular adenosine to activate erythropoiesis when given jointly with G-CSF. To demonstrate these interactions, the effects of the drugs on the recovery from erythropoietic damage induced in mice by a single dose of 5-fluorouracil (5-FU) were investigated. Elevation of extracellular adenosine and thus activation of adenosine receptors was induced by joint administration of dipyridamole (DP), a drug inhibiting the cellular uptake of adenosine, and adenosine monophosphate (AMP), an adenosine prodrug. The drugs were injected in a 4-d treatment regimen starting 2 h after 5-FU injection. Both DP+AMP and G-CSF alone induced only weak effects. However, the combination of the three drugs produced significant elevation of erythrocytes in the peripheral blood which pertained in the posttreatment period. Stimulation of proliferation of erythroid progenitor cells (BFU-E) in femoral bone marrow and increased levels of reticulocytes in the peripheral blood were observed in the course of the 4-d treatment regimen. In addition, significantly decreased mean cell haemoglobin accompanying the elevated numbers of erythrocytes in the combination-treated mice was found. This effect could be interpreted as the result of a sublethal 5-FU-induced damage to erythroid progenitor and precursor cells forced to proliferate intensively by the combination therapy. The observed additivity and synergism of G-CSF with elevated extracellular adenosine in terms of erythropoiesis is an interesting finding with potential implications in clinical practice.
Citace poskytuje Crossref.org
Lack of adenosine A3 receptors causes defects in mouse peripheral blood parameters
The role of adenosine receptor agonists in regulation of hematopoiesis