Enhancement of hematopoietic recovery in gamma-irradiated mice by the joint use of diclofenac, an inhibitor of prostaglandin production, and glucan, a macrophage activator
Language English Country Netherlands Media print
Document type Journal Article
PubMed
1628707
Knihovny.cz E-resources
- MeSH
- Macrophage Activation drug effects MeSH
- Cell Division drug effects MeSH
- Bone Marrow Cells MeSH
- Whole-Body Irradiation * MeSH
- Diclofenac pharmacology MeSH
- Glucans pharmacology MeSH
- Hematopoiesis radiation effects MeSH
- Drug Therapy, Combination MeSH
- Bone Marrow radiation effects MeSH
- Mice MeSH
- Premedication MeSH
- Radiation-Protective Agents pharmacology MeSH
- Spleen cytology radiation effects MeSH
- Drug Synergism MeSH
- Gamma Rays MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Diclofenac MeSH
- Glucans MeSH
- Radiation-Protective Agents MeSH
The effects of diclofenac (inhibitor of prostaglandin production) and carboxymethylglucan (immunomodulator and an agent stimulating hematopoiesis), when given to mice 1 day before gamma-irradiation, were studied. Both of the agents were administered either alone or in combination. The investigations included the assessment of post-irradiation hematopoietic recovery in terms of bone marrow and spleen cellularity and endogenous spleen colony formation, as well as the determination of the survival of lethally irradiated mice. The results demonstrated at least additive radioprotective effects when mice were given diclofenac and carboxymethylglucan in combination. Experimental evidence provided by the increased 125iodo-deoxyuridine incorporation into the spleen and elevated hydroxyurea kill of endogenous spleen colony-forming units indicated that the beneficial action of the combined treatment could be a consequence of increased cell proliferation in the hematopoietic tissue. It is likely that the inhibition of prostaglandin production (diclofenac action) and the concomitant increased release of growth factors (glucan action) shift the regulatory balance towards the predominance of positive hematopoietic control.
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