Stimulatory action of cyclooxygenase inhibitors on hematopoiesis: a review
Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články, práce podpořená grantem, přehledy
PubMed
22576231
PubMed Central
PMC6268959
DOI
10.3390/molecules17055615
PII: molecules17055615
Knihovny.cz E-zdroje
- MeSH
- antiflogistika nesteroidní terapeutické užití MeSH
- cyklooxygenasa 2 metabolismus MeSH
- dinoproston metabolismus MeSH
- faktor stimulující kolonie granulocytů biosyntéza krev MeSH
- hematopoéza účinky léků účinky záření MeSH
- inhibitory cyklooxygenasy 2 terapeutické užití MeSH
- lidé MeSH
- meloxikam MeSH
- myelopoéza účinky léků účinky záření MeSH
- myši MeSH
- thiaziny terapeutické užití MeSH
- thiazoly terapeutické užití MeSH
- záření gama MeSH
- zpětná vazba fyziologická účinky léků účinky záření MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- přehledy MeSH
- Názvy látek
- antiflogistika nesteroidní MeSH
- cyklooxygenasa 2 MeSH
- dinoproston MeSH
- faktor stimulující kolonie granulocytů MeSH
- inhibitory cyklooxygenasy 2 MeSH
- meloxikam MeSH
- thiaziny MeSH
- thiazoly MeSH
The presented review summarizes experimental data obtained with a mouse model when investigating the relationship between inhibition of prostaglandin production and hematopoiesis. While prostaglandin E2 acts in a negative feedback control of myelopoiesis, inhibition of cyclooxygenases, responsible for its production, shifts the feedback to positive control. Based on these relationships, agents inhibiting cyclo-oxygenases, known as non-steroidal anti-inflammatory drugs (NSAIDs), can activate hematopoiesis and be protective or curative under myelosuppressive states. The effectiveness of therapeutic use of NSAIDs in these situations is expressive especially under the selective inhibition of cyclooxygenase-2 (COX-2), when undesirable side effects of cyclooxygenase-1 inhibition, like gastrointestinal damage, are absent. The effects of the clinically approved selective COX-2 inhibitor, meloxicam, were investigated and demonstrated significant hematopoiesis-stimulating and survival-enhancing actions of this drug in sublethally or lethally γ-irradiated mice. These effects were connected with the ability of meloxicam to increase serum levels of the granulocyte colony-stimulating factor. It can be inferred from these findings that selective COX-2 inhibitors might find their use in the treatment of myelosuppressions of various etiologies.
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