Stimulation of haemopoiesis and protection of mice against radiation injury by synthetic analogues of muramyldipeptide incorporated in liposomes
Jazyk angličtina Země Velká Británie, Anglie Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
9637362
DOI
10.1016/s0192-0561(98)00003-4
PII: S0192-0561(98)00003-4
Knihovny.cz E-zdroje
- MeSH
- acetylmuramyl-alanyl-isoglutamin aplikace a dávkování analogy a deriváty farmakologie MeSH
- adjuvancia imunologická aplikace a dávkování farmakologie MeSH
- analýza kolonii tvořících jednotek MeSH
- experimentální radiační poranění prevence a kontrola MeSH
- glykopeptidy aplikace a dávkování farmakologie MeSH
- hematopoéza účinky léků účinky záření MeSH
- liposomy MeSH
- myši inbrední C57BL MeSH
- myši inbrední CBA MeSH
- myši MeSH
- radioprotektivní látky aplikace a dávkování farmakologie MeSH
- záření gama MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- acetylmuramyl-alanyl-isoglutamin MeSH
- adjuvancia imunologická MeSH
- Glc-(1-4)-norMurNAc-Abu-isoGln MeSH Prohlížeč
- GlcNstearoyl-(1-4)-norMurNAc-Abu-isoGln MeSH Prohlížeč
- glykopeptidy MeSH
- liposomy MeSH
- radioprotektivní látky MeSH
Protection from undesirable effects of radiotherapy or chemotherapy, primarily from myelosuppression, remains still a crucial problem to be studied. Attention has been therefore paid to various immunomodulatory agents that through the monocyte/macrophage system induced production of cytokines, which can induce and operate restoration of haemopoiesis and thus act radioprotectively. Some synthetic analogues of MDP free of undesirable side-effects, were synthesized in the Czech Republic. Lipophilic beta-D-GlcNstearoyl-(1- > 4)-norMurNAc-L-Abu-D-isoGln (DDD-St) was designed to be easily entrapped into liposomes and this liposomal DDD-St protected efficiently mice against irradiation, when administered i.p., i.v. or s.c. 24 h prior to lethal irradiation (survival rate in the range of 30-80% compared with 0% in control). Especially the subcutaneous application of liposomal DDD-St was very efficient. The parameters characteristic of recovery of haemopoiesis in bone marrow on day 10 after 6.5 Gy irradiation were significantly improved in comparison with the controls. Very high radioprotective effect of s.c. administered liposomal DDD-St can be explained (together with induction of haemopoiesis) by an effective and long-lasting activation of nonspecific immunity, which is able to withhold an onset of septicemia in early days after irradiation. In conclusion, the liposomal DDD-St should be therapeutically beneficial in moderating the haemopoietic damage, which is an undesirable effect of radiotherapy or chemotherapy.
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