Unbound MEDLINE

Effect of mineral trioxide aggregate on cytokine production by peritoneal macrophages. International endodontic journal. [Int Endod J] Journal article

 
TitleEffect of mineral trioxide aggregate on cytokine production by peritoneal macrophages.
Author(s)Rezende TM, Vargas DL, Cardoso FP, Sobrinho AP, Vieira LQ 
InstitutionDepartamento de Dentística Restauradora, Faculdade de Odontologia, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
SourceInt Endod J 2005 Dec; 38(12):896-903.
MeSHAluminum Compounds
Animals
Calcium Compounds
Cell Survival
Cells, Cultured
Drug Combinations
Female
Fusobacterium nucleatum
Interferon Type II
Interleukin-10
Interleukin-12
Macrophages, Peritoneal
Male
Mice
Mice, Inbred C57BL
Mice, Inbred Strains
Oxides
Peptostreptococcus
Protein Subunits
Research Support, Non-U.S. Gov't
Root Canal Filling Materials
Silicates
Tumor Necrosis Factor-alpha
AbstractAIM: To test the effect of two commercial brands of grey mineral trioxide aggregate (ProRoot and MTA-Angelus) on cytokine production by M1 and M2 inflammatory macrophages.
METHODOLOGY: M1 (from C57BL/6 mice) and M2 peritoneal inflammatory macrophages (from C57BL/6 IL12p40-/- mice) were obtained and cultured in vitro in the presence of MTA. The cellular viability and the production of tumour necrosis factor-alpha, interleukin (IL)-12 and IL-10 in response to stimulation with interferon-gamma and Fusobacterium nucleatum or Peptostreptococcus anaerobius were evaluated. Data were analysed by Mann-Whitney, Kruskal-Wallis and anova tests.
RESULTS: The cements did not interfere with cellular viability or with cytokine production by either type of macrophage. However, M2 macrophages produced higher levels of IL-10 when stimulated with F. nucleatum than M1 macrophages (P < 0.05).
CONCLUSIONS: The brands of MTA evaluated did not interfere in the cytokine response by M1 or M2 macrophages to the two bacteria tested. However, a difference in cytokine production between the two types of macrophages was found.
Languageeng
Pub Type(s)Journal Article
PubMed ID16343117
  
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