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10.1016/j.intimp.2013.12.012

http://scihub22266oqcxt.onion/10.1016/j.intimp.2013.12.012
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24374021!ä!24374021

suck abstract from ncbi


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pmid24374021      Int+Immunopharmacol 2014 ; 18 (2): 373-8
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  • Effects of P-MAPA immunomodulator on Toll-like receptor 2, ROS, nitric oxide, MAPKp38 and IKK in PBMC and macrophages from dogs with visceral leishmaniasis #MMPMID24374021
  • Melo LM; Perosso J; Almeida BF; Silva KL; Somenzari MA; de Lima VM
  • Int Immunopharmacol 2014[Feb]; 18 (2): 373-8 PMID24374021show ga
  • Leishmania (L.) chagasi is the etiologic agent of visceral leishmaniasis (VL) that can be transmitted to humans and dogs. VL in Brazil represents a serious public health problem; therefore, it is important to study new alternatives to treat infected dogs. In dogs, the therapeutic arsenal against canine VL is limited. The immunomodulator protein aggregate magnesium-ammonium phospholinoleate-palmitoleate anhydride (P-MAPA) improves immunocompetence when the immune system is impaired, but its dependence on Toll-like receptors (TLRs) and the mechanisms involved in immune response remain unclear. The in vitro action of P-MAPA on the expression of TLR2 and TLR4, reactive oxygen species (ROS), nitric oxide (NO) and p38 mitogen-activated protein kinase (p38 MAPK) and IKK phosphorylation was studied in mononuclear cells from peripheral blood and macrophages from healthy and Leishmania-infected dogs. The PBMC or macrophages were isolated and cultured with different concentrations of P-MAPA (20,100 and 200 mug/ml) in a humid environment at 37 degrees C with 5% CO(2). Observation revealed that Leishmania-infected dogs showed a decrease in TLR2 in macrophages compared with healthy dogs and in induction with P-MAPA. ROS were increased in PBMCs from Leishmania spp.-infected dogs compared with healthy dogs and P-MAPA improved ROS production. NO production was increased in culture supernatant from macrophages stimulated by P-MAPA in both healthy and Leishmania spp. infected dogs. Treatment of macrophages from healthy dogs with immunomodulatory P-MAPA induced p38 MAPK and IKK phosphorylation, suggesting signal transduction by this pathway. These findings suggest that P-MAPA has potential as a therapeutic drug in the treatment of canine visceral leishmaniasis.
  • |Animals[MESH]
  • |Dog Diseases/*immunology[MESH]
  • |Dogs[MESH]
  • |Female[MESH]
  • |Immunologic Factors/*pharmacology[MESH]
  • |Kruppel-Like Transcription Factors/immunology[MESH]
  • |Leishmaniasis, Visceral/*immunology/veterinary[MESH]
  • |Leukocytes, Mononuclear/*drug effects/immunology[MESH]
  • |Macrophages/*drug effects/immunology[MESH]
  • |Male[MESH]
  • |Nitric Oxide/immunology[MESH]
  • |Reactive Oxygen Species/immunology[MESH]
  • |Toll-Like Receptor 2/immunology[MESH]


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