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1.
Sci Rep ; 12(1): 452, 2022 01 10.
Artículo en Inglés | MEDLINE | ID: mdl-35013585

RESUMEN

Macrophages are a heterogeneous population of mononuclear phagocytes abundantly distributed throughout the intestinal compartments that adapt to microenvironmental specific cues. In adult mice, the majority of intestinal macrophages exhibit a mature phenotype and are derived from blood monocytes. In the steady-state, replenishment of these cells is reduced in the absence of the chemokine receptor CCR2. Within the intestine of mice with colitis, there is a marked increase in the accumulation of immature macrophages that demonstrate an inflammatory phenotype. Here, we asked whether CCR2 is necessary for the development of colitis in mice lacking the receptor for IL10. We compared the development of intestinal inflammation in mice lacking IL10RA or both IL10RA and CCR2. The absence of CCR2 interfered with the accumulation of immature macrophages in IL10R-deficient mice, including a novel population of rounded submucosal Iba1+ cells, and reduced the severity of colitis in these mice. In contrast, the absence of CCR2 did not reduce the augmented inflammatory gene expression observed in mature intestinal macrophages isolated from mice lacking IL10RA. These data suggest that both newly recruited CCR2-dependent immature macrophages and CCR2-independent residual mature macrophages contribute to the development of intestinal inflammation observed in IL10R-deficient mice.


Asunto(s)
Colitis/inmunología , Subunidad alfa del Receptor de Interleucina-10/inmunología , Intestinos/inmunología , Monocitos/inmunología , Receptores CCR2/inmunología , Animales , Colitis/genética , Femenino , Humanos , Subunidad alfa del Receptor de Interleucina-10/genética , Macrófagos/inmunología , Masculino , Ratones , Ratones Noqueados , Receptores CCR2/genética
2.
Comp Immunol Microbiol Infect Dis ; 66: 101334, 2019 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-31437688

RESUMEN

Administration of antibiotics as feed additives in broilers resulted in prompting of some undesirable effects such as the rising emergence of multi-drug resistant (MDR) bacteria, so scrutinizing for new alternatives like herbs is the up to date task for global health. This study was designed to determine the in-vitro antibacterial and ex-vivo immunomodulatory efficacy of garlic (Allium sativum) and ginger (Zingiber officinale) extracts post dietary supplementation for 900-one-day-old Sasso broiler chicks. The in-vivo protective actions of these extracts against avian pathogenic MDR Escherichia coli (E. coli) O78 challenge was evaluated after 21 days of extracts supplementation. Garlic extract exhibited broader antimicrobial spectra against MDR E. coli O78 and S. aureus isolates. Through the 21 days of garlic or ginger dietary supplementation, the chicks' innate immune response was modulated via various mechanisms including phagocytosis augmentation, bactericidal activity enhancement and nitric oxide (NO) production reduction, together with triggering the IL-1ß, IL-6 and IFN-γ cytokines expression levels in comparison with the non-supplemented chicks. It is tempting to speculate that protection against pathogenic E. coli O78 challenge was high in chicks supplemented with each individual extract with severe reduction in the bacterial colony forming units in chicks' vital organs that confirm the extracts immunomodulatory activity and provide a mechanism(s) of their protective actions. Our data suggest promising useful insights to garlic and ginger dietary supplementation in broilers that may be safe for consumers from antibiotic toxic metabolites' residues and protective against the risk of infection with bacterial pathogens.


Asunto(s)
Infecciones por Escherichia coli/veterinaria , Escherichia coli/efectos de los fármacos , Ajo/química , Inmunidad Innata , Extractos Vegetales/farmacología , Zingiber officinale/química , Animales , Pollos/inmunología , Citocinas/inmunología , Suplementos Dietéticos , Farmacorresistencia Bacteriana Múltiple , Infecciones por Escherichia coli/prevención & control , Inmunomodulación
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