Adamdec1, Ednrb and Ptgs1/Cox1, inflammation genes upregulated in the intestinal mucosa of obese rats, are downregulated by three probiotic strains
Metadatos
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Plaza Díaz, Julio; Robles-Sánchez, Candido; Abadía Molina, Francisco; Morón Calvente, Virginia; Sáez Lara, María José; Ruiz-Bravo López, Alfonso; Jiménez Valera, María Manuela; Gil Hernández, Ángel; Gómez Llorente, Carolina; Fontana Gallego, LuisEditorial
Springer Nature
Fecha
2017-05-16Referencia bibliográfica
Plaza-Díaz, J., Robles-Sánchez, C., Abadía-Molina, F. et al. Adamdec1, Ednrb and Ptgs1/Cox1, inflammation genes upregulated in the intestinal mucosa of obese rats, are downregulated by three probiotic strains. Sci Rep 7, 1939 (2017). https://doi.org/10.1038/s41598-017-02203-3
Patrocinador
Company Hero Spain, S. A. (grant #3545 managed by Fundación General Empresa-Universidad de Granada); CEIBiotic, University of Granada, Spain (grant CEI2013P-11)Resumen
We have previously reported that administration of Lactobacillus paracasei CNCM I-4034,
Bifidobacterium breve CNCM I-4035 and Lactobacillus rhamnosus CNCM I-4036 to obese Zucker-Leprfa/fa
rats attenuates liver steatosis and exerts anti-inflammatory effects. The goal of the present work
was to investigate the modulation of gene expression in intestinal mucosa samples of obese Zucker-
Leprfa/fa rats fed the probiotic strains using a DNA microarray and postgenomic techniques. We also
measured secretory IgA content in the gut and lipopolysaccharide (LPS)-binding protein (LBP) in serum.
Expression of three genes (Adamdec1, Ednrb and Ptgs1/Cox1) was up-regulated in the intestinal mucosa
of the obese rats compared with that in the rats when they were still lean. Probiotic administration
down-regulated expression of Adamdec1 and Ednrb at the mRNA and protein levels and that of
Ptgs1/Cox1 at the mRNA level, and this effect was in part mediated by a decrease in both macrophage
and dendritic cell populations. Probiotic treatment also increased secretory IgA content and diminished
the LBP concentration. Based on results reported in this work and else where, we propose a possible
mechanism of action for these bacterial strains.