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1.
Protein Pept Lett ; 28(10): 1164-1179, 2021.
Article in English | MEDLINE | ID: mdl-34315363

ABSTRACT

BACKGROUND: It is well known that alcohol can trigger inflammatory effects in the gastrointestinal tract (GIT), interfering with mucosal homeostasis. OBJECTIVES: This study evaluated the effectiveness of Lactococcus lactis treatment in controlling the increase in molecular biomarkers related to allergic inflammation and the effect on the diversity and abundance of the Enterobacteriaceae family in the GIT after high-dose acute administration of ethanol. METHODS: Mice received ethanol or saline solution by gavage for four consecutive days, and 24 h after the last administration, the animals were given L. lactis or M17 broth orally ad libitum for two consecutive days. The animals were subsequently sacrificed and dissected. RESULTS: L. lactis treatment was able to restore basal levels of secretory immunoglobulin A in the gastric mucosa, serum total immunoglobulin E, interleukin (IL)-4 production in gastric and intestinal tissues, and IL-10 levels in gastric tissue. L. lactis treatment encouraged the diversification of the Enterobacteriaceae population, particularly the commensal species, in the GIT. CONCLUSION: This research opens a field of studies regarding the modulatory effect of L. lactis on immunological and microbial changes induced after alcohol intake.


Subject(s)
Enterobacteriaceae/metabolism , Ethanol/metabolism , Immunoglobulin E/metabolism , Interleukin-4/metabolism , Lactococcus lactis/metabolism , Administration, Oral , Alcohol Drinking , Animals , Cytokines/metabolism , Ethanol/administration & dosage , Female , Gastrointestinal Tract , Humans , Immunoglobulin A/metabolism , Immunoglobulin E/blood , Inflammation/metabolism , Interleukin-4/blood , Intestinal Mucosa/metabolism , Mice , Mice, Inbred C57BL
2.
Protein Pept Lett ; 28(7): 761-768, 2021.
Article in English | MEDLINE | ID: mdl-33302826

ABSTRACT

BACKGROUND: The microbiome is now known for its important role in whole-body homeostasis. A dysbiosis of the normal microbiota is correlated with metabolic disorders. In this sense, the search for compounds able to modulate the microbiome is needed. Resveratrol, a natural compound found in grapes seems to be a promising candidate. OBJECTIVE: In this study, our motivation was to evaluate the effects of the association between Resveratrol and Lactococcus lactis, a probiotic, on the composition of the gastrointestinal microbiota and body weight of mice. METHODS: Twenty female mice were divided into 4 groups: (1) standard diet, (2) standard diet plus Lactococcus lactis, (3) standard diet plus resveratrol, and (4) standard diet plus Lactococcus lactis and resveratrol. At the end of the treatment period, samples of blood, mucus, stomach, and small and large intestines were collected for analysis. Total levels of Immunoglobulin A and Immunoglobulin E, Lac+ and Lac- bacteria and Lactobacillus were measured. RESULTS: The main results indicate that the association between resveratrol and probiotics was able to decrease mice body weight, as compared to the other groups, in addition to decrease the number of Lac- bacteria and increasing the number of Lac+ bacteria. The levels of secretory IgA were also decreased, compared to the animals treated with only probiotics or resveratrol. CONCLUSION: We observed potential synergism between Resveratrol and Lactococcus lactis mainly in modulating the stomach and intestinal microbiota.


Subject(s)
Body Weight/drug effects , Enterobacteriaceae/drug effects , Gastrointestinal Microbiome/drug effects , Lactococcus lactis/immunology , Probiotics/administration & dosage , Resveratrol/administration & dosage , Animals , Body Weight/immunology , Diet/methods , Enterobacteriaceae/growth & development , Enterobacteriaceae/immunology , Female , Gastrointestinal Microbiome/immunology , Immunoglobulin A/biosynthesis , Immunoglobulin E/blood , Intestine, Large/drug effects , Intestine, Large/immunology , Intestine, Large/microbiology , Intestine, Small/drug effects , Intestine, Small/immunology , Intestine, Small/microbiology , Mice , Mice, Inbred C57BL , Stomach/drug effects , Stomach/immunology , Stomach/microbiology
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