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1.
J Dairy Sci ; 96(1): 89-95, 2013 Jan.
Article in English | MEDLINE | ID: mdl-23164226

ABSTRACT

Based on animal studies, intake of probiotic bacteria was suggested to improve insulin sensitivity by reducing endotoxinemia and inflammation. The objective of this study was to determine the effects of supplementation with the probiotic strain Lactobacillus casei Shirota (LcS) over 12 wk on insulin sensitivity, ß-cell function, inflammation, and endothelial dysfunction parameters in subjects with metabolic syndrome. In a randomized-controlled study, 30 subjects with metabolic syndrome either received Lactobacillus casei Shirota 3 times daily for 12 wk or served as controls with standard medical therapy. Fasting blood samples were taken and a 75-g oral glucose tolerance test was performed to derive indices for insulin sensitivity and ß-cell function. In addition, parameters to assess endothelial function and inflammation markers were determined. Even though the insulin sensitivity index significantly improved after 3 mo of probiotic supplementation (0.058±0.021 vs. 0.038±0.025), the change was not significantly different compared with the control group. No improvements were seen in additional indices of insulin sensitivity (quantitative insulin sensitivity check index, insulin sensitivity by oral glucose tolerance test, and homeostasis model assessment for insulin resistance) and ß-cell function (first and second phase insulin secretion, and homeostasis model assessment for ß-cell function). Probiotic supplementation resulted in a significant reduction in soluble vascular cell adhesion molecule-1 (sVCAM-1) level (1,614±343 vs. 1,418±265 ng/mL). No significant changes in parameters used to assess low-grade inflammation or endothelial dysfunction were observed. Intake of LcS for 12 wk in subjects with metabolic syndrome did not improve insulin sensitivity, ß-cell function, endothelial function, or inflammation markers in this trial.


Subject(s)
Endothelium, Vascular/drug effects , Inflammation/drug therapy , Insulin Resistance , Insulin-Secreting Cells/drug effects , Lacticaseibacillus casei/metabolism , Metabolic Syndrome/drug therapy , Probiotics/pharmacology , Dietary Supplements , Endothelium, Vascular/physiology , Glucose Tolerance Test , Humans , Insulin Resistance/physiology , Insulin-Secreting Cells/physiology , Male , Middle Aged , Pilot Projects
2.
Eur J Clin Nutr ; 66(10): 1110-5, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22872030

ABSTRACT

BACKGROUND/OBJECTIVES: Obesity and metabolic disorders are linked to inflammation via gut microbiota and/or gut permeability. Gut-derived endotoxin triggers inflammation leading to metabolic syndrome (MetS) and contributing to oxidative stress. We intended to investigate the effect of Lactobacillus casei Shirota on gut permeability, presence of endotoxin and neutrophil function in MetS. SUBJECTS/METHODS: Patients with MetS were randomized to receive 3 × 6.5 × 109 CFU L. casei Shirota (probiotic group) or not for 3 months. Gut permeability was assessed by a differential sugar absorption method and by determination of diaminooxidase serum levels, endotoxin by an adapted limulus amoebocyte lysate assay, neutrophil function and toll-like receptor (TLR) expression by flow cytometry and ELISA was used to detect lipopolysaccharide-binding protein (LBP) and soluble CD14 (sCD14) levels. RESULTS: Twenty-eight patients and 10 healthy controls were included. Gut permeability was significantly increased in MetS compared with controls but did not differ between patient groups. None of the patients were positive for endotoxin. LBP and sCD14 levels were not significantly different from healthy controls. High-sensitive C-reactive protein and LBP levels slightly but significantly increased after 3 months within the probiotics group. Neutrophil function and TLR expression did not differ from healthy controls or within the patient groups. CONCLUSIONS: Gut permeability of MetS patients was increased significantly compared with healthy controls. L. casei Shirota administration in the MetS patients did not have any influence on any parameter tested possibly due to too-short study duration or underdosing of L. casei Shirota.


Subject(s)
Intestinal Mucosa/metabolism , Intestinal Mucosa/microbiology , Metabolic Syndrome/diet therapy , Metabolic Syndrome/metabolism , Probiotics/therapeutic use , Acute-Phase Proteins , Adult , Aged , Amine Oxidase (Copper-Containing)/blood , C-Reactive Protein/analysis , Carrier Proteins/blood , Cohort Studies , Endotoxins/blood , Female , Humans , Intestinal Mucosa/immunology , Lacticaseibacillus casei/growth & development , Lacticaseibacillus casei/immunology , Lacticaseibacillus casei/metabolism , Lipopolysaccharide Receptors/blood , Male , Membrane Glycoproteins/blood , Metabolic Syndrome/immunology , Metabolic Syndrome/microbiology , Middle Aged , Neutrophils/immunology , Neutrophils/metabolism , Permeability , Pilot Projects , Solubility , Young Adult
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