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Benef Microbes ; 11(4): 361-373, 2020 Aug 12.
Article in English | MEDLINE | ID: mdl-32755263

ABSTRACT

Excessive body fat and the related dysmetabolic diseases affect both developed and developing countries. The aim of this study was to investigate the beneficial role of a bacterial culture supernatant (hereafter: BS) of Lactobacillus and Bifidobacterium and their potential mechanisms of action on white-fat browning and lipolysis. For selection of four candidates among 55 Lactic acid producing bacteria (LAB) from human infant faeces, we evaluated by Oil Red O staining and Ucp1 mRNA quantitation in 3T3-L1 preadipocytes. The expression of browning and lipolysis markers was examined along with in vitro assays. The possible mechanism was revealed by molecular and biological experiments including inhibitor and small interfering RNA (siRNA) assays. In a mouse model, physiological, histological, and biochemical parameters and expression of some thermogenesis-related genes were compared among six experimental groups fed a high-fat diet and one normal-diet control group. The results allow us to speculate that BS treatment promotes browning and lipolysis both in vitro and in vivo. Moreover, the BS may activate thermogenic programs via a mechanism involving PKA-CREB signaling in 3T3-L1 cells. According to our data, we can propose that two LAB strains, Bifidobacterium longum DS0956 and Lactobacillus rhamnosus DS0508, may be good candidates for a dietary supplement against obesity and metabolic diseases; however, further research is required for the development as dietary supplements or drugs.


Subject(s)
Bifidobacterium longum/metabolism , Lacticaseibacillus rhamnosus/metabolism , Obesity/therapy , Thermogenesis/drug effects , 3T3-L1 Cells , Adipocytes/cytology , Adipocytes/drug effects , Adipocytes/metabolism , Adipose Tissue, White/drug effects , Adipose Tissue, White/metabolism , Adipose Tissue, White/pathology , Animals , Cell Differentiation/drug effects , Culture Media, Conditioned/metabolism , Culture Media, Conditioned/pharmacology , Cyclic AMP-Dependent Protein Kinases/metabolism , Diet, High-Fat/adverse effects , Gene Expression Regulation/drug effects , Humans , Lipolysis/drug effects , Lipolysis/genetics , Mice , Mice, Inbred C57BL , Mitochondria/drug effects , Mitochondria/metabolism , Obesity/etiology , Obesity/genetics , Obesity/metabolism , Oxidation-Reduction/drug effects , Signal Transduction/drug effects , Thermogenesis/genetics
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