2019
DOI: 10.1016/j.jnutbio.2018.10.020
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Gut microbiota: a potential manipulator for host adipose tissue and energy metabolism

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Cited by 49 publications
(39 citation statements)
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“…NAFLD and obesity are associated with higher gut barrier permeability, causing metabolic endotoxemia and an increase in the blood levels of LPS. Subsequently, it also causes hepatic and systemic inflammation as well as alterations in gene expression, hormone secretion, and energy consumption in distal peripheral tissues, such as the white adipose tissue [27]. This LPS role was corroborated in a preclinical study in which mice injected with LPS showed a similar phenotype than those obtained after a high fat diet (body weight gain, IR and increased NAFLD progression) [15].…”
Section: Role Of Lps In Gut Microbiota Dysbiosismentioning
confidence: 80%
“…NAFLD and obesity are associated with higher gut barrier permeability, causing metabolic endotoxemia and an increase in the blood levels of LPS. Subsequently, it also causes hepatic and systemic inflammation as well as alterations in gene expression, hormone secretion, and energy consumption in distal peripheral tissues, such as the white adipose tissue [27]. This LPS role was corroborated in a preclinical study in which mice injected with LPS showed a similar phenotype than those obtained after a high fat diet (body weight gain, IR and increased NAFLD progression) [15].…”
Section: Role Of Lps In Gut Microbiota Dysbiosismentioning
confidence: 80%
“…Recently, the gut microbiota (GM) has emerged as a new contributor to weight gain and immune/inflammatory system imbalances. This concept has been demonstrated through fecal transfer experiments using mice 21 or human 22 donors and germ-free mice recipients, and suggests that fecal GM may impact energy metabolism and immune cell activation in the AT (reviewed in 23 ). An increasing number of studies has further demonstrated that a nonnegligible proportion of obese subjects exhibit GM dysbiosis.…”
Section: Introductionmentioning
confidence: 99%
“…Micro-organisms extract energy from foods that humans cannot digest, producing bioactive compounds such as short-chain fatty acids (SCFAs)-mainly acetate, propionate and butyrate-which supply energy to the intestinal epithelium and liver, providing~10% of the daily caloric requirement [213]. The microbiota regulates energy balance through different mechanisms: gut-brain axis control at both the level of intestinal nutrient-sensing mechanisms, as well as at the central nervous system integration sites; development of a low-grade chronic systemic and adipose inflammation together with abnormal gut permeability by an increased relative abundance of pathogenic bacteria; effects on the metabolism of bile acids, with the production of secondary bile acids activating thyroid hormones and oxygen consumption; and impaired secretion of gut peptides and hormones implicated in appetite regulation [214][215][216]. Alterations in gut-brain signaling can affect the regulation of food intake and SCFAs impact on the incretins and hormones implicated in energy homeostasis, such as glucagon-like-peptide 1, gastric inhibitory peptide, peptide YY, leptin and insulin [217].…”
Section: The Impact Of the Gut Microbiota On The Human Energy Balancementioning
confidence: 99%