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Guillermou's avatar

Endothelial cells like epithelial cells are tightly linked by intercellular adhesion proteins, called tight junctions, which are key regulators of intestinal barrier permeability and integrity. Various dietary or lifestyle agents, such as alcohol consumption, toxic diet or chronic diseases, modulate intestinal permeability; In addition to the direct effect on the epithelium, these factors modulate the intestinal microbiota, inducing dysbiosis. This is the driving force for increased intestinal permeability, with consequent systemic inflammation related to bacterial translocation (BT) and lipopolysaccharide (LPS) endotoxemia overload.

Unhealthy diets and metabolic disorders, such as obesity and type 2 diabetes mellitus, are associated with intestinal barrier dysfunction and dysbiosis, resulting in increased circulating LPS, a condition called metabolic endotoxemia. The low-grade inflammation caused by MS, in turn, establishes a vicious cycle associated with worsening glucose and lipid metabolism, the development of insulin resistance, and nonalcoholic fatty liver disease (NAFLD). and generates a favorable environment for cancer cell transformation and tumor progression [ 42 ]. The combination of dysbiosis and metabolic changes in microbial metabolites and cellular energy pathways promote a pro-inflammatory environment in intestinal cancer.

Short-chain fatty acids (SCFAs) derived from dietary fermentation of dietary fibers are recognized as protective agents against chronic intestinal inflammation, and experimental studies demonstrated that fiber intake improves the composition of the intestinal microbiota, glucose metabolism and lipids and body weight, all recognized factors involved in tumorigenesis.

Both hyperglycemia and intestinal barrier impairment have a recognized oncogenic potential in the development of colorectal cancer (CRC). ME also increases the formation of reactive oxygen species (ROS) and DNA damage, favoring the process of tumorigenesis. The translocation of LPS into the bloodstream triggers molecular pathways involved in cytokine release and immune dysregulation. This is a critical step in the exacerbation of many diseases, including metabolic disorders and cancer. Indeed, the role of LPS in cancer development is widely recognized, and examples include gastric tumor related to Helicobacter pylori infection and hepatocellular carcinoma, both preceded by prolonged inflammatory injury; Furthermore, the risk of recurrence and development of metastasis appears to be associated with endotoxemia.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9963870/ (2023).-------

https://www.thelancet.com/journals/ebiom/article/PIIS2352-3964(23)00131-7/fulltext (2023)

https://www.sciencedirect.com/science/article/pii/S277263202100009X (2022).----

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8082020/ (2021).----

https://karger.com/dig/article/102/4/508/100644/Gut-Microbiota-Dysbiosis-Drives-the-Development-of (2020).-----

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Guillermou's avatar

The gastrointestinal tract is the most important source of endotoxins. Once endotoxins pass the intestinal barrier, through paracellular or transcellular pathways, they trigger an inflammatory response that consumes energy and nutrients necessary for growth and production. Heat stress, mycotoxins, pathogens, feed changes, weaning) increase intestinal permeability and promote the leakage of endotoxins.

https://www.nutrex.eu/insights/endotoxins-explained/

This prospective study included 393 young people and examined the associations of endotoxin biomarkers at baseline with adiposity, body mass index (, visceral adipose tissue, subcutaneous adipose tissue, skinfolds, waist circumference) and cardiometabolic risk ( insulin, glucose, adipokines, lipid profile, blood pressure) at both visits using mixed effects regression and with liver fat fraction (HFF) at follow-up using linear regression.

Higher lipopolysaccharide (LPS) and its binding protein, LPS-binding protein (LBP), predicted higher levels of the studied biomarkers. Metabolic endotoxemia may be a shared mechanism underlying childhood obesity and early-onset cardiometabolic diseases.

https://academic.oup.com/jcem/article/107/7/e3018/6547256?login=false (2022)

This study examines dysregulation of intestinal tight junctions, increased permeability of the intestinal barrier, and apoptosis of epithelial cells during the development of intestinal inflammation. The results showed that glycolysis, Krebs cycle and pyrimidine metabolism were affected by intestinal inflammation. In particular, the activity of complex I of the hepatic mitochondrial respiratory chain was significantly increased. Pathogenic bacteria in the intestine, as well as plasma LPS, significantly increased the dysfunctional metabolism of the liver is related to the dislocation of LPS.

https://www.frontiersin.org/articles/10.3389/fimmu.2022.981917/full (2022)

In this meta-analysis. Blood endotoxin levels were higher in patients with simple steatosis versus controls with healthy liver as well as in patients with non-alcoholic steatohepatitis versus patients with non-alcoholic fatty liver/non-alcoholic steatohepatitis. Consistently, higher levels of endotoxin were observed in patients with more advanced histopathological grades of steatosis and liver fibrosis. An increase in blood endotoxin levels was partially attributed to an increase in body mass index in patients with NAFLD compared to controls. Increases in blood endotoxin levels were associated with increases in C-reactive protein concentrations and, in most cases, were paralleled by an increase in markers of intestinal permeability. Results support blood endotoxin levels as relevant diagnostic biomarkers for NAFLD, both for disease detection and staging during disease progression, and could serve as a surrogate marker for increased intestinal permeability in NAFLD. .

BLOOD ENDOTOXIN LEVELS AS BIOMARKER OF NON-ALCOHOLIC FATTY LIVER DISEASE: A SYSTEMATIC REVIEW AND META-ANALYSIS

https://www.cghjournal.org/article/S1542-3565(22)01110-7/fulltext (2022)

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