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obesity

Liver Injury in Non-Alcoholic Fatty Liver Disease Is Associated with Urea Cycle Enzyme Dysregulation

[Scientific Reports] Scientists evaluated changes in urea cycle enzymes in non-alcoholic fatty liver disease (NAFLD) patients and in two preclinical animal models mimicking this entity. Seventeen liver specimens from NAFLD patients were included for immunohistochemistry and gene expression analysis.

Methionine Adenosyltransferase 1a Antisense Oligonucleotides Activate the Liver-Brown Adipose Tissue Axis Preventing Obesity and Associated Hepatosteatosis

[Nature Communications] Targeting Mat1a activated the liver-brown adipose tissue axis by increasing NRF2-mediated FGF21 secretion, which prevented obesity, insulin resistance and hepatosteatosis.

Reduced Production of Isoprostanes by Peri-Pancreatic Adipose Tissue from Zucker Fa/Fa Rats as a New Mechanism for β-Cell Compensation in Insulin Resistance and Obesity

[Free Radical Biology and Medicine] Researchers investigated whether peri-pancreatic white adipose tissue produced oxygenated lipids, namely isoprostanes and neuroprostanes and whether they can influence β-cell function in obesity.

FXR: Structures, Biology, and Drug Development for NASH and Fibrosis Diseases

[Acta Pharmacologica Sinica] Scientists discuss potential strategies for developing future therapeutic farnesoid-X-receptor (FXR) modulators to overcome current limitations for fibrosis diseases, providing new perspectives for enterohepatic and metabolic diseases treatment.

Bile Acid and Receptors: Biology and Drug Discovery for Nonalcoholic Fatty Liver Disease

[Acta Pharmacologica Sinica] Scientists summarize the current knowledge on the role of bile acids and the receptors in the development of nonalcoholic fatty liver disease and nnonalcoholic steatohepatitis, especially the functions of farnesoid X receptor in different tissues including liver and intestine.

lncRNA TUG1 Protects Intestinal Epithelial Cells from Damage Induced by High Glucose and High Fat via AMPK/SIRT1

[Molecular Medicine Reports] Protein expression was detected by western blotting. Cell Counting Kit‑8 assays were performed to analyze cell viability, and flow cytometry and a TUNEL assay was performed to evaluate cell apoptosis.

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