2015
DOI: 10.1016/j.jnutbio.2015.05.011
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Diets rich in fructose, fat or fructose and fat alter intestinal barrier function and lead to the development of nonalcoholic fatty liver disease over time

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Cited by 141 publications
(113 citation statements)
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“…It has been clearly demonstrated that a high rate of hepatocyte apoptosis was developed in a NASH rat model induced by a HFD. Our observation is in agreement with findings from both human studies of NASH patients [22, 87] and an animal model of NASH [88]. These results suggest that increased hepatocyte apoptosis could contribute to NASH pathogenesis.…”
Section: Discussionsupporting
confidence: 93%
“…It has been clearly demonstrated that a high rate of hepatocyte apoptosis was developed in a NASH rat model induced by a HFD. Our observation is in agreement with findings from both human studies of NASH patients [22, 87] and an animal model of NASH [88]. These results suggest that increased hepatocyte apoptosis could contribute to NASH pathogenesis.…”
Section: Discussionsupporting
confidence: 93%
“…A significant decrease in hepatic IκBα1 protein in the HF-EFr-fed rats was observed. The activation of NF-κB and TLR4-CD14 cascade presumably resulted from an activation of CD68 + macrophages, as the chronic intake of HF-EFr enhances the influx of endotoxin to portal blood [26,38,39]. …”
Section: Discussionmentioning
confidence: 99%
“…Fasting blood glucose was measured by using a standard glucometer (Contour; Bayer Vital GmbH). Paraffinembedded sections of liver (5 mm) were stained with hematoxylin and eosin (Sigma Aldrich Chemie GmbH) and analyzed as previously described (17). Neutrophil granulocytes were stained in paraffinembedded liver sections (5 mm) by using a commercially available naphthol AS-D chloroacetate esterase staining kit (Sigma Aldrich Chemie GmbH) and counted as detailed previously (17).…”
Section: Methodsmentioning
confidence: 99%
“…Paraffin-embedded duodenal sections (4 mm) were stained by using a specific antibody against the tight junction protein occludin (Invitrogen). Staining intensities in all liver and duodenal sections were determined as previously detailed (17). To determine means, data from 8 fields (liver: 2003 magnification; duodenum: 4003 magnification) of each tissue section (e.g., liver or duodenum) were used.…”
Section: Methodsmentioning
confidence: 99%