To determine the contributions of galactose and fructose to glucose formation, 6 subjects (26 +/- 2 years old; body mass index, 22.4 +/- 0.2 kg/m(2)) (mean +/- SE) were studied during fasting conditions. Three subjects received a primed constant intravenous infusion of [6,6-(2)H(2)]glucose for 3 hours followed by oral bolus ingestion of galactose labeled to 2% with [U-(13)C]galactose (0.72 g/kg); the other 3 subjects received a primed constant intravenous infusion of [6,6-(2)H(2)]glucose followed by either a bolus ingestion of fructose alone (0.72 g/kg) (labeled to 2% with [U-(13)C]fructose) or coingestion of fructose (labeled with [U-(13)C]fructose) (0.72 g/kg) and unlabeled glucose (0.72 g/kg). Four hours after ingestion, subjects received 1 mg of glucagon intravenously to stimulate glycogenolysis. When galactose was ingested alone, the area under the curve (AUC) of [(13)C(6)]glucose and [(13)C(3)]glucose was 7.28 +/- 0.39 and 3.52 +/- 0.05 mmol/L per 4 hours, respectively. When [U-(13)C]fructose was ingested with unlabeled fructose or unlabeled fructose plus glucose, no [(13)C(6)]glucose was detected in plasma. The AUC of [(13)C(3)]glucose after fructose and fructose plus glucose ingestion was 20.21 +/- 2.41 and 6.25 +/- 0.34 mmol/L per 4 hours, respectively. Comparing the AUC for the (13)C(3) vs (13)C(6) enrichments, 67% of oral galactose enters the systemic circulation via a direct route and 33% via an indirect route. In contrast, fructose only enters the systemic circulation via the indirect route. Finally, when ingested alone, fructose and galactose contribute little to glycogen synthesis. After the coingestion of fructose and glucose with the resultant insulin response from the glucose, fructose is a significant contributor to glycogen synthesis.
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http://dx.doi.org/10.1016/j.metabol.2009.02.018 | DOI Listing |
Am J Reprod Immunol
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Laboratory of Molecular Genetics and Experimentation in Animal Reproduction, University of Western São Paulo (Unoeste), Presidente Prudente, São Paulo, Brazil.
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January 2025
Biochemistry, Molecular, Cellular, and Developmental Graduate Group, University of California, Davis, Davis, CA, 95616, USA; Department of Chemistry, University of California, Davis, Davis, CA, 95616, USA. Electronic address:
D-allose is a rare monosaccharide, found naturally in low abundances. Due to its low-calorie profile and similar taste to sucrose, D-allose has the potential to become an ideal sugar substitute. D-allose also displays unique properties and health benefits that can be applied to various fields, including food and medicine.
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Zoology Department, Faculty of Science, Damietta University, New Damietta 34517, Egypt. Electronic address:
Maternal obesity predisposes offspring to type 2 diabetes (T2D) through a direct chronic effect of lipids on pancreatic β-cell neogenesis. β-cells produce FABP3 to bind and metabolize fatty acids. Ferulic acid (FA) is a natural product that may inhibit fatty acids' binding to FABP3, preventing their toxicity.
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Department of Pediatrics, Center for Inherited Metabolic Diseases Copenhagen University Hospital, Rigshospitalet Copenhagen Denmark.
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View Article and Find Full Text PDFJ Food Sci
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Department of Analytical and Food Chemistry, Faculty of Sciences, University of Vigo, Ourense, Spain.
This work aimed to study the production, for the first time, of three fermented products of chestnut puree (CP) with milk kefir grains, a higher nisin-producing (Lactococcus (L.) lactis CECT 539) and a higher lactic acid-producing (Lactobacillus (Lb.) casei CECT 4043) lactic acid bacteria (LAB).
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