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Fructose metabolism and metabolic disease
Sarah A. Hannou, … , Nicola M. McKeown, Mark A. Herman
Sarah A. Hannou, … , Nicola M. McKeown, Mark A. Herman
Published February 1, 2018
Citation Information: J Clin Invest. 2018;128(2):545-555. https://doi.org/10.1172/JCI96702.
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Fructose metabolism and metabolic disease

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Abstract

Increased sugar consumption is increasingly considered to be a contributor to the worldwide epidemics of obesity and diabetes and their associated cardiometabolic risks. As a result of its unique metabolic properties, the fructose component of sugar may be particularly harmful. Diets high in fructose can rapidly produce all of the key features of the metabolic syndrome. Here we review the biology of fructose metabolism as well as potential mechanisms by which excessive fructose consumption may contribute to cardiometabolic disease.

Authors

Sarah A. Hannou, Danielle E. Haslam, Nicola M. McKeown, Mark A. Herman

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Figure 1

Fructose biochemistry.

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Fructose biochemistry.
Upon entering hepatocytes, fructose is phosphoryl...
Upon entering hepatocytes, fructose is phosphorylated by KHK to F1P. F1P is cleaved to DHAP and glyceraldehyde by ALDOB. Glyceraldehyde is phosphorylated by triose-kinase (TKFC, also known as dihydroxyacetone kinase 2 or DAK) to form the glycolytic intermediate glyceraldehyde 3-phosphate (GA3P). Both fructose-derived DHAP and GA3P enter the glycolytic/gluconeogenic metabolite pool at the triose-phosphate level, and these metabolites have numerous metabolic fates. F1P also allosterically regulates metabolic enzymes (red and green lines) to regulate the disposition of fructose-derived substrate and other metabolic products like uric acid. AMPD3, adenosine deaminase; GA, glyceraldehyde; IMP, inosine monophosphate; MTTP, microsomal triglyceride transfer protein; PYGL, glycogen phosphorylase L; GYS2, glycogen synthase 2; PKLR, pyruvate kinase, liver and red blood cell; PEP, phosphoenolpyruvate; TAG, triacylglycerol.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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