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Sci Rep. 2019 Jan 29;9(1):854. doi: 10.1038/s41598-018-36674-9.

Diverse metabolic reactions activated during 58-hr fasting are revealed by non-targeted metabolomic analysis of human blood.

Author information

1
G0 Cell Unit, Okinawa Institute of Science and Technology Graduate University (OIST), Okinawa, Japan.
2
Gunma University Initiative for Advanced Research (GIAR), Gunma University, Gunma, Japan.
3
G0 Cell Unit, Okinawa Institute of Science and Technology Graduate University (OIST), Okinawa, Japan. myanagid@gmail.com.
4
Geriatric unit, Department of Community Network and Collaborative Medicine, Graduate School of Medicine, Kyoto University, Kyoto, Japan. hkondoh@kuhp.kyoto-u.ac.jp.

Abstract

During human fasting, metabolic markers, including butyrates, carnitines, and branched-chain amino acids, are upregulated for energy substitution through gluconeogenesis and use of stored lipids. We performed non-targeted, accurate semiquantitative metabolomic analysis of human whole blood, plasma, and red blood cells during 34-58 hr fasting of four volunteers. During this period, 44 of ~130 metabolites increased 1.5~60-fold. Consistently fourteen were previously reported. However, we identified another 30 elevated metabolites, implicating hitherto unrecognized metabolic mechanisms induced by fasting. Metabolites in pentose phosphate pathway are abundant, probably due to demand for antioxidants, NADPH, gluconeogenesis and anabolic metabolism. Global increases of TCA cycle-related compounds reflect enhanced mitochondrial activity in tissues during fasting. Enhanced purine/pyrimidine metabolites support RNA/protein synthesis and transcriptional reprogramming, which is promoted also by some fasting-related metabolites, possibly via epigenetic modulations. Thus diverse, pronounced metabolite increases result from greatly activated catabolism and anabolism stimulated by fasting. Anti-oxidation may be a principal response to fasting.

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