Oxalic acid and diacylglycerol 36:3 are cross-species markers of sleep debt

Abstract

Reduced sleep duration is a hallmark of modern-day society and is increasingly associated with medical conditions, such as diabetes, obesity, metabolic syndrome, and cardiovascular disease. Here we present data from a rat model and human clinical study of chronic sleep restriction, both revealing that two metabolites in blood, oxalic acid and diacylglycerol 36:3, are quantitatively depleted under sleep-restricted conditions and restored after recovery sleep. Our findings also reveal a significant overall shift in lipid metabolism, with higher levels of phospholipids in both species and evidence of a systemic oxidative environment. This work provides a potential link between the known pathologies of reduced sleep duration and metabolic dysfunction.

Document Details

Document Type
Pub Defense Publication
Publication Date
Feb 09, 2015
Source ID
10.1073/pnas.1417432112

Entities

People

  • Aalim M. Weljie
  • Amita Sehgal
  • Arjun Sengupta
  • David F. Dinges
  • Matthew S Kayser
  • Morris J. Birnbaum
  • Namni Goel
  • Peter Meerlo
  • Ted Abel

Organizations

  • Howard Hughes Medical Institute
  • National Aeronautics and Space Administration
  • National Institute of Nursing Research
  • University of Groningen
  • University of Pennsylvania

Tags

Fields of Study

  • Biology

Readers

  • Circadian Sleep-Wake Regulation and Chronobiology
  • Prostate Cancer Biology.
  • Toxicology/Environmental Toxicology