ROS and hypoxia signaling regulate periodic metabolic arousal during insect dormancy to coordinate glucose, amino acid, and lipid metabolism

Proc Natl Acad Sci U S A. 2021 Jan 5;118(1):e2017603118. doi: 10.1073/pnas.2017603118.

Abstract

Metabolic suppression is a hallmark of animal dormancy that promotes overall energy savings. Some diapausing insects and some mammalian hibernators have regular cyclic patterns of substantial metabolic depression alternating with periodic arousal where metabolic rates increase dramatically. Previous studies, largely in mammalian hibernators, have shown that periodic arousal is driven by an increase in aerobic mitochondrial metabolism and that many molecules related to energy metabolism fluctuate predictably across periodic arousal cycles. However, it is still not clear how these rapid metabolic shifts are regulated. We first found that diapausing flesh fly pupae primarily use anaerobic glycolysis during metabolic depression but engage in aerobic respiration through the tricarboxylic acid cycle during periodic arousal. Diapausing pupae also clear anaerobic by-products and regenerate many metabolic intermediates depleted in metabolic depression during arousal, consistent with patterns in mammalian hibernators. We found that decreased levels of reactive oxygen species (ROS) induced metabolic arousal and elevated ROS extended the duration of metabolic depression. Our data suggest ROS regulates the timing of metabolic arousal by changing the activity of two critical metabolic enzymes, pyruvate dehydrogenase and carnitine palmitoyltransferase I by modulating the levels of hypoxia inducible transcription factor (HIF) and phosphorylation of adenosine 5'-monophosphate-activated protein kinase (AMPK). Our study shows that ROS signaling regulates periodic arousal in our insect diapasue system, suggesting the possible importance ROS for regulating other types of of metabolic cycles in dormancy as well.

Keywords: ROS; diapause; hibernation; hypoxia signaling; periodic arousal.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Amino Acids / metabolism
  • Animals
  • Cell Respiration
  • Citric Acid Cycle
  • Diapause / physiology
  • Energy Metabolism
  • Glucose / metabolism
  • Glycolysis / physiology
  • Hypoxia / metabolism*
  • Insecta / metabolism
  • Lipid Metabolism / physiology
  • Lipids / physiology
  • Mitochondria / metabolism
  • Phosphorylation
  • Reactive Oxygen Species / metabolism*
  • Sarcophagidae / metabolism
  • Signal Transduction
  • Torpor / physiology*

Substances

  • Amino Acids
  • Lipids
  • Reactive Oxygen Species
  • Glucose