Preventive effect of L-carnitine on the disorder of lipid metabolism and circadian clock of mice subjected to chronic jet-lag

Physiol Res. 2017 Nov 24;66(5):801-810. doi: 10.33549/physiolres.933543. Epub 2017 Jul 18.

Abstract

Circadian clock plays an essential role in orchestrating daily physiology, and its disruption can evoke metabolic diseases such as obesity. L-Carnitine can reduce blood lipid levels, and ameliorate fatty liver through regulating lipid metabolism. However, whether L-Carnitine administration may affect the disturbance of lipid metabolism and circadian rhythm of mice induced by prolonged circadian disruption is still unknown. Herein, we investigated the effects of L-Carnitine on conditions of circadian clock and lipid metabolism through a chronic jet-lag mice model which was developed by reversing 12 h light/12 h dark cycle every 4 days for a continuous 12 weeks. Results showed that L-Carnitine administration significantly decreased levels of serum glutamic-oxaloacetic transaminase (GOT) and triglycerides (TG), which were remarkably elevated by chronic jet-lag. More importantly, quantitative real-time polymerase chain reaction (qRT-PCR) analysis indicated that L-Carnitine supplementation would effectively counteract the negative alterations in gene expression which related to lipid metabolism (Srebp1, Acaca, Fasn, and Scd1), metabolic regulator (mTOR) and circadian rhythm (Bmal1, Per1, Cry1 and Dec1) in the liver of mice subjected to the chronic jet-lag. As a conclusion, L-Carnitine was partly effective in preventing the disruption of circadian clock and lipid metabolic disorders induced by the chronic jet-lag.

MeSH terms

  • Animals
  • Carnitine / pharmacology
  • Carnitine / therapeutic use*
  • Chronic Disease
  • Circadian Clocks / drug effects*
  • Circadian Clocks / physiology
  • Circadian Rhythm / drug effects*
  • Circadian Rhythm / physiology
  • Jet Lag Syndrome / blood
  • Jet Lag Syndrome / drug therapy*
  • Jet Lag Syndrome / genetics
  • Lipid Metabolism / drug effects*
  • Lipid Metabolism / physiology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Random Allocation
  • Treatment Outcome

Substances

  • Carnitine