Fasting-induced reduction in locomotor activity and reduced response of orexin neurons in carnitine-deficient mice

Neurosci Res. 2006 May;55(1):78-86. doi: 10.1016/j.neures.2006.02.003. Epub 2006 Mar 15.

Abstract

We found reduced locomotor activity (LA) under fasting in systemic carnitine-deficient juvenile visceral steatosis (jvs(-/-)) mice. When food was withdrawn at 8:00 a.m. (lights-off at 7:00 p.m., 12h/cycle), the nocturnal LA of jvs(-/-) mice was much less than the control (jvs(+/+) and jvs(+/-)) mice. LA recovered under carnitine or sucrose administration, but not under medium-chain triglyceride. In addition, fasted jvs(-/-) mice, without any energy supply, were activated by modafinil, a stimulator of the dopamine pathway. These results suggest that the reduced LA is not adequately explained by energy deficit. As the fasted jvs(-/-) mice showed lower body core temperature (BT), we examined the central nervous system regulating LA and BT. We found lower percentage of c-Fos positive orexin neurons in the lateral hypothalamus and reduced orexin-A concentration in the cerebrospinal fluid of fasted jvs(-/-) mice. Sleep analysis revealed that fasted jvs(-/-) mice had disruption of prolonged wakefulness, with a higher frequency of brief episodes of non-REM sleep during the dark period than fasted jvs(+/+) mice. These results strongly suggest that the reduced LA in fasted jvs(-/-) mice is related to the inhibition of orexin neuronal activity.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Behavior, Animal
  • Blood Glucose
  • Body Temperature / drug effects
  • Body Temperature / physiology
  • Carnitine / administration & dosage
  • Carnitine / deficiency*
  • Electroencephalography / methods
  • Fasting / physiology*
  • Fatty Acids, Nonesterified / blood
  • Female
  • Glucose / administration & dosage
  • Immunohistochemistry / methods
  • Intracellular Signaling Peptides and Proteins / metabolism*
  • Mice
  • Mice, Knockout
  • Motor Activity / genetics*
  • Neurons / drug effects
  • Neurons / physiology*
  • Neuropeptides / metabolism*
  • Orexins
  • Polysomnography / methods
  • Proto-Oncogene Proteins c-fos / metabolism
  • Sleep, REM / drug effects
  • Sleep, REM / physiology
  • Sucrose / administration & dosage
  • Time Factors

Substances

  • Blood Glucose
  • Fatty Acids, Nonesterified
  • Intracellular Signaling Peptides and Proteins
  • Neuropeptides
  • Orexins
  • Proto-Oncogene Proteins c-fos
  • Sucrose
  • Glucose
  • Carnitine