Effects of 24-hr fasting on methamphetamine- and apomorphine-induced locomotor activities, and on monoamine metabolism in mouse corpus striatum and nucleus accumbens

Pharmacol Biochem Behav. 1990 Feb;35(2):391-6. doi: 10.1016/0091-3057(90)90175-h.

Abstract

The effects of 24-hr fasting on the vertical (VMA) and horizontal (HMA) locomotor activities, on cage climbing activity and on brain monoamine-related substances, were examined using male ddY mice. Both the VMA and HMA increased with fasting, but not the cage climbing activity. Methamphetamine (2 mg/kg, SC) increased the VMA and HMA in both the feeding and fasting mice, whereas with apomorphine (0.1 mg/kg, SC) both decreased. Furthermore, pretreatment with haloperidol (0.025 mg/kg, SC) showed no influence on the methamphetamine-induced VMA increase in both the feeding and fasting mice. However, pretreatment with haloperidol inhibited the methamphetamine-induced HMA increase in both the feeding and fasting mice and showed a higher level of HMA in fasting mice than in feeding mice. When measuring brain monoamine-related substances, the DA, NE, 5-HT, and 5-HIAA levels in the corpus striatum increased, whereas the 3-MT levels decreased. The monoamine levels in the nucleus accumbens of fasting mice were the same as those in feeding mice, except for a decrease of the 3-MT level. These results suggest that the locomotor activity in fasting mice may be increased by a change in the sensitivity of dopaminergic neurons in the corpus striatum.

MeSH terms

  • Animals
  • Apomorphine / pharmacology*
  • Biogenic Monoamines / metabolism*
  • Brain / metabolism*
  • Corpus Striatum / metabolism
  • Drug Interactions
  • Fasting / physiology*
  • Haloperidol / pharmacology
  • Male
  • Methamphetamine / pharmacology*
  • Mice
  • Motor Activity / drug effects*
  • Motor Activity / physiology
  • Nucleus Accumbens / metabolism

Substances

  • Biogenic Monoamines
  • Methamphetamine
  • Haloperidol
  • Apomorphine