Effects of Irregular Feeding on the Daily Fluctuations in mRNA Expression of the Neurosecretory Protein GL and Neurosecretory Protein GM Genes in the Mouse Hypothalamus

Int J Mol Sci. 2021 Feb 20;22(4):2109. doi: 10.3390/ijms22042109.

Abstract

Circadian desynchrony induced by a long period of irregular feeding leads to metabolic diseases, such as obesity and diabetes mellitus. The recently identified neurosecretory protein GL (NPGL) and neurosecretory protein GM (NPGM) are hypothalamic small proteins that stimulate food intake and fat accumulation in several animals. To clarify the mechanisms that evoke feeding behavior and induce energy metabolism at the appropriate times in accordance with a circadian rhythm, diurnal fluctuations in Npgl and Npgm mRNA expression were investigated in mice. Quantitative RT-PCR analysis revealed that the mRNAs of these two genes were highly expressed in the mediobasal hypothalamus during the active dark phase under ad libitum feeding. In mice restricted to 3 h of feeding during the inactive light phase, the Npgl mRNA level was augmented in the moment prior to the feeding period and the midnight peak of Npgm mRNA was attenuated. Moreover, the mRNA expression levels of clock genes, feeding regulatory neuropeptides, and lipid metabolic enzymes in the central and peripheral tissues were comparable to those of central Npgl and Npgm. These data suggest that Npgl and Npgm transcription fluctuates daily and likely mediates feeding behavior and/or energy metabolism at an appropriate time according to the meal timing.

Keywords: environmental light/dark cycle; fat accumulation; feeding restriction; food intake; neurosecretory protein GL; neurosecretory protein GM; rhythmicity.

MeSH terms

  • Analysis of Variance
  • Animals
  • Anorexia / blood
  • Anorexia / genetics
  • Blood Glucose / metabolism
  • CLOCK Proteins / genetics
  • CLOCK Proteins / metabolism
  • Feeding Behavior / physiology*
  • Gene Expression Profiling
  • Gene Expression Regulation*
  • Hypothalamus / metabolism*
  • Insulin / blood
  • Lipid Metabolism / genetics
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism*
  • Orexins / metabolism
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Time Factors

Substances

  • Blood Glucose
  • Insulin
  • NPGM protein, mouse
  • Nerve Tissue Proteins
  • Orexins
  • RNA, Messenger
  • neurosecretory protein GL, mouse
  • CLOCK Proteins