Effects of fasting and re-feeding on the expression of Dec1, Per1, and other clock-related genes

Takeshi Kawamoto1, Mitsuhide Noshiro, Masae Furukawa

  • 1Department of Dental and Medical Biochemistry and Department of Prosthetic Dentistry, Hiroshima University Graduate School of Biomedical Sciences, Hiroshima 734-8553.

Insights

Fasting and re-feeding alter circadian rhythms of clock genes in mouse peripheral tissues. These changes, including Dec1 and Per1 expression, link to metabolic activity, revealing food

Area of Science:

  • Chronobiology
  • Molecular Biology
  • Metabolic Regulation

Background:

  • Peripheral clock systems regulate tissue-specific circadian rhythms.
  • Food availability is a key environmental cue influencing these rhythms.
  • Understanding clock gene regulation by feeding is crucial for metabolic health.

Purpose of the Study:

  • To investigate the impact of fasting and re-feeding on circadian clock gene expression in mouse peripheral tissues.
  • To elucidate the role of Dec1 and Dec2 in the food-entrainable oscillator mechanism.
  • To determine the relationship between clock gene expression and tissue metabolic activity.

Main Methods:

  • Mice were subjected to 2-day fasting, followed by re-feeding or restriction feeding.
  • Quantitative real-time PCR was used to measure mRNA levels of clock genes (Dec1, Dec2, Per1, Per2, Bmal1, Rev-erbalpha).
  • Gene expression profiles were analyzed across various tissues (liver, heart, etc.) at different time points.

Main Results:

  • Fasting decreased Dec1 mRNA in all examined tissues, while Per1 mRNA increased.
  • Per2 expression was reduced in liver and heart after prolonged fasting.
  • Re-feeding partially reversed fasting effects, and restriction feeding shifted gene expression phases.

Conclusions:

  • Short-term fasting and re-feeding differentially modulate peripheral circadian clock gene rhythms.
  • Dec1, Per1, and other clock genes are closely linked to tissue metabolic activity.
  • These findings highlight the intricate interplay between metabolism and circadian timing in peripheral organs.