Altered body mass regulation in male mPeriod mutant mice on high-fat diet

Robert Dallmann1, David R Weaver

  • 1Department of Neurobiology, University of Massachusetts Medical School, Worcester, Massachusetts, USA. Robert@dallmanns.de

Insights

The circadian clock regulates mammalian physiology. This study found that disrupting Period (mPer) genes, particularly mPer3, significantly increases body mass gain in mice fed a high-fat diet, suggesting a role in obesity.

Area of Science:

  • Chronobiology
  • Metabolic Regulation
  • Genetics

Background:

  • The mammalian circadian clock controls physiological processes, and its disruption is linked to obesity and metabolic syndrome.
  • Period (mPer) genes mPer1 and mPer2 are crucial for core clock function in mice, while mPer3's role is less understood.

Purpose of the Study:

  • To investigate the impact of mPer gene disruption on body mass regulation.
  • To assess the role of mPer1, mPer2, and mPer3 in diet-induced obesity.

Main Methods:

  • Generation of mPer1/2/3 triple-deficient mice and mPer3 single-deficient mice.
  • Feeding mutant and control mice a high-fat diet.
  • Monitoring body mass gain.

Main Results:

  • Male mPer1/2/3 triple-deficient mice exhibited significantly greater body mass gain compared to wild-type controls when fed a high-fat diet.
  • Mice deficient in only mPer3 also showed increased body mass gain, similar to the triple-deficient group.
  • These findings highlight a previously unrecognized role for mPer3 in regulating body mass.

Conclusions:

  • The Period genes, including mPer3, play a significant role in regulating body mass.
  • Disruption of mPer3 alone can lead to increased body mass gain on a high-fat diet, suggesting its importance in preventing obesity.
  • Circadian clock genes are critical targets for understanding and potentially treating metabolic disorders like obesity.

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