Melatonin administered during the fetal stage affects circadian clock in the suprachiasmatic nucleus but not in the liver

  • Pavel Houdek
    Department of Neurohumoral Regulations Institute of Physiology, v.v.i., Academy of Science of the Czech Republic Videnska 1083 14220 Prague Czech Republic
  • Lenka Polidarová
    Department of Neurohumoral Regulations Institute of Physiology, v.v.i., Academy of Science of the Czech Republic Videnska 1083 14220 Prague Czech Republic
  • Marta Nováková
    Department of Neurohumoral Regulations Institute of Physiology, v.v.i., Academy of Science of the Czech Republic Videnska 1083 14220 Prague Czech Republic
  • Kristýna Matějů
    Department of Neurohumoral Regulations Institute of Physiology, v.v.i., Academy of Science of the Czech Republic Videnska 1083 14220 Prague Czech Republic
  • Štěpán Kubík
    Department of Neurophysiology of Memory Institute of Physiology, v.v.i., Academy of Science of the Czech Republic Videnska 1083 14220 Prague Czech Republic
  • Alena Sumová
    Department of Neurohumoral Regulations Institute of Physiology, v.v.i., Academy of Science of the Czech Republic Videnska 1083 14220 Prague Czech Republic

書誌事項

公開日
2014-07-23
権利情報
  • http://onlinelibrary.wiley.com/termsAndConditions#vor
DOI
  • 10.1002/dneu.22213
公開者
Wiley

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説明

<jats:title>ABSTRACT</jats:title><jats:p>The mammalian circadian system develops gradually during ontogenesis, and after birth, the system is already set to a phase of the mothers. The role of maternal melatonin in the entrainment of fetal circadian clocks has been suggested, but direct evidence is lacking. In our study, intact or pinealectomized pregnant rats were exposed to constant light (LL) throughout pregnancy to suppress the endogenous melatonin and behavioral rhythms. During the last 5 days of gestation, the rats were injected with melatonin or vehicle or were left untreated. After delivery, daily expression profiles of <jats:italic>c‐fos</jats:italic> and <jats:italic>Avp</jats:italic> in the suprachiasmatic nuclei (SCN), and <jats:italic>Per1</jats:italic>, <jats:italic>Per2, Rev‐erbα</jats:italic>, and <jats:italic>Bmal1</jats:italic> in the liver were measured in 1‐day‐old pups. Due to the LL exposure, no gene expression rhythms were detected in the SCN of untreated pregnant rats or in the SCN and liver of the pups. The administration of melatonin to pregnant rats entrained the pups' gene expression profiles in the SCN, but not in the liver. Melatonin did not affect the maternal behavior during pregnancy. Vehicle injections also synchronized the gene expression in the SCN but not in the liver. Melatonin and vehicle entrained the gene expression profiles to different phases, demonstrating that the effect of melatonin was apparently not due to the treatment procedure <jats:italic>per se</jats:italic>. The data demonstrate that in pregnant rats with suppressed endogenous melatonin levels, pharmacological doses of melatonin affect the fetal clock in the SCN but not in the liver. © 2014 Wiley Periodicals, Inc. Develop Neurobiol 75: 131–144, 2015</jats:p>

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