Alteration of intrinsic biological rhythms during interferon treatment and its possible mechanism

研究成果: Contribution to journalArticle

58 被引用数 (Scopus)

抄録

One of the most indispensable biological functions for all living organisms is the circadian clock, which acts like a multifunctional timer to regulate the homeostatic system, including sleep and wakefulness, hormonal secretions, and various other bodily functions with a 24-h cycle. We reported previously that interferon (IFN) has the ability to modulate the biological clock system at the genetic level. In the present study, this mechanism was investigated further by evaluating the effects of IFN-α on circadian output function. Treatment of cultured hepatic cells (HepG2) with IFN-α significantly decreased the protein levels of CLOCK and BMAL1, which are positive regulators of circadian output rhythm, then their mRNA levels. Aurintricarboxylic acid, a ligand inhibitor of IFN-α, dose dependently inhibited the IFN-α-induced phosphorylation of the signal transducer and activator of transcription 1 (STAT1) protein in HepG2 cells, accompanied by the restoration of Clock and Bmal1 mRNA levels. The continuous administration of IFN-α significantly decreased CLOCK and BMAL1 protein levels in the suprachiasmatic nucleus and liver of mice, thereby preventing oscillations in the expression of clock and clock-controlled output genes. These results reveal a possible pharmacological action by IFN-α on the core circadian oscillation mechanism and indicate that the disruptive effect of IFN-α on circadian output function is the underlying cause of its adverse effects on 24-h rhythms in physiology and behavior.

本文言語英語
ページ(範囲)1393-1399
ページ数7
ジャーナルMolecular Pharmacology
62
6
DOI
出版ステータス出版済み - 12 1 2002

All Science Journal Classification (ASJC) codes

  • Molecular Medicine
  • Pharmacology

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