Alterations of circadian expressions of clock genes in Dahl salt-sensitive rats fed a high-salt diet

Hypertension. 2003 Aug;42(2):189-94. doi: 10.1161/01.HYP.0000082766.63952.49. Epub 2003 Jun 30.

Abstract

In mammals, behavioral and physiologic processes display 24-hour rhythms that are regulated by a circadian system consisting of central and peripheral oscillators. Because various cardiovascular functions show diurnal variations and abnormal patterns of circadian blood pressure variation carry a high risk of cardiovascular complications, we investigated whether the expression of clock genes is altered in an animal model of hypertension. In Dahl salt-sensitive rats fed a high-salt (4% NaCl) diet for 6 weeks (DS-H), radiotelemetry monitoring showed increased amplitude of circadian variations in blood pressure. The ratio of heart weight to body weight and the ratio of kidney weight to body weight were higher in DS-H. Echocardiographic data showed that the wall thickness of the left ventricle was greater in DS-H. Northern blot analysis and single cosinor analysis revealed that the amplitudes of circadian expression changes of the clock genes (mPer2, Bmal1, and dbp) in the heart, liver, and kidney were significantly decreased in DS-H rats compared with a normal-salt-diet group, except for Bmal1 in the liver. The circadian expression changes of plasminogen activator inhibitor-1, a clock-regulated gene, were attenuated in the hearts of DS-H. The present results demonstrate that DS-H show altered circadian expression of peripheral clock genes. Detailed analyses of the relation between circadian expression of clock genes and blood pressure regulation might reveal a role for chronologic therapy of cardiovascular disease.

MeSH terms

  • ARNTL Transcription Factors
  • Administration, Oral
  • Animals
  • Basic Helix-Loop-Helix Transcription Factors
  • Blood Pressure
  • Cell Cycle Proteins
  • Circadian Rhythm*
  • DNA-Binding Proteins*
  • Gene Expression Regulation*
  • Heart Rate
  • Hypertension / etiology
  • Hypertension / genetics*
  • Hypertension / metabolism
  • Hypertension / physiopathology
  • Hypertrophy, Left Ventricular / diagnostic imaging
  • Kidney / pathology
  • Male
  • Myocardium / metabolism
  • Myocardium / pathology
  • Nuclear Proteins / biosynthesis
  • Nuclear Proteins / genetics
  • Organ Size
  • Period Circadian Proteins
  • Plasminogen Activator Inhibitor 1 / biosynthesis
  • Plasminogen Activator Inhibitor 1 / genetics
  • RNA, Messenger / biosynthesis
  • Rats
  • Rats, Inbred Dahl
  • Sodium Chloride / administration & dosage
  • Sodium Chloride / pharmacology
  • Telemetry
  • Transcription Factors / biosynthesis
  • Transcription Factors / genetics
  • Ultrasonography

Substances

  • ARNTL Transcription Factors
  • Basic Helix-Loop-Helix Transcription Factors
  • Cell Cycle Proteins
  • DBP protein, rat
  • DNA-Binding Proteins
  • Nuclear Proteins
  • Per2 protein, rat
  • Period Circadian Proteins
  • Plasminogen Activator Inhibitor 1
  • RNA, Messenger
  • Transcription Factors
  • Sodium Chloride