Short communication: Ischemia/reperfusion tolerance is time-of-day- dependent: Mediation by the cardiomyocyte circadian clock

David J. Durgan, Thomas Pulinilkunnil, Carolina Villegas-Montoya, Merissa E. Garvey, Nikolaos G. Frangogiannis, Lloyd H. Michael, Chi Wing Chow, Jason R B Dyck, Martin E. Young

Research output: Contribution to journalArticle

129 Citations (Scopus)

Abstract

Rationale: Cardiovascular physiology and pathophysiology vary dramatically over the course of the day. For example, myocardial infarction onset occurs with greater incidence during the early morning hours in humans. However, whether myocardial infarction tolerance exhibits a time-of-day dependence is unknown. Objective: To investigate whether time of day of an ischemic insult influences clinically relevant outcomes in mice. METHODS AND RESULTS: Wild-type mice were subjected to ischemia/reperfusion (I/R) (45 minutes of ischemia followed by 1 day or 1 month of reperfusion) at distinct times of the day, using the closed-chest left anterior descending coronary artery occlusion model. Following 1 day of reperfusion, hearts subjected to ischemia at the sleep-to-wake transition (zeitgeber time [ZT]12) resulted in 3.5-fold increases in infarct size compared to hearts subjected to ischemia at the wake-to-sleep transition (ZT0). Following 1 month of reperfusion, prior ischemic event at ZT12 versus ZT0 resulted in significantly greater infarct volume, fibrosis, and adverse remodeling, as well as greater depression of contractile function. Genetic ablation of the cardiomyocyte circadian clock (termed cardiomyocyte-specific circadian clock mutant [CCM] mice) attenuated/abolished time-of-day variations in I/R outcomes observed in wild-type hearts. Investigation of Akt and glycogen synthase kinase-3β in wild-type and CCM hearts identified these kinases as potential mechanistic ties between the cardiomyocyte circadian clock and I/R tolerance. Conclusions: We expose a profound time-of-day dependence for I/R tolerance, which is mediated by the cardiomyocyte circadian clock. Further understanding of I/R tolerance rhythms will potentially provide novel insight regarding the etiology and treatment of ischemia-induced cardiac dysfunction.

Original languageEnglish (US)
Pages (from-to)546-550
Number of pages5
JournalCirculation Research
Volume106
Issue number3
DOIs
StatePublished - Feb 2010
Externally publishedYes

Fingerprint

Circadian Clocks
Cardiac Myocytes
Reperfusion
Ischemia
Communication
Sleep
Myocardial Infarction
Cardiovascular Physiological Phenomena
Glycogen Synthase Kinase 3
Coronary Occlusion
Coronary Vessels
Fibrosis
Phosphotransferases
Thorax
Incidence

Keywords

  • Chronobiology
  • Ischemia/reperfusion
  • Myocardium

ASJC Scopus subject areas

  • Physiology
  • Cardiology and Cardiovascular Medicine

Cite this

Short communication : Ischemia/reperfusion tolerance is time-of-day- dependent: Mediation by the cardiomyocyte circadian clock. / Durgan, David J.; Pulinilkunnil, Thomas; Villegas-Montoya, Carolina; Garvey, Merissa E.; Frangogiannis, Nikolaos G.; Michael, Lloyd H.; Chow, Chi Wing; Dyck, Jason R B; Young, Martin E.

In: Circulation Research, Vol. 106, No. 3, 02.2010, p. 546-550.

Research output: Contribution to journalArticle

Durgan, DJ, Pulinilkunnil, T, Villegas-Montoya, C, Garvey, ME, Frangogiannis, NG, Michael, LH, Chow, CW, Dyck, JRB & Young, ME 2010, 'Short communication: Ischemia/reperfusion tolerance is time-of-day- dependent: Mediation by the cardiomyocyte circadian clock', Circulation Research, vol. 106, no. 3, pp. 546-550. https://doi.org/10.1161/CIRCRESAHA.109.209346
Durgan, David J. ; Pulinilkunnil, Thomas ; Villegas-Montoya, Carolina ; Garvey, Merissa E. ; Frangogiannis, Nikolaos G. ; Michael, Lloyd H. ; Chow, Chi Wing ; Dyck, Jason R B ; Young, Martin E. / Short communication : Ischemia/reperfusion tolerance is time-of-day- dependent: Mediation by the cardiomyocyte circadian clock. In: Circulation Research. 2010 ; Vol. 106, No. 3. pp. 546-550.
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AU - Frangogiannis, Nikolaos G.

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