4.7 Article

Circadian Dependence of the Acute Immune Response to Myocardial Infarction

期刊

FRONTIERS IN PHARMACOLOGY
卷 13, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fphar.2022.869512

关键词

myocardial infarction; immune response; inflammation; circadian rhythms; leukocytes; neutrophils

资金

  1. Alexandre Suerman program for MD/PhD students of the University Medical Center Utrecht, Netherlands
  2. HUSTCare grant from the Netherlands CardioVascular Research Initiative (CVON): the Dutch Heart Foundation
  3. Dutch Federation of University Medical Centers
  4. Netherlands Organization for Health Research and Development
  5. Royal Netherlands Academy of Sciences, Veni [ZonMW91612147]
  6. Netherlands Heart Foundation [2013T056]
  7. Dekker Senior Clinical Scientist 2019 [2019T056]
  8. EU's H2020 research and innovation programme under Marie S. Curie co-fund RESCUE Grant [801540]

向作者/读者索取更多资源

Circadian rhythms play a crucial role in the hyperacute immune response after a myocardial infarction (MI). The levels of immune cells and cardiac damage vary throughout the day, indicating the circadian influence on the immune response. These findings align with the clinical observation that patients who experience an MI early in the morning have worse outcomes.
Circadian rhythms influence the recruitment of immune cells and the onset of inflammation, which is pivotal in the response to ischemic cardiac injury after a myocardial infarction (MI). The hyperacute immune response that occurs within the first few hours after a MI has not yet been elucidated. Therefore, we characterized the immune response and myocardial damage 3 hours after a MI occurs over a full twenty-four-hour period to investigate the role of the circadian rhythms in this response. MI was induced at Zeitgeber Time (ZT) 2, 8, 14, and 20 by permanent ligation of the left anterior descending coronary artery. Three hours after surgery, animals were terminated and blood and hearts collected to assess the immunological status and cardiac damage. Blood leukocyte numbers varied throughout the day, peaking during the rest-phase (ZT2 and 8). Extravasation of leukocytes was more pronounced during the active-phase (ZT14 and 20) and was associated with greater chemokine release to the blood and expression of adhesion molecules in the heart. Damage to the heart, measured by Troponin-I plasma levels, was elevated during this time frame. Clock gene oscillations remained intact in both MI-induced and sham-operated mice hearts, which could explain the circadian influence of the hyperacute inflammatory response after a MI. These findings are in line with the clinical observation that patients who experience a MI early in the morning (i.e., early active phase) have worse clinical outcomes. This study provides further insight on the immune response occurring shortly after an MI, which may contribute to the development of novel and optimization of current therapeutic approaches.

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