CXCR2 antagonism or neutrophil-specific CXCR2 knockout during the active phase (ZT13) significantly reduced infarct size and improved cardiac function after myocardial infarction.
Myocardial infarction (MI) is the leading cause of death in Western countries. Epidemiological studies show acute MI to be more prevalent in the morning and to be associated with a poorer outcome in terms of mortality and recovery. The mechanisms behind this association are not fully understood. Here, we report that circadian oscillations of neutrophil recruitment to the heart determine infarct size, healing, and cardiac function after MI Preferential cardiac neutrophil recruitment during the active phase (Zeitgeber time, ZT13) was paralleled by enhanced myeloid progenitor production, increased circulating numbers of CXCR2(hi) neutrophils as well as upregulated cardiac adhesion molecule and chemokine expression. MI at ZT13 resulted in significantly higher cardiac neutrophil infiltration compared to ZT5, which was inhibited by CXCR2 antagonism or neutrophil-specific CXCR2 knockout. Limiting exaggerated neutrophilic inflammation at this time point significantly reduced the infarct size and improved cardiac function.
Schloss et al. (Wed,) conducted a other in Myocardial infarction. CXCR2 antagonism or neutrophil-specific CXCR2 knockout was evaluated on Infarct size and cardiac function. CXCR2 antagonism or neutrophil-specific CXCR2 knockout during the active phase (ZT13) significantly reduced infarct size and improved cardiac function after myocardial infarction.
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