Key result
Cardiomyocyte-specific MAO-B knockout reduces infarct size after ischemia/reperfusion in male but not female mice.
Why the study?
Because sex hormones strongly impact MAO metabolic pathways, the in vivo impact of cardiomyocyte-specific MAO-B knockout on myocardial infarct size following ischemia/reperfusion in male versus female mice remained to be determined.
Does cardiomyocyte-specific knockout of MAO-B reduce myocardial infarct size following ischemia/reperfusion in male and female mice?
Does cardiomyocyte-specific knockout of MAO-B reduce myocardial infarct size following ischemia/reperfusion in male and female mice?
Cardiomyocyte-specific MAO-B knockout provides sex-specific cardioprotection against acute myocardial infarction, reducing infarct size in male but not female mice.
Answers are grounded in this paper and cite their sources.
Should not alter clinical I/R management; hypothesis-generating for sex-specific MAO-B effects in preclinical models.
The cardiomyocyte-specific knockout (KO) of monoamine oxidase (MAO)-B, an enzyme involved in the formation of reactive oxygen species (ROS), reduced myocardial ischemia/reperfusion (I/R) injury in vitro. Because sex hormones have a strong impact on MAO metabolic pathways, we analyzed the myocardial infarct size (IS) following I/R in female and male MAO-B KO mice in vivo. METHOD AND RESULTS: littermates) were fed with tamoxifen for 2 weeks followed by 10 weeks of normal mice chow. Myocardial infarction (assessed by TTC staining and expressed as a percentage of the area at risk as determined by Evans blue staining)) was induced by 45 min coronary occlusion followed by 120 min of reperfusion. RESULTS: The mortality following I/R was higher in male compared to female mice, with the lowest mortality found in MAO-B KO female mice. IS was significantly higher in male WT mice compared to female WT mice. MAO-B KO reduced IS in male mice but had no further impact on IS in female MAO-B KO mice. Interestingly, there was no difference in the plasma estradiol levels among the groups. CONCLUSION: The cardiomyocyte-specific knockout of MAO-B protects male mice against acute myocardial infarction but had no effect on the infarct size in female mice.
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Heger et al. (2023) studied Acute Myocardial Infarction. Cardiomyocyte-specific knockout of MAO-B vs. Wild-type (WT) mice was evaluated on Myocardial infarct size (IS) following ischemia/reperfusion. Cardiomyocyte-specific knockout of MAO-B reduced myocardial infarct size in male mice following ischemia/reperfusion, but had no effect on infarct size in female mice.
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