Human cardiac ischemia‐reperfusion injury: Blunted stress response with age. Issue 10 (11th July 2021)

• Record Type: Journal Article
• Authors: Oliveira, Ashley N.; Yanagawa, Bobby; Quan, Adrian; Verma, Subodh; Hood, David A.
• Is Part Of: Journal of cardiac surgery. Volume 36:Issue 10(2021)
• Page Start: 3643
• Page End: 3651
• Publication Date: 2021-07-11
• Subjects: aging myocardium -- autophagy -- ischemia‐reperfusion -- mitochondria -- mitophagy; Heart -- Surgery -- Periodicals; 617.412005
• DOI: 10.1111/jocs.15807
• Languages: English
• ISSNs: 0886-0440

Abstract

Abstract: Background and Aim: Autophagy is a cytoprotective recycling mechanism, capable of digesting dysfunctional cellular components, and this process is associated with pro‐survival outcomes. Autophagy may decline in the aging myocardium, thereby contributing to cardiac dysfunction. However, it remains to be established how autophagy responds to ischemia‐reperfusion stress with age. Methods: Samples from the right atrium were collected from young (≤50 years; n = 5) and aged (≥70 years; n = 11) patients before and immediately following cardioplegic arrest during coronary artery bypass grafting surgery, a model of human ischemia‐reperfusion injury. Results: Mitochondrial content, as assessed by a cohort of mitochondrial markers, exhibited an overall decrease in the aging myocardium ( p = 0.01). In response to IR, COX‐I (0.63 vs. 0.91, p = 0.01) increased in young, but not in aged patients (interaction effect p = 0.08). Reductions in LC3‐I (0.48 vs. 0.28, p = 0.02) along with declines in TFEB and TFE3 (0.63 vs. 0.20, p = 0.05; 0.71 vs. 0.20, p = 0.01) were observed with age suggesting an impairment in the aged myocardium. Aged patients also displayed an inability to mount an appropriate response to IR compared to their young counterparts, specifically, increases in v‐ATPase and NIX (1.06 vs 0.69, p = .01; 1.15 vs 0.69, p = .001) were not seen in the aged. Conclusion: Our data demonstrate a reduced cardiac mitochondrial content and a blunted mitochondrial response to ischemia with age, accompanied by a possible impairment in mitophagy. These findings support an age‐associated inability of the atrial myocardium to mount appropriate adaptive responses to stress.