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冠状动脉微血管功能障碍中的跨心肌ω-3脂肪酸梯度

Trans-myocardial omega-3 fatty acid gradient in coronary microvascular dysfunction.

作者信息

Keeley Ellen C, Handberg Eileen M, Noel Bairey Merz C, Pepine Carl J

机构信息

Department of Medicine, Division of Cardiovascular Medicine, University of Florida, Gainesville, FL, United States of America.

Barbra Streisand Heart Center, Smidt Heart Institute, Cedars-Sinai Medical Center, Los Angeles, CA, United States of America.

出版信息

Am Heart J Plus. 2022 Oct;22. doi: 10.1016/j.ahjo.2022.100213. Epub 2022 Sep 28.

DOI:10.1016/j.ahjo.2022.100213
PMID:37377675
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10297500/
Abstract

BACKGROUND

Cardiac remodeling is a process mediated, in part, by 18-hydroxyeicosapentaenoic acid (HEPE), a metabolite of the omega-3 polyunsaturated fatty acid, eicosapentaenoic acid (EPA). We hypothesized that trans-myocardial levels of 18-HEPE could inform the pathophysiologic processes involved in heart failure with preserved ejection fraction (HFpEF).

METHODS

We measured the concentration of 18-HEPE and EPA in trans-myocardial plasma samples from 10 subjects enrolled in The Women's Ischemia Syndrome Evaluation [WISE] Mechanisms of Coronary Microvascular Dysfunction Leading to Pre-HFpEF project.

RESULTS

Concentrations of 18-HEPE were significantly lower in coronary venous compared to the aortic plasma (270.5 pg/mL [212.8-480.8] vs. 430.5 pg/mL [299.5-655.8], = 0.0039). There was a significant correlation between the concentrations of coronary venous EPA and aortic 18-HEPE ( = 0.94, = 0.0002), and aortic EPA and aortic 18-HEPE ( = 0.82, = 0.0058).

CONCLUSIONS

Results of this small pilot study support the suggestion that 18-HEPE is synthesized outside the heart and utilized within the myocardial bed.

摘要

背景

心脏重塑是一个部分由18-羟基二十碳五烯酸(18-HEPE)介导的过程,18-HEPE是ω-3多不饱和脂肪酸二十碳五烯酸(EPA)的一种代谢产物。我们假设经心肌的18-HEPE水平可以反映射血分数保留的心力衰竭(HFpEF)所涉及的病理生理过程。

方法

我们测量了参与“女性缺血综合征评估[WISE]导致HFpEF前期的冠状动脉微血管功能障碍机制”项目的10名受试者经心肌血浆样本中18-HEPE和EPA的浓度。

结果

与主动脉血浆相比,冠状动脉静脉血中18-HEPE的浓度显著降低(270.5 pg/mL [212.8 - 480.8] vs. 430.5 pg/mL [299.5 - 655.8],P = 0.0039)。冠状动脉静脉血EPA浓度与主动脉18-HEPE浓度之间存在显著相关性(r = 0.94,P = 0.0002),以及主动脉EPA与主动脉18-HEPE之间也存在显著相关性(r = 0.82,P = 0.0058)。

结论

这项小型初步研究的结果支持以下观点,即18-HEPE在心脏外合成并在心肌床内被利用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a073/10978403/8c03090b3d53/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a073/10978403/33cc595def59/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a073/10978403/8c03090b3d53/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a073/10978403/33cc595def59/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a073/10978403/8c03090b3d53/gr2.jpg

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本文引用的文献

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Specialized Proresolving Mediators in Symptomatic Women With Coronary Microvascular Dysfunction (from the Women's Ischemia Trial to Reduce Events in Nonobstructive CAD [WARRIOR] Trial).有症状的女性冠状动脉微血管功能障碍患者中的特异性促解决介质(来自女性缺血试验以减少非阻塞性 CAD 中的事件[WARRIOR]试验)。
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Inflammatory biomarkers as predictors of heart failure in women without obstructive coronary artery disease: A report from the NHLBI-sponsored Women's Ischemia Syndrome Evaluation (WISE).
炎症生物标志物作为无阻塞性冠状动脉疾病女性心力衰竭的预测指标:美国国立心肺血液研究所资助的女性缺血综合征评估(WISE)报告
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18-HEPE, an n-3 fatty acid metabolite released by macrophages, prevents pressure overload-induced maladaptive cardiac remodeling.18-HEPE,一种由巨噬细胞释放的 n-3 脂肪酸代谢物,可预防压力超负荷引起的适应性心脏重构。
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Identification and signature profiles for pro-resolving and inflammatory lipid mediators in human tissue.在人体组织中鉴定和特征分析促修复和促炎脂质介质。
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