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在心肌梗死后重构的性别差异彩虹的某个地方:激素、染色体、炎性小体,哦,我的天。

Somewhere over the sex differences rainbow of myocardial infarction remodeling: hormones, chromosomes, inflammasome, oh my.

机构信息

Department of Medicine, Division of Cardiology, Medical University of South Carolina, and Research Service, Ralph H. Johnson Veterans Affairs Medical Center, Charleston, SC, USA.

Department of Cellular and Integrative Physiology, Center for Heart and Vascular Research, University of Nebraska Medical Center, and Research Service, Nebraska-Western Iowa Health Care System, Omaha, NE, USA.

出版信息

Expert Rev Proteomics. 2019 Nov-Dec;16(11-12):933-940. doi: 10.1080/14789450.2019.1664293. Epub 2019 Sep 11.

DOI:10.1080/14789450.2019.1664293
PMID:31483157
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7007969/
Abstract

: Cardiovascular disease is a major cause of death in both men and women. While women are protected until the onset of menopause, after menopause women have increased risk of adverse cardiovascular disease events. Animal models of myocardial infarction recapitulate many of the sex differences observed in humans, and proteomics evaluations offer mechanistic insights to explain sex differences.: In this review, we will discuss how proteomics has helped us understand the hormonal, chromosomal, and immune mechanisms behind sex differences in response to ischemic injury and the development of heart failure.: There are a number of ways in which proteomics has and will continue to facilitate our understanding of sex differences in cardiac remodeling after myocardial infarction.

摘要

: 心血管疾病是男性和女性死亡的主要原因。虽然女性在绝经前受到保护,但绝经后女性患心血管疾病不良事件的风险增加。心肌梗死的动物模型再现了许多在人类中观察到的性别差异,蛋白质组学评估提供了机制上的见解,以解释对缺血性损伤和心力衰竭发展的反应中的性别差异。在这篇综述中,我们将讨论蛋白质组学如何帮助我们理解激素、染色体和免疫机制背后的性别差异,以及对缺血性损伤的反应和心力衰竭的发展。蛋白质组学有许多方法可以帮助我们理解心肌梗死后心脏重构的性别差异,并且还将继续这样做。

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本文引用的文献

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The Number of X Chromosomes Influences Inflammatory Cytokine Production Following Toll-Like Receptor Stimulation.X 染色体数量影响 Toll 样受体刺激后的炎症细胞因子产生。
Front Immunol. 2019 May 9;10:1052. doi: 10.3389/fimmu.2019.01052. eCollection 2019.
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Inorganic arsenic exposure induces sex-disparate effects and exacerbates ischemia-reperfusion injury in the female heart.无机砷暴露会引发性别差异效应,并加剧雌性心脏的缺血再灌注损伤。
Am J Physiol Heart Circ Physiol. 2019 May 1;316(5):H1053-H1064. doi: 10.1152/ajpheart.00364.2018. Epub 2019 Mar 1.
3
G protein-coupled estrogen receptor activation improves contractile and diastolic functions in rat renal interlobular artery to protect against renal ischemia reperfusion injury.G 蛋白偶联雌激素受体激活可改善大鼠肾小叶间动脉的收缩和舒张功能,防止肾缺血再灌注损伤。
Biomed Pharmacother. 2019 Apr;112:108666. doi: 10.1016/j.biopha.2019.108666. Epub 2019 Feb 20.
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LXR/RXR signaling and neutrophil phenotype following myocardial infarction classify sex differences in remodeling.心肌梗死后 LXR/RXR 信号和中性粒细胞表型可分类重塑的性别差异。
Basic Res Cardiol. 2018 Aug 21;113(5):40. doi: 10.1007/s00395-018-0699-5.
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Metabolic Modulation in Macrophage Effector Function.巨噬细胞效应功能的代谢调节
Front Immunol. 2018 Feb 19;9:270. doi: 10.3389/fimmu.2018.00270. eCollection 2018.
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Heart Disease and Stroke Statistics-2018 Update: A Report From the American Heart Association.《2018年心脏病和中风统计数据更新:美国心脏协会报告》
Circulation. 2018 Mar 20;137(12):e67-e492. doi: 10.1161/CIR.0000000000000558. Epub 2018 Jan 31.
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Gender-related differences in heart failure with preserved ejection fraction.射血分数保留的心力衰竭中的性别相关差异。
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