Suppr超能文献

成年系统性原发性高血压的早期编程。

Early Programming of Adult Systemic Essential Hypertension.

机构信息

Department of Physiology, Instituto Nacional de Cardiología "Ignacio Chávez", Mexico City 14080, Mexico.

Nutrition Biochemistry Laboratory, Research and Food Development Unit. Veracruz Technological Institute, National Technological of Mexico, Veracruz 91897, Mexico.

出版信息

Int J Mol Sci. 2020 Feb 11;21(4):1203. doi: 10.3390/ijms21041203.

Abstract

Cardiovascular diseases are being included in the study of developmental origins of health and disease (DOHaD) and essential systemic hypertension has also been added to this field. Epigenetic modifications are one of the main mechanisms leading to early programming of disease. Different environmental factors occurring during critical windows in the early stages of life may leave epigenetic cues, which may be involved in the programming of hypertension when individuals reach adulthood. Such environmental factors include pre-term birth, low weight at birth, altered programming of different organs such as the blood vessels and the kidney, and living in disadvantageous conditions in the programming of hypertension. Mechanisms behind these factors that impact on the programming include undernutrition, oxidative stress, inflammation, emotional stress, and changes in the microbiota. These factors and their underlying causes acting at the vascular level will be discussed in this paper. We also explore the establishment of epigenetic cues that may lead to hypertension at the vascular level such as DNA methylation, histone modifications (methylation and acetylation), and the role of microRNAs in the endothelial cells and blood vessel smooth muscle which participate in hypertension. Since epigenetic changes are reversible, the knowledge of this type of markers could be useful in the field of prevention, diagnosis or epigenetic drugs as a therapeutic approach to hypertension.

摘要

心血管疾病被纳入健康与疾病的发育起源(DOHaD)研究中,原发性高血压也被纳入这一领域。表观遗传修饰是导致疾病早期程序化的主要机制之一。在生命早期的关键窗口期发生的不同环境因素可能会留下表观遗传线索,当个体进入成年期时,这些线索可能与高血压的编程有关。这些环境因素包括早产、出生体重低、血管和肾脏等不同器官的编程改变,以及在编程中生活在不利条件下导致的高血压。影响编程的这些因素背后的机制包括营养不足、氧化应激、炎症、情绪压力和微生物群的改变。本文将讨论这些因素及其在血管水平上对编程的影响。我们还探讨了可能导致血管水平高血压的表观遗传线索的建立,如 DNA 甲基化、组蛋白修饰(甲基化和乙酰化)以及参与高血压的内皮细胞和血管平滑肌中 microRNAs 的作用。由于表观遗传变化是可逆的,因此了解这种类型的标记物可能有助于预防、诊断或作为治疗高血压的一种治疗方法。

相似文献

4
Hypertensive epigenetics: from DNA methylation to microRNAs.高血压表观遗传学:从DNA甲基化到微小RNA
J Hum Hypertens. 2015 Oct;29(10):575-82. doi: 10.1038/jhh.2014.132. Epub 2015 Jan 29.
7
The Role of DNA Methylation in Hypertension.DNA甲基化在高血压中的作用。
Adv Exp Med Biol. 2017;956:583-598. doi: 10.1007/5584_2016_80.
10
Early programming of hypertension.高血压的早期编程。
Arch Argent Pediatr. 2022 Feb;120(1):e8-e16. doi: 10.5546/aap.2022.eng.e8. Epub 2021 Dec 17.

引用本文的文献

2
The Update of Fetal Growth Restriction Associated with Biomarkers.与生物标志物相关的胎儿生长受限研究进展
Matern Fetal Med. 2022 Jul 22;4(3):210-217. doi: 10.1097/FM9.0000000000000156. eCollection 2022 Jul.
9

本文引用的文献

3
Role of T-cell activation in salt-sensitive hypertension.T细胞激活在盐敏感性高血压中的作用。
Am J Physiol Heart Circ Physiol. 2019 Jun 1;316(6):H1345-H1353. doi: 10.1152/ajpheart.00096.2019. Epub 2019 Mar 22.
7
Epigenetics of chronic inflammatory diseases.慢性炎症性疾病的表观遗传学
J Inflamm Res. 2018 Dec 20;12:1-14. doi: 10.2147/JIR.S129027. eCollection 2019.
10
Preterm Birth: Long Term Cardiovascular and Renal Consequences.早产:长期心血管和肾脏后果。
Curr Pediatr Rev. 2018;14(4):219-226. doi: 10.2174/1573396314666180813121652.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验