• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

心脏发育与转录因子:胰岛素信号传导、胰岛素抵抗与心血管疾病的宫内营养编程

Cardiac Development and Transcription Factors: Insulin Signalling, Insulin Resistance, and Intrauterine Nutritional Programming of Cardiovascular Disease.

作者信息

Govindsamy Annelene, Naidoo Strinivasen, Cerf Marlon E

机构信息

Discipline of Pharmaceutical Sciences, University of KwaZulu-Natal, Durban, South Africa.

Biomedical Research and Innovation Platform, South African Medical Research Council, Cape Town, South Africa.

出版信息

J Nutr Metab. 2018 Feb 1;2018:8547976. doi: 10.1155/2018/8547976. eCollection 2018.

DOI:10.1155/2018/8547976
PMID:29484207
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5816854/
Abstract

Programming with an insult or stimulus during critical developmental life stages shapes metabolic disease through divergent mechanisms. Cardiovascular disease increasingly contributes to global morbidity and mortality, and the heart as an insulin-sensitive organ may become insulin resistant, which manifests as micro- and/or macrovascular complications due to diabetic complications. Cardiogenesis is a sequential process during which the heart develops into a mature organ and is regulated by several cardiac-specific transcription factors. Disrupted cardiac insulin signalling contributes to cardiac insulin resistance. Intrauterine under- or overnutrition alters offspring cardiac structure and function, notably cardiac hypertrophy, systolic and diastolic dysfunction, and hypertension that precede the onset of cardiovascular disease. Optimal intrauterine nutrition and oxygen saturation are required for normal cardiac development in offspring and the maintenance of their cardiovascular physiology.

摘要

在关键的发育生命阶段受到侮辱或刺激进行编程,会通过不同机制引发代谢性疾病。心血管疾病对全球发病率和死亡率的影响日益增加,心脏作为一个对胰岛素敏感的器官可能会出现胰岛素抵抗,这会表现为糖尿病并发症导致的微血管和/或大血管并发症。心脏发生是一个连续的过程,在此过程中,心脏发育成为一个成熟的器官,并受到多种心脏特异性转录因子的调控。心脏胰岛素信号传导中断会导致心脏胰岛素抵抗。子宫内营养不足或营养过剩会改变后代的心脏结构和功能,特别是在心血管疾病发作之前出现的心脏肥大、收缩和舒张功能障碍以及高血压。后代正常的心脏发育及其心血管生理功能的维持需要最佳的子宫内营养和氧饱和度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0238/5816854/ab5c86d35ac3/JNME2018-8547976.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0238/5816854/ab5c86d35ac3/JNME2018-8547976.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0238/5816854/ab5c86d35ac3/JNME2018-8547976.001.jpg

相似文献

1
Cardiac Development and Transcription Factors: Insulin Signalling, Insulin Resistance, and Intrauterine Nutritional Programming of Cardiovascular Disease.心脏发育与转录因子:胰岛素信号传导、胰岛素抵抗与心血管疾病的宫内营养编程
J Nutr Metab. 2018 Feb 1;2018:8547976. doi: 10.1155/2018/8547976. eCollection 2018.
2
High fat programming of beta cell compensation, exhaustion, death and dysfunction.β细胞代偿、耗竭、死亡及功能障碍的高脂肪编程
Pediatr Diabetes. 2015 Mar;16(2):71-8. doi: 10.1111/pedi.12137. Epub 2014 Apr 3.
3
Metabolic imprinting by prenatal, perinatal, and postnatal overnutrition: a review.产前、围生期和产后过度营养导致的代谢印迹:综述。
Semin Reprod Med. 2011 May;29(3):266-76. doi: 10.1055/s-0031-1275521. Epub 2011 Jul 18.
4
High fat programming of beta-cell failure.高脂肪编程导致β细胞衰竭。
Adv Exp Med Biol. 2010;654:77-89. doi: 10.1007/978-90-481-3271-3_5.
5
HORSE SPECIES SYMPOSIUM: Nutritional programming and the impact on mare and foal performance.马种研讨会:营养编程及其对母马和马驹性能的影响。
J Anim Sci. 2015 Jul;93(7):3261-7. doi: 10.2527/jas.2015-9057.
6
Cardiac insulin-resistance and decreased mitochondrial energy production precede the development of systolic heart failure after pressure-overload hypertrophy.心脏胰岛素抵抗和线粒体能量产生减少先于压力超负荷肥厚后收缩性心力衰竭的发展。
Circ Heart Fail. 2013 Sep 1;6(5):1039-48. doi: 10.1161/CIRCHEARTFAILURE.112.000228. Epub 2013 Jul 16.
7
Puerarin Improves Vascular Insulin Resistance and Cardiovascular Remodeling in Salt-Sensitive Hypertension.葛根素改善盐敏感性高血压血管胰岛素抵抗和心血管重塑。
Am J Chin Med. 2017;45(6):1169-1184. doi: 10.1142/S0192415X17500641. Epub 2017 Aug 22.
8
Developmental Programming of Renal Function and Re-Programming Approaches.肾功能的发育编程与重编程方法
Front Pediatr. 2018 Feb 27;6:36. doi: 10.3389/fped.2018.00036. eCollection 2018.
9
Postnatal undernutrition alters adult female mouse cardiac structure and function leading to limited exercise capacity.产后营养不良改变成年雌性小鼠的心脏结构和功能,导致运动能力受限。
J Physiol. 2019 Apr;597(7):1855-1872. doi: 10.1113/JP277637. Epub 2019 Mar 3.
10
Leptin as mediator of the effects of developmental programming.瘦素作为发育编程效应的中介物。
Best Pract Res Clin Endocrinol Metab. 2012 Oct;26(5):677-87. doi: 10.1016/j.beem.2012.03.005. Epub 2012 May 22.

引用本文的文献

1
Harnessing developmental cues for cardiomyocyte production.利用发育线索产生心肌细胞。
Development. 2023 Aug 1;150(15). doi: 10.1242/dev.201483. Epub 2023 Aug 10.
2
Made in the Womb: Maternal Programming of Offspring Cardiovascular Function by an Obesogenic Womb.子宫内形成:致肥胖子宫对后代心血管功能的母体编程
Metabolites. 2023 Jul 13;13(7):845. doi: 10.3390/metabo13070845.
3
Identification of the metabolic state of surviving cardiomyocytes in the human infarcted heart by spatial single-cell transcriptomics.通过空间单细胞转录组学鉴定人类梗死心脏中存活心肌细胞的代谢状态

本文引用的文献

1
Experimentally induced intrauterine growth restriction in rabbits leads to differential remodelling of left versus right ventricular myocardial microstructure.实验诱导的兔子宫内生长受限导致左心室与右心室心肌微观结构的差异重塑。
Histochem Cell Biol. 2017 Nov;148(5):557-567. doi: 10.1007/s00418-017-1587-z. Epub 2017 Jul 10.
2
Intrauterine Growth Restriction: Antenatal and Postnatal Aspects.宫内生长受限:产前和产后情况
Clin Med Insights Pediatr. 2016 Jul 14;10:67-83. doi: 10.4137/CMPed.S40070. eCollection 2016.
3
Influence of paternal preconception exposures on their offspring: through epigenetics to phenotype.
Cardiol Plus. 2023 Jan-Mar;8(1):18-26. doi: 10.1097/CP9.0000000000000038. Epub 2023 Apr 4.
4
Amniotic Fluid Mesenchymal Stromal Cells Derived from Fetuses with Isolated Cardiac Defects Exhibit Decreased Proliferation and Cardiomyogenic Potential.源自患有孤立性心脏缺陷胎儿的羊水间充质基质细胞表现出增殖能力降低和成心肌潜力下降。
Biology (Basel). 2023 Apr 5;12(4):552. doi: 10.3390/biology12040552.
5
Pregestational diabetes alters cardiac structure and function of neonatal rats through developmental plasticity.孕前糖尿病通过发育可塑性改变新生大鼠的心脏结构和功能。
Front Cardiovasc Med. 2022 Sep 13;9:919293. doi: 10.3389/fcvm.2022.919293. eCollection 2022.
6
Sexual dimorphism in testosterone programming of cardiomyocyte development in sheep.绵羊心肌细胞发育过程中睾酮的性别二态性编程。
Am J Physiol Heart Circ Physiol. 2022 Apr 1;322(4):H607-H621. doi: 10.1152/ajpheart.00691.2021. Epub 2022 Feb 4.
7
Programming With Varying Dietary Fat Content Alters Cardiac Insulin Receptor, Glut4 and FoxO1 Immunoreactivity in Neonatal Rats, Whereas High Fat Programming Alters Cebpa Gene Expression in Neonatal Female Rats.改变膳食脂肪含量编程会改变新生大鼠心脏胰岛素受体、Glut4 和 FoxO1 的免疫反应,而高脂肪编程会改变新生雌性大鼠 Cebpa 基因的表达。
Front Endocrinol (Lausanne). 2022 Jan 5;12:772095. doi: 10.3389/fendo.2021.772095. eCollection 2021.
8
Cardiac magnetic resonance imaging: insights into developmental programming and its consequences for aging.心脏磁共振成像:对发育编程及其对衰老影响的深入了解。
J Dev Orig Health Dis. 2021 Apr;12(2):203-219. doi: 10.1017/S2040174420001233. Epub 2020 Dec 22.
9
Human Induced Pluripotent Stem-Cell-Derived Cardiomyocytes as Models for Genetic Cardiomyopathies.人诱导多能干细胞衍生心肌细胞作为遗传性心肌病模型。
Int J Mol Sci. 2019 Sep 6;20(18):4381. doi: 10.3390/ijms20184381.
10
SIRT6 Suppresses NFATc4 Expression and Activation in Cardiomyocyte Hypertrophy.SIRT6在心肌细胞肥大中抑制NFATc4的表达和激活。
Front Pharmacol. 2019 Jan 8;9:1519. doi: 10.3389/fphar.2018.01519. eCollection 2018.
父亲孕前暴露对其后代的影响:从表观遗传学到表型
Am J Stem Cells. 2016 May 15;5(1):11-8. eCollection 2016.
4
Intrauterine growth restriction: impact on cardiovascular development and function throughout infancy.宫内生长受限:对婴儿期心血管发育和功能的影响
Pediatr Res. 2016 Jun;79(6):821-30. doi: 10.1038/pr.2016.24. Epub 2016 Feb 11.
5
Maternal high-fat diet impairs cardiac function in offspring of diabetic pregnancy through metabolic stress and mitochondrial dysfunction.孕期糖尿病母亲的高脂饮食通过代谢应激和线粒体功能障碍损害子代心脏功能。
Am J Physiol Heart Circ Physiol. 2016 Mar 15;310(6):H681-92. doi: 10.1152/ajpheart.00795.2015. Epub 2016 Jan 22.
6
The programming of cardiovascular disease.心血管疾病的编程
J Dev Orig Health Dis. 2015 Oct;6(5):366-76. doi: 10.1017/S2040174415001300. Epub 2015 Jul 15.
7
Intrauterine programming.宫内编程。
Iran J Basic Med Sci. 2015 Mar;18(3):212-20.
8
DNA methylation mediates the effect of maternal smoking during pregnancy on birthweight of the offspring.DNA甲基化介导孕期母亲吸烟对后代出生体重的影响。
Int J Epidemiol. 2015 Aug;44(4):1224-37. doi: 10.1093/ije/dyv048. Epub 2015 Apr 10.
9
Epigenomics: Roadmap for regulation.表观基因组学:调控路线图
Nature. 2015 Feb 19;518(7539):314-6. doi: 10.1038/518314a.
10
Developmental programming of cardiovascular disease following intrauterine growth restriction: findings utilising a rat model of maternal protein restriction.宫内生长受限后心血管疾病的发育编程:利用母体蛋白质限制大鼠模型的研究结果
Nutrients. 2014 Dec 29;7(1):119-52. doi: 10.3390/nu7010119.