Suppr超能文献

孕期接触亚砷酸盐会改变妊娠晚期的母体心脏重塑。

Prenatal arsenite exposure alters maternal cardiac remodeling during late pregnancy.

作者信息

Taube Nicole, Kabir Raihan, Ebenebe Obialunanma V, Garbus Haley, Alam El Din Sarah-Marie, Illingworth Emily, Fitch Michael, Wang Nadan, Kohr Mark J

机构信息

Department of Environmental Health and Engineering, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, United States.

Cardiology Division, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, United States.

出版信息

Toxicol Appl Pharmacol. 2024 Feb;483:116833. doi: 10.1016/j.taap.2024.116833. Epub 2024 Jan 23.

Abstract

Exposure to inorganic arsenic through drinking water is widespread and has been linked to many chronic diseases, including cardiovascular disease. Arsenic exposure has been shown to alter hypertrophic signaling in the adult heart, as well as in utero offspring development. However, the effect of arsenic on maternal cardiac remodeling during pregnancy has not been studied. As such, there is a need to understand how environmental exposure contributes to adverse pregnancy-related cardiovascular events. This study seeks to understand the impact of trivalent inorganic arsenic exposure during gestation on maternal cardiac remodeling in late pregnancy, as well as offspring outcomes. C57BL/6 J mice were exposed to 0 (control), 100 or 1000 μg/L sodium arsenite (NaAsO) beginning at embryonic day (E) 2.5 and continuing through E17.5. Maternal heart function and size were assessed via transthoracic echocardiography, gravimetric measurement, and histology. Transcript levels of hypertrophic markers were probed via qRT-PCR and confirmed by western blot. Offspring outcomes were assessed through echocardiography and gravimetric measurement. We found that maternal heart size was smaller and transcript levels of Esr1 (estrogen receptor alpha), Pgrmc1 (progesterone receptor membrane component 1) and Pgrmc2 (progesterone receptor membrane component 2) reduced during late pregnancy with exposure to 1000 μg/L iAs vs. non-exposed pregnant controls. Both 100 and 1000 μg/L iAs also reduced transcription of Nppa (atrial natriuretic peptide). Akt protein expression was also significantly reduced after 1000 μg/L iAs exposure in the maternal heart with no change in activating phosphorylation. This significant abrogation of maternal cardiac hypertrophy suggests that arsenic exposure during pregnancy can potentially contribute to cardiovascular disease. Taken together, our findings further underscore the importance of reducing arsenic exposure during pregnancy and indicate that more research is needed to assess the impact of arsenic and other environmental exposures on the maternal heart and adverse pregnancy events.

摘要

通过饮用水接触无机砷的情况很普遍,并且与许多慢性疾病有关,包括心血管疾病。研究表明,砷暴露会改变成年心脏以及子宫内子代发育中的肥厚信号。然而,砷对孕期母体心脏重塑的影响尚未得到研究。因此,有必要了解环境暴露如何导致与妊娠相关的不良心血管事件。本研究旨在了解妊娠期三价无机砷暴露对妊娠晚期母体心脏重塑以及子代结局的影响。从胚胎第2.5天开始,将C57BL/6 J小鼠暴露于0(对照)、100或1000μg/L的亚砷酸钠(NaAsO)中,并持续至胚胎第17.5天。通过经胸超声心动图、重量测量和组织学评估母体心脏功能和大小。通过qRT-PCR检测肥厚标志物的转录水平,并通过蛋白质印迹法进行确认。通过超声心动图和重量测量评估子代结局。我们发现,与未暴露的怀孕对照组相比,暴露于1000μg/L无机砷的妊娠晚期母体心脏尺寸较小,Esr1(雌激素受体α)、Pgrmc1(孕激素受体膜成分1)和Pgrmc2(孕激素受体膜成分2)的转录水平降低。100和1000μg/L的无机砷也降低了Nppa(心钠素)的转录。在母体心脏中暴露于1000μg/L无机砷后,Akt蛋白表达也显著降低,而激活磷酸化没有变化。母体心脏肥大的这种显著消除表明,孕期砷暴露可能会导致心血管疾病。综上所述,我们的研究结果进一步强调了孕期减少砷暴露的重要性,并表明需要更多研究来评估砷和其他环境暴露对母体心脏和不良妊娠事件的影响。

相似文献

1
Prenatal arsenite exposure alters maternal cardiac remodeling during late pregnancy.
Toxicol Appl Pharmacol. 2024 Feb;483:116833. doi: 10.1016/j.taap.2024.116833. Epub 2024 Jan 23.
2
Prenatal Arsenite Exposure Alters Maternal Cardiac Remodeling During Late Pregnancy.
bioRxiv. 2023 Sep 29:2023.09.28.559986. doi: 10.1101/2023.09.28.559986.
3
Gestational arsenite exposure alters maternal postpartum heart size and induces Ca-handling dysregulation in cardiomyocytes.
Am J Physiol Heart Circ Physiol. 2025 Mar 1;328(3):H460-H471. doi: 10.1152/ajpheart.00266.2024. Epub 2025 Jan 31.
5
Inorganic arsenic induces sex-dependent pathological hypertrophy in the heart.
Am J Physiol Heart Circ Physiol. 2021 Apr 1;320(4):H1321-H1336. doi: 10.1152/ajpheart.00435.2020. Epub 2021 Jan 22.
6
Effects of maternal exposure to arsenic on social behavior and related gene expression in F2 male mice.
Environ Health Prev Med. 2021 Mar 11;26(1):34. doi: 10.1186/s12199-021-00956-y.
8
Inorganic arsenic exposure induces sex-disparate effects and exacerbates ischemia-reperfusion injury in the female heart.
Am J Physiol Heart Circ Physiol. 2019 May 1;316(5):H1053-H1064. doi: 10.1152/ajpheart.00364.2018. Epub 2019 Mar 1.
10
In utero exposure to arsenite contributes to metabolic and reproductive dysfunction in male offspring of CD-1 mice.
Reprod Toxicol. 2020 Aug;95:95-103. doi: 10.1016/j.reprotox.2020.05.006. Epub 2020 May 17.

引用本文的文献

1
Gestational arsenite exposure alters maternal postpartum heart size and induces Ca-handling dysregulation in cardiomyocytes.
Am J Physiol Heart Circ Physiol. 2025 Mar 1;328(3):H460-H471. doi: 10.1152/ajpheart.00266.2024. Epub 2025 Jan 31.

本文引用的文献

1
Effects of Sodium Arsenite on the Myocardial Differentiation in Mouse Embryonic Bodies.
Toxics. 2023 Feb 1;11(2):142. doi: 10.3390/toxics11020142.
3
Arsenic exposure during juvenile and puberty significantly affected reproductive system development of female SD rats.
Ecotoxicol Environ Saf. 2022 Sep 1;242:113857. doi: 10.1016/j.ecoenv.2022.113857. Epub 2022 Jul 7.
4
Associations of exposure to lead and cadmium with risk of all-cause and cardiovascular disease mortality among patients with type 2 diabetes.
Environ Sci Pollut Res Int. 2022 Nov;29(51):76805-76815. doi: 10.1007/s11356-022-21273-z. Epub 2022 Jun 7.
5
Arsenic Exposure, Blood DNA Methylation, and Cardiovascular Disease.
Circ Res. 2022 Jul 8;131(2):e51-e69. doi: 10.1161/CIRCRESAHA.122.320991. Epub 2022 Jun 6.
6
Metabolic signatures of pregnancy-induced cardiac growth.
Am J Physiol Heart Circ Physiol. 2022 Jul 1;323(1):H146-H164. doi: 10.1152/ajpheart.00105.2022. Epub 2022 May 27.
7
Maternal obesity causes fetal cardiac hypertrophy and alters adult offspring myocardial metabolism in mice.
J Physiol. 2022 Jul;600(13):3169-3191. doi: 10.1113/JP282462. Epub 2022 May 11.
8
Indoxyl Sulfate Activates NLRP3 Inflammasome to Induce Cardiac Contractile Dysfunction Accompanied by Myocardial Fibrosis and Hypertrophy.
Cardiovasc Toxicol. 2022 Apr;22(4):365-377. doi: 10.1007/s12012-021-09718-2. Epub 2022 Jan 28.
9
The Relationship Between Preeclampsia and Arsenic Concentration in the Peripheral Blood.
Biol Trace Elem Res. 2022 Sep;200(9):3965-3974. doi: 10.1007/s12011-021-02988-5. Epub 2022 Jan 7.
10
Maternal exposure to arsenic in drinking water and risk of congenital heart disease in the offspring.
Environ Int. 2022 Feb;160:107051. doi: 10.1016/j.envint.2021.107051. Epub 2021 Dec 20.

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