Prenatal high-sucrose diet affects pulmonary artery contractile functions via MT receptors

IF 3.3 4区 医学 Q2 REPRODUCTIVE BIOLOGY
Xueqin Feng , Hongwei Fu , Xiao Sun , Hua Shu , Yongning Zhu , Yanyan Bai , Qinggui Ren , Xinying Liu , Meng Liu , Fanyong Zhang , Yanping Wang
{"title":"Prenatal high-sucrose diet affects pulmonary artery contractile functions via MT receptors","authors":"Xueqin Feng ,&nbsp;Hongwei Fu ,&nbsp;Xiao Sun ,&nbsp;Hua Shu ,&nbsp;Yongning Zhu ,&nbsp;Yanyan Bai ,&nbsp;Qinggui Ren ,&nbsp;Xinying Liu ,&nbsp;Meng Liu ,&nbsp;Fanyong Zhang ,&nbsp;Yanping Wang","doi":"10.1016/j.reprotox.2024.108760","DOIUrl":null,"url":null,"abstract":"<div><div>A high sucrose diet during pregnancy may generate profound effects on vascular diseases in offspring later in life. Pulmonary artery (PA) functions is closely related to pulmonary hypertension, but whether and how prenatal high-sucrose diet (HS) affect pulmonary vasoreactivity in adult offspring remains unknown. We investigated the alterations of PA reactivity in postnatal offspring exposed to prenatal HS. Pregnant Sprague-Dawley rats were fed either a tap water or 20 % high sucrose solution throughout pregnancy. Pulmonary arteries from adult offspring were isolated and tested for all experiments. Prenatal HS increased vascular wall thickness, resulted in swollen mitochondria, and altered myofilament distribution in vascular smooth muscle layers of PA. Notably, the offspring's PAs from HS group showed increased vasoconstriction, but reduced PKC function and expression, suggesting that the dysfunction was not primary linked to PKC signals. RNA-Seq analysis of PA revealed that the MT1R and MT2AR genes were significantly increased in the HS group, but their protein levels decreased. This suggests that MT receptors, rather than PKC signaling, are the key factors to influencing vascular contraction of PAs exposure to prenatal HS.</div></div>","PeriodicalId":21137,"journal":{"name":"Reproductive toxicology","volume":"132 ","pages":"Article 108760"},"PeriodicalIF":3.3000,"publicationDate":"2024-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Reproductive toxicology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0890623824002272","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"REPRODUCTIVE BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

A high sucrose diet during pregnancy may generate profound effects on vascular diseases in offspring later in life. Pulmonary artery (PA) functions is closely related to pulmonary hypertension, but whether and how prenatal high-sucrose diet (HS) affect pulmonary vasoreactivity in adult offspring remains unknown. We investigated the alterations of PA reactivity in postnatal offspring exposed to prenatal HS. Pregnant Sprague-Dawley rats were fed either a tap water or 20 % high sucrose solution throughout pregnancy. Pulmonary arteries from adult offspring were isolated and tested for all experiments. Prenatal HS increased vascular wall thickness, resulted in swollen mitochondria, and altered myofilament distribution in vascular smooth muscle layers of PA. Notably, the offspring's PAs from HS group showed increased vasoconstriction, but reduced PKC function and expression, suggesting that the dysfunction was not primary linked to PKC signals. RNA-Seq analysis of PA revealed that the MT1R and MT2AR genes were significantly increased in the HS group, but their protein levels decreased. This suggests that MT receptors, rather than PKC signaling, are the key factors to influencing vascular contraction of PAs exposure to prenatal HS.
产前高糖饮食通过MT受体影响肺动脉收缩功能
怀孕期间的高蔗糖饮食可能对后代以后的血管疾病产生深远的影响。肺动脉(PA)功能与肺动脉高压密切相关,但产前高糖饮食(HS)是否以及如何影响成年后代的肺血管反应性尚不清楚。我们研究了暴露于产前HS的产后后代PA反应性的变化。怀孕的Sprague-Dawley大鼠在整个怀孕期间被喂食自来水或20% %高蔗糖溶液。分离成年后代的肺动脉,并对所有实验进行检测。产前HS增加了血管壁厚度,导致线粒体肿胀,改变了PA血管平滑肌层的肌丝分布。值得注意的是,HS组后代的PAs血管收缩增加,但PKC功能和表达减少,表明功能障碍与PKC信号无关。PA的RNA-Seq分析显示,HS组MT1R和MT2AR基因显著升高,但蛋白水平降低。这表明MT受体,而不是PKC信号,是影响PAs暴露于产前HS血管收缩的关键因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Reproductive toxicology
Reproductive toxicology 生物-毒理学
CiteScore
6.50
自引率
3.00%
发文量
131
审稿时长
45 days
期刊介绍: Drawing from a large number of disciplines, Reproductive Toxicology publishes timely, original research on the influence of chemical and physical agents on reproduction. Written by and for obstetricians, pediatricians, embryologists, teratologists, geneticists, toxicologists, andrologists, and others interested in detecting potential reproductive hazards, the journal is a forum for communication among researchers and practitioners. Articles focus on the application of in vitro, animal and clinical research to the practice of clinical medicine. All aspects of reproduction are within the scope of Reproductive Toxicology, including the formation and maturation of male and female gametes, sexual function, the events surrounding the fusion of gametes and the development of the fertilized ovum, nourishment and transport of the conceptus within the genital tract, implantation, embryogenesis, intrauterine growth, placentation and placental function, parturition, lactation and neonatal survival. Adverse reproductive effects in males will be considered as significant as adverse effects occurring in females. To provide a balanced presentation of approaches, equal emphasis will be given to clinical and animal or in vitro work. Typical end points that will be studied by contributors include infertility, sexual dysfunction, spontaneous abortion, malformations, abnormal histogenesis, stillbirth, intrauterine growth retardation, prematurity, behavioral abnormalities, and perinatal mortality.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信