Postnatal development in the rat: Changes in Na+ flux, sodium pump molecular activity and membrane lipid composition

IF 2.6 Q2 Medicine Mechanisms of Development Pub Date : 2020-06-01 DOI:10.1016/j.mod.2020.103610
Paul L. Else
{"title":"Postnatal development in the rat: Changes in Na+ flux, sodium pump molecular activity and membrane lipid composition","authors":"Paul L. Else","doi":"10.1016/j.mod.2020.103610","DOIUrl":null,"url":null,"abstract":"<div><p>The cellular mechanisms underpinning changes in metabolism during postnatal development in young mammals have not been extensively examined. This study examines changes in sodium pump capacity (Na<sup>+</sup>, K<sup>+</sup>-ATPase activity), number and molecular activity, as well as, Na<sup>+</sup> flux, cholesterol level and fatty acid composition in a number of major organs during postnatal development in the rat. In liver, Na<sup>+</sup> flux was highest (2.6 times) in the youngest rats (3-day old) and decreased with increasing age, whereas Na<sup>+</sup>, K<sup>+</sup>-ATPase activity increased with age (up to 9–28 days) in liver, kidney and brain, but not in heart. Increases in Na<sup>+</sup>, K<sup>+</sup>-ATPase activity where primarily driven by increases in molecular activity, 4-fold in brain and 7-fold in kidney, rather than by increases in sodium pump number. Membrane polyunsaturation increased in both kidney and brain during development, with kidney becoming increasingly dominated by omega-6 (18:2n-6 and 20:4n-6) and brain by omega-3 (22:6n-3) fatty acids. Membrane reconstitution experiments support the concept that changes in membrane composition might underpin higher sodium molecular activities in the adult. In conclusion, at birth rats possess high Na<sup>+</sup> flux but a lower sodium pump capacity that increases with age being driven by increases in molecular activities associate with changes in membrane lipid composition.</p></div>","PeriodicalId":49844,"journal":{"name":"Mechanisms of Development","volume":"162 ","pages":"Article 103610"},"PeriodicalIF":2.6000,"publicationDate":"2020-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.mod.2020.103610","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Mechanisms of Development","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0925477320300150","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 2

Abstract

The cellular mechanisms underpinning changes in metabolism during postnatal development in young mammals have not been extensively examined. This study examines changes in sodium pump capacity (Na+, K+-ATPase activity), number and molecular activity, as well as, Na+ flux, cholesterol level and fatty acid composition in a number of major organs during postnatal development in the rat. In liver, Na+ flux was highest (2.6 times) in the youngest rats (3-day old) and decreased with increasing age, whereas Na+, K+-ATPase activity increased with age (up to 9–28 days) in liver, kidney and brain, but not in heart. Increases in Na+, K+-ATPase activity where primarily driven by increases in molecular activity, 4-fold in brain and 7-fold in kidney, rather than by increases in sodium pump number. Membrane polyunsaturation increased in both kidney and brain during development, with kidney becoming increasingly dominated by omega-6 (18:2n-6 and 20:4n-6) and brain by omega-3 (22:6n-3) fatty acids. Membrane reconstitution experiments support the concept that changes in membrane composition might underpin higher sodium molecular activities in the adult. In conclusion, at birth rats possess high Na+ flux but a lower sodium pump capacity that increases with age being driven by increases in molecular activities associate with changes in membrane lipid composition.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
大鼠出生后发育:Na+通量、钠泵分子活性和膜脂组成的变化
年轻哺乳动物出生后发育过程中代谢变化的细胞机制尚未得到广泛研究。本研究考察了大鼠出生后发育过程中钠泵能力(Na+、K+- atp酶活性)、数量和分子活性,以及Na+通量、胆固醇水平和脂肪酸组成在一些主要器官中的变化。在肝脏中,Na+通量在最小的大鼠(3日龄)中最高(2.6倍),并随着年龄的增长而下降,而Na+, K+- atp酶活性在肝,肾和脑中随着年龄的增长(可达9-28日龄)而增加,但在心脏中没有。Na+, K+- atp酶活性的增加主要是由分子活性的增加引起的,在大脑中是4倍,在肾脏中是7倍,而不是钠泵数量的增加。在发育过程中,肾和脑的膜多不饱和增加,肾脏越来越多地被omega-6 (18:2n-6和20:4n-6)支配,脑越来越多地被omega-3 (22:6n-3)脂肪酸支配。膜重构实验支持这样一个概念,即膜组成的变化可能支持成人较高的钠分子活性。综上所述,在出生时,大鼠具有较高的Na+通量,但钠泵能力较低,随着年龄的增长,由膜脂组成变化相关的分子活性增加所驱动。
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 去求助
来源期刊
Mechanisms of Development
Mechanisms of Development 生物-发育生物学
CiteScore
3.60
自引率
0.00%
发文量
0
审稿时长
12.4 weeks
期刊介绍: Mechanisms of Development is an international journal covering the areas of cell biology and developmental biology. In addition to publishing work at the interphase of these two disciplines, we also publish work that is purely cell biology as well as classical developmental biology. Mechanisms of Development will consider papers in any area of cell biology or developmental biology, in any model system like animals and plants, using a variety of approaches, such as cellular, biomechanical, molecular, quantitative, computational and theoretical biology. Areas of particular interest include: Cell and tissue morphogenesis Cell adhesion and migration Cell shape and polarity Biomechanics Theoretical modelling of cell and developmental biology Quantitative biology Stem cell biology Cell differentiation Cell proliferation and cell death Evo-Devo Membrane traffic Metabolic regulation Organ and organoid development Regeneration Mechanisms of Development does not publish descriptive studies of gene expression patterns and molecular screens; for submission of such studies see Gene Expression Patterns.
期刊最新文献
Editorial Board Publisher's note Outside Front Cover Regulatory functions of gga-miR-218 in spermatogonial stem cells meiosis by targeting Stra8 Improved early development potence of in vitro fertilization embryos by treatment with tubacin increasing acetylated tubulin of matured porcine oocytes
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1