Unexpected effects of voluntary exercise training on natriuretic peptide and receptor mRNA expression in the ob/ob mouse heart

Tom L. Broderick , Donghao Wang , Marek Jankowski , Jolanta Gutkowska
{"title":"Unexpected effects of voluntary exercise training on natriuretic peptide and receptor mRNA expression in the ob/ob mouse heart","authors":"Tom L. Broderick ,&nbsp;Donghao Wang ,&nbsp;Marek Jankowski ,&nbsp;Jolanta Gutkowska","doi":"10.1016/j.regpep.2013.12.005","DOIUrl":null,"url":null,"abstract":"<div><p><span>Regular exercise is generally recommended for the treatment of obesity and type 2 diabetes. Exercise reduces body weight, improves glycemic control and cardiovascular (CV) function. This study was designed to determine the impact of voluntary wheel running on the cardiac oxytocin (OT)–natriuretic peptide (NP) system and plasma CV risk factors in the </span><em>ob/ob</em> mouse, a model of insulin resistance coupled with severe obesity. Five-week-old male <em>ob/ob</em><span> mice and non-obese heterozygote control littermates were assigned to either a sedentary or running group. Voluntary running was performed using a wheel system for a period of 8</span> <!-->weeks. Compared to non-obese mice, daily running activity expressed in kilometers, was significantly lower in <em>ob/ob</em><span><span> mice. In these mice, voluntary running improved body weight, but exacerbated CV markers, including plasma glucose and triglyceride levels. </span>OT receptor gene expression was decreased in hearts of </span><em>ob/ob</em> mice compared to non-obese mice, and no improvement in the expression of this receptor was observed after voluntary running. Hearts from <em>ob/ob</em> mice also expressed lower BNP mRNA, whereas no differences in A- and C-type NP were observed between non-obese and <em>ob/ob</em> mice. After voluntary running, a downregulation in the expression of all three NPs coupled with increased apoptosis was observed in <em>ob/ob</em> hearts. Our results show that voluntary exercise running activity was decreased in the <em>ob/ob</em> mouse. Surprisingly, this was associated with a worsening of common CV plasma markers, reduced expression of peptides linked to the cardioprotective OT–NP system, and increased expression of cardiac apoptotic markers.</p></div>","PeriodicalId":20853,"journal":{"name":"Regulatory Peptides","volume":"188 ","pages":"Pages 52-59"},"PeriodicalIF":0.0000,"publicationDate":"2014-01-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.regpep.2013.12.005","citationCount":"20","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Regulatory Peptides","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0167011513001730","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 20

Abstract

Regular exercise is generally recommended for the treatment of obesity and type 2 diabetes. Exercise reduces body weight, improves glycemic control and cardiovascular (CV) function. This study was designed to determine the impact of voluntary wheel running on the cardiac oxytocin (OT)–natriuretic peptide (NP) system and plasma CV risk factors in the ob/ob mouse, a model of insulin resistance coupled with severe obesity. Five-week-old male ob/ob mice and non-obese heterozygote control littermates were assigned to either a sedentary or running group. Voluntary running was performed using a wheel system for a period of 8 weeks. Compared to non-obese mice, daily running activity expressed in kilometers, was significantly lower in ob/ob mice. In these mice, voluntary running improved body weight, but exacerbated CV markers, including plasma glucose and triglyceride levels. OT receptor gene expression was decreased in hearts of ob/ob mice compared to non-obese mice, and no improvement in the expression of this receptor was observed after voluntary running. Hearts from ob/ob mice also expressed lower BNP mRNA, whereas no differences in A- and C-type NP were observed between non-obese and ob/ob mice. After voluntary running, a downregulation in the expression of all three NPs coupled with increased apoptosis was observed in ob/ob hearts. Our results show that voluntary exercise running activity was decreased in the ob/ob mouse. Surprisingly, this was associated with a worsening of common CV plasma markers, reduced expression of peptides linked to the cardioprotective OT–NP system, and increased expression of cardiac apoptotic markers.

自愿运动训练对ob/ob小鼠心脏利钠肽和受体mRNA表达的意外影响
经常锻炼通常被推荐用于治疗肥胖和2型糖尿病。运动可以减轻体重,改善血糖控制和心血管功能。本研究旨在确定自主跑轮运动对ob/ob小鼠心脏催产素-利钠肽(NP)系统和血浆CV危险因素的影响,ob/ob小鼠是胰岛素抵抗合并严重肥胖的模型。五周大的雄性ob/ob小鼠和非肥胖杂合子对照鼠被分配到久坐组或跑步组。使用车轮系统进行自愿跑步,为期8周。与非肥胖小鼠相比,肥胖/肥胖小鼠的日跑步活动量(以公里表示)显著降低。在这些小鼠中,自愿跑步改善了体重,但加重了CV指标,包括血浆葡萄糖和甘油三酯水平。与非肥胖小鼠相比,ob/ob小鼠心脏中OT受体基因表达降低,并且在自愿跑步后未观察到该受体表达的改善。ob/ob小鼠的心脏也表达较低的BNP mRNA,而非肥胖小鼠和ob/ob小鼠的A型和c型NP没有差异。在自愿跑步后,观察到ob/ob心脏中所有三种NPs的表达下调并伴有细胞凋亡增加。我们的研究结果表明,ob/ob小鼠的自愿运动跑步活动减少。令人惊讶的是,这与常见CV血浆标志物的恶化、与心脏保护OT-NP系统相关肽的表达减少以及心脏凋亡标志物的表达增加有关。
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
Regulatory Peptides
Regulatory Peptides 医学-内分泌学与代谢
自引率
0.00%
发文量
0
审稿时长
2 months
期刊介绍: Regulatory Peptides provides a medium for the rapid publication of interdisciplinary studies on the physiology and pathology of peptides of the gut, endocrine and nervous systems which regulate cell or tissue function. Articles emphasizing these objectives may be based on either fundamental or clinical observations obtained through the disciplines of morphology, cytochemistry, biochemistry, physiology, pathology, pharmacology or psychology.
×
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