Effects of Epicatechin on the Expression of MyomiRs−31, −133, −136, −206, −296, and −486 in the Skeletal Muscle of the Offspring of Obese Mothers

IF 2.5 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Cell Biochemistry and Biophysics Pub Date : 2025-02-27 DOI:10.1007/s12013-025-01700-x
Paola B. Zárate-Segura, Ana Luisa Alvarez-Chávez, Sergio De los Santos, Fernando G. Bastida-Gonzalez, José Manuel Hernández-Hernández, Elena Zambrano, Ramón Mauricio Coral-Vázquez, Patricia Canto
{"title":"Effects of Epicatechin on the Expression of MyomiRs−31, −133, −136, −206, −296, and −486 in the Skeletal Muscle of the Offspring of Obese Mothers","authors":"Paola B. Zárate-Segura,&nbsp;Ana Luisa Alvarez-Chávez,&nbsp;Sergio De los Santos,&nbsp;Fernando G. Bastida-Gonzalez,&nbsp;José Manuel Hernández-Hernández,&nbsp;Elena Zambrano,&nbsp;Ramón Mauricio Coral-Vázquez,&nbsp;Patricia Canto","doi":"10.1007/s12013-025-01700-x","DOIUrl":null,"url":null,"abstract":"<div><p><b>Specific myogenic microRNAs termed “myomiRNAs”</b> are involved in skeletal muscle development and regeneration, and an obesogenic environment <i>in utero</i> may affect these processes. The present study aimed to determine whether this environment induced variations in the expression levels of myomiRs-31, −133, −136, −206, and −296 and whether the administration of (-)-epicatechin (Epi), an exercise mimetic, could modify these variations. Rat Wistar male offspring from control mothers (C) or obese mothers (MO) were treated (C+Epi and MO+Epi) or not treated with Epi (C and MO). MyomiRNA expression in the gastrocnemius and soleus muscles was analyzed via RT‒qPCR, and bioinformatic analysis was used to predict the participation of these miRNAs in different skeletal muscle signal transduction pathways. The expression of myomiRNA-31-5p in the gastrocnemius and soleus was significantly lower in the Epi-treated groups (C+Epi and MO+Epi vs. C and MO). The expression of myomiRNA-206 increased in the gastrocnemius muscles of the MO and MO+Epi groups but decreased in the soleus muscles of the MO and MO+Epi groups. The expression of myomiRNA-296 was increased in the MO group in the gastrocnemius and soleus but was reduced in the Epi stimulus group. The expression of myomiRNA-486 increased in the gastrocnemius of the C+Epi group and decreased in the soleus of the MO+Epi group (<i>p</i> = 0.028 vs. MO). In conclusion, we show that an intrauterine obesogenic environment differentially affects the expression levels of some myomiRNAs and that this effect is modified by epicatechin.</p></div>","PeriodicalId":510,"journal":{"name":"Cell Biochemistry and Biophysics","volume":"83 3","pages":"3177 - 3185"},"PeriodicalIF":2.5000,"publicationDate":"2025-02-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s12013-025-01700-x.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cell Biochemistry and Biophysics","FirstCategoryId":"99","ListUrlMain":"https://link.springer.com/article/10.1007/s12013-025-01700-x","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Specific myogenic microRNAs termed “myomiRNAs” are involved in skeletal muscle development and regeneration, and an obesogenic environment in utero may affect these processes. The present study aimed to determine whether this environment induced variations in the expression levels of myomiRs-31, −133, −136, −206, and −296 and whether the administration of (-)-epicatechin (Epi), an exercise mimetic, could modify these variations. Rat Wistar male offspring from control mothers (C) or obese mothers (MO) were treated (C+Epi and MO+Epi) or not treated with Epi (C and MO). MyomiRNA expression in the gastrocnemius and soleus muscles was analyzed via RT‒qPCR, and bioinformatic analysis was used to predict the participation of these miRNAs in different skeletal muscle signal transduction pathways. The expression of myomiRNA-31-5p in the gastrocnemius and soleus was significantly lower in the Epi-treated groups (C+Epi and MO+Epi vs. C and MO). The expression of myomiRNA-206 increased in the gastrocnemius muscles of the MO and MO+Epi groups but decreased in the soleus muscles of the MO and MO+Epi groups. The expression of myomiRNA-296 was increased in the MO group in the gastrocnemius and soleus but was reduced in the Epi stimulus group. The expression of myomiRNA-486 increased in the gastrocnemius of the C+Epi group and decreased in the soleus of the MO+Epi group (p = 0.028 vs. MO). In conclusion, we show that an intrauterine obesogenic environment differentially affects the expression levels of some myomiRNAs and that this effect is modified by epicatechin.

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
表儿茶素对肥胖母亲后代骨骼肌中myomir -31、-133、-136、-206、-296和-486表达的影响
被称为“myomiRNAs”的特异性肌源性小rna参与骨骼肌的发育和再生,而子宫内的致肥环境可能会影响这些过程。本研究旨在确定这种环境是否会诱导myomir -31、-133、-136、-206和-296表达水平的变化,以及(-)-表儿茶素(Epi)(一种运动模拟物)的施用是否可以改变这些变化。对照母鼠(C)和肥胖母鼠(MO)的Wistar雄性后代分别给予(C+Epi和MO+Epi)或不给予Epi (C和MO)。通过RT-qPCR分析腓肠肌和比目鱼肌中MyomiRNA的表达,并利用生物信息学分析预测这些mirna参与不同骨骼肌信号转导通路。Epi处理组腓肠肌和比目鱼肌myomiRNA-31-5p的表达明显降低(C+Epi和MO+Epi vs C和MO)。肌irna -206在MO和MO+Epi组腓肠肌中表达升高,而在MO和MO+Epi组比目鱼肌中表达降低。肌irna -296在MO组腓肠肌和比目鱼肌的表达升高,Epi刺激组肌irna -296的表达降低。myomiRNA-486在C+Epi组腓肠肌中表达升高,在MO+Epi组比目鱼肌中表达降低(p = 0.028 vs MO)。总之,我们发现宫内致肥环境对一些myomirna的表达水平有不同的影响,而这种影响是由表儿茶素修饰的。
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
Cell Biochemistry and Biophysics
Cell Biochemistry and Biophysics 生物-生化与分子生物学
CiteScore
4.40
自引率
0.00%
发文量
72
审稿时长
7.5 months
期刊介绍: Cell Biochemistry and Biophysics (CBB) aims to publish papers on the nature of the biochemical and biophysical mechanisms underlying the structure, control and function of cellular systems The reports should be within the framework of modern biochemistry and chemistry, biophysics and cell physiology, physics and engineering, molecular and structural biology. The relationship between molecular structure and function under investigation is emphasized. Examples of subject areas that CBB publishes are: · biochemical and biophysical aspects of cell structure and function; · interactions of cells and their molecular/macromolecular constituents; · innovative developments in genetic and biomolecular engineering; · computer-based analysis of tissues, cells, cell networks, organelles, and molecular/macromolecular assemblies; · photometric, spectroscopic, microscopic, mechanical, and electrical methodologies/techniques in analytical cytology, cytometry and innovative instrument design For articles that focus on computational aspects, authors should be clear about which docking and molecular dynamics algorithms or software packages are being used as well as details on the system parameterization, simulations conditions etc. In addition, docking calculations (virtual screening, QSAR, etc.) should be validated either by experimental studies or one or more reliable theoretical cross-validation methods.
期刊最新文献
Healing mechanisms of Galectin-1 in the ischemic heart. Comparative Transcriptome Analysis Reveals Tissue-Specific Expression and Conservation of Mitochondrial Metal and Cofactor Genes in Buffalo. Experimental Validation and Computational Deconstruction of Downstream Mutations in MIR5195: Integrating Whole-Exome Sequencing, Structural Dynamics, and Molecular Docking to Decipher Transcriptional Reprogramming in CML. Breaking the Inflammatory Loop: Caffeic Acid Inhibits LPS/NF-κB/MMPs pathway and Preserves ALP-Iodine Crosstalk in LPS Induced Murine Endocrinopathy. FGFRL1 Modulates Glucose-Glycogen Homeostasis and Signaling Pathway Genes to Suppress Chemoresistance in Esophageal Carcinoma.
×
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:604180095
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