Unpacking the multimodal, multi-scale data of the fast and slow lanes of the cardiac vagus through computational modelling.

IF 2.6 4区 医学 Q2 PHYSIOLOGY Experimental Physiology Pub Date : 2024-12-01 Epub Date: 2023-04-30 DOI:10.1113/EP090865
Michelle M Gee, Eden Hornung, Suranjana Gupta, Adam J H Newton, Zixi Jack Cheng, William W Lytton, Abraham M Lenhoff, James S Schwaber, Rajanikanth Vadigepalli
{"title":"Unpacking the multimodal, multi-scale data of the fast and slow lanes of the cardiac vagus through computational modelling.","authors":"Michelle M Gee, Eden Hornung, Suranjana Gupta, Adam J H Newton, Zixi Jack Cheng, William W Lytton, Abraham M Lenhoff, James S Schwaber, Rajanikanth Vadigepalli","doi":"10.1113/EP090865","DOIUrl":null,"url":null,"abstract":"<p><p>The vagus nerve is a key mediator of brain-heart signaling, and its activity is necessary for cardiovascular health. Vagal outflow stems from the nucleus ambiguus, responsible primarily for fast, beat-to-beat regulation of heart rate and rhythm, and the dorsal motor nucleus of the vagus, responsible primarily for slow regulation of ventricular contractility. Due to the high-dimensional and multimodal nature of the anatomical, molecular and physiological data on neural regulation of cardiac function, data-derived mechanistic insights have proven elusive. Elucidating insights has been complicated further by the broad distribution of the data across heart, brain and peripheral nervous system circuits. Here we lay out an integrative framework based on computational modelling for combining these disparate and multi-scale data on the two vagal control lanes of the cardiovascular system. Newly available molecular-scale data, particularly single-cell transcriptomic analyses, have augmented our understanding of the heterogeneous neuronal states underlying vagally mediated fast and slow regulation of cardiac physiology. Cellular-scale computational models built from these data sets represent building blocks that can be combined using anatomical and neural circuit connectivity, neuronal electrophysiology, and organ/organismal-scale physiology data to create multi-system, multi-scale models that enable in silico exploration of the fast versus slow lane vagal stimulation. The insights from the computational modelling and analyses will guide new experimental questions on the mechanisms regulating the fast and slow lanes of the cardiac vagus toward exploiting targeted vagal neuromodulatory activity to promote cardiovascular health.</p>","PeriodicalId":12092,"journal":{"name":"Experimental Physiology","volume":" ","pages":"1994-2000"},"PeriodicalIF":2.6000,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10613580/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Experimental Physiology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1113/EP090865","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/4/30 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"PHYSIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

The vagus nerve is a key mediator of brain-heart signaling, and its activity is necessary for cardiovascular health. Vagal outflow stems from the nucleus ambiguus, responsible primarily for fast, beat-to-beat regulation of heart rate and rhythm, and the dorsal motor nucleus of the vagus, responsible primarily for slow regulation of ventricular contractility. Due to the high-dimensional and multimodal nature of the anatomical, molecular and physiological data on neural regulation of cardiac function, data-derived mechanistic insights have proven elusive. Elucidating insights has been complicated further by the broad distribution of the data across heart, brain and peripheral nervous system circuits. Here we lay out an integrative framework based on computational modelling for combining these disparate and multi-scale data on the two vagal control lanes of the cardiovascular system. Newly available molecular-scale data, particularly single-cell transcriptomic analyses, have augmented our understanding of the heterogeneous neuronal states underlying vagally mediated fast and slow regulation of cardiac physiology. Cellular-scale computational models built from these data sets represent building blocks that can be combined using anatomical and neural circuit connectivity, neuronal electrophysiology, and organ/organismal-scale physiology data to create multi-system, multi-scale models that enable in silico exploration of the fast versus slow lane vagal stimulation. The insights from the computational modelling and analyses will guide new experimental questions on the mechanisms regulating the fast and slow lanes of the cardiac vagus toward exploiting targeted vagal neuromodulatory activity to promote cardiovascular health.

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
通过计算建模,解开心脏迷走神经快通道和慢通道的多模式、多尺度数据。
新发现:这篇综述的主题是什么?迷走神经是心血管稳态的重要调节器,其活动与心脏健康有关。迷走神经活动源于两个脑干核:模糊核(快速通道)和迷走神经背侧运动核(慢速通道),因其传输信号所需的时间尺度而得名。它强调了哪些进步?计算模型是以生理学意义的方式组织快车道和慢车道上多尺度、多模式数据的强大工具。针对这些模型如何指导旨在利用快速通道和慢速通道差异激活对心血管健康益处的实验,制定了一项策略。摘要:迷走神经是脑心信号传导的关键介质,其活动对心血管健康至关重要。迷走神经流出源于迷走神经核,主要负责心率和节律的快速逐搏调节,迷走神经背侧运动核主要负责心室收缩力的缓慢调节。由于心脏功能神经调节的解剖、分子和生理数据具有高维和多模式的性质,数据衍生的机制见解已被证明是难以捉摸的。由于数据在心脏、大脑和外周神经系统回路中的广泛分布,阐明见解变得更加复杂。在这里,我们提出了一个基于计算建模的综合框架,用于将心血管系统的两个迷走神经控制通道上的这些不同的多尺度数据相结合。最新可用的分子尺度数据,特别是单细胞转录组分析,增强了我们对迷走神经介导的心脏生理快速和慢速调节背后的异质神经元状态的理解。由这些数据集构建的细胞尺度计算模型代表了可以使用解剖和神经回路连接、神经元电生理学和器官/生物体尺度生理学数据组合的构建块,以创建多系统、多尺度模型,从而能够对快通道和慢通道迷走神经刺激进行计算机探索。计算模型和分析的见解将指导关于调节心脏迷走神经快通道和慢通道的机制的新实验问题,以利用有针对性的迷走神经神经调节活动来促进心血管健康。
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
Experimental Physiology
Experimental Physiology 医学-生理学
CiteScore
5.10
自引率
3.70%
发文量
262
审稿时长
1 months
期刊介绍: Experimental Physiology publishes research papers that report novel insights into homeostatic and adaptive responses in health, as well as those that further our understanding of pathophysiological mechanisms in disease. We encourage papers that embrace the journal’s orientation of translation and integration, including studies of the adaptive responses to exercise, acute and chronic environmental stressors, growth and aging, and diseases where integrative homeostatic mechanisms play a key role in the response to and evolution of the disease process. Examples of such diseases include hypertension, heart failure, hypoxic lung disease, endocrine and neurological disorders. We are also keen to publish research that has a translational aspect or clinical application. Comparative physiology work that can be applied to aid the understanding human physiology is also encouraged. Manuscripts that report the use of bioinformatic, genomic, molecular, proteomic and cellular techniques to provide novel insights into integrative physiological and pathophysiological mechanisms are welcomed.
期刊最新文献
Neural control of coronary artery blood flow by non-adrenergic and non-cholinergic mechanisms. Unpacking the multimodal, multi-scale data of the fast and slow lanes of the cardiac vagus through computational modelling. Selective efferent vagal stimulation in heart failure. Correction to 'Pulmonary diffusing capacity to nitric oxide and carbon monoxide during exercise and in the supine position: A test-retest reliability study'. CTRP6-mediated cardiac protection in heart failure via the AMPK/SIRT1/PGC-1α signalling pathway.
×
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