Hippocampal Neurogenesis via Light-Intensity Running and Its Mechanism.

Q3 Neuroscience
Koshiro Inoue, Hideaki Soya
{"title":"Hippocampal Neurogenesis via Light-Intensity Running and Its Mechanism.","authors":"Koshiro Inoue, Hideaki Soya","doi":"10.1007/978-981-95-0066-6_3","DOIUrl":null,"url":null,"abstract":"<p><p>Adult hippocampal neurogenesis (AHN) is the process of generating new neurons in the adult hippocampal dentate gyrus (DG). Exercise promotes AHN and improves hippocampal function through neuroplastic enhancement. The underlying regulatory factors of this process are currently being vigorously studied. However, many previous studies have used a rodent wheel-running model, in which the exercise condition (e.g., volume, intensity, duration) cannot be controlled. In contrast, treadmill running (TR) allows the precise regulation of conditions such that animals can run according to specific experimental aims. Understanding the intensity-dependent effects of exercise on AHN and hippocampal functions, and the underlying mechanisms, is crucial for the development of exercise prescriptions for humans in diverse educational and clinical fields. Based on the lactate threshold (LT), an inflection point at which blood lactate accumulation drastically rises during incremental exercise, exercise can be defined as minimal-stress light-intensity exercise (below LT) and exercise-derived-stress vigorous-intensity exercise (above LT). This chapter begins with a brief overview of AHN, followed by a discussion of LT-based exercise effects on AHN and hippocampal function as they vary with exercise intensity, primarily following the findings from the TR models, and closing with the molecular factors involved in AHN and hippocampal function regulation.</p>","PeriodicalId":7360,"journal":{"name":"Advances in neurobiology","volume":"44 ","pages":"39-82"},"PeriodicalIF":0.0000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advances in neurobiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/978-981-95-0066-6_3","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Neuroscience","Score":null,"Total":0}
引用次数: 0

Abstract

Adult hippocampal neurogenesis (AHN) is the process of generating new neurons in the adult hippocampal dentate gyrus (DG). Exercise promotes AHN and improves hippocampal function through neuroplastic enhancement. The underlying regulatory factors of this process are currently being vigorously studied. However, many previous studies have used a rodent wheel-running model, in which the exercise condition (e.g., volume, intensity, duration) cannot be controlled. In contrast, treadmill running (TR) allows the precise regulation of conditions such that animals can run according to specific experimental aims. Understanding the intensity-dependent effects of exercise on AHN and hippocampal functions, and the underlying mechanisms, is crucial for the development of exercise prescriptions for humans in diverse educational and clinical fields. Based on the lactate threshold (LT), an inflection point at which blood lactate accumulation drastically rises during incremental exercise, exercise can be defined as minimal-stress light-intensity exercise (below LT) and exercise-derived-stress vigorous-intensity exercise (above LT). This chapter begins with a brief overview of AHN, followed by a discussion of LT-based exercise effects on AHN and hippocampal function as they vary with exercise intensity, primarily following the findings from the TR models, and closing with the molecular factors involved in AHN and hippocampal function regulation.

通过光强度跑步的海马神经发生及其机制。
成体海马神经发生(AHN)是成体海马齿状回(DG)产生新神经元的过程。运动促进AHN并通过神经可塑性增强改善海马功能。目前正在积极研究这一过程的潜在调节因素。然而,以往的许多研究使用的是啮齿类动物的轮跑模型,在这种模型中,运动条件(如体积、强度、持续时间)无法控制。相比之下,跑步机跑步(TR)允许精确调节条件,这样动物就可以根据特定的实验目标跑步。了解运动对AHN和海马功能的强度依赖性影响及其潜在机制,对于在不同的教育和临床领域开发人类运动处方至关重要。根据乳酸阈值(LT),即在增量运动过程中血乳酸积累急剧上升的拐点,可以将运动定义为最小应激轻强度运动(低于LT)和运动衍生应激大强度运动(高于LT)。本章首先简要概述了AHN,然后讨论了基于lt的运动对AHN和海马功能的影响,因为它们随着运动强度的变化而变化,主要是根据TR模型的发现,最后讨论了AHN和海马功能调节中涉及的分子因素。
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
Advances in neurobiology
Advances in neurobiology Neuroscience-Neurology
CiteScore
2.80
自引率
0.00%
发文量
0
×
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:604180095
Book学术官方微信