The intake of monosodium aspartate attenuates aggression induced by post-weaning social isolation in an ADHD rat model.

IF 3.3 4区 医学 Q2 PHYSIOLOGY
Journal of Physiological Sciences Pub Date : 2026-03-01 Epub Date: 2026-01-09 DOI:10.1016/j.jphyss.2026.100056
Yu Nishimura, Dewi Mustika, Shinya Ueno, Shiori Tominaga, Mariko Shindo, Naoki Tajiri, Cha-Gyun Jung, Hideki Hida
{"title":"The intake of monosodium aspartate attenuates aggression induced by post-weaning social isolation in an ADHD rat model.","authors":"Yu Nishimura, Dewi Mustika, Shinya Ueno, Shiori Tominaga, Mariko Shindo, Naoki Tajiri, Cha-Gyun Jung, Hideki Hida","doi":"10.1016/j.jphyss.2026.100056","DOIUrl":null,"url":null,"abstract":"<p><p>We investigated whether monosodium aspartate (MSA), an umami compound structurally analogous to monosodium glutamate (MSG), influences aggressive behavior in a rat model of attention-deficit/hyperactivity disorder. Spontaneously hypertensive rats (SHR/Izm) were subjected to post-weaning social isolation and assessed using the resident-intruder paradigm. MSA ingestion significantly reduced aggression, particularly the frequency and duration of attacks, while the open field test showed no differences in anxiety-like behavior. c-Fos immunohistochemistry revealed increased neuronal activation in the intermediate nucleus of the solitary tract (iNTS) and decreased activation in the central amygdala (CeA) following MSA ingestion. This effect, along with the reduction in aggression, was abolished by vagotomy, suggesting gut-brain involvement. These findings indicate that MSA, like MSG, can reduce aggression via the gut-brain axis, implicating the vagus nerve, iNTS and CeA as key mediators. This highlights that the modulation of aggression by ingested amino acids is a broader effect acting through shared mechanisms.</p>","PeriodicalId":16832,"journal":{"name":"Journal of Physiological Sciences","volume":"76 1","pages":"100056"},"PeriodicalIF":3.3000,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12856302/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Physiological Sciences","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.jphyss.2026.100056","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/9 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"PHYSIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

We investigated whether monosodium aspartate (MSA), an umami compound structurally analogous to monosodium glutamate (MSG), influences aggressive behavior in a rat model of attention-deficit/hyperactivity disorder. Spontaneously hypertensive rats (SHR/Izm) were subjected to post-weaning social isolation and assessed using the resident-intruder paradigm. MSA ingestion significantly reduced aggression, particularly the frequency and duration of attacks, while the open field test showed no differences in anxiety-like behavior. c-Fos immunohistochemistry revealed increased neuronal activation in the intermediate nucleus of the solitary tract (iNTS) and decreased activation in the central amygdala (CeA) following MSA ingestion. This effect, along with the reduction in aggression, was abolished by vagotomy, suggesting gut-brain involvement. These findings indicate that MSA, like MSG, can reduce aggression via the gut-brain axis, implicating the vagus nerve, iNTS and CeA as key mediators. This highlights that the modulation of aggression by ingested amino acids is a broader effect acting through shared mechanisms.

在ADHD大鼠模型中,摄入天冬氨酸钠可减轻断奶后社会隔离引起的攻击行为。
我们研究了一种结构类似于味精(MSG)的鲜味化合物天冬氨酸钠(MSA)是否会影响注意缺陷/多动障碍大鼠模型的攻击行为。对自发性高血压大鼠(SHR/Izm)进行断奶后社会隔离,并采用居民-入侵者范式进行评估。摄入MSA显著减少了攻击行为,特别是攻击的频率和持续时间,而开放场地测试显示焦虑样行为没有差异。c-Fos免疫组化显示,摄取MSA后,孤立束中间核(iNTS)的神经元激活增加,中央杏仁核(CeA)的神经元激活减少。这种影响,连同攻击性的减少,被迷走神经切开术消除了,这表明肠-脑参与其中。这些发现表明,MSA和味精一样,可以通过肠脑轴减少攻击行为,其中迷走神经、iNTS和CeA是关键的介质。这突出表明,通过摄入氨基酸对攻击的调节是一种更广泛的效应,通过共享机制起作用。
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
CiteScore
4.40
自引率
4.30%
发文量
27
审稿时长
6-12 weeks
期刊介绍: The Journal of Physiological Sciences publishes peer-reviewed original papers, reviews, short communications, technical notes, and letters to the editor, based on the principles and theories of modern physiology and addressed to the international scientific community. All fields of physiology are covered, encompassing molecular, cellular and systems physiology. The emphasis is on human and vertebrate physiology, but comparative papers are also considered. The process of obtaining results must be ethically sound. Fields covered: Adaptation and environment Autonomic nervous function Biophysics Cell sensors and signaling Central nervous system and brain sciences Endocrinology and metabolism Excitable membranes and neural cell physiology Exercise physiology Gastrointestinal and kidney physiology Heart and circulatory physiology Molecular and cellular physiology Muscle physiology Physiome/systems biology Respiration physiology Senses.
×
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
小红书