Anethole via increase in the gene expression of PI3K/AKT/mTOR mitigates the autistic-like behaviors induced by maternal separation stress in mice

IF 2 Q3 NEUROSCIENCES
Yasaman Yadollahi-Farsani, Vahid Reisi Vanani, Zahra Lorigooini, Anahita Farahzad, Hossein Amini-Khoei
{"title":"Anethole via increase in the gene expression of PI3K/AKT/mTOR mitigates the autistic-like behaviors induced by maternal separation stress in mice","authors":"Yasaman Yadollahi-Farsani,&nbsp;Vahid Reisi Vanani,&nbsp;Zahra Lorigooini,&nbsp;Anahita Farahzad,&nbsp;Hossein Amini-Khoei","doi":"10.1016/j.ibneur.2023.11.009","DOIUrl":null,"url":null,"abstract":"<div><p>Autism spectrum disorder (ASD) is a neurodegenerative disease with increasing incidence in the world. The maternal separation (MS) stress at early life with its own neuroendocrine and neurostructural changes can provide the basis for development of ASD. Previously it has been reported neuroprotective characteristics for anethole. The PI3K/AKT/mTOR signaling pathway has pivotal role in the function of central nervous system (CNS). This study aimed to evaluate the possible effects of anethole on the autistic-like behaviors in the maternally separated (MS) mice focusing on the potential role of the PI3K/AKT/mTOR pathway. Forty male Naval Medical Research Institute (NMRI) mice were assigned to five groups (n = 8) comprising a control group (treated with normal saline) and four groups subjected to MS and treated with normal saline and or anethole at doses of 31.25, 62.5 and 125 mg/kg, respectively. All gents were administrated via intraperitoneal (i.p.) route for 14 constant days. Behavioral tests were conducted, including the three-chamber test, shuttle box and resident-intruder test. The gene expression of the PI3K, AKT and mTOR assessed in the hippocampus by qRT-PCR. Findings indicated that MS is associated with autistic-like behaviors. Anethole increased the sociability and social preference indexes in the three-chamber test, increased duration of secondary latency in the shuttle box test and decreased aggressive behaviors in the resident-intruder test. Also, anethole increased the gene expression of PI3K, AKT and mTOR in the hippocampus of MS mice. We concluded that anethole through increase in the gene expression of PI3K/ AKT/mTOR mitigated autistic-like behaviors induced by MS in mice.</p></div>","PeriodicalId":13195,"journal":{"name":"IBRO Neuroscience Reports","volume":null,"pages":null},"PeriodicalIF":2.0000,"publicationDate":"2023-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2667242123022868/pdfft?md5=83a766f84f65f427d6cd7aac5da533b3&pid=1-s2.0-S2667242123022868-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"IBRO Neuroscience Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2667242123022868","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Autism spectrum disorder (ASD) is a neurodegenerative disease with increasing incidence in the world. The maternal separation (MS) stress at early life with its own neuroendocrine and neurostructural changes can provide the basis for development of ASD. Previously it has been reported neuroprotective characteristics for anethole. The PI3K/AKT/mTOR signaling pathway has pivotal role in the function of central nervous system (CNS). This study aimed to evaluate the possible effects of anethole on the autistic-like behaviors in the maternally separated (MS) mice focusing on the potential role of the PI3K/AKT/mTOR pathway. Forty male Naval Medical Research Institute (NMRI) mice were assigned to five groups (n = 8) comprising a control group (treated with normal saline) and four groups subjected to MS and treated with normal saline and or anethole at doses of 31.25, 62.5 and 125 mg/kg, respectively. All gents were administrated via intraperitoneal (i.p.) route for 14 constant days. Behavioral tests were conducted, including the three-chamber test, shuttle box and resident-intruder test. The gene expression of the PI3K, AKT and mTOR assessed in the hippocampus by qRT-PCR. Findings indicated that MS is associated with autistic-like behaviors. Anethole increased the sociability and social preference indexes in the three-chamber test, increased duration of secondary latency in the shuttle box test and decreased aggressive behaviors in the resident-intruder test. Also, anethole increased the gene expression of PI3K, AKT and mTOR in the hippocampus of MS mice. We concluded that anethole through increase in the gene expression of PI3K/ AKT/mTOR mitigated autistic-like behaviors induced by MS in mice.

茴香醚通过增加 PI3K/AKT/mTOR 的基因表达缓解小鼠因母体分离压力而诱发的类似自闭症的行为
自闭症谱系障碍(ASD)是一种神经退行性疾病,在全球的发病率越来越高。幼年时期的母体分离(MS)应激及其自身的神经内分泌和神经结构变化可为 ASD 的发展提供基础。以前曾有报道称茴香醚具有神经保护特性。PI3K/AKT/mTOR 信号通路在中枢神经系统(CNS)的功能中起着关键作用。本研究旨在评估茴香硫醚对母体分离(MS)小鼠自闭症样行为的可能影响,重点研究 PI3K/AKT/mTOR 通路的潜在作用。40 只雄性海军医学研究所(NMRI)小鼠被分成 5 组(n = 8),其中一组为对照组(用生理盐水治疗),另外 4 组为 MS 组,分别用生理盐水和或茴香醚治疗,剂量分别为 31.25、62.5 和 125 毫克/千克。所有实验鼠均通过腹腔注射给药,连续注射 14 天。行为试验包括三室试验、穿梭箱试验和驻留闯入者试验。通过qRT-PCR技术评估了海马中PI3K、AKT和mTOR基因的表达。研究结果表明,多发性硬化症与类似自闭症的行为有关。茴香醚能提高三室试验中的交际性和社会偏好指数,延长穿梭盒试验中的次级潜伏期,并减少驻留-入侵者试验中的攻击行为。此外,茴香醚还能增加多发性硬化症小鼠海马中 PI3K、AKT 和 mTOR 的基因表达。我们的结论是,茴香硫醚通过增加 PI3K/ AKT/mTOR 的基因表达,减轻了多发性硬化症诱发的小鼠自闭症样行为。
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
IBRO Neuroscience Reports
IBRO Neuroscience Reports Neuroscience-Neuroscience (all)
CiteScore
2.80
自引率
0.00%
发文量
99
审稿时长
14 weeks
文献相关原料
公司名称 产品信息 采购帮参考价格
×
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