Caenorhabditis Intervention Testing Program: the putative mTOR inhibitors Cinnarizine and Meclizine do not extend lifespan in C. elegans.

microPublication biology Pub Date : 2026-09-14 eCollection Date: 2026-01-01 DOI:10.17912/micropub.biology.002198
Erik Johnson, Christine A Sedore, Anna L Coleman-Hulbert, Brian D Onken, Vijaya Madhuri Achanta, Yuhua Song, Gino Cortopassi, Gordon J Lithgow, Monica Driscoll, Patrick C Phillips
{"title":"<i>Caenorhabditis</i> Intervention Testing Program: the putative mTOR inhibitors Cinnarizine and Meclizine do not extend lifespan in <i>C. elegans</i>.","authors":"Erik Johnson, Christine A Sedore, Anna L Coleman-Hulbert, Brian D Onken, Vijaya Madhuri Achanta, Yuhua Song, Gino Cortopassi, Gordon J Lithgow, Monica Driscoll, Patrick C Phillips","doi":"10.17912/micropub.biology.002198","DOIUrl":null,"url":null,"abstract":"<p><p>The mechanistic target of rapamycin (mTOR), a protein kinase and master cell regulator, is one of the most validated longevity drug targets: mTOR inhibition by compounds like rapamycin has been shown to significantly extend lifespan in numerous model organisms. Here, we tested whether the novel putative mTOR-inhibiting compounds cinnarizine and meclizine could likewise increase lifespan in the nematode <i>C. elegans</i> , following standardized protocols from the <i>Caenorhabditis</i> Intervention Testing Program (CITP). Our results indicate that cinnarizine and meclizine have no effect on <i>C. elegans</i> lifespan at lower doses, and that both compounds exert a toxic effect at higher doses, significantly shortening lifespan.</p>","PeriodicalId":74192,"journal":{"name":"microPublication biology","volume":"2026 ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2026-09-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13617457/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"microPublication biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.17912/micropub.biology.002198","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

The mechanistic target of rapamycin (mTOR), a protein kinase and master cell regulator, is one of the most validated longevity drug targets: mTOR inhibition by compounds like rapamycin has been shown to significantly extend lifespan in numerous model organisms. Here, we tested whether the novel putative mTOR-inhibiting compounds cinnarizine and meclizine could likewise increase lifespan in the nematode C. elegans , following standardized protocols from the Caenorhabditis Intervention Testing Program (CITP). Our results indicate that cinnarizine and meclizine have no effect on C. elegans lifespan at lower doses, and that both compounds exert a toxic effect at higher doses, significantly shortening lifespan.

隐杆线虫炎干预试验计划:假定的mTOR抑制剂Cinnarizine和Meclizine不能延长秀丽隐杆线虫的寿命。
雷帕霉素(mTOR)的机制靶点是一种蛋白激酶和主细胞调节剂,是最有效的长寿药物靶点之一:雷帕霉素等化合物抑制mTOR已被证明可以显着延长许多模式生物的寿命。在这里,我们测试了新的假定的mtor抑制化合物cinnarizine和meclizine是否同样可以延长秀丽隐杆线虫的寿命,遵循秀丽隐杆线虫炎干预测试计划(CITP)的标准化方案。我们的研究结果表明,肉桂利嗪和美甲利嗪在低剂量下对秀丽隐杆线虫的寿命没有影响,而在高剂量下,这两种化合物都有毒性作用,显著缩短线虫的寿命。
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
自引率
0.00%
发文量
0
审稿时长
3 weeks
×
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