• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

橙皮苷通过调节22 - 26月龄小鼠的炎症衰老及AKT/mTOR/FoxO3a信号通路改善肌肉减少症

Hesperidin Ameliorates Sarcopenia through the Regulation of Inflammaging and the AKT/mTOR/FoxO3a Signaling Pathway in 22-26-Month-Old Mice.

作者信息

Oh Hyun-Ji, Jin Heegu, Lee Boo-Yong

机构信息

Department of Food Science and Biotechnology, College of Life Science, CHA University, Seongnam 13488, Gyeonggi, Republic of Korea.

出版信息

Cells. 2023 Aug 7;12(15):2015. doi: 10.3390/cells12152015.

DOI:10.3390/cells12152015
PMID:37566094
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10417333/
Abstract

Faced with a globally aging society, the maintenance of health and quality of life in older people is very important. The age-related loss of muscle mass and strength, known as sarcopenia, severely reduces quality of life and increases the risks of various diseases. In this study, we investigated the inhibitory effect of hesperidin (HES) on inflammaging, with the intention of evaluating its potential use as a treatment for sarcopenia. We studied 22-26-month-old mice, corresponding to humans aged ≥70 years, with aging-related sarcopenia, and young mice aged 3-6 months. The daily administration of HES for 8 weeks resulted in greater muscle mass and strength and increased the fiber size of the old mice. HES also restored the immune homeostasis that had been disrupted by aging, such as the imbalance in M1/M2 macrophage ratio. In addition, we found that HES ameliorated the sarcopenia by regulating AKT/mammalian target of rapamycin/forkhead box 3a signaling through an increase in insulin-like growth factor (IGF)-1 expression in the old mice. Therefore, HES represents a promising candidate inhibitor of sarcopenia in older people, and its effects are achieved through the maintenance of immune homeostasis.

摘要

面对全球老龄化社会,维持老年人的健康和生活质量非常重要。与年龄相关的肌肉质量和力量丧失,即肌肉减少症,会严重降低生活质量并增加各种疾病的风险。在本研究中,我们研究了橙皮苷(HES)对炎症衰老的抑制作用,旨在评估其作为肌肉减少症治疗方法的潜在用途。我们研究了相当于人类70岁及以上的22 - 26月龄患有与衰老相关肌肉减少症的小鼠,以及3 - 6月龄的年轻小鼠。每天给予HES 8周可使老年小鼠的肌肉质量和力量增加,并增大其纤维尺寸。HES还恢复了因衰老而被破坏的免疫稳态,如M1/M2巨噬细胞比例失衡。此外,我们发现HES通过增加老年小鼠胰岛素样生长因子(IGF)-1的表达来调节AKT/雷帕霉素哺乳动物靶蛋白/叉头框蛋白3a信号通路,从而改善肌肉减少症。因此,HES是老年人肌肉减少症的一种有前景的候选抑制剂,其作用是通过维持免疫稳态来实现的。

相似文献

1
Hesperidin Ameliorates Sarcopenia through the Regulation of Inflammaging and the AKT/mTOR/FoxO3a Signaling Pathway in 22-26-Month-Old Mice.橙皮苷通过调节22 - 26月龄小鼠的炎症衰老及AKT/mTOR/FoxO3a信号通路改善肌肉减少症
Cells. 2023 Aug 7;12(15):2015. doi: 10.3390/cells12152015.
2
Silk Peptide Ameliorates Sarcopenia through the Regulation of Akt/mTOR/FoxO3a Signaling Pathways and the Inhibition of Low-Grade Chronic Inflammation in Aged Mice.丝胶肽通过调节 Akt/mTOR/FoxO3a 信号通路和抑制老年小鼠低度慢性炎症改善肌肉减少症。
Cells. 2023 Sep 12;12(18):2257. doi: 10.3390/cells12182257.
3
Signalling pathways regulating muscle mass in ageing skeletal muscle: the role of the IGF1-Akt-mTOR-FoxO pathway.调控衰老骨骼肌质量的信号通路:IGF1-Akt-mTOR-FoxO 通路的作用。
Biogerontology. 2013 Jun;14(3):303-23. doi: 10.1007/s10522-013-9432-9. Epub 2013 May 19.
4
Losartan restores skeletal muscle remodeling and protects against disuse atrophy in sarcopenia.氯沙坦可恢复骨骼肌重塑,防止废用性萎缩。
Sci Transl Med. 2011 May 11;3(82):82ra37. doi: 10.1126/scitranslmed.3002227.
5
Soluble Whey Protein Hydrolysate Ameliorates Muscle Atrophy Induced by Immobilization via Regulating the PI3K/Akt Pathway in C57BL/6 Mice.可溶性乳清蛋白水解物通过调节 PI3K/Akt 通路改善 C57BL/6 小鼠的固定化诱导的肌肉萎缩。
Nutrients. 2020 Nov 1;12(11):3362. doi: 10.3390/nu12113362.
6
Testosterone regulation of Akt/mTORC1/FoxO3a signaling in skeletal muscle.睾酮对骨骼肌中 Akt/mTORC1/FoxO3a 信号通路的调节作用。
Mol Cell Endocrinol. 2013 Jan 30;365(2):174-86. doi: 10.1016/j.mce.2012.10.019. Epub 2012 Oct 29.
7
Chronic resistance training activates autophagy and reduces apoptosis of muscle cells by modulating IGF-1 and its receptors, Akt/mTOR and Akt/FOXO3a signaling in aged rats.慢性抗阻训练通过调节 IGF-1 及其受体、Akt/mTOR 和 Akt/FOXO3a 信号通路,激活自噬并减少老年大鼠肌肉细胞的凋亡。
Exp Gerontol. 2013 Apr;48(4):427-36. doi: 10.1016/j.exger.2013.02.009. Epub 2013 Feb 16.
8
The non-saponin fraction of Korean Red Ginseng ameliorates sarcopenia by regulating immune homeostasis in 22-26-month-old C57BL/6J mice.高丽红参的非皂苷组分通过调节22 - 26月龄C57BL/6J小鼠的免疫稳态来改善肌肉减少症。
J Ginseng Res. 2022 Nov;46(6):809-818. doi: 10.1016/j.jgr.2022.05.007. Epub 2022 May 23.
9
Testosterone supplementation reverses sarcopenia in aging through regulation of myostatin, c-Jun NH2-terminal kinase, Notch, and Akt signaling pathways.睾酮补充通过调节肌肉生长抑制素、c-Jun NH2-末端激酶、Notch 和 Akt 信号通路逆转衰老导致的肌肉减少症。
Endocrinology. 2010 Feb;151(2):628-38. doi: 10.1210/en.2009-1177. Epub 2009 Dec 18.
10
Age-related differences in insulin-like growth factor-1 receptor signaling regulates Akt/FOXO3a and ERK/Fos pathways in vascular smooth muscle cells.胰岛素样生长因子-1受体信号传导中的年龄相关差异调节血管平滑肌细胞中的Akt/FOXO3a和ERK/Fos通路。
J Cell Physiol. 2008 Nov;217(2):377-87. doi: 10.1002/jcp.21507.

引用本文的文献

1
Unraveling the Metabolic Pathways Between Metabolic-Associated Fatty Liver Disease (MAFLD) and Sarcopenia.解析代谢相关脂肪性肝病(MAFLD)与肌肉减少症之间的代谢途径
Int J Mol Sci. 2025 May 14;26(10):4673. doi: 10.3390/ijms26104673.
2
Epigenetic factors and inflammaging: FOXO3A as a potential biomarker of sarcopenia and upregulation of DNMT3A and SIRT3 in older adults.表观遗传因素与炎症衰老:FOXO3A作为肌肉减少症的潜在生物标志物以及老年人中DNMT3A和SIRT3的上调
Front Immunol. 2025 Feb 17;16:1467308. doi: 10.3389/fimmu.2025.1467308. eCollection 2025.
3
Fermented red ginseng extract improves sarcopenia-related muscle atrophy in old mice through regulation of muscle protein metabolism.

本文引用的文献

1
Aging and aging-related diseases: from molecular mechanisms to interventions and treatments.衰老和与衰老相关的疾病:从分子机制到干预和治疗。
Signal Transduct Target Ther. 2022 Dec 16;7(1):391. doi: 10.1038/s41392-022-01251-0.
2
Inflammaging: Implications in Sarcopenia.慢性炎症与肌肉减少症
Int J Mol Sci. 2022 Nov 30;23(23):15039. doi: 10.3390/ijms232315039.
3
Forkhead Box O Signaling Pathway in Skeletal Muscle Atrophy.叉头框蛋白 O 信号通路在骨骼肌萎缩中的作用。
发酵红参提取物通过调节肌肉蛋白质代谢改善老年小鼠的少肌症相关肌肉萎缩。
Food Sci Biotechnol. 2024 Sep 23;34(3):793-802. doi: 10.1007/s10068-024-01702-0. eCollection 2025 Feb.
4
Insights into the Therapeutic Potential of Active Ingredients of in Combatting Sarcopenia: An In Silico Approach.探讨 治疗肌少症的活性成分的治疗潜力:一种计算机模拟方法。
Int J Mol Sci. 2024 Oct 25;25(21):11451. doi: 10.3390/ijms252111451.
5
The essential role of dual-energy x-ray absorptiometry in the prediction of subclinical cardiovascular disease.双能X线吸收法在亚临床心血管疾病预测中的重要作用。
Front Cardiovasc Med. 2024 Aug 29;11:1377299. doi: 10.3389/fcvm.2024.1377299. eCollection 2024.
6
Type 2 diabetes mellitus related sarcopenia: a type of muscle loss distinct from sarcopenia and disuse muscle atrophy.2 型糖尿病相关肌少症:一种有别于废用性肌肉萎缩的肌肉丢失类型。
Front Endocrinol (Lausanne). 2024 May 24;15:1375610. doi: 10.3389/fendo.2024.1375610. eCollection 2024.
7
Age Is Just a Number: Progress and Obstacles in the Discovery of New Candidate Drugs for Sarcopenia.年龄只是一个数字:肌少症新候选药物发现的进展和障碍。
Cells. 2023 Nov 11;12(22):2608. doi: 10.3390/cells12222608.
Am J Pathol. 2022 Dec;192(12):1648-1657. doi: 10.1016/j.ajpath.2022.09.003. Epub 2022 Sep 27.
4
High Intensity Interval Training: A Potential Method for Treating Sarcopenia.高强度间歇训练:治疗肌肉减少症的一种潜在方法。
Clin Interv Aging. 2022 May 26;17:857-872. doi: 10.2147/CIA.S366245. eCollection 2022.
5
Low-Grade Systemic Inflammation Interferes with Anabolic and Catabolic Characteristics of the Aged Human Skeletal Muscle.低水平系统性炎症会干扰老年人类骨骼肌的合成代谢和分解代谢特性。
Oxid Med Cell Longev. 2021 Dec 7;2021:8376915. doi: 10.1155/2021/8376915. eCollection 2021.
6
Exercise-Induced Autophagy Suppresses Sarcopenia Through Akt/mTOR and Akt/FoxO3a Signal Pathways and AMPK-Mediated Mitochondrial Quality Control.运动诱导的自噬通过Akt/mTOR和Akt/FoxO3a信号通路以及AMPK介导的线粒体质量控制来抑制肌肉减少症。
Front Physiol. 2020 Nov 2;11:583478. doi: 10.3389/fphys.2020.583478. eCollection 2020.
7
Pharmacological Interventions for Treatment of Sarcopenia: Current Status of Drug Development for Sarcopenia.治疗肌肉减少症的药物干预:肌肉减少症药物研发的现状
Ann Geriatr Med Res. 2019 Sep;23(3):98-104. doi: 10.4235/agmr.19.0028. Epub 2019 Sep 23.
8
The role of FOXOs and autophagy in cancer and metastasis-Implications in therapeutic development.FOXOs 和自噬在癌症和转移中的作用——对治疗开发的影响。
Med Res Rev. 2020 Nov;40(6):2089-2113. doi: 10.1002/med.21695. Epub 2020 May 31.
9
Inflammaging as a common ground for the development and maintenance of sarcopenia, obesity, cardiomyopathy and dysbiosis.炎症性衰老作为肌肉减少症、肥胖症、心肌病和肠道菌群失调发展和维持的共同基础。
Ageing Res Rev. 2019 Dec;56:100980. doi: 10.1016/j.arr.2019.100980. Epub 2019 Nov 11.
10
The Role of the IGF-1 Signaling Cascade in Muscle Protein Synthesis and Anabolic Resistance in Aging Skeletal Muscle.胰岛素样生长因子-1信号级联在衰老骨骼肌肌肉蛋白质合成及合成代谢抵抗中的作用
Front Nutr. 2019 Sep 10;6:146. doi: 10.3389/fnut.2019.00146. eCollection 2019.