• 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

衰老过程中热量限制对白色脂肪组织和棕色脂肪组织的差异反应。

Differential Responses of White Adipose Tissue and Brown Adipose Tissue to Calorie Restriction During Aging.

机构信息

Division of Geriatric Endocrinology, the First Affiliated Hospital of Nanjing Medical University, People's Republic of China.

Division of Geriatric Respiratory, the First Affiliated Hospital of Nanjing Medical University, People's Republic of China.

出版信息

J Gerontol A Biol Sci Med Sci. 2021 Feb 25;76(3):393-399. doi: 10.1093/gerona/glaa070.

DOI:10.1093/gerona/glaa070
PMID:32222773
Abstract

Age-related adipose tissue dysfunction is potentially important in the development of insulin resistance and metabolic disorder. Caloric restriction (CR) is a robust intervention to reduce adiposity, improve metabolic health, and extend healthy life span. Both white adipose tissue (WAT) and brown adipose tissue (BAT) are involved in energy homeostasis. CR triggers the beiging of WAT in young mice; however, the effects of CR on beiging of WAT and function of BAT during aging are unclear. This study aimed to investigate how age and CR impact the beiging of WAT, the function of BAT, and metabolic health in mice. C57BL/6 mice were fed CR diet (40% less than the ad libitum [AL] diet) for 3 months initiated in young (3 months), middle-aged (12 months), and old (19 months) stage. We found age-related changes in different types of adipose tissue, including adipocyte enlargement, declined beiging of WAT, and declined thermogenic and β-oxidational function of BAT. Moreover, CR attenuated age-associated adipocyte enlargement and prevented the age-related decline in beiging potential of WAT. These protective effects on the beiging potential were significant in inguinal WAT at all three ages, which were significant in epididymal WAT at young and old age. In contrast, thermogenic and β-oxidational function of BAT further declined after CR in the young age group. In conclusion, our findings reveal the contribution of WAT beiging decline to age-related metabolic disorder and suggest nutritional intervention, specifically targeting WAT beiging, as an effective approach to metabolic health during aging.

摘要

年龄相关的脂肪组织功能障碍在胰岛素抵抗和代谢紊乱的发展中具有重要意义。热量限制(CR)是一种减少肥胖、改善代谢健康和延长健康寿命的强大干预措施。白色脂肪组织(WAT)和棕色脂肪组织(BAT)都参与能量稳态。CR 可引发年轻小鼠 WAT 的褐色化;然而,CR 对衰老过程中 WAT 的褐色化和 BAT 功能的影响尚不清楚。本研究旨在探讨年龄和 CR 如何影响 WAT 的褐色化、BAT 的功能和小鼠的代谢健康。C57BL/6 小鼠在年轻(3 个月)、中年(12 个月)和老年(19 个月)阶段开始接受 CR 饮食(比自由进食[AL]饮食少 40%)3 个月。我们发现不同类型脂肪组织的年龄相关变化,包括脂肪细胞增大、WAT 褐色化减少以及 BAT 的产热和β-氧化功能下降。此外,CR 减弱了与年龄相关的脂肪细胞增大,并防止了 WAT 褐色化潜力随年龄的下降。这些对褐色化潜力的保护作用在所有三个年龄段的腹股沟 WAT 中均显著,在年轻和老年的附睾 WAT 中也显著。相比之下,在年轻年龄组中,CR 后 BAT 的产热和β-氧化功能进一步下降。总之,我们的研究结果揭示了 WAT 褐色化减少对与年龄相关的代谢紊乱的贡献,并表明营养干预,特别是针对 WAT 褐色化,是衰老过程中代谢健康的有效方法。

相似文献

1
Differential Responses of White Adipose Tissue and Brown Adipose Tissue to Calorie Restriction During Aging.衰老过程中热量限制对白色脂肪组织和棕色脂肪组织的差异反应。
J Gerontol A Biol Sci Med Sci. 2021 Feb 25;76(3):393-399. doi: 10.1093/gerona/glaa070.
2
Long-term caloric restriction ameliorates deleterious effects of aging on white and brown adipose tissue plasticity.长期热量限制可改善衰老对白色和棕色脂肪组织可塑性的有害影响。
Aging Cell. 2019 Jun;18(3):e12948. doi: 10.1111/acel.12948. Epub 2019 Mar 28.
3
Depot-specific regulation of NAD/SIRTs metabolism identified in adipose tissue of mice in response to high-fat diet feeding or calorie restriction.高脂饮食喂养或热量限制后,在小鼠脂肪组织中鉴定到了 depot 特异性调节 NAD/SIRTs 代谢的作用。
J Nutr Biochem. 2020 Jun;80:108377. doi: 10.1016/j.jnutbio.2020.108377. Epub 2020 Mar 19.
4
Transient p53 inhibition sensitizes aged white adipose tissue for beige adipocyte recruitment by blocking mitophagy.短暂抑制 p53 通过阻断线粒体自噬使衰老的白色脂肪组织对米色脂肪细胞的募集敏感。
FASEB J. 2019 Jan;33(1):844-856. doi: 10.1096/fj.201800577R. Epub 2018 Jul 27.
5
Differential responses of white adipose tissue and brown adipose tissue to caloric restriction in rats.热量限制对大鼠白色脂肪组织和棕色脂肪组织的反应差异。
Mech Ageing Dev. 2012 May;133(5):255-66. doi: 10.1016/j.mad.2012.02.003. Epub 2012 Mar 10.
6
Helminth antigens counteract a rapid high-fat diet-induced decrease in adipose tissue eosinophils.蠕虫抗原可对抗高脂饮食快速诱导的脂肪组织嗜酸性粒细胞减少。
J Mol Endocrinol. 2017 Oct;59(3):245-255. doi: 10.1530/JME-17-0112. Epub 2017 Jul 10.
7
Aging leads to a programmed loss of brown adipocytes in murine subcutaneous white adipose tissue.衰老导致小鼠皮下白色脂肪组织中棕色脂肪细胞的程序性丧失。
Aging Cell. 2012 Dec;11(6):1074-83. doi: 10.1111/acel.12010. Epub 2012 Oct 24.
8
Adrenomedullin 2 Enhances Beiging in White Adipose Tissue Directly in an Adipocyte-autonomous Manner and Indirectly through Activation of M2 Macrophages.肾上腺髓质素2以脂肪细胞自主的方式直接增强白色脂肪组织的米色化,并通过激活M2巨噬细胞间接增强米色化。
J Biol Chem. 2016 Nov 4;291(45):23390-23402. doi: 10.1074/jbc.M116.735563. Epub 2016 Sep 12.
9
Adiponectin stimulates Sca1CD34-adipocyte precursor cells associated with hyperplastic expansion and beiging of brown and white adipose tissue.脂联素刺激与棕色和白色脂肪组织的增生性扩张及米色化相关的Sca1CD34脂肪细胞前体细胞。
Metabolism. 2024 Feb;151:155716. doi: 10.1016/j.metabol.2023.155716. Epub 2023 Nov 2.
10
Beiging of white adipose tissue as a therapeutic strategy for weight loss in humans.白色脂肪组织褐变作为人类减肥的一种治疗策略。
Horm Mol Biol Clin Investig. 2017 Jun 23;31(2):/j/hmbci.2017.31.issue-2/hmbci-2017-0016/hmbci-2017-0016.xml. doi: 10.1515/hmbci-2017-0016.

引用本文的文献

1
Potential downsides of calorie restriction.热量限制的潜在不利之处。
Nat Rev Endocrinol. 2025 Apr 17. doi: 10.1038/s41574-025-01111-1.
2
Drug-Based Lifespan Extension in Mice Strongly Affects Lipids Across Six Organs.基于药物的小鼠寿命延长对六个器官的脂质有强烈影响。
Aging Cell. 2025 May;24(5):e14465. doi: 10.1111/acel.14465. Epub 2025 Mar 24.
3
Sarcopenia and cachexia: molecular mechanisms and therapeutic interventions.肌肉减少症和恶病质:分子机制与治疗干预
MedComm (2020). 2025 Jan 5;6(1):e70030. doi: 10.1002/mco2.70030. eCollection 2025 Jan.
4
Rapid modulation of interscapular brown adipose tissue mitochondrial activity by ketosis induced by 1,3-butanediol administration to rats.1,3-丁二醇给药诱导酮症快速调节肩胛间棕色脂肪组织线粒体活性。
FASEB J. 2024 Nov 30;38(22):e70195. doi: 10.1096/fj.202401592RR.
5
Brown Fat and Nutrition: Implications for Nutritional Interventions.棕色脂肪与营养:营养干预的影响
Nutrients. 2023 Sep 20;15(18):4072. doi: 10.3390/nu15184072.
6
Aging adipose tissue, insulin resistance, and type 2 diabetes.衰老的脂肪组织、胰岛素抵抗和 2 型糖尿病。
Biogerontology. 2024 Feb;25(1):53-69. doi: 10.1007/s10522-023-10067-6. Epub 2023 Sep 19.
7
Plasticity of adipose tissues in response to fasting and refeeding declines with aging in mice.随着小鼠年龄的增长,其脂肪组织对禁食和再喂养的反应能力会逐渐降低。
Aging (Albany NY). 2023 May 23;15(10):4319-4333. doi: 10.18632/aging.204734.
8
FGF21 has a sex-specific role in calorie-restriction-induced beiging of white adipose tissue in mice.成纤维细胞生长因子21在小鼠白色脂肪组织的卡路里限制诱导米色化过程中具有性别特异性作用。
Aging Biol. 2022;1.
9
The effects of caloric restriction on adipose tissue and metabolic health are sex- and age-dependent.热量限制对脂肪组织和代谢健康的影响具有性别和年龄依赖性。
Elife. 2023 Apr 25;12:e88080. doi: 10.7554/eLife.88080.
10
Dietary patterns and cardiometabolic health: Clinical evidence and mechanism.饮食模式与心脏代谢健康:临床证据与机制
MedComm (2020). 2023 Feb 5;4(1):e212. doi: 10.1002/mco2.212. eCollection 2023 Feb.