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热量限制会影响皮肤屏障功能,并减轻增生性皮肤病的发展。

Caloric restriction impacts skin barrier function and attenuates the development of hyperplasia skin disease.

作者信息

Tang Huihao, Li Jianzhou, Jin Mengyu, Li Chengliang, Zhai Chuntao, Wang Juan, Huang Taomin, Ding Xiaolei

机构信息

Institute of Geriatrics, Affiliated Nantong Hospital of Shanghai University (The Sixth People's Hospital of Nantong), School of Medicine, Shanghai University, Nantong, China.

Shanghai Engineering Research Center of Organ Repair, School of Medicine, Shanghai University, Shanghai, China.

出版信息

Front Nutr. 2024 Sep 20;11:1423524. doi: 10.3389/fnut.2024.1423524. eCollection 2024.

DOI:10.3389/fnut.2024.1423524
PMID:39371941
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11449767/
Abstract

Caloric restriction (CR) stands out as one of the most potent interventions that prolong lifespan and mitigate age-associated diseases. Despite its well-established systemic effects, the impact of CR on skin physiological function remains poorly understood, and whether the intervention can alleviate the progression of inflammatory skin diseases remains uncertain. Here, we investigated the effects of CR on mouse skin barrier function and inflammatory response. Our results revealed that CR led to dramatic atrophy in the skin subcutaneous layer. The expression of barrier proteins and trans-epidermal water loss remain largely unchanged. Intriguingly, skin from CR mice exhibited reduced expression of inflammatory cytokines under steady conditions. In an imiquimod (IMQ)-induced mouse model of psoriasis, CR treatment attenuated the pathogenesis of psoriasis phenotypes, accompanied by a reduced activation of mTOR signaling in the psoriatic skin. Taken together, our findings shed light on the complex interplay between metabolic interventions and skin health, suggesting that CR has the potential to serve as a modulator of inflammatory responses in the skin.

摘要

热量限制(CR)是延长寿命和减轻与年龄相关疾病的最有效干预措施之一。尽管其全身性作用已得到充分证实,但CR对皮肤生理功能的影响仍知之甚少,且该干预措施能否缓解炎症性皮肤病的进展仍不确定。在此,我们研究了CR对小鼠皮肤屏障功能和炎症反应的影响。我们的结果显示,CR导致皮肤皮下层显著萎缩。屏障蛋白的表达和经表皮水分流失基本保持不变。有趣的是,在稳定状态下,CR小鼠的皮肤炎症细胞因子表达降低。在咪喹莫特(IMQ)诱导的银屑病小鼠模型中,CR治疗减轻了银屑病表型的发病机制,同时银屑病皮肤中mTOR信号的激活减少。综上所述,我们的研究结果揭示了代谢干预与皮肤健康之间的复杂相互作用,表明CR有潜力作为皮肤炎症反应的调节剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96d8/11449767/4d129086b660/fnut-11-1423524-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96d8/11449767/9134aabf3ca3/fnut-11-1423524-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96d8/11449767/73f4f6338a77/fnut-11-1423524-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96d8/11449767/e859a5882a6f/fnut-11-1423524-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96d8/11449767/0999757e971f/fnut-11-1423524-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96d8/11449767/40aff98dae2f/fnut-11-1423524-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96d8/11449767/4d129086b660/fnut-11-1423524-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96d8/11449767/9134aabf3ca3/fnut-11-1423524-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96d8/11449767/73f4f6338a77/fnut-11-1423524-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96d8/11449767/e859a5882a6f/fnut-11-1423524-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96d8/11449767/0999757e971f/fnut-11-1423524-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96d8/11449767/40aff98dae2f/fnut-11-1423524-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96d8/11449767/4d129086b660/fnut-11-1423524-g006.jpg

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本文引用的文献

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Epithelial-derived interleukin-23 promotes oral mucosal immunopathology.上皮细胞衍生的白细胞介素-23 促进口腔黏膜免疫病理学。
Immunity. 2024 Apr 9;57(4):859-875.e11. doi: 10.1016/j.immuni.2024.02.020. Epub 2024 Mar 20.
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Effects of dietary intervention on human diseases: molecular mechanisms and therapeutic potential.饮食干预对人类疾病的影响:分子机制与治疗潜力。
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Nuclear translocation of PKM2 mediates keratinocyte metabolic reprogramming in psoriasis.
PKM2 的核转位介导银屑病角质形成细胞代谢重编程。
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Short-Term Caloric Restriction and Subsequent Re-Feeding Compromise Liver Health and Associated Lipid Mediator Signaling in Aged Mice.短期热量限制和随后的再喂养会损害老年小鼠的肝脏健康和相关脂质介质信号转导。
Nutrients. 2023 Aug 21;15(16):3660. doi: 10.3390/nu15163660.
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Association of Nutrition, Obesity and Skin.营养、肥胖与皮肤关联
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Modulation of Dietary Fatty Acids in an Open-Label Study Improves Psoriasis and Dampens the Inflammatory Activation Status.在一项开放标签研究中,调节饮食中的脂肪酸可改善银屑病,并减轻炎症激活状态。
Nutrients. 2023 Mar 30;15(7):1698. doi: 10.3390/nu15071698.
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Monocytes re-enter the bone marrow during fasting and alter the host response to infection.在禁食期间,单核细胞重新进入骨髓,并改变宿主对感染的反应。
Immunity. 2023 Apr 11;56(4):783-796.e7. doi: 10.1016/j.immuni.2023.01.024. Epub 2023 Feb 23.
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Do Sleep Disorders and Western Diet Influence Psoriasis? A Scoping Review.睡眠障碍和西方饮食会影响银屑病吗?范围综述。
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mTORC1 Activity in Psoriatic Lesions Is Mediated by Aberrant Regulation through the Tuberous Sclerosis Complex.银屑病皮损中 mTORC1 的活性是通过结节性硬化复合物的异常调节介导的。
Cells. 2022 Sep 13;11(18):2847. doi: 10.3390/cells11182847.