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Antioxidants (Basel). 2023 Apr 10;12(4):902. doi: 10.3390/antiox12040902.
2
TRPV1 alleviates osteoarthritis by inhibiting M1 macrophage polarization via Ca/CaMKII/Nrf2 signaling pathway.TRPV1 通过 Ca/CaMKII/Nrf2 信号通路抑制 M1 巨噬细胞极化缓解骨关节炎。
Cell Death Dis. 2021 May 18;12(6):504. doi: 10.1038/s41419-021-03792-8.
3
Adipogenesis as a Potential Anti-Obesity Target: A Review of Pharmacological Treatment and Natural Products.脂肪生成作为潜在的抗肥胖靶点:药物治疗与天然产物综述
Diabetes Metab Syndr Obes. 2021 Jan 8;14:67-83. doi: 10.2147/DMSO.S281186. eCollection 2021.
4
NRF2 as a regulator of cell metabolism and inflammation in cancer.NRF2 作为癌症中细胞代谢和炎症的调节剂。
Carcinogenesis. 2020 Jun 17;41(4):405-416. doi: 10.1093/carcin/bgaa039.
5
Antioxidant treatment induces reductive stress associated with mitochondrial dysfunction in adipocytes.抗氧化处理诱导脂肪细胞中与线粒体功能障碍相关的还原性应激。
J Biol Chem. 2019 Feb 15;294(7):2340-2352. doi: 10.1074/jbc.RA118.004253. Epub 2018 Dec 17.
6
Novel Neohesperidin Dihydrochalcone Analogue Inhibits Adipogenic Differentiation of Human Adipose-Derived Stem Cells through the Nrf2 Pathway.新型橙皮苷二氢查尔酮类似物通过 Nrf2 通路抑制人脂肪干细胞的成脂分化。
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7
Nrf2-ARE pathway: An emerging target against oxidative stress and neuroinflammation in neurodegenerative diseases.Nrf2-ARE 通路:一种针对神经退行性疾病中氧化应激和神经炎症的新兴靶点。
Pharmacol Ther. 2016 Jan;157:84-104. doi: 10.1016/j.pharmthera.2015.11.003. Epub 2015 Nov 23.
8
Antioxidant responses and cellular adjustments to oxidative stress.抗氧化反应及细胞对氧化应激的调节
Redox Biol. 2015 Dec;6:183-197. doi: 10.1016/j.redox.2015.07.008. Epub 2015 Jul 21.
9
The emerging role of Nrf2 in mitochondrial function.Nrf2在线粒体功能中的新作用。
Free Radic Biol Med. 2015 Nov;88(Pt B):179-188. doi: 10.1016/j.freeradbiomed.2015.04.036. Epub 2015 May 11.
10
UV, stress and aging.紫外线、压力与衰老。
Dermatoendocrinol. 2012 Jul 1;4(3):236-40. doi: 10.4161/derm.23652.

济州岛火山熔岩海水通过人成纤维细胞中Nrf2的易位产生的抗氧化活性。

Antioxidant activity of Jeju lava seawater through translocation of Nrf2 in human fibroblast.

作者信息

Heo Hee Sun, Kim Yeong Eun, Lee Jong Hun

机构信息

Department of Food Science and Biotechnology, College of Life Sciences, CHA University, Gyeonggi-do, 11160 Republic of Korea.

Orion Jeju Yongamsoo, Jeju, 63359 Republic of Korea.

出版信息

Food Sci Biotechnol. 2024 Feb 25;33(11):2653-2661. doi: 10.1007/s10068-023-01510-y. eCollection 2024 Aug.

DOI:10.1007/s10068-023-01510-y
PMID:39144193
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11319678/
Abstract

Reactive oxygen species (ROS) are associated with various pathological conditions, including atherosclerosis and cancer. Photoaging, mainly caused by UVB-induced ROS, accelerates skin aging and collagen degradation. Nuclear factor erythroid 2-related factor 2 (Nrf2) regulates antioxidant enzymes and has demonstrated protective effects against chronic diseases. Jeju lava seawater (JLS), which is rich in minerals, is attracting attention for its health benefits. The current study investigates the antioxidant properties of JLS in human dermal fibroblasts (HDFs). experiments were conducted by culturing HDFs in JLS with different water hardness levels and irradiating UVB. The results show that JLS does not affect HDF viability, especially at high water hardness. JLS treatment enhances collagen production and upregulates Nrf2 and antioxidant enzymes such as NQO1 and HO-1. This mechanism involves the translocation of Nrf2 to the cell nucleus. JLS shows promise as an antioxidant, potentially mitigating the effects of oxidative stress and promoting collagen synthesis.

摘要

活性氧(ROS)与多种病理状况相关,包括动脉粥样硬化和癌症。光老化主要由紫外线B(UVB)诱导的ROS引起,会加速皮肤老化和胶原蛋白降解。核因子红细胞2相关因子2(Nrf2)调节抗氧化酶,并已证明对慢性疾病具有保护作用。富含矿物质的济州岛火山熔岩海水(JLS)因其对健康有益而受到关注。当前研究调查了JLS在人皮肤成纤维细胞(HDFs)中的抗氧化特性。通过在不同水硬度水平的JLS中培养HDFs并照射UVB来进行实验。结果表明,JLS不影响HDF的活力,尤其是在高水硬度下。JLS处理可增强胶原蛋白的产生,并上调Nrf2以及NQO1和HO-1等抗氧化酶。该机制涉及Nrf2向细胞核的转位。JLS有望作为一种抗氧化剂,潜在地减轻氧化应激的影响并促进胶原蛋白合成。