Nrf2 cell signaling pathway is responsible for the antioxidant effect of resveratrol in aging

被引:3
作者
Franco, Filipe Nogueira [1 ]
Arrieta, Orlando Alfredo Pineda [2 ]
de Mello Silva, Breno [2 ]
Aragao, Matheus Motta [3 ]
Nagem, Ronaldo Alves Pinto [3 ]
de Araujo, Glaucy Rodrigues [1 ]
Chaves, Miriam Martins [1 ]
机构
[1] Univ Fed Minas Gerais, Biol Sci Inst, Dept Biochem & Immunol, Biochem Lab Aging & Correlated Dis, Belo Horizonte, MG, Brazil
[2] Univ Fed Ouro Preto, Inst Exact & Biol Sci, Dept Biol Sci, Microorganism Biol & Technol Lab, Ouro Preto, Brazil
[3] Univ Fed Minas Gerais, Biol Sci Inst, Dept Biochem & Immunol, Struct Biol Lab, Belo Horizonte, MG, Brazil
关键词
aging; AMPK; Nrf2; pathway; oxidative stress; resveratrol; AMPK; ACTIVATION; PROTECTS; STRESS;
D O I
10.1111/ggi.14939
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Introduction One of the markers of aging is oxidative stress, a condition characterized by an increase in free radicals concomitant with a reduction in antioxidant defenses. Within this, resveratrol is a compound that has been shown to act as a potent antioxidant. However, few studies highlight the cellular signaling pathways that are activated or inhibited during aging and that are responsible for this biological effect. Aim To verify the antioxidant profile of resveratrol (5 mu M) in leukocytes from donors in different age groups. Methods The project was approved by the Ethics Committee. Individuals were divided into three groups: 20-39, 40-59, and 60-80 years old. After separating the leukocytes, assays were performed to evaluate the AMPK (AMP-activated protein kinase) and Nrf2 (erythroid nuclear factor 2-related factor 2) pathways. In addition, luciferase assay and enzyme-linked immunosorbent assay were performed to evaluate transcription factor activation and Nrf2 expression, respectively. The analysis between age and treatment was performed using Pearson correlation (*P < 0.05). Results There was a reduction in the antioxidant effect of resveratrol during the aging process. In leukocytes from donors over 60 years of age, the AMPK pathway was silenced. Nrf2 was active at all ages. There was an increase in the activation of the transcription factor and phosphorylated protein in all age groups. Conclusions Nrf2 is an important biochemical mechanism responsible for the antioxidant effect of resveratrol. This effect diminishes with aging but is still observed.
引用
收藏
页码:954 / 961
页数:8
相关论文
共 30 条
[1]  
Abdollahi M., 2014, ENCYCL TOXICOL 3, P967, DOI [10.1016/B978-0-12-386454-3.00736-3, DOI 10.1016/B978-0-12-386454-3.00736-3]
[2]   Biomarkers of non-communicable chronic disease: an update on contemporary methods [J].
Al-Hadlaq, Solaiman M. ;
Balto, Hanan A. ;
Hassan, Wail M. ;
Marraiki, Najat A. ;
El-Ansary, Afaf K. .
PEERJ, 2022, 10
[3]  
[Anonymous], PROMEGA PRL RENILLA
[4]   The therapeutic potential of resveratrol: a review of clinical trials [J].
Berman, Adi Y. ;
Motechin, Rachel A. ;
Wiesenfeld, Maia Y. ;
Holz, Marina K. .
NPJ PRECISION ONCOLOGY, 2017, 1
[5]   Resveratrol: Change of SIRT 1 and AMPK signaling pattern during the aging process [J].
Caldeira, Camila Amaro ;
Santos, Milena Almeida ;
Araujo, Glaucy Rodrigues ;
Lara, Raquel Cunha ;
Franco, Filipe Nogueira ;
Chaves, Miriam Martins .
EXPERIMENTAL GERONTOLOGY, 2021, 146
[6]   Age-Associated Proinflammatory Secretory Phenotype in Vascular Smooth Muscle Cells From the Non-human Primate Macaca mulatta: Reversal by Resveratrol Treatment [J].
Csiszar, Anna ;
Sosnowska, Danuta ;
Wang, Mingyi ;
Lakatta, Edward G. ;
Sonntag, William E. ;
Ungvari, Zoltan .
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES, 2012, 67 (08) :811-820
[7]  
Cui Hang, 2012, J Signal Transduct, V2012, P646354, DOI 10.1155/2012/646354
[8]   Resveratrol stimulates AMP kinase activity in neurons [J].
Dasgupta, Biplab ;
Milbrandt, Jeffrey .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (17) :7217-7222
[9]   Reduction of AMP-Activated Protein Kinase α2 Increases Endoplasmic Reticulum Stress and Atherosclerosis In Vivo [J].
Dong, Yunzhou ;
Zhang, Miao ;
Liang, Bin ;
Xie, Zhonglin ;
Zhao, Zhengxing ;
Asfa, Sima ;
Choi, Hyoung Chul ;
Zou, Ming-Hui .
CIRCULATION, 2010, 121 (06) :792-803
[10]   Specific SIRT1 Activation Mimics Low Energy Levels and Protects against Diet-induced Metabolic Disorders by Enhancing Fat Oxidation [J].
Feige, Jerome N. ;
Lagouge, Marie ;
Canto, Carles ;
Strehle, Axelle ;
Houten, Sander M. ;
Milne, Jill C. ;
Lambert, Philip D. ;
Mataki, Chikage ;
Elliott, Peter J. ;
Auwerx, Johan .
CELL METABOLISM, 2008, 8 (05) :347-358