Generic placeholder image

Current Pharmaceutical Design

Editor-in-Chief

ISSN (Print): 1381-6128
ISSN (Online): 1873-4286

General Research Article

Protective Effect of Anthocyanins on Radiation-induced Hippocampal Injury through Activation of SIRT3

Author(s): Chenchen Wang, Shuna Yu , Jiying Jiang, Huiting Li, Yitong Pan, Wanzhen Li, Chen Bai, Ming Li, Peitong Xie, Jiao Liu* and Jianguo Li*

Volume 28, Issue 13, 2022

Published on: 11 August, 2021

Page: [1103 - 1108] Pages: 6

DOI: 10.2174/1381612827666210603151224

Price: $65

Abstract

Background: Neuronal cell apoptosis is associated with radiation exposure. It is urgent to study the radiation protection of hippocampal neurons.

Objective: The purpose of this study was to investigate the protective effect of anthocyanins on radiation and its potential mechanism.

Materials and Methods: The irradiation was carried out at room temperature with 4-Gy dose. Anthocyanins were intraperitoneally administered to rats prior to radiation exposure. The immunohistology and survival of neurons within the hippocampi, neuroprotective effects of anthocyanin, mean ROS accumulation and SIRT3 expression by Western Blot and qRTPCR were performed.

Results: Anthocyanins inhibit radiation-induced apoptosis by activating SIRT3. SIRT3 mRNA increased 24 hours after anthocyanin performed, accompanied by an increase in SIRT3 protein and activity.

Conclusion: Anthocyanin can effectively resist radiation-induced oxidation and support its role in scavenging cellular reactive oxygen species. The results showed that anthocyanin protected hippocampal neurons from apoptosis through the activity of SIRT3 after irradiation.

Keywords: Anthocyanins, hippocampus, sirtuin 3, radiation, reactive oxygen species, apoptosis, oxidative stress.

« Previous
[1]
Verreet T, Verslegers M, Quintens R, Baatout S, Benotmane MA. Current evidence for developmental, structural, and functional brain defects following prenatal radiation exposure. Neural Plast 2016; 2016: 1243527.
[http://dx.doi.org/10.1155/2016/1243527] [PMID: 27382490]
[2]
Du C, Fang M, Li Y, Li L, Wang X. Smac, a mitochondrial protein that promotes cytochrome c-dependent caspase activation by eliminating IAP inhibition. Cell 2000; 102(1): 33-42.
[http://dx.doi.org/10.1016/S0092-8674(00)00008-8] [PMID: 10929711]
[3]
Azzam EI, Jay-Gerin JP, Pain D. Ionizing radiation-induced metabolic oxidative stress and prolonged cell injury. Cancer Lett 2012; 327(1-2): 48-60.
[http://dx.doi.org/10.1016/j.canlet.2011.12.012] [PMID: 22182453]
[4]
Wang G, Fu XL, Wang JJ, Guan R, Sun Y, Tony SST. Inhibition of glycolytic metabolism in glioblastoma cells by Pt3glc combinated with PI3K inhibitor via SIRT3-mediated mitochondrial and PI3K/Akt-MAPK pathway. J Cell Physiol 2019; 234(5): 5888-903.
[http://dx.doi.org/10.1002/jcp.26474] [PMID: 29336479]
[5]
Maes M, Anderson G, Betancort Medina SR, Seo M, Ojala JO. Integrating autism spectrum disorder pathophysiology: Mitochondria, vitamin A, CD38, oxytocin, serotonin and melatonergic alterations in the placenta and gut. Curr Pharm Des 2019; 25(41): 4405-20.
[http://dx.doi.org/10.2174/1381612825666191102165459] [PMID: 31682209]
[6]
Kabziński J, Walczak A, Mik M, Majsterek I. Sirt3 regulates the level of mitochondrial DNA repair activity through deacetylation of NEIL1, NEIL2, OGG1, MUTYH, APE1 and LIG3 in colorectal cancer. Pol Przegl Chir 2019; 92(1): 1-4.
[http://dx.doi.org/10.5604/01.3001.0013.5539] [PMID: 32312920]
[7]
Diaconeasa Z, Ayvaz H, Ruginǎ D, et al. Melanoma inhibition by anthocyanins is associated with the reduction of oxidative stress biomarkers and changes in mitochondrial membrane potential. Plant Foods Hum Nutr 2017; 72(4): 404-10.
[http://dx.doi.org/10.1007/s11130-017-0638-x] [PMID: 29129015]
[8]
Salvatori I, Valle C, Ferri A, Carrì MT. SIRT3 and mitochondrial metabolism in neurodegenerative diseases. Neurochem Int 2017; 109: 184-92.
[http://dx.doi.org/10.1016/j.neuint.2017.04.012] [PMID: 28449871]
[9]
Li R, Xin T, Li D, Wang C, Zhu H, Zhou H. Therapeutic effect of Sirtuin 3 on ameliorating nonalcoholic fatty liver disease: The role of the ERK-CREB pathway and Bnip3-mediated mitophagy. Redox Biol 2018; 18: 229-43.
[http://dx.doi.org/10.1016/j.redox.2018.07.011] [PMID: 30056271]
[10]
Kempf SJ, Janik D, Barjaktarovic Z, et al. Chronic low-dose-rate ionising radiation affects the hippocampal phosphoproteome in the ApoE-/- Alzheimer’s mouse model. Oncotarget 2016; 7(44): 71817-32.
[http://dx.doi.org/10.18632/oncotarget.12376] [PMID: 27708245]
[11]
Baltaci SB, Mogulkoc R, Baltaci AK. Resveratrol and exercise. Biomed Rep 2016; 5(5): 525-30.
[http://dx.doi.org/10.3892/br.2016.777] [PMID: 27882212]
[12]
Poulose SM, Rabin BM, Bielinski DF, et al. Neurochemical differences in learning and memory paradigms among rats supplemented with anthocyanin-rich blueberry diets and exposed to acute doses of 56Fe particles. Life Sci Space Res (Amst) 2017; 12: 16-23.
[http://dx.doi.org/10.1016/j.lssr.2016.12.002] [PMID: 28212704]
[13]
Fan ZL, Wang ZY, Zuo LL, Tian SQ. Protective effect of anthocyanins from lingonberry on radiation-induced damages. Int J Environ Res Public Health 2012; 9(12): 4732-43.
[http://dx.doi.org/10.3390/ijerph9124732] [PMID: 23249859]
[14]
Lou H, Yao J, Sun Y, et al. Role of blueberry anthocyanin extract in the expression of SIRT1 and NF-κB in rat lens epithelial cells in experimentally induced DM. Curr Eye Res 2021; 46(1): 45-51.
[http://dx.doi.org/10.1080/02713683.2020.1776879] [PMID: 32478572]
[15]
Han L, Yang Q, Li J, et al. Protocatechuic acid-ameliorated endothelial oxidative stress through regulating acetylation level via CD36/AMPK pathway. J Agric Food Chem 2019; 67(25): 7060-72.
[http://dx.doi.org/10.1021/acs.jafc.9b02647] [PMID: 31240928]
[16]
Afzal M, Redha A, AlHasan R. Anthocyanins potentially contribute to defense against Alzheimer’s disease. Molecules 2019; 24(23): 4255.
[http://dx.doi.org/10.3390/molecules24234255] [PMID: 31766696]
[17]
Shah SA, Amin FU, Khan M, et al. Anthocyanins abrogate glutamate-induced AMPK activation, oxidative stress, neuroinflammation, and neurodegeneration in postnatal rat brain. J Neuroinflammation 2016; 13(1): 286.
[http://dx.doi.org/10.1186/s12974-016-0752-y] [PMID: 27821173]
[18]
Pacheco SM, Soares MSP, Gutierres JM, et al. Anthocyanins as a potential pharmacological agent to manage memory deficit, oxidative stress and alterations in ion pump activity induced by experimental sporadic dementia of Alzheimer’s type. J Nutr Biochem 2018; 56: 193-204.
[http://dx.doi.org/10.1016/j.jnutbio.2018.02.014] [PMID: 29587242]
[19]
Bendokas V, Stanys V, Mažeikienė I, Trumbeckaite S, Baniene R, Liobikas J. Anthocyanins: From the Field to the Antioxidants in the Body. Antioxidants 2020; 9(9): 819.
[http://dx.doi.org/10.3390/antiox9090819] [PMID: 32887513]
[20]
Park SW, Choi J, Kim J, et al. Anthocyanins from black soybean seed coat prevent radiation-induced skin fibrosis by downregulating TGF-β and Smad3 expression. Arch Dermatol Res 2018; 310(5): 401-12.
[http://dx.doi.org/10.1007/s00403-018-1827-7] [PMID: 29556751]
[21]
Li J, Meng Z, Zhang G, et al. N-acetylcysteine relieves oxidative stress and protects hippocampus of rat from radiation-induced apoptosis by inhibiting caspase-3. Biomed Pharmacother 2015; 70: 1-6.
[http://dx.doi.org/10.1016/j.biopha.2014.12.029] [PMID: 25776470]
[22]
Dudek SM, Garcia JG. Cytoskeletal regulation of pulmonary vascular permeability. J Appl Physiol (1985) 2001; 91(4): 1487-500.
[23]
Wilke C, Grosshans D, Duman J, Brown P, Li J. Radiation-induced cognitive toxicity: pathophysiology and interventions to reduce toxicity in adults. Neuro-oncol 2018; 20(5): 597-607.
[http://dx.doi.org/10.1093/neuonc/nox195] [PMID: 29045710]
[24]
Xiao Z, Yang S, Su Y, et al. Alteration of the inflammatory molecule network after irradiation of soft tissue. Adv Exp Med Biol 2013; 765: 335-41.
[http://dx.doi.org/10.1007/978-1-4614-4989-8_47] [PMID: 22879053]
[25]
Jęśko H, Wencel P, Strosznajder RP, Strosznajder JB. Sirtuins and their roles in brain aging and neurodegenerative disorders. Neurochem Res 2017; 42(3): 876-90.
[http://dx.doi.org/10.1007/s11064-016-2110-y] [PMID: 27882448]
[26]
Epperly MW, Franicola D, Shields D, et al. Screening of antimicrobial agents for in vitro radiation protection and mitigation capacity, including those used in supportive care regimens for bone marrow transplant recipients. In Vivo 2010; 24(1): 9-19.
[PMID: 20133970]
[27]
Kalt W, Cassidy A, Howard LR, et al. Recent research on the health benefits of blueberries and their anthocyanins. Adv Nutr 2020; 11(2): 224-36.
[PMID: 31329250]
[28]
Winter AN, Bickford PC. Anthocyanins and their metabolites as therapeutic agents for neurodegenerative disease. Antioxidants 2019; 8(9): 333.
[http://dx.doi.org/10.3390/antiox8090333] [PMID: 31443476]
[29]
Lumniczky K, Szatmári T, Sáfrány G. Ionizing radiation-induced immune and inflammatory reactions in the brain. Front Immunol 2017; 8: 517.
[http://dx.doi.org/10.3389/fimmu.2017.00517] [PMID: 28529513]

Rights & Permissions Print Cite
© 2024 Bentham Science Publishers | Privacy Policy