Photoperiod affects oxidative stress in the liver of Cricetulus barabensis through the Nrf2-Keap1 signaling pathway

References

• Atgié C, Le GS, Marti L, Hanoun N, Casteilla L, Pénicaud L, Ambid L, Carpéné C. 1998 Mar. Lipolytic and antilipolytic responses of the Siberian hamster (Phodopus sungorus) white adipocytes after weight loss induced by short photoperiod exposure. Comp Biochem Physiol A. 119(2):503–510. doi: 10.1016/s1095-6433(97)00457-1.
   PubMed Web of Science ®Google Scholar
• Baydaş G, Erçel E, Canatan H, Dönder E, Akyol A. 2001. Effect of melatonin on oxidative status of rat brain, liver and kidney tissues under constant light exposure. Cell Biochem Funct. 19(1):37–41. doi: 10.1002/cbf.897.
   PubMed Web of Science ®Google Scholar
• Bellezza I, Giambanco I, Minelli A, Donato R. 2018 May. Nrf2-Keap1 signaling in oxidative and reductive stress. Bba-Mol Cell Res. 1865(5):721–733. doi: 10.1016/j.bbamcr.2018.02.010
   PubMed Web of Science ®Google Scholar
• Chainy GB, Paital B, Dandapat J. 2016. An overview of seasonal changes in oxidative stress and antioxidant defence parameters in some invertebrate and vertebrate species. Scientifica. 2016:1–8. doi:10.1155/2016/6126570.
   Google Scholar
• Cichoż-Lach H, Michalak A. 2014 Jul 7. Oxidative stress as a crucial factor in liver diseases. World J Gastroentero. 20(25):8082–8091. doi: 10.3748/wjg.v20.i25.8082.
   PubMed Web of Science ®Google Scholar
• Circu ML, Aw TY. 2010 Mar 15. Reactive oxygen species, cellular redox systems, and apoptosis. Free Radic Biol Med. 48(6):749–762. doi: 10.1016/j.freeradbiomed.2009.12.022.
   PubMed Web of Science ®Google Scholar
• Cruz A, Padillo FJ, Granados J, Túnez I, Muñoz MC, Briceño J, Pera-Madrazo C, Montilla P. 2003 Dec. Effect of melatonin on cholestatic oxidative stress under constant light exposure. Cell Biochem Funct. 21(4):377–380. doi: 10.1002/cbf.1046
   PubMed Web of Science ®Google Scholar
• de la Vega MR, Chapman E, Zhang DD. 2018 Jul 9. NRF2 and the Hallmarks of cancer. Cancer Cell. 34(1):21–43. doi: 10.1016/j.ccell.2018.03.022.
   PubMed Web of Science ®Google Scholar
• Djordjevic A, Kotnik P, Horvat D, Knez Z, Antonic M. 2020 Dec. Pharmacodynamics of malondialdehyde as indirect oxidative stress marker after arrested-heart cardiopulmonary bypass surgery. Biomed Pharmacother. 132:132. doi:10.1016/j.biopha.2020.110877.
   Web of Science ®Google Scholar
• Escribano BM, Díaz-Moreno A, Tasset I, Túnez I, Ashton N. 2014. Impact of light/dark cycle patterns on oxidative stress in an adriamycin-induced nephropathy model in rats. PLoS One. 9(5):e97713. doi: 10.1371/journal.pone.0097713.
   PubMed Web of Science ®Google Scholar
• Farooqui MY, Ahmed AE. 1984 Jun 11. Circadian periodicity of tissue glutathione and its relationship with lipid peroxidation in rats. Life Sci. 34(24):2413–2418. doi: 10.1016/0024-3205(84)90430-2.
   PubMed Web of Science ®Google Scholar
• Fukai T, Ushio-Fukai M. 2011 Sep 15. Superoxide dismutases: role in redox signaling, vascular function, and diseases. Antioxid Redox Signal. 15(6):1583–1606. doi: 10.1089/ars.2011.3999.
   PubMed Web of Science ®Google Scholar
• Galasso M, Gambino S, Romanelli MG, Donadelli M, Scupoli MT. 2021. Browsing the oldest antioxidant enzyme: catalase and its multiple regulation in cancer. Free Radical Bio Med. Aug 20. 172:264–272. doi: 10.1016/j.freeradbiomed.2021.06.010.
   PubMed Web of Science ®Google Scholar
• He L, He T, Farrar S, Ji LB, Liu TY, Ma X. 2017. Antioxidants maintain cellular redox homeostasis by elimination of reactive oxygen species. Cell Physiol Biochem. 44(2):532–553. doi: 10.1159/000485089.
   PubMedGoogle Scholar
• Jakubczyk K, Dec K, Kaldunska J, Kawczuga D, Kochman J, Janda K. 2020 Apr 22. Reactive oxygen species - sources, functions, oxidative damage. Pol Merkur Lekarski. 48(284):124–127.
   PubMedGoogle Scholar
• Jaramillo MC, Zhang DD. 2013 Oct 15 . The emerging role of the Nrf2–Keap1 signaling pathway in cancer. Genes Dev. 27(20):2179–2191. doi: 10.1101/gad.225680.113.
   PubMed Web of Science ®Google Scholar
• Juarez-Tapia CR, Torres-Mendoza D, Duran P, Miranda-Anaya M. 2015 Nov. Short-day photoperiod disrupts daily activity and facilitates anxiety–depressive behaviours in gerbil Meriones unguiculatus. Biol Rhythm Res. 46(6):919–927. doi: 10.1080/09291016.2015.1066545
   Web of Science ®Google Scholar
• Kattoor AJ, Pothineni NVK, Palagiri D, Mehta JL. 2017 Nov 19. Oxidative stress in atherosclerosis. Curr Atheroscler Rep. 19(11). doi: 10.1007/s11883-017-0678-6.
   PubMed Web of Science ®Google Scholar
• Mas-Bargues C, Escriva C, Dromant M, Borras C, Vina J. 2021. Lipid peroxidation as measured by chromatographic determination of malondialdehyde. Human plasma reference values in health and disease. Arch Biochem Biophys. 709:108941. doi: 10.1016/j.abb.2021.108941.
   PubMed Web of Science ®Google Scholar
• Matzkin ME, Valchi P, Riviere E, Rossi SP, Tavalieri YE, de Toro MM M, Mayerhofer A, Bartke A, Calandra RS, Frungieri MB. 2019 Sep. Aging in the Syrian hamster testis: Inflammatory-oxidative status and the impact of photoperiod. Exp Gerontol. 124:110649. doi:10.1016/j.exger.2019.110649.
   PubMed Web of Science ®Google Scholar
• Moustafa A. 2021 Apr 15. Chronic exposure to continuous brightness or darkness modulates immune responses and ameliorates the antioxidant enzyme system in male rats. Front Vet Sci. 8. doi: 10.3389/fvets.2021.621188.
   Web of Science ®Google Scholar
• Nemmiche S. 2017. Oxidative signaling response to Cadmium exposure. Toxicol Sci Mar. 156:4–10. doi:10.1093/toxsci/kfw222.
   PubMed Web of Science ®Google Scholar
• Nguyen T, Nioi P, Pickett CB. 2009 May 15. The Nrf2-antioxidant response element signaling pathway and its activation by oxidative stress. J Biol Chem. 284(20):13291–13295. doi: 10.1074/jbc.R900010200.
   PubMed Web of Science ®Google Scholar
• Pal S, Haldar C, Verma R. 2022 Oct. Impact of photoperiod on uterine redox/inflammatory and metabolic status of golden hamster, Mesocricetus auratus. J Exp Zool Part A. 337(8):812–822. doi: 10.1002/jez.2638
   Google Scholar
• Panday A, Sahoo MK, Osorio D, Batra S. 2015 Jan. NADPH oxidases: an overview from structure to innate immunity-associated pathologies. Cell Mol Immunol. 12(1):5–23. doi: 10.1038/cmi.2014.89
   PubMed Web of Science ®Google Scholar
• Pizzino G, Irrera N, Cucinotta M, Pallio G, Mannino F, Arcoraci V, Squadrito F, Altavilla D, Bitto A. 2017. Oxidative stress: harms and benefits for human health. Oxid Med Cell Longev. 2017:1–13. doi:10.1155/2017/8416763.
   Web of Science ®Google Scholar
• Porcu A, Riddle M, Dulcis D, Welsh DK. 2018. Photoperiod-induced Neuroplasticity in the Circadian System. Neural Plast. 2018:1–13. doi:10.1155/2018/5147585.
   Web of Science ®Google Scholar
• Rada P, Rojo AI, Chowdhry S, McMahon M, Hayes JD, Cuadrado A. 2011 Mar. SCF/β-TrCP promotes glycogen synthase kinase 3-dependent degradation of the Nrf2 transcription factor in a Keap1-independent manner. Mol Cell Biol. 31(6):1121–1133. doi: 10.1128/MCB.01204-10.
   PubMed Web of Science ®Google Scholar
• Robinson MW, Harmon C, O’Farrelly C. 2016 May. Liver immunology and its role in inflammation and homeostasis. Cell Mol Immunol. 13(3):267–276. doi: 10.1038/cmi.2016.3.
   PubMed Web of Science ®Google Scholar
• Rojo AI, Medina-Campos ON, Rada P, Zúñiga-Toalá A, López-Gazcón A, Espada S, Pedraza-Chaverri J, Cuadrado A. 2012 Jan 15. Signaling pathways activated by the phytochemical nordihydroguaiaretic acid contribute to a Keap1-independent regulation of Nrf2 stability: role of glycogen synthase kinase-3. Free Radic Biol Med. 52(2):473–487. doi: 10.1016/j.freeradbiomed.2011.11.003.
   PubMed Web of Science ®Google Scholar
• Schieber M, Chandel NS. 2014 May 19. ROS function in redox signaling and oxidative stress. Curr Biol. 24(10):R453–462. doi: 10.1016/j.cub.2014.03.034.
   PubMed Web of Science ®Google Scholar
• Shin SK, Cho HW, Song SE, Song DK. 2018 Dec. Catalase and nonalcoholic fatty liver disease. Pflugers Arch -European J Physiol. 470(12):1721–1737. doi: 10.1007/s00424-018-2195-z
   PubMed Web of Science ®Google Scholar
• Singh SS, Deb A, Sutradhar S. 2020 Nov. Effect of melatonin on arsenic-induced oxidative stress and expression of MT1 and MT2 receptors in the kidney of laboratory mice. Biol Rhythm Res. 51(8):1216–1230. doi: 10.1080/09291016.2019.1566993
   Web of Science ®Google Scholar
• Sun HJ, Ding S, Guan DX, Ma LQ. 2022 Sep. Nrf2/Keap1 pathway in countering arsenic-induced oxidative stress in mice after chronic exposure at environmentally-relevant concentrations. Chemosphere. 303:303. doi:10.1016/j.chemosphere.2022.135256.
   Web of Science ®Google Scholar
• Suzuki T, Yamamoto M. 2015 Nov. Molecular basis of the Keap1-Nrf2 system. Free Radic Biol Med. 88:93–100. doi:10.1016/j.freeradbiomed.2015.06.006.
   PubMed Web of Science ®Google Scholar
• Wang CL, Wang Z, Mou JJ, Wang S, Zhao XY, Feng YZ, Xue HL, Wu M, Chen L, Xu JH, et al. 2022. Short photoperiod reduces oxidative stress by Up-Regulating the Nrf2–Keap1 signaling pathway in hamster Kidneys. J Evol Biochem Physiol. 58(2):418–429. doi: 10.1134/S0022093022020107.
   Web of Science ®Google Scholar
• Wang Z, Xu JH, Mou JJ, Kong XT, Wu M, Xue HL, Xu LX. 2020. Photoperiod affects Harderian gland morphology and secretion in female Cricetulus barabensis: Autophagy, Apoptosis, and Mitochondria. Front Physiol. 11(11):408. doi: 10.3389/fphys.2020.00408.
   PubMedGoogle Scholar
• Wang S, Xu JH, Zhao XY, Feng YZ, Xu WL, Xue HL, Wu M, Xu LX. 2023. Small RNA-seq and hormones in the testes of dwarf hamsters (Cricetulus barabensis) reveal the potential pathways in photoperiod regulated reproduction. Heliyon. 9(5):15687. doi: 10.1016/j.heliyon.2023.e15687.
   Web of Science ®Google Scholar
• Zhao ZJ, Chi QS, Cao J, Wang DH. 2014 Mar-Apr. Seasonal changes of body mass and energy budget in striped hamsters: the role of leptin. Physiol Biochem Zool. 87(2):245–256. doi: 10.1086/674974.
   PubMed Web of Science ®Google Scholar
• Zhao XY, Wang S, Xu JH, Wang CL, Feng YZ, Xue HL, Wu M, Chen L, Xu LX. 2022. Effects of short daylight and mild low temperature on mitochondrial degeneration in the testis of Cricetulus barabensis. Molecular Reproduction Devel. 89(9):413–422. doi: 10.1002/mrd.23632.
   PubMed Web of Science ®Google Scholar