The effect of antioxidants on the morphology and function of ovaries in rats inflammatory process (pregnancy) within the framework of the analysis of the assessment of their action and effectiveness on nuclear and cytoplasmic maturation of oocytes

Authors

DOI:

https://doi.org/10.63341/bmbr/4.2024.45

Keywords:

post-ovulatory ageing, egg, antioxidant, oxidative imbalance, citrus coumarin

Abstract

The study aimed to investigate the effect of various antioxidants on the morphological and functional characteristics of ovaries in pregnant Wistar rats under conditions of systemic inflammation. The experimental research was conducted on a total of 20 sexually mature female rats of the Wistar strain, which were divided into five subgroups with four animals in each. The rats were categorised into the following groups: a control group (no treatment), an inflammation-induced group (lipopolysaccharide treatment), and three antioxidant-treated groups, where systemic inflammation was induced and the females were treated with resveratrol, quercetin, or lycopene. Systemic inflammation was induced using lipopolysaccharide, and different antioxidants were administered to the treated subgroups over a specified period from May to June 2023. The research focused on examining the impact of these antioxidants on oocyte morphology, mitochondrial function, and the levels of reactive oxygen species and glutathione. Results indicated that antioxidant treatment significantly improved oocyte morphology by reducing abnormalities and restoring normal mitochondrial distribution. Rats in the antioxidant-treated group exhibited reduced levels of reactive oxygen species
and elevated concentrations of glutathione, signalling a reduction in oxidative stress. Additionally, an increase in the expression of genes associated with antioxidant defence was observed, suggesting an enhanced antioxidant response. These findings imply that antioxidants can improve oocyte quality in cases of inflammation-induced oxidative stress, offering new insights for reproductive biology. The practical relevance of this work lies in its potential application in reproductive medicine, particularly for patients with inflammation-related infertility, where antioxidant therapies could contribute to improving oocyte quality and reproductive outcomes

Received: 13.07.2024 | Revised: 18.10.2024 | Accepted: 26.11.2024

Author Biography

Angelina Stewart, Bogomoletz Institute of Physiology of the National Academy of Sciences of Ukraine

Postgraduate Student, Researcher 01024, 4 Bogomoletz Str., Kyiv, Ukraine

References

Bibak B, Shakeri F, Barreto GE, Keshavarzi Z, Sathyapalan T, Sahebkar A. A review of the pharmacological and therapeutic effects of auraptene. Biofactors. 2019;45(6):867–79. DOI: 10.1002/biof.1550

Askari VR, Rahimi VB, Rezaee SA, Boskabady MH. Auraptene regulates Th1/Th2/TReg balances, NF-kB nuclear localization and nitric oxide production in normal and Th2 provoked situations in human isolated lymphocytes. Phytomedicine. 2018;43:1–10. DOI: 10.1016/j.phymed.2018.03.049

Askari VR, Rahimi VB, Zargarani R, Ghodsi R, Boskabady M, Boskabady MH. Anti-oxidant and anti-inflammatory effects of auraptene on phytohemagglutinin (PHA)-induced inflammation in human lymphocytes. Pharmacol Rep. 2021;73(1):154–62. DOI: 10.1007/s43440-020-00083-5

Fiorito S, Epifano F, Palumbo L, Genovese S. A novel auraptene-enriched citrus peels-based blend with enhanced antioxidant activity. Plant Foods Hum Nutr. 2021;76:397–8. DOI: 10.1007/s11130-021-00911-w

Keshavarzi Z, Amiresmaili S, Shahrokhi N, Bibak B, Shakeri F. Neuroprotective effects of auraptene following traumatic brain injury in male rats: The role of oxidative stress. Brain Res Bull. 2021;177:203–9. DOI: 10.1016/j.brainresbull.2021.09.021

Tayarani-Najaran Z, Tayarani-Najaran N, Eghbali S. A review of auraptene as an anticancer agent. Front Pharmacol. 2021;12:698352. DOI: 10.3389/fphar.2021.698352

Vakili T, Iranshahi M, Arab H, Riahi B, Roshan NM, Karimi G. Safety evaluation of auraptene in rats in acute and subacute toxicity studies. Regul Toxicol Pharmacol. 2017;91:159–64. DOI: 10.1016/j.yrtph.2017.10.025

Igase M, Okada Y, Ochi M, Igase K, Ochi H, Okuyama S, et al. Auraptene in the peels of citrus Kawachiensis (Kawachibankan) contributes to the preservation of cognitive function: A randomized, placebo-controlled, double-blind study in healthy volunteers. J Prev Alzheimers Dis. 2018;5:197–201. DOI: 10.14283/jpad.2017.47

Galluzzi S, Zanardini R, Ferrari C, Gipponi S, Passeggia I, Rampini M, et al. Cognitive and biological effects of citrus phytochemicals in subjective cognitive decline: A 36-week, randomized, placebo-controlled trial. Nutr. J. 2022;21:64. DOI: 10.1186/s12937-022-00817-6

Abizadeh M, Novin MG, Amidi F, Ziaei SA, Abdollahifar MA, Nazarian H. Potential of auraptene in improvement of oocyte maturation, fertilization rate, and inflammation in polycystic ovary syndrome mouse model. Reprod Sci. 2020;27(9):1742–51. DOI: 10.1007/s43032-020-00168-9

Jang Y, Choo H, Lee MJ, Han J, Kim SJ, Ju X, et al. Auraptene mitigates Parkinson’s disease-like behavior by protecting inhibition of mitochondrial respiration and scavenging reactive oxygen species. Int J Mol Sci. 2019;20(14):3409. DOI: 10.3390/ijms20143409

Lee MJ, Jang Y, Zhu J, Namgung E, Go D, Seo C, et al. Auraptene enhances junction assembly in cerebrovascular endothelial cells by promoting resilience to mitochondrial stress through activation of antioxidant enzymes and mtUPR. Antioxidants. 2021;10(3):475. DOI: 10.3390/antiox10030475

Hassanein EH, Sayed AM, Hussein OE, Mahmoud AM. Coumarins as modulators of the Keap1/Nrf2/ARE signaling pathway. Oxidative Med Cell Longev. 2020;2020:1675957. DOI: 10.1155/2020/1675957

Akino N, Wada-Hiraike O, Isono W, Terao H, Honjo H, Miyamoto Y, et al. Activation of Nrf2/Keap1 pathway by oral Dimethylfumarate administration alleviates oxidative stress and age-associated infertility might be delayed in the mouse ovary. Reprod Biol Endocrinol. 2019;17:23. DOI: 10.1186/s12958-019-0466-y

Di Nisio V, Antonouli S, Damdimopoulou P, Salumets A, Cecconi S. In vivo and in vitro postovulatory aging: When time works against oocyte quality? J Assist Reprod Genet. 2022;39(4):905–18. DOI: 10.1007/s10815-022-02418-y

Yu C, Xiao JH. The Keap1-Nrf2 system: A mediator between oxidative stress and aging. Oxid Med Cell Longev. 2021;2021:6635460. DOI: 10.1155/2021/6635460

Kim KH, Kim EY, Lee KA. GAS6 ameliorates advanced age-associated meiotic defects in mouse oocytes by modulating mitochondrial function. Aging. 2021;13(14):18018–32. DOI: 10.18632/aging.203328

Almansa-Ordonez A, Bellido R, Vassena R, Barragan M, Zambelli F. Oxidative stress in reproduction: A mitochondrial perspective. Biol. 2020;9(9):269. DOI: 10.3390/biology9090269

Khazaei M, Aghaz F. Reactive oxygen species generation and use of antioxidants during in vitro maturation of oocytes. Int J Fertil Steril. 2017;11(2):63–70. doi: DOI: 10.22074/ijfs.2017.4995

Cecchele A, Cermisoni GC, Giacomini E, Pinna M, Vigano P. Cellular and molecular nature of fragmentation of human embryos. Int J Mol Sci. 2022;23(3):1349. DOI: 10.3390/ijms23031349

van der Reest J, Cecchino GN, Haigis MC, Kordowitzki P. Mitochondria: Their relevance during oocyte ageing. Ageing Res Rev. 2021;70:101378. DOI: 10.1016/j.arr.2021.101378

Lu J, Wang Z, Cao J, Chen Y, Dong Y. A novel and compact review on the role of oxidative stress in female reproduction. Reprod Biol Endocrinol. 2018;16:80. DOI: 10.1186/s12958-018-0391-5

Perkins AT, Greig MM, Sontakke AA, Peloquin AS, McPeek MA, Bickel SE. Increased levels of superoxide dismutase suppress meiotic segregation errors in aging oocytes. Chromosoma. 2019;128(3):215–22. DOI: 10.1007/s00412-019-00702-y

Armstrong S, Bhide P, Jordan V, Pacey A, Marjoribanks J, Farquhar C. Time-lapse systems for embryo incubation and assessment in assisted reproduction. Cochrane Database Syst Rev. 2019;5:CD011320. DOI: 10.1002/14651858.CD011320.pub4

Bellusci G, Mattiello L, Iannizzotto V, Ciccone S, Maiani E, Villani V, et al. Kinase-independent inhibition of cyclophosphamide-induced pathways protects the ovarian reserve and prolongs fertility. Cell Death Dis. 2019;10(10):726. DOI: 10.1038/s41419-019-1961-y

Fonseca É, Marques CC, Pimenta J, Jorge J, Baptista MC, Gonçalves AC, et al. Anti-aging effect of urolithin a on bovine oocytes in vitro. Animals. 2021;11(7):2048. DOI: 10.3390/ani11072048

Furukawa Y, Washimi YS, Hara RI, Yamaoka M, Okuyama S, Sawamoto A, et al. Citrus auraptene induces expression of brain-derived neurotrophic factor in Neuro2a cells. Molecules. 2020;25(5):1117. DOI: 10.3390/molecules25051117

Shimoi G, Tomita M, Kataoka M, Kameyama Y. Destabilization of spindle assembly checkpoint causes aneuploidy during meiosis II in murine post-ovulatory aged oocytes. J Reprod Dev. 2019;65(1):57–66. DOI: 10.1262/jrd.2018-056

Zhang D, Keilty D, Zhang ZF, Chian RC. Mitochondria in oocyte aging: Current understanding. Facts Views Vis Obgyn. 2017;9(1):29–38.

Lagalla C, Coticchio G, Sciajno R, Tarozzi N, Zaca C, Borini A. Alternative patterns of partial embryo compaction: Prevalence, morphokinetic history and possible implications. Reprod Biomed Online. 2020;40(3):347–54. DOI: 10.1016/j.rbmo.2019.11.011

Tamura H, Jozaki M, Tanabe M, Shirafuta Y, Mihara Y, Shinagawa M, et al. Importance of melatonin in assisted reproductive technology and ovarian aging. Int J Mol Sci. 2020;21(3):1135. DOI: 10.3390/ijms21031135

Council of Europe. European Convention for the Protection of Vertebrate Animals Used for Experimental and Other Scientific Purposes [Internet]. 1986 [cited 2024 Nov 28]. ETS No. 123. 1986 Mar 18. Available from: https://rm.coe.int/168007a67b

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Published

2025-01-14

How to Cite

Stewart, A. (2025). The effect of antioxidants on the morphology and function of ovaries in rats inflammatory process (pregnancy) within the framework of the analysis of the assessment of their action and effectiveness on nuclear and cytoplasmic maturation of oocytes. Bulletin of Medical and Biological Research, (4), 45–54. https://doi.org/10.63341/bmbr/4.2024.45