Effect of Different Doses of Cerium Oxide Nanoparticles (CeO2 NPs) on In vitro Maturation, Cleavage and Embryo Development of Buffalo Oocytes
DOI:
https://doi.org/10.6000/1927-520X.2026.15.07Keywords:
CeO2 NPs, buffalo oocytes, IVM, IVFAbstract
The present study investigated the effects of different concentrations of cerium oxide nanoparticles (CeO2 NPs) on viability, in vitro maturation (IVM), fertilization (IVF), and subsequent embryo development of buffalo oocytes. Cumulus-oocyte complexes (COCs) were collected from slaughtered female buffalo and cultured in IVM medium. COCs were incubated in an in vitro maturation (IVM) medium supplemented with different concentrations of cerium oxide nanoparticles (CeO2 NPs) (10, 20, and 100µg/ml), alongside an untreated control group(0), for 22-24 hours under controlled conditions (39 °C, 5% CO2, and 95% relative humidity). At 0, 8, and 24 hours of incubation, oocytes from all experimental groups were collected, and their viability was determined using the trypan blue exclusion method. Following maturation, oocytes from both control and CeO2 NPs -treated groups were subsequently used for in vitro fertilization with frozen-thawed buffalo spermatozoa. The gametes were co-cultured for an additional 24 hours at 39°C in 5% CO2, following the protocol. Fertilization success was initially determined by the appearance of a second polar body and further verified by cleavage to the two-cell stage. The viability of developing embryos was assessed using the trypan blue exclusion method. The results demonstrated that supplementation of the IVM medium with 20 µg/ml CeO2 NPs significantly enhanced nuclear maturation of oocytes, yielding the highest value (95%) compared with the control and other treated groups. Moreover, the development of fertilized oocytes, as evidenced by the progression into the two-cell stage, was significantly higher at the 20 µg/ml concentration (85%) than in the other treatments. Additionally, the percentage of non-developed (degenerated) zygotes was significantly reduced at this concentration, with the lowest value recorded (15%). In conclusion, the addition of 20 µg/ml cerium oxide nanoparticles to the IVM medium appears to improve the in vitro developmental competence of buffalo oocytes.
References
FAOSTAT. Crop and livestock products [Internet]. Rome: Food and Agriculture Organization of the United Nations; 2024 [cited 2024 Apr 22]. Available from: https://www.fao.org/faostat/en/#data/QCL
FAOSTAT. Food and agriculture data: Crop statistics [Internet]. Rome: Food and Agriculture Organization of the United Nations; 2024. Available from: https://www.fao.org/faostat/en/#data/QCL
Presicce GA, Gasparrini B, Salzano A, Neglia G, Campanile G, Zicarelli L. Reproductive technologies in the buffalo (Bubalus bubalis). In: Reproductive Technologies in Animals 2020; pp. 81-98. DOI: https://doi.org/10.1016/B978-0-12-817107-3.00006-0
El-Wishy AB. The postpartum buffalo: II. Acyclicity and anestrus. Anim Reprod Sci 2007; 97: 216-36. DOI: https://doi.org/10.1016/j.anireprosci.2006.03.003
Kumar S, Chaves M, Ferreira-Silva JC, Melo LM, Freitas VJF. Factors affecting the in vitro embryo production in buffalo (Bubalus bubalis): A review. Vet Med (Praha) 2023; 68: 45-56. DOI: https://doi.org/10.17221/48/2022-VETMED
Arias-Álvarez M, García-García RM, López-Tello J, Rebollar P, Gutiérrez-Adán A, Lorenzo PL. In vitro and in vivo maturation of rabbit oocytes differently affect the gene expression profile, mitochondrial distribution, apoptosis, and early embryo development. Reprod Fertil Dev 2017; 29: 1667-79. DOI: https://doi.org/10.1071/RD15553
Kakkassery MP, Vijayakumaran V, Sreekumaran T. Effect of cumulus oocyte complex morphology on in vitro maturation of bovine oocytes. J Vet Anim Sci 2010; 41: 12-7.
Landim-Alvarenga F, Maziero R. Control of oocyte maturation. Anim Reprod 2014; 11: 150-8.
Ferreira EM, Vireque AA, Adona PR, Meirelles FV, Ferriani RA, Navarro PA. Cytoplasmic maturation of bovine oocytes: Structural and biochemical modifications and acquisition of developmental competence. Theriogenology 2009; 71: DOI: https://doi.org/10.1016/j.theriogenology.2008.10.023
-48.
Agarwal A, Gupta S, Sikka S. The role of free radicals and antioxidants in reproduction. Curr Opin Obstet Gynecol 2006; 18: 325-32. DOI: https://doi.org/10.1097/01.gco.0000193003.58158.4e
Khoudja RY, Xu Y, Li T, Zhou C. Better IVF outcomes following improvements in laboratory air quality. J Assist Reprod Genet 2013; 30: 69-76.
Brunet S, Maro B. Cytoskeleton and cell cycle control during meiotic maturation of the mouse oocyte: Integrating time and space. Reproduction 2005; 130: 801-11. DOI: https://doi.org/10.1530/rep.1.00364
Guisbiers G, Mejía-Rosales S, Deepak FL. Nanomaterial properties: Size and shape dependencies. J Nanomater 2012; 2012: 180976. DOI: https://doi.org/10.1155/2012/180976
Jeevanandam J, Barhoum A, Chan YS, Dufresne A, Danquah MK. Review on nanoparticles and nanostructured materials: History, sources, toxicity and regulations. Beilstein J Nanotechnol 2018; 9: 1050-74. DOI: https://doi.org/10.3762/bjnano.9.98
Tawfik HN, Kandil OM, Ahmad IM, Mansour M, El-Debaky HA, Ali KA, et al. Effect of melatonin-loaded chitosan nanoparticles on gene expression of in-vitro matured buffalo oocyte. J Adv Vet Res 2023; 13: 656-63.
Remião MH, Lucas CG, Domingues WB, Silveira T, Barther NN, Komninou ER, et al. Melatonin delivery by nanocapsules during in vitro bovine oocyte maturation decreased the reactive oxygen species of oocytes and embryos. Reprod Toxicol 2016; 63: 70-81. DOI: https://doi.org/10.1016/j.reprotox.2016.05.016
Roy PK, Qamar AY, Tanga BM, Bang S, Seong G, Fang X, et al. Modified Spirulina maxima nanoparticles improve the developmental competence of in vitro-matured porcine oocytes. Animals (Basel) 2021; 11: 2483. DOI: https://doi.org/10.3390/ani11092483
Ahmed HA, Aboul-Enein AM, Abou-Elella F, Salem S, Aly HF, Nassrallah A, et al. Nano-formulations of hesperidin and essential oils extracted from sweet orange peel: Chemical properties and biological activities. Egypt J Chem 2021; 64: 5373-85. DOI: https://doi.org/10.21608/ejchem.2021.84783.4139
Taylor U, Barchanski A, Kues W, Barcikowski S, Rath D. Impact of metal nanoparticles on germ cell viability and functionality. Reprod Domest Anim 2012; 47: 359-68. DOI: https://doi.org/10.1111/j.1439-0531.2012.02099.x
Pirmohamed T, Dowding JM, Singh S, Wasserman B, Heckert E, Karakoti AS, et al. Nanoceria exhibit redox state-dependent catalase mimetic activity. Chem Commun (Camb) 2010; 46: 2736-8. DOI: https://doi.org/10.1039/b922024k
Parimi D, Sundararajan V, Sadak O, Gunasekaran S, Mohideen SS, Sundaramurthy A. Synthesis of positively and negatively charged CeO2 nanoparticles: Investigation of the role of surface charge on growth and development of Drosophila melanogaster. ACS Omega 2019; 4(1): 104-13. DOI: https://doi.org/10.1021/acsomega.8b02747
Abd-Allah S. Laboratory production of buffalo embryos. 1st ed. Germany: LAP Publishing House 2015; p. 217.
Abd-Allah SM. In vitro fertilization in buffaloes: A review. J Buffalo Sci 2015; 4: 11-4. DOI: https://doi.org/10.6000/1927-520X.2015.04.01.2
Ariu F, Bogliolo L, Pinna A, Malfatti L, Innocenzi P, Falchi L, et al. Cerium oxide nanoparticles (CeO2 NPs) improve the developmental competence of in vitro-matured prepubertal ovine oocytes. Reprod Fertil Dev 2017; 29(5): 1046-56. DOI: https://doi.org/10.1071/RD15521
Ciofani G, Genchi GG, Mazzolai B, Mattoli V. Transcriptional profile of genes involved in oxidative stress and antioxidant defense in PC12 cells following treatment with cerium oxide nanoparticles. Biochim Biophys Acta 2014; 1840: 495-506. DOI: https://doi.org/10.1016/j.bbagen.2013.10.009
Celardo I, Traversa E, Ghibelli L. Cerium oxide nanoparticles: A promise for applications in therapy. J Exp Ther Oncol 2011; 9: 47-51.
Nakayama T, Noda Y, Goto Y, Mori T. Effects of visible light and other environmental factors on the production of oxygen radicals by hamster embryos. Theriogenology. 1994; 41: 499-510. DOI: https://doi.org/10.1016/0093-691X(94)90086-X
Liebel F, Kaur S, Ruvolo E, Kollias N, Southall MD. Irradiation of skin with visible light induces reactive oxygen species and matrix-degrading enzymes. J Invest Dermatol 2012; 132: 1901-7. DOI: https://doi.org/10.1038/jid.2011.476
Khoudja RY, Xu Y, Li T, Zhou C. Better IVF outcomes following improvements in laboratory air quality. J Assist Reprod Genet 2013; 30: 69-76. DOI: https://doi.org/10.1007/s10815-012-9900-1
Agarwal A, Said TM, Bedaiwy MA, Banerjee J, Alvarez JG. Oxidative stress in an assisted reproductive techniques setting. Fertil Steril 2006; 86: 503-12. DOI: https://doi.org/10.1016/j.fertnstert.2006.02.088
Downloads
Published
How to Cite
Issue
Section
License
Policy for Journals/Articles with Open Access
Authors who publish with this journal agree to the following terms:
- Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution License that allows others to share the work with an acknowledgment of the work's authorship and initial publication in this journal.
- Authors are permitted and encouraged to post links to their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work