The effects of fenugreek seeds on the albino rat male reproductive system, MDA and SOD levels, and CD16 responses to Al2O3 NPs administration

Palavras-chave: aluminum oxide; MDA; SOD; CD16; Fenugreek.

Resumo

Aluminum is widely distributed in the environment and enters the body via air, water, food, medications, and manmade objects. Some studies suggest that aluminum toxicity increases the rate of lipid peroxidation and consequently the generation of free radicals. However, the impact of nanoparticles on human health is still not fully understood. An indicator of lipid peroxidation in serum and tissues is an increased MDA. At the same time, there was a decrease in the level SOD and detection CD16 using the immunohistochemistry technique, objectives evaluating the impact of Al₂O₃ NPs on oxidative stress markers (MDA and SOD) and immune responses (CD16) in the testes, as well as the protective effects of fenugreek seed extract it was observed that these changes in levels recovered when given the plant extract of fenugreek seeds,65 albino rats were divided into 13 groups, including the control group Two concentrations of fenugreek extract (2 and 4 gm kg-1) and two concentrations of Al₂O₃ NPs solution (70 and 140 mg kg-1) were given orally to the rats for 21 and 35 days, respectively. The amino-histochemistry method was used to detect CD16, and its presence was checked along with the concentrations of oxidative stress markers like SOD and MDA. Immunohistochemical findings revealed a significant increase in CD16 in testicular cells; fenugreek extract doses significantly decreased MDA and slightly raised SOD. Al₂O₃ NPs. were shown to significantly raise MDA and decrease SOD at (p ≤ 0.05), according to the study's findings. and Immunohistochemical results detected a significant increase in CD16 in testicular cells, and doses of fenugreek extract reduced the MDA was significant, and a slightly significant increase in SOD. The study concluded Al₂O₃ NPs led to an imbalance in the testicle by generating oxidative stress and the fenugreek extract succeeded in alleviating the harmful effects of Al₂O₃ and by curbing MOD and strengthening the antioxidant defense system SOD, at the same time significantly influenced the histopathological and toxicological change responses through expression CD16.

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Referências

Abduljabbar, A. A., & Ismail, P. A. (2019). Investigation of Malondialdehyde (MDA), Homocysteine (Hcy) and C- reactive protein (CRP) in sera of patients with Angina Pectoris. Al-Mustansiriyah Journal of Science, 30(1), 68-74. DOI: https://doi.org/10.23851/mjs.v30i1.463

Aguilar, O. A., Gonzalez-Hinojosa, M. D. R., Arakawa-Hoyt, J. S., Millan, A. J., Gotthardt, D., Nabekura, T., & Lanier, L. L. (2023). The CD16 and CD32b Fc-gamma receptors regulate antibody-mediated responses in mouse natural killer cells. Journal of Leukocyte Biology, 113(1), 27-40. DOI: https://doi.org/10.1093/jleuko/qiac003

Al Mashkor, I. M. A. (2014). Phenolic content and antioxidant activity of fenugreek seeds extract. International Journal of Pharmacognosy and Phytochemical Research, 6(4), 841-844.

Al-Musawi, M. M. S., Al-Shmgani, H., & Al-Bairuty, G. A. (2022). Histopathological and biochemical comparative study of copper oxide nanoparticles and copper sulphate toxicity in male albino mice reproductive system. International Journal Biomaterials, 2022, 4877637. DOI: https://doi.org/10.1155/2022/4877637

Attarilar, S., Yang, J., Ebrahimi, M., Wang, Q., Liu, J., Tang, Y., & Yang, J. (2020). The toxicity phenomenon and the related occurrence in metal and metal oxide nanoparticles: a brief review from the biomedical perspective. Frontiers in Bioengineering and Biotechnology, 8, 822. DOI: https://doi.org/10.3389/fbioe.2020.00822

Banerjee, M. S., & Saxena, M. (2014). Genetic polymorphisms of cytokine genes in type 2 diabetes mellitus. World Journal of Diabetes, 5(4), 493-504. DOI: https://doi.org/10.4239/wjd.v5.i4.493

Benson, A. K., Kelly, S. A., Legge, R., Ma, F., Low, S. J., Kim, J., ... Pomp, D. (2010). Individuality in gut microbiota composition is a complex polygenic trait shaped by multiple environmental and host genetic factors. Proceedings of the National Academy of Sciences, 107(44), 18933-18938. DOI: https://doi.org/10.1073/pnas.1007028107

Bisht, S., Faiq, M., Tolahunase, M., & Dada, R. (2017). Oxidative stress and male infertility. Nature Reviews Urology, 14(8), 470-485. DOI: https://doi.org/10.1038/nrurol.2017.69

Bolourian, A., & Mojtahedi, Z. (2017). Possible damage to immune-privileged sites in natural killer cell therapy in cancer patients: side effects of natural killer cell therapy. Immunotherapy, 9(3), 281-288. DOI: https://doi.org/10.2217/imt-2016-0137

Boots, M., Donnelly, R., & White, A. (2013). Optimal immune defence in the light of variation in lifespan. Parasite Immunology, 35(11), 331-338. DOI: https://doi.org/10.1111/pim.12055

Chatterjee, S., Goswami, N., Bhatnagar, P., Kumar, M., & Kumar, A. (2013). Antimutagenic and chemopreventive potentialities of fenugreek Trigonella foenum graecum seed extract. Oxidants and Antioxidants in Medical Science, 2(1), 1. DOI: https://doi.org/10.5455/oams.020313.or.028

Cocchia, N., Pasolini, M. P., Mancini, R., Petrazzuolo, O., Cristofaro, I., Rosapane, I., ... Mancini, A. (2011). Effect of sod (superoxide dismutase) protein supplementation in semen extenders on motility, viability, acrosome status and ERK (extracellular signal-regulated kinase) protein phosphorylation of chilled stallion spermatozoa. Theriogenology, 75(7), 1201-1210.

De, A., Ghosh, S., Chakrabarti, M., Ghosh, I., Banerjee, R., & Mukherjee, A. (2020). Effect of low-dose exposure of aluminium oxide nanoparticles in Swiss albino mice: histopathological changes and oxidative damage. Toxicology and Industrial Health, 36(8), 567-579. DOI: https://doi.org/10.1177/0748233720936828

Devasena, T., & Menon, P. V. (2007). Fenugreek seeds modulate 1,2-dimethylhydrazine-induced hepatic oxidative stress during colon carcinogenesis. Italian Journal of Biochemistry, 56(1), 28-34.

Eggert-Kruse, W., Zwick, E.-M., Batschulat, K., Rohr, G., Armbruster, F. P., Petzoldt, D., & Strowitzki, T. (2002). Are zinc levels in seminal plasma associated with seminal leukocytes and other determinants of semen quality? Fertility and Sterility, 77(2), 260-269.

El-Gendy, A. M. (2011). Amelioration of aluminium-intake oxidative stress by some antioxidants in male albino rats. The Egyptian Journal of Hospital Medicine, 45(1), 536-546. DOI: https://doi.org/10.21608/ejhm.2011.16384

El-Sisy, G. A., El-Nattat, W. S., & El-Sheshtawy, R. I. (2008). Effect of superoxide dismutase and catalase on viability of cryopreserved buffalo spermatozoa. Global Veterinaria, 2(2), 56-61.

Exley, C. (2013). Human exposure to aluminium. Environmental Science: Processes & Impacts, 15(10), 1807-1816. DOI: https://doi.org/10.1039/C3EM00374D

Fu, B., Zhou, Y., Ni, X., Tong, X., Xu, X., Dong, Z., ... Wei, H. (2017). Natural killer cells promote fetal development through the secretion of growth-promoting factors. Immunity, 47(6), 1100-1113. DOI: https://doi.org/10.1016/j.immuni.2017.11.018

Gamal, A., Kortam, L. E., El Ghareeb, A. E. W., & El Rahman, H. A. A. (2022). Assessment of the potential toxic effect of magnetite nanoparticles on the male reproductive system based on immunological and molecular studies. Andrologia, 54(11), e14613. DOI: https://doi.org/10.1111/and.14613

Godfrey, D. I., Pellicci, D. G., Patel, O., Kjer-Nielsen, L., McCluskey, J., & Rossjohn, J. (2010). Antigen recognition by CD1d-restricted NKT T cell receptors. Seminars in Immunology, 22(2), 61-67. DOI: https://doi.org/10.1016/j.smim.2009.10.004

Griffith, A. (2007). SPSS FOR Dummies. Indianapolis, IN: Wiley publishing-Inc.

Habas, K., Demir, E., Guo, C., Brinkworth, M. H., & Anderson, D. (2021). Toxicity mechanisms of nanoparticles in the male reproductive system. Drug Metabolism Reviews, 53(4), 604-617. DOI: https://doi.org/10.1080/03602532.2021.1917597

Hamdi, H. (2020). Testicular dysfunction induced by aluminum oxide nanoparticle administration in albino rats and the possible protective role of the pumpkin seed oil. The Journal of Basic and Applied Zoology, 81(1), 42. DOI: https://doi.org/10.1186/s41936-020-00178-8

Herman, S., Lipiński, P., Ogórek, M., Starzyński, R., Grzmil, P., Bednarz, A., & Lenartowicz, M. (2020). Molecular regulation of copper homeostasis in the male gonad during the process of spermatogenesis. International Journal of Molecular Sciences, 21(23), 9053. DOI: https://doi.org/10.3390/ijms21239053

Hossain, M. M., Begum, M., & Kim, I. H. (2018). Effects of fenugreek (Trigonella foenum-graecum L.) seed extract supplementation in different energy density diets on growth performance, nutrient digestibility, blood characteristics, fecal microbiota, and fecal gas emission in growing pigs. Canadian Journal of Animal Science, 98(2), 289-298. DOI: https://doi.org/10.1139/cjas-2016-0076

Huang, H., Wang, X., Yang, L., He, W., Meng, T., Zheng, K., … Xiao, D. (2022). The effects of fenugreek extract on growth performance, serum biochemical indexes, immunity and NF-κB signaling pathway in broiler. Frontiers in Veterinary Science, 9, 882754. DOI: https://doi.org/10.3389/fvets.2022.882754

Ibraheem, S. R., & Ibrahim, M. R. (2016). Physiological and histological effects of (zinc and iron) oxide nanoparticles on some fertility parameters in female mice. Al-Mustansiriyah Journal of Science, 27(5), 1-10.

Jagadeesan, J., Nandakumar, N., Rengarajan, T., & Balasubramanian, M. P. (2012). Diosgenin, a steroidal saponin, exhibits anticancer activity by attenuating lipid peroxidation via enhancing antioxidant defense system during NMU-induced breast carcinoma. Journal of Environmental Pathology, Toxicology and Oncology, 31(2), 121-129. DOI: https://doi.org/10.1615/jenvironpatholtoxicoloncol.v31.i2.40

Ktari, N., Trabelsi, I., Bardaa, S., Triki, M., Bkhairia, I., Salem, R. B. S. B., ... Salah, R. B. (2017). Antioxidant and hemolytic activities, and effects in rat cutaneous wound healing of a novel polysaccharide from fenugreek (Trigonella foenum-graecum) seeds. International Journal of Biological Macromolecules, 95, 625-634. DOI: https://doi.org/10.1016/j.ijbiomac.2016.11.091

Lawniczak, M. K. N., Barnes, A. I., Linklater, J. R., Boone, J. M., Wigby, S., & Chapman, T. (2007). Mating and immunity in invertebrates. Trends in Ecology & Evolution, 22(1), 48-55. DOI: https://doi.org/10.1016/j.tree.2006.09.012

Laurent, S., Forge, D., Port, M., Roch, A., Robic, C., Vander Elst, L., & Muller, R. N. (2008). Magnetic iron oxide nanoparticles: synthesis, stabilization, vectorization, physicochemical characterizations, and biological applications. Chemical Reviews, 108(6), 2064-2110. DOI: https://doi.org/10.1021/cr068445e

Lawniczak, M. K., Barnes, A. I., Linklater, J. R., Boone, J. M., Wigby, S., & Chapman, T. (2007). Mating and immunity in invertebrates. Trends in Ecology & Evolution, 22(1), 48-55. DOI: https://doi.org/10.1016/j.tree.2006.09.012

Li, J. J., Hartono, D., Ong, C.-N., Bay, B.-H., & Yung, L.-Y. L. (2010). Autophagy and oxidative stress associated with gold nanoparticles. Biomaterials, 31(23), 5996-6003. DOI: https://doi.org/10.1016/j.biomaterials.2010.04.014

McGarry, T., Biniecka, M., Veale, D. J., & Fearon, U. (2018). Hypoxia, oxidative stress and inflammation. Free Radical Biology and Medicine, 125, 15-24. DOI: https://doi.org/10.1016/10.1016/j.freeradbiomed.2018.03.042

McCrank, J. (2009). Nanotechnology applications in the forest sector. Ottawa, CA: Natural Resources Canada.

Michael, A. J., Alexopoulos, C., Pontiki, E. A., Hadjipavlou-Litina, D. J., Saratsis, P., Ververidis, H. N., & Boscos, C. M. (2009). Effect of antioxidant supplementation in semen extenders on semen quality and reactive oxygen species of chilled canine spermatozoa. Animal Reproduction Science, 112(1-2), 119-135. DOI: https://doi.org/10.1016/j.anireprosci.2008.04.007

Mohsen, G. L., Abdula, A. M., Jassim, A. M., Rodhan, W. F., & Ayrim, N. B. (2021). New 3,5-disubstituted-4,5-dihydroisoxazole derivatives: Synthesis, antimicrobial, antioxidant and docking study against glucosamine-6-phosphate synthase. The International Conference of Chemistry, 1853, 012042. DOI: https://doi.org/10.1088/1742-6596/1853/1/012042

O’Brien, K. L., & Finlay, D. K. (2019). Immunometabolism and Natural Killer cell responses. Nature Reviews Immunology, 19(5), 282-290. DOI: https://doi.org/10.1038/s41577-019-0139-2

Oku, K., Price, T. A. R., & Wedell, N. (2019). Does mating negatively affect female immune defences in insects? Animal Biology, 69(1), 117-136. DOI: https://doi.org/10.1163/15707563-20191082

Park, E.-J., Bae, E., Yi, J., Kim, Y., Choi, K., Lee, S. H., ... Park, K. (2010). Repeated-dose toxicity and inflammatory responses in mice by oral administration of silver nanoparticles. Environmental Toxicology and Pharmacology, 30(2), 162-168. DOI: https://doi.org/10.1016/j.etap.2010.05.004

Perez-Sepulveda, A., Torres, M. J., Khoury, M., & Illanes, S. E. (2014). Innate immune system and preeclampsia. Frontiers in Immunology, 5, 244. DOI: https://doi.org/10.3389/fimmu.2014.00244

Poli, A., Michel, T., Thérésine, M., Andrès, E., Hentges, F., & Zimmer, J. (2009). CD56bright natural killer (NK) cells: an important NK cell subset. Immunology, 126(4), 458-465. DOI: https://doi.org/10.1111/j.1365-2567.2008.03027.x

Pournamdari, M., Mandegary, A., Sharififar, F., Zarei, G., Zareshahi, R., Asadi, A., & Mehdipour, M. (2018). Anti-inflammatory subfractions separated from acidified chloroform fraction of fenugreek seeds (Trigonella foenum-graecum L.). Journal of Dietary Supplements, 15(1), 98-107. DOI: https://doi.org/10.1080/19390211.2017.1326431

Prabhakar, P. V., Reddy, U. A., Singh, S. P., Balasubramanyam, A., Rahman, M. F., Kumari, S. I., … Mahboob, M. (2012). Retracted: oxidative stress induced by aluminum oxide nanomaterials after acute oral treatment in Wistar rats. Journal of Applied Toxicology, 32(6), 436-445. DOI: https://doi.org/10.1002/jat.1775

Ramesh, G., & Reeves, W. B. (2002). TNF-α mediates chemokine and cytokine expression and renal injury in cisplatin nephrotoxicity. The Journal of Clinical Investigation, 110(6), 835-842. DOI: https://doi.org/10.1172/JCI15606

Rolff, J., & Reynolds, S. (2009). Insect infection and immunity: evolution, ecology, and mechanisms (No. 25). Oxford, UK: Oxford University Press. (NÃO CITADO – RETIRAR)

Schuppe, H. C., Meinhardt, A., Allam, J.P., Bergmann, M., Weidner, W., & Haidl, G. (2008). Chronic orchitis: a neglected cause of male infertility? Andrologia, 40, 84-91. DOI: https://doi.org/10.1111/j.1439-0272.2008.00837.x

Schwenke, R. A., Lazzaro, B. P., & Wolfner, M. F. (2016). Reproduction-immunity trade-offs in insects. Annual Review of Entomology, 61, 239-256. DOI: https://doi.org/10.1146/annurev-ento-010715-023924

Sharma, N., Suresh, S., Debnath, A., & Jha, S. (2017). Trigonella seed extract ameliorates inflammation via regulation of the inflammasome adaptor protein, ASC. Frontiers In Bioscience, 9(2), 246-257. DOI: https://doi.org/10.2741/E799

Shrestha, B., Schaefer, A., Zhu, Y., Saada, J., Jacobs, T. M., Chavez, E. C., ... Lai, S. K. (2021). Engineering sperm-binding IgG antibodies for the development of an effective nonhormonal female contraception. Science Translational Medicine, 13(606), eabd5219. DOI: https://doi.org/10.1126/scitranslmed.abd5219

Silva-Holguín, P. N., Ruíz-Baltazar, Á. J., Medellín-Castillo, N. A., Labrada-Delgado, G. J., & Reyes-López, S. Y. (2022). Synthesis and characterization of α-Al2O3/Ba-β-Al2O3 spheres for cadmium ions removal from aqueous solutions. Materials, 15(19), 6809. DOI: https://doi.org/10.3390/ma15196809

Sindhu, G., Ratheesh, M., Shyni, G. L., Nambisan, B., Helen, A. (2012). Anti-in flammatory and antioxidative effects of mucilage of Trigonella foenum graecum (Fenugreek) on adjuvant induced arthritic rats. International Immunopharmacology, 12(1), 205-211. DOI: https://doi.org/10.1016/j.intimp.2011.11.012

Sioutas, C., Delfino, R. J., & Singh, M. (2005). Exposure assessment for atmospheric ultrafine particles (UFPs) and implications in epidemiologic research. Environmental Health Perspectives, 113(8), 947-955. DOI: https://doi.org/10.1289/ehp.7939

Siva-Jothy, M. T. (2009). Reproductive immunity. Oxford, UK: Oxford University Press,

Taylor, A. A., Tsuji, J. S., Garry, M. R., McArdle, M. E., Goodfellow Jr., W. L., Adams, W. J., & Menzie, C. A. (2020). Critical review of exposure and effects: implications for setting regulatory health criteria for ingested copper. Environmental Management, 65(1), 131-159. DOI: https://doi.org/10.1007/s00267-019-01234-y

Terayama, H., Yoshimoto, T., Hirai, S., Naito, M., Qu, N., Hatayama, N., ... Itoh, M. (2014). Contribution of IL-12/IL-35 common subunit p35 to maintaining the testicular immune privilege. PLoS One, 9(4), e96120. DOI: https://doi.org/10.1371/journal.pone.0096120

Trinchieri, G., & Valiante, N. (1993). Receptors for the Fc fragment of IgG on natural killer cells. Natural Immunity, 12(4-5), 218-234.

Vivier, E. (2006). What is natural in natural killer cells? Immunology Letters, 107(1), 1-7. DOI: https://doi.org/10.1016/j.imlet.2006.07.004

Wigby, S., Suarez, S. S., Lazzaro, B. P., Pizzari, T., & Wolfner, M. F. (2019). Chapter eight - sperm success and immunity. Current Topics in Developmental Biology, 135, 287-313. DOI: https://doi.org/10.1016/bs.ctdb.2019.04.002

Zhao, X., Wang, S., Wu, Y., You, H., & Lv, L. (2013). Acute ZnO nanoparticles exposure induces developmental toxicity, oxidative stress and DNA damage in embryo-larval zebrafish. Aquatic Toxicology, 136-137, 49-59. DOI: https://doi.org/10.1016/j.aquatox.2013.03.019

Publicado
2024-11-13
Como Citar
Hameed, Z. R., Zabbon, A., & Al-Bairuty, G. (2024). The effects of fenugreek seeds on the albino rat male reproductive system, MDA and SOD levels, and CD16 responses to Al2O3 NPs administration . Acta Scientiarum. Animal Sciences, 47(1), e71295. https://doi.org/10.4025/actascianimsci.v47i1.71295
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Produção Animal

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