Ameliorative Potential of Pumpkin Seeds Against Lead-Induced Toxicity in Poultry Chicken (Gallus gallus domesticus)
DOI:
https://doi.org/10.70749/ijbr.v2i02.367Keywords:
Lead Toxicity, Pumpkin Seeds, Oxidative Stress, HepatorenalAbstract
Objective: This study aimed to evaluate the protective effects of pumpkin seed supplementation against lead-induced hepatorenal toxicity in Gallus gallus domesticus. Material and Methods: Young chickens were divided into four groups: control (G0), lead-exposed (G1), pumpkin seed-treated (G2), and combined lead and pumpkin seed-treated (G3). Lead acetate (0.4 mg/kg body weight) and pumpkin seed powder (300 mg/kg body weight) were administered for four weeks. Liver and kidney function tests (ALT, AST, ALP, bilirubin, urea, creatinine), lipid profiles (LDL, HDL, cholesterol, triglycerides), and antioxidant enzymes (CAT, GPx, GR, SOD) were analyzed. Histopathological evaluations of liver and kidney tissues were conducted. Data were analyzed using SPSS 25, with P < 0.05 considered significant. Results: Lead exposure increased ALT (14.6 ± 0.01 IU/L), AST (2210.7 ± 10.31 IU/L), ALP (1970.4 ± 1.07 IU/L), bilirubin (0.7 ± 0.00 mg/dL), and LDL (56.9 ± 0.91 mg/dL). Pumpkin seed supplementation reduced AST (110.1 ± 8.84 IU/L), ALP (1360.5 ± 1.00 IU/L), and LDL (22.9 ± 1.04 mg/dL), and improved antioxidant enzyme activities. Conclusion: Pumpkin seed supplementation mitigates lead-induced oxidative stress and improves hepatorenal function, presenting a natural strategy to reduce heavy metal toxicity in poultry.
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Ghosh, D., Firdaus, S. B., Dey, M., & Mitra, E.(2012). Protective Effect of Aqueous Leaf Extract of Murraya Koe Against Lead-Induced Oxidative Stress in Rat Liver, Heart, and Kidney: A Dose Response Study. Asian Journal of Pharmaceutical and Clinical Research, 5(Suppl. 4), 54–58.
Flora, G., Mittal, M., & Flora, S. J. (2015). Medical countermeasures—Chelation therapy. Handbook of Arsenic Toxicology, 589-626. https://doi.org/10.1016/b978-0-12-418688-0.00026-5
Zalups, R. K., & Lash, L. H. (2023). Interactions between Glutathione and mercury in the kidney, liver, and blood. Toxicology of Metals, Volume I, 145-163. https://doi.org/10.1201/9781003418917-14
Zhang, Q., Li, Y., Liu, Z., & Chen, Q. (2016). Reproductive toxicity of inorganic mercury exposure in adult zebrafish: Histological damage, oxidative stress, and alterations of sex hormone and gene expression in the hypothalamic-pituitary-gonadal axis. Aquatic Toxicology, 177, 417-424. https://doi.org/10.1016/j.aquatox.2016.06.018
Adams, D. H., Sonne, C., Basu, N., Dietz, R., Nam, D., Leifsson, P. S., & Jensen, A. L. (2010). Mercury contamination in spotted seatrout, Cynoscion nebulosus: An assessment of liver, kidney, blood, and nervous system health. Science of The Total Environment, 408(23), 5808-5816. https://doi.org/10.1016/j.scitotenv.2010.08.019
Ito, C., Itoigawa, M., Nakao, K., Murata, T., Tsuboi, M., Kaneda, N., & Furukawa, H. (2006). Induction of apoptosis by carbazole alkaloids isolated from Murraya koenigii. Phytomedicine, 13(5), 359-365. https://doi.org/10.1016/j.phymed.2005.03.010
Mitra, A., & Mahadevappa, M. (2010). Antidiabetic and hypolipidemic effects of mahanimbine (carbazole alkaloid) from Murraya koenigii (rutaceae) leaves. Int. J. Phytomedicine, 2, 22-30. https://doi.org/10.5138/ijpm.2010.0975.0185.02004
Mishra, B., Singh, R., Srivastava, A., Tripathi, V., & Tiwari, V. (2009). Fighting against leishmaniasis: Search of alkaloids as future true potential anti-leishmanial agents. Mini-Reviews in Medicinal Chemistry, 9(1), 107-123. https://doi.org/10.2174/138955709787001758
Shukla, S., Mehta, A., Bajpai, V. K., & Shukla, S. (2009). In vitro antioxidant activity and total phenolic content of ethanolic leaf extract of Stevia rebaudiana Bert. Food and Chemical Toxicology, 47(9), 2338-2343. https://doi.org/10.1016/j.fct.2009.06.024
HUANG, C., HSU, C., LIU, S., & LINSHIAU, S. (2008). Neurotoxicological mechanism of methylmercury induced by low-dose and long-term exposure in mice: Oxidative stress and down-regulated Na+/k+-atpase involved. Toxicology Letters, 176(3), 188-197. https://doi.org/10.1016/j.toxlet.2007.11.004
Gado, A., & Aldahmash, B. (2013). Antioxidant effect of Arabic gum against mercuric chloride-induced nephrotoxicity. Drug Design, Development and Therapy, 1245. https://doi.org/10.2147/dddt.s50928
Afridi, H. I., Talpur, F. N., Kazi, T. G., & Brabazon, D. (2014). Assessment of toxic elements in the samples of different cigarettes and their effect on the essential elemental status in the biological samples of Irish hypertensive consumers. Journal of Human Hypertension, 29(5), 309-315. https://doi.org/10.1038/jhh.2014.87
Abdel-Moneim, A. E., Dkhil, M. A., & Al-Quraishy, S. (2010). The redox status in rats treated with flaxseed oil and lead-induced Hepatotoxicity. Biological Trace Element Research, 143(1), 457-467. https://doi.org/10.1007/s12011-010-8882-z
Franciscato, C., Moraes-Silva, L., Duarte, F., Oliveira, C., Ineu, R., Flores, E., Dressler, V., Peixoto, N., & Pereira, M. (2011). Delayed biochemical changes induced by mercury intoxication are prevented by zinc pre-exposure. Ecotoxicology and Environmental Safety, 74(3), 480-486. https://doi.org/10.1016/j.ecoenv.2010.11.011
Reitman, S., & Frankel, S. (1957). A Colorimetric method for the determination of serum glutamic Oxalacetic and glutamic pyruvic transaminases. American Journal of Clinical Pathology, 28(1), 56-63. https://doi.org/10.1093/ajcp/28.1.56
Paglia, D. E., & Valentine, W. N. (1967). Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase. The Journal of laboratory and clinical medicine, 70(1), 158-169.
Abosrea, A. M., Aboul Ezz, H. S., Mahmoud, S. M., Mousa, M. R., & Ahmed, N. A. (2023). The potential role of pumpkin seeds oil on methotrexate-induced lung toxicity. Scientific Reports, 13(1). https://doi.org/10.1038/s41598-023-34143-6
Almohaimeed, H. M., Hamed, S., Seleem, H. S., Batawi, A. H., Mohammedsaleh, Z. M., Balgoon, M. J., Ali, S. S., Al Jaouni, S., & Ayuob, N. (2021). An Ethanolic extract of Cucurbita pepo L. Seeds modifies neuroendocrine disruption in chronic stressed rats and adrenal expression of inflammatory markers and HSP70. Frontiers in Pharmacology, 12. https://doi.org/10.3389/fphar.2021.749766
Kaur, N., Kishore, L., Farooq, S. A., Kajal, A., Singh, R., Agrawal, R., Mannan, A., & Singh, T. G. (2023). Cucurbita pepo seeds improve peripheral neuropathy in diabetic rats by modulating the inflammation and oxidative stress in rats. Environmental Science and Pollution Research, 30(36), 85910-85919. https://doi.org/10.1007/s11356-023-28339-6
Sánchez-Velázquez, O. A., Luna-Vital, D. A., Morales-Hernandez, N., Contreras, J., Villaseñor-Tapia, E. C., Fragoso-Medina, J. A., & Mojica, L. (2023). Nutritional, bioactive components and health properties of the milpa triad system seeds (corn, common bean and pumpkin). Frontiers in Nutrition, 10. https://doi.org/10.3389/fnut.2023.1169675
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