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Hepato-Preventive Effects of Hydroethanolic Leaves Extract of Persea americana Mill. (Lauraceae) “Avocado” against Antouka SuperInduced Damage in Male Japanese Quail (Coturnix coturnix Japonica)

DOI: 10.4236/ojvm.2021.111003, PP. 41-56

Keywords: Antouka Super (AS), Hepatoprotective, Toxicity, Hydroethanolic Leaves Extract, Persea americana, Japanese Quail

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Abstract:

The present study was undertaken to evaluate the protective effects of Hydroethanolic leaves extract of Persea americana (HEPA) against Antouka Super?(AS) induced hepatotoxicity in male Japanese quail. In total, 40 immature male Japanese quails aged 28 days were used and divided equally into 5 groups. The groups were designed as the control group (received only a 10 ml/kg of distilled water) and the AS group (75 mg/kg b.w). Other three groups received AS (75 mg of AS/kg b.w) plus HEPA (50, 100, and 200 mg/kg b.w/day respectively) by the oral route. After 60 days of the experiment, the crushed liver was performed to obtain homogenate. The protective effects of HEPA on the biochemical parameters, oxidative stress biomarkers and histology changes in the liver were evaluated. The results indicated that AS treatment caused significant alterations in the clinical signs and behavior. It induces the increase in the content of Urea, Creatinine, Protein, AST and ALT in liver tissues and serum. The activities of enzymatic oxidative stress markers such as Superoxide Dismutase (SOD); Catalase (CAT) and Total Peroxidase (POD) also showed significant perturbations in AS-treated quails. Histopathological examination of the liver of AS-treated quails revealed liver lesions characterized by moderate to severe degenerative changes showing a number of hepatocytes undergo fatty changes, focal aggregation of the lymphocytes, multiple necrotic changes and inflammatory infiltrate. The administration of HEPA however, markedly ameliorated the toxicity of AS by protecting the levels of aforesaid biomarkers to near normal levels. These results suggested that HEPA due to its phytochemical constituents with antioxidant properties possesses significant effects against AS-induced toxicity. However, these effects were more pronounced at a dose of 200 mg/kg bw.

References

[1]  Ngoumtsop, V.H., Ngoula, F., Kenfack, A., et al. (2017) Effects of Oxidative Stress Induced by Antouka Super? (Insecticide) on Some Reproductive Parameters of Male Japanese Quail (Coturnix coturnix Japonica) and Mitigation Strategies Using Aqueous Leaves Extract of Persea americana. Global Veterinaria, 18, 242-249.
[2]  Abel, E., Arslan-Acaroz, D., Demirel, H.H., Kucukkurt, I. and Ince, S. (2018) The Subchronic Exposure to Malathion, an Organophosphate Pesticide, Causes Lipid Peroxidation, Oxidative Stress, and Tissue Damage in Rats: The Protective Role of Resveratrol. Toxicology Research, 7, 503-512.
https://doi.org/10.1039/C8TX00030A
[3]  Nessiem, A.L., Bassily, N.S. and Metwally, S.A. (2003) Comparative Histopathological Evaluation of Permethrin, Pirimiphos Methyl and Bendiocarb Toxicities in Testes, Liver and Kidney of Rat. Egyptian Journal of Hospital Medicine, 11, 58-73.
[4]  Hallenbeck, W.H. and Cunningham-Burns, K.M. (2014) Pesticides and Human Health. Springer-Verlag, New York.
[5]  Kingsley, C. and Patrick-Iwuanyanwu (2014) Biochemical and Histological Changes in Liver and Kidney in Male Wistar Albino Rats Following Exposure to Solignum: A Permethrin Containing Wood Preservative Iniobong A. Charles. Journal of Xenobiotics, 4, 45-96.
https://doi.org/10.4081/xeno.2014.4596
[6]  Heikal, A.T., Mossa, H., Ibrahim, A.W. and Abdel-Hamid, H.F. (2014) Hepato-Renal Damage and Oxidative Stress Associated with Pirimiphos-Methyl Exposure in Male Mice. Oxidative and Antioxidant Medicine Sciences, 3, 109-117.
https://doi.org/10.5455/oams.260514.or.064
[7]  Mansour, S.A. and Mossa, A.H. (2009) Lipid Peroxidation and Oxidative Stress in Rat Erythrocytes Induced by Chlorpyrifos and the Protective Effect of Zinc. Pesticide Biochemical Physiological, 9, 4-9.
[8]  Arslan, H.O., Herrera, C., Malama, E., Siuda, M., Leiding, C. and Bollwein, H. (2019) Effect of the Addition of Different Catalase Concentrations to a TRIS-Egg Yolk Extender on Quality and In Vitro Fertilization Rate of Frozen-Thawed Bull Sperm. Cryobiology, 91, 40-52.
https://doi.org/10.1016/j.cryobiol.2019.10.200
[9]  Mossa, A.T., Refaie, A.A., Ramadan, A. and Bouajila, J. (2003) Amelioration of Prallethrin-Induced Oxidative Stress and Hepatotoxicity in Rat by the Administration of Origanum majorana Essential Oil. Biomedical Research International, 1, 11.
https://doi.org/10.1155/2013/859085
[10]  Mossa, A.H., Swelam, E.S. and Mohafrash, S.M.M. (2015) Sub-Chronic Exposure to Fipronil Induced Oxidative Stress, Biochemical and Histopathological Changes in the Liver and Kidney of Male Albino Rats. Toxicology Reports, 2, 775-784.
https://doi.org/10.1016/j.toxrep.2015.02.009
[11]  Gutteridge, J.M. and Halliwell, B. (2010) Antioxidants: Molecules, Medicines, and Myths. Biochemical and Biophysical Research Communications, 393, 561-564.
https://doi.org/10.1016/j.bbrc.2010.02.071
[12]  Acaroz, U., Ince, S., Arslan-Acaroz, D., et al. (2018) The Ameliorative Effects of Boron against Acrylamide-Induced Oxidative Stress, Inflammatory Response, and Metabolic Changes in Rats. Food and Chemical Toxicology, 118, 745-752.
https://doi.org/10.1016/j.fct.2018.06.029
[13]  Mimić-Oka, J., Simić, T., Djukanović, L., Reljić, Z. and Davicević, Z. (1999) Alteration in Plasma Antioxidant Capacity in Various Degrees of Chronic Renal Failure. Clinical Nephrology, 5, 233-241.
[14]  Nice, D. (1997) Antioxidant Based Nutraceuticals. In: Yalpani, M., Ed., New Technologies for Healthy Foods and Nutraceuticals, Science Publishers, Shrewsbury, 23-105.
[15]  Adeyemi, O.O., Okpo, O.S. and Ogunti, O.O. (2012) Analgesic and Anti-Inflammatory Effects of the Aqueous Extract of Leaves of Persea americana Mill. (Lauraceae). Fitoterapia, 73, 375-380.
https://doi.org/10.1016/S0367-326X(02)00118-1
[16]  Korać, R.R. and Khambholja, K.M. (2011) Potential of Herbs in Skin Protection from Ultraviolet Radiation. Pharmacognosy Reviews, 5, 164-173.
https://doi.org/10.4103/0973-7847.91114
[17]  Raharjo, S.H.T., Gomez-Lim, W.M.A., Padilla, G. and Litz, R.E. (2008) Recovery of Avocado (Persea americana Mill.) Plants Transformed with the Antifungal Plant Defense in Gene PDF12. In Vitro Cellular Developmental Biology, 44, 254-262.
https://doi.org/10.1007/s11627-008-9117-2
[18]  Anaka, O.A., Ozolua, R.I. and Okpo, S.O. (2009) Effect of the Aqueous Seed Extract of Persea americana Mill. (Lauraceae) on the Blood Pressure of Sprague Dawley Rats. African Journal Pharmacy Pharmacology, 3, 485-490.
[19]  Kosińska, A., Karamác, M., Estrella, I., Hernández, T., Bartolomé, B. and Dykes, A.G. (2012) Phenolic Compound Profiles and Antioxidant Capacity of Persea americana Mill. Peels and Seeds of Two Varieties. Journal Agricultural Food Chemistry, 60, 4613-4619.
https://doi.org/10.1021/jf300090p
[20]  Hidalgo, M., Sánchez-Moreno, C. and Pascual-Teresa, S. (2010) Flavonoid-Flavonoid Interaction and Its Effect on Their Antioxidant Activity. Food Chemistry, 12, 691-696.
https://doi.org/10.1016/j.foodchem.2009.12.097
[21]  Rodríguez-Carpena, J., Morcuende, D., Andrade, M.J., Kylli, P. and Estéve, M. (2011) Avocado (Persea americana Mill.) Phenolics, in Vitro Antioxidante and Antimicrobial Activities, and Inhibition of Lipid and Protein Oxidation in Porcine Patties. Journal Agricultural Food Chemistry, 59, 5625-5635.
https://doi.org/10.1021/jf1048832
[22]  Ekor, M., Adepoju, G.K.A. and Epoyun, A.A. (2006) Protective Effect of the Methanolic Leaf Extract of Persea americana (Avocado) against Paracetamol-Induced Acute Hepatotoxicity in Rats. International Journal of Pharmacology, 2, 416-420.
https://doi.org/10.3923/ijp.2006.416.420
[23]  Owolabi, M.A., Coker, B.A.H. and Jaja, S.I. (2010) Bioactivity of the Phytoconstituents of the Leaves of Persea americana. Journal of Medicinal Plants Research, 4, 1130-1135.
[24]  Rice-Evans, C. (1995) Plant Polyphenols: Free Radical Scavengers or Chain-Breaking Antioxidants. Biochemical and Social Symposium, 6, 103-116.
https://doi.org/10.1042/bss0610103
[25]  Rice-Evans, C.A. and Miller, N.J. (1996) Antioxidant Activities of Flavonoids as Bioactive Components of Food. Biochemical and Social Transdisciplinary, 24, 790-795. https://doi.org/10.1042/bst0240790
[26]  Rice-Evans, C.A., Miller, N.J. and Paganga, G. (1996) Structure-Antioxidant Activity Relationships of Flavonoids and Phenolic Acid. Free Radical Biology & Medicine, 20, 933-956.
https://doi.org/10.1016/0891-5849(95)02227-9
[27]  Bruck, R., Hershkoviz, R., Lider, O., Aeed, H., Zaidel, L. and Matas, Z. (2007) Flavonoid Metabolites in Urine after Oral Administration of the Aqueous Extract of Persea americana to Rats.
[28]  Conwell, D.G., Jones, K.H., Jiang, Z., Lantry, L.E., Kohar, et al. (1998) Cytotoxicity of Tocopherols and Their Quinines in Drug-Sensitive and Multidrug-Resistant Leukemia Cells. Lipids Journal, 3, 295-301.
https://doi.org/10.1007/s11745-998-0208-8
[29]  Cook, N.C. and Samman, S. (1996) Flavonoids Chemistry, Metabolism, Cardioprotective Effects, and Dietary Sources. Journal of Nutrition and Biochemical, 7, 66-76.
https://doi.org/10.1016/S0955-2863(95)00168-9
[30]  Owolabi, M.A., Bruck, R., Hershkoviz, R., Lider, et al. (2007) Flavonoid Metabolites in Urine after Oral Administration of the Aqueous Extract of Persea americana to Rats. Journal of Natural Medicine, 6, 200-204.
https://doi.org/10.1007/s11418-006-0122-7
[31]  Rame-Tiendrebeogo, A.A., Tibiri, A., Lompo, M., Millogo-Kone, H. and Guissou, P. (2012) Antioxidative and Bacterial Activities of Phenolics Compounds from Ficus sur Forssk and Fircus sycomorus L. (Moraceae): Potential for Sickle Cell Disease Treatment in Burkina Faso. International Journal of Biological and Chemistry Sciences, 6, 328-336.
https://doi.org/10.4314/ijbcs.v6i1.29
[32]  EEC (1986) Council Directive 86/609/EEC of 24 November 1986 on the Approximation of Laws, Regulations and Administration Provisions of the Member States Regarding the Protection of Animals Used for Experimental and Other Scientific Purposes. Official Journal European Committed, 35, 1-29.
[33]  Hayes, W.J. and Laws, E.R. (1998) Handbook of Pesticide Toxicology. Academic Press, Cambridge, 185.
[34]  Tchoffo, H., Kana, J.R., Ngoula, F., Ngoumtsop, V.H., et al. (2019) Effects of Ginger (Zingiber officinale, Roscoe) Essential Oil on Growth and Laying Performances, Serum Metabolites, and Egg Yolk Antioxidant and Cholesterol Status in Laying Japanese Quail. Journal of Veterinary Medicine, 2019, Article ID: 7857504.
https://doi.org/10.1155/2019/7857504
[35]  Habbu, P.V., Shastry, R.A., Mahadevan, K.M., Hanumanthachar, J. and Das, S.K. (2008) Protective and Antioxidant Effects of Argyreia speciosa in Quails. African Journal and Alternative Medicine, 5, 158-164.
https://doi.org/10.4314/ajtcam.v5i2.31268
[36]  Dimo, T., Tsala, D.E., Dzeufiet, D.P.D., Penlap, B.V. and Njifutie, N. (2006) Effects of Alafia multiflora Stap on Lipid Peroxidation and Antioxidant Enzyme Status in Carbon Tetrachloride-Treated Quails. Pharmacology Online, 2, 76-89.
[37]  Kodjo, N., Atsafack, S.S., Njateng, S.S.G., Sokoudjou, B.J. and Kuiate, R.J. (2016) Antioxidant Effect of Aqueous Extract of Curcuma longa Rhizomes (Zingiberaceae) in the Typhoid Fever Induced in Wistar Rats Model. Journal of Applied Medicine and Pharmacological Sciences, 7, 1-13.
https://doi.org/10.9734/JAMPS/2016/24949
[38]  Sajeeth, C.I., Manna, P.K. and Manavalan, R. (2011) Antioxidant Activity of Polyherbal Formulation on Streptozotocin Induced Diabetes in Experimental Animals. Der Pharmacia Sinica, 2, 220-226.
[39]  Prakash, P.J., Rajashekher, G., Krishnappa, H., Sulaiman, S.M. and Rao, K.V. (2009) Acute Toxic Effects of Endosulfan 35 EC (Endocel) upon Oral Gavage and Dietary Admixture in Japanese Quails. Research Journal of Environmental Toxicology, 3, 124-131.
https://doi.org/10.3923/rjet.2009.124.131
[40]  Sarkar, R., Mohana, K.P. and Chowdhury, H. (2000) Effects of an Organophosphate Pesticide, Quinalphos, on the Hypothalamo-Pituitary-Gonadal Axis in Adult Male Rats. Journal of Reproduction and Fertility, 118, 29-38.
https://doi.org/10.1530/jrf.0.1180029
[41]  Rastogi, S.K., Satyanarayan, P.V.V., Ravishankar, D. and Tripathi, S. (2007) A Study on Oxidative Stress and Antioxidant Status of Agricultural Workers Exposed to Organophosphorus Insecticides during Spraying. Indian Journal of Occupational Environmental Medicine, 13, 131-134.
https://doi.org/10.4103/0019-5278.58916
[42]  Naudi, A.M., Jove, V., Ayala, R., Cabre, M., Portero-Otin, et al. (2013) Non-Enzymatic Modification of Aminophospholipids by Carbonyl-Amine Reactions. International Journal of Molecular Sciences, 14, 3285-3313.
https://doi.org/10.3390/ijms14023285
[43]  Kumar, V., Tripathi, V.K., Singh, A.K., Lohani, M. and Kuddus, M. (2013) Trans-Resveratrol Restores the Damages Induced by Organophosphate Pesticide-Monocrotophos in Neuronal Cells. Toxicology International, 20, 48-55.
https://doi.org/10.4103/0971-6580.111571
[44]  Umosen, J.A., Ambali, S.F., Ayo, J.O., Mohammed, B. and Uchendu, C. (2012) Alleviating Effects of Melatonin on Oxidative Changes in the Testes and Pituitary Glands Evoked by Subacute Chlorpyrifos Administration in Wistar Rats. Asian Pacific Journal Tropical Biomedicine, 2, 645-850.
https://doi.org/10.1016/S2221-1691(12)60113-0
[45]  EL-Hossary, G.G., Mansour, S.M. and Mohamed, A.S. (2009) Neurotoxic Effects of Chlorpyrifos and the Possible Protective Role of Antioxidant Supplements: An Experimental Study. Journal of Applied Sciences Research, 5, 1218-1222.
[46]  Raquel, J., Gabriel, L.O., Celso, P. and Claudriana, L. (2012) Attribution Evaluation of Biochemical, Hematological and Oxidative Parameters in Mice Exposed to the Herbicide Glyphosate-Roundup. Interdisciplinary Toxicology, 5, 133-140.
https://doi.org/10.2478/v10102-012-0022-5
[47]  Lin, S.C., Yao, C.J., Lin, C.C. and Lin, H.Y. (1996) Hepatoprotective Activity of Taiwan Folk Medicine: Eclipta prostrata Linn. against Various Hepatotoxins Induced Acute Hepatotoxicity. Phytotherapy Research, 10, 483-490.
[48]  Moss, D.W. and Butterworth, P.J. (1974) Enzymology and Medicine. 139.
[49]  Saraswat, B., Visen, P.K., Patnaik, K.G. and Dhawan, N.B. (1993) Anticholestatic Effect of Picroliv, Active Hepatoprotective Principle of Picrorhiza kurrooa, against Carbon Tetrachloride Induced Cholestasis. Indian Journal of Experimental Biology, 31, 316-318.
[50]  Gupta, M., Mazumder, U.K., Kumar, S.T., Gomathi, P. and Kumar, S.R. (2004) Antioxidant and Hepatoprotective Effects of Bauhinia racemosa against paracetamol and carbon tetrachloride induced liver damage in rats. Iranian Journal of Pharmacological Therapeutics, 3, 12-20.
[51]  Iniaghe, O.S., Malomo, O.J., Adebayo and Arise, O.R. (2008) Evaluation of the Antioxidant and Hepatoprotective Properties of the Methanolic Extract of Acalypha racemosa Leaf in Carbon Tetrachloride-Treated Rats. African Journal of Biotechnology, 7, 1716-1720.
https://doi.org/10.5897/AJB08.229
[52]  Adesanoye, A.O. and Farombi, O.E. (2010) Hepatoprotective Effects of Vernonia amygdalina (Astereaceae) in Rats Treated with Carbon Tetrachloride. Experimental Toxicology and Pathology, 62, 197-206.
https://doi.org/10.1016/j.etp.2009.05.008
[53]  Maksimovic, Z., Kovacevic, N., Lakusic, B. and Cebovic, T. (2011) Antioxidant Activity of Yellow Dock (Rumex crispus L., Polygonaceae) Fruit Extract. Phytotherapy Research, 25, 101-105.
https://doi.org/10.1002/ptr.3234
[54]  Shenoy, A.K., Somayaji, N.S. and Bairy, L.K. (2001) Hepatoprotective Effect of Ginkgo biloba against CCl4-Induced Hepatic Injury in Rats. Indian Journal of Pharmacology, 33, 260-266.
[55]  Wang, J.B., Liu, T.C., Tseng, Y.C., Wu, P.C. and Yu, R.Z. (2004) Hepatoprotective and Antioxidant Effects of Bupleurum kaoi Liu (Chao et Chuang) Extract and Its Fractions Fractionated Using Supercritical CO2 on CCl4-Induced Liver Damage. Food Chemical and Toxicology, 42, 609-617.
https://doi.org/10.1016/j.fct.2003.11.011
[56]  Arukwe, U., Amadi, A.B., Duru, C.K.M., Aguomo, et al. (2012) Chemical Composition of Persea americana Leaf, Fruit and Seed. International Journal Research and Applied Sciences, 11, 349-356.
[57]  Khalid, J.H., Sheikh, S.A. and Anwar, G.H. (2002) Protective Effect of Rutin on Paracetamol- and CCl4-Induced Hepatotoxicity in Rodents. Fitoterapia, 73, 557-563.
https://doi.org/10.1016/S0367-326X(02)00217-4
[58]  Al-Qarawi, A.A., Mousa, M.H., Ali, H.B., Abdel-Rahman, H. and El-Moug, A.S. (2004) Protective Effect of Extracts from Dates (Phoenix dactylifera L.) on Carbon Tetrachloride-Induced Hepatotoxicity in Rats. International Journal of Applied Research Veterinary Medicine, 2, 176-180.
[59]  Mankani, L.K., Krishna, V., Manjunatha, B.K., MVidya, et al. (2005) Evaluation of Hepatoprotective Activity of Stem Bark of Pterocarpus marsupium Roxb. Indian Journal of Pharmacology, 37, 165-168.
https://doi.org/10.4103/0253-7613.16213
[60]  Harisch, G. and Meyer, W. (1985) Studies on Tissue Distribution of Glutathione and on Activities of Glutathione-Related Enzymes after Carbon Tetrachlo-ride-Induced Liver Injury. Research Communications in Chemical Pathology and Pharmacology, 47, 399-414.
[61]  Halliwell, B. (2000) The Antioxidant Paradox. The Lancet, 355, 1179-1180.
https://doi.org/10.1016/S0140-6736(00)02075-4
[62]  Kyle, E.M., Miccadei, S., Nakae, D. and Farber, L.J. (1987) Superoxide Dismutase and Catalase Protect Cultured Hepatocytes from the Cytotoxicity of Acetaminophen. Biochemical and Biophysical Research Communications, 149, 889-896.
https://doi.org/10.1016/0006-291X(87)90491-8
[63]  John, S., Kale, M., Rathore, N. and Bhatnagar, D. (2001) Protective Effect of Vitamin E in Dimethoate and Malathion Induced Oxidative Stress in Rat Erythrocytes. Journal of Nutrition and Biochemical, 12, 500-504.
https://doi.org/10.1016/S0955-2863(01)00160-7

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