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Evaluation of the Protective Effect of Citrullus lanatus (Water Melon) Fruit-Parts Extracts on the Liver of Acetaminophen-Intoxicated Albino Rats

DOI: 10.4236/oalib.1106807, PP. 1-23

Subject Areas: Biochemistry

Keywords: Citrullus lanatus, Acetaminophen, Mesocarp, Endocarp, Seeds, Liver

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Abstract

There is always the need to study the bioactive components present in the various parts of edible fruits. This will go a long way to providing an idea of its potential biological benefits when consumed. The current study evaluated the protective effect of C. lanatus fruit’s endocarp/exocarp, mesocarp and seed extracts on the liver of albino rats. The qualitative and quantitative phytochemical analysis was also done following standard methods. The albino rats were divided into nine groups of five per group and treated thus; group 1 (normal control), group 2, Acetaminophen (2 g/kg), group 3, 200 mg/kg silymarin 2 g/kg Acetaminophen, group 4, 200 mg/kg mesocarp 2 g/kg Acetaminophen, group 5, 400 mg/kg, group 6, 200 mg/kg exocarp, group 7, 400 mg/kg exocarp, group 8, 200 mg/kg seeds, group 9, 400 mg/kg seeds. The pre-treatment with the extracts lasted for 14 days then acetaminophen administered. The rats were sacrificed after 48 hours of intoxication. Results showed the presence of alkaloids, phenolics, Tannins, steroids and terpenoids and glycosides while saponins and flavonoids were not detected in the endocarp. In the mesocarp, glycosides, phenolics, steroids and terpenoids and tannins were present while Saponins and flavonoids were not detected. Seed extract showed the presence of alkaloids, flavonoids, phenolics, tannins, steroids and terpenoids. Glycosides and saponins were not detected. The activities of AST, ALT and ALP were significantly (p < 0.05) increased in group 2 (55.80 ± 3.11, 20.80 ± .84 and 27.00 ± 1.22 respectively) when compared to the normal control group (group 1) (32.00 ± 2.12, 9.00 ± 1.00 and 19.80 ± 4.49 respectively). The administration of the extracts (group 4, 5, 6, 7, 8 and 9) led to a significant decrease in the serum activities of AST (51.40 ± 1.14, 48.60 ± 7.57, 39.20 ± 1.79, 48.00 ± 1.73, 51.00 ± 0.00 and 47.00 ± 2.74) and ALT (10.20 ± 1.30, 11.20 ± 1.30, 17.20 ± 2.77, 20.00 ± 0.71, 17.60 ± 0.55 and 18.20 ± 1.64) when compared with the acetaminophen group (group 2). Photomicrograph images showed normal liver morphology in the control groups 1 and 3, 200 mg/kg mesocarp and 400 mg/kg seed extract administered groups, indicating that the two extract doses better protected the liver against damage occasioned by acetaminophen.

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Enemali, M. O. , Asogwa, M. E. , Nweze, C. C. , Haruna, G. S. and Ijeomah, A. U. (2020). Evaluation of the Protective Effect of Citrullus lanatus (Water Melon) Fruit-Parts Extracts on the Liver of Acetaminophen-Intoxicated Albino Rats. Open Access Library Journal, 7, e6807. doi: http://dx.doi.org/10.4236/oalib.1106807.

References

[1]  Bailey, L.H. (1930) Three Discussions in Cucurbitaceae. Gentes Herbarum, 2, 175-186.
[2]  Chomicki, G. and Renner, S.S. (2014) Watermelon Origin Solved with Molecular Phylogenetics Including Linnaean Material: Another Example of Museomics. New Phytologist, 205, 526-532. https://doi.org/10.1111/nph.13163
[3]  Maynard, D. and Donald, N. (2012) 6: Cucumbers, Melons and Watermelons. In: Kiple, K.F. and Ornelas, K.C., Eds., The Cambridge World History of Food, Part 2, Medical History, 46, Cambridge University Press, Cambridge, 267-270.
[4]  Erhirhie, E.O. and Ekene, N.E. (2013) Medicinal Values on Citrullus lanatus (Watermelon): Pharmacological Review. International Journal of Research in Pharmaceutical and Biomedical Sciences, 4, 1305-1312.
[5]  Charoensiri, R., Kongkachuichai, R., Suknicom, S. and Sungpuag, P. (2009) Beta-Carotene, Lycopene, and Alpha-Tocopherol Contents of Selected Thai Fruits. Food Chemistry, 113, 202-207. https://doi.org/10.1016/j.foodchem.2008.07.074
[6]  Altaş, S., Kizil, G., Kizil, M., Ketani, A. and Haris, P.I. (2011) Protective Effect of Diyarbakir Watermelon Juice on Carbon Tetrachloride-Induced Toxicity in Rats. Food and Chemical Toxicology, 49, 2433-2438. https://doi.org/10.1016/j.fct.2011.06.064
[7]  Collins, J.K., Wu, G., Perkins-Veazie, P., Spears, K., Claypool, P.L., Baker, R.A. and Clevidence, B.A. (2007) Watermelon Consumption Increases Plasma Arginine Concentrations in Adults. Nutrition, 23, 261-266. https://doi.org/10.1016/j.nut.2007.01.005
[8]  Perkins-Veazie, P., Collins, J.K., Pair, S.D. and Roberts, W.(2001) Lycopene Content Differs Among Red-Fleshed Watermelon Cultivars. Journal of the Science of Food and Agriculture, 81, 983-987. https://doi.org/10.1002/jsfa.880
[9]  Akashi, K., Nishimura, N., Ishida, Y. and Yokota, A. (2004) Potent Hydroxyl Radical-Scavenging Activity of Drought-Induced Type-2 Metallothionein in Wild Watermelon. Biochemical and Biophysical Research Communications, 323, 72-78. https://doi.org/10.1016/j.bbrc.2004.08.056
[10]  Chaturvedi, P., Pipedi-Tshekiso, M. and Tumedi, A. (2014) Supplementation with Watermelon Renders Protection Against Toxicity Induced by Paracetamol in Albino Rats: The Mutual and Fine Interaction of Antioxidants Prevented the Cellular Damage. International Journal of Food, Agriculture & Veterinary Sciences, 4, 102-111.
[11]  Alok, B.R.K., Vivek, D. and Niyaz, A. (2012) Evaluation of Anti-Ulcer Activity of Citrallus lanatus Seed Extract in Wistar Rats. Journal of Pharmaceutical Sciences, 4, 135-139.
[12]  National Plant Data Center, NRCS, USDA (2000) Baton Rouge, LA 70874-4490 USA. Citrullus lanatus var. lanatus, the Plants Database, Database (Version 5.1.1). http://plants.usda.gov
[13]  Van Gulik, T.M., De Graaf, W, Dinant, S., Busch, O.R.C. and Gouma, D.J. (2007) Vascular Occlusion Techniques during Liver Resection. Digestive Surgery, 24, 274-281. https://doi.org/10.1159/000103658
[14]  Tortora, G., Derrickson, J. and Bryan, H. (2008) Principles of Anatomy and Physiology. 12th Edition, John Wiley & Sons, Hoboken, 945.
[15]  Maton, A., Jean, H., Charles, W., Mclaughlin, S. Johnson, M., Quon, W., David, L. and Jill, D.W. (1993) Human Biology and Health. Prentice Hall, Englewood Cliffs.
[16]  Mamta S., Jyoti, S., Rajeev, N., Dhatmendra, S. and Abhishek, G. (2013) Phytochemistry of Medicinal Plants. Journal of Pharmacognosy and Phytochemistry, 1, 168-182.
[17]  Narasinga, R. (2003) Bioactive Phytochemicals in Indian Foods and Their Potential in Health Promotion and Disease Prevention. Asia Pacific Journal of Clinical Nutrition, 12, 9-22.
[18]  Harborne, J.B. (1973) Phytochemical Methods: A Guide to Modern Technique of Plant Analysis. Chapman and Hall, London, 107-150.
[19]  Trease, G.E. and Evans, W.C. (1989) Pharmacognosy. 13th Edition, Bailliere Tindall Books Publishers, London, 1-105.
[20]  Sofowora, A. (1993) Screening Plants for Bioactive Agents. In: Medicinal Plants and Traditional Medical in Africa. 2nd Edition, Spectrum Books Ltd., Sunshine House, 134-156.
[21]  Reitman, S. and Frankel, S. (1957) A Colorimetric Determination of Oxaloacetic and Glutamic Pyruvic Transaminases. American Journal of Clinical Pathology, 28, 56-63. https://doi.org/10.1093/ajcp/28.1.56
[22]  Bancroft, J.D. and Stevens, M. (2002) Theory and Practice of Histological Techniques. Churchill Livingstone, Edinburgh, 16-64.
[23]  Nita, Y., Rajesh, Y. and Anju, G. (2014) Chemistry of Terpenoids. International Journal of Pharmaceutical Sciences Review and Research, 27, 272-278.
[24]  Leist, M., Gantner, F., Bohlinger, I., Tiegs, G., Germann, P.G. and Wendel, A. (1995) Tumor Necrosis Factor-Induced Hepatocyte Apoptosis Precedes Liver Failure in Experiment Murine Shock Models. The American Journal of Pathology, 146, 1220-1234.
[25]  Lawson, J.A., Fisher, M.A., Simmons, C.A., Farhood, A. and Jaeschke, H. (1998) Parenchymal Cell Apoptosis as a Signal for Sinusoidal Sequestration and Transendothelial Migration of Neutrophils in Murine Models of Endotoxin and Fas-Antibody-Induced Liver Injury. Hepatology, 28, 761-767. https://doi.org/10.1002/hep.510280324
[26]  Lemasters, J.J., Ji, S. and Thurman, R.G. (1981) Centrilobular Injury Following Hypoxia in Isolated, Perfused Rat Liver. Science, 213, 661-663. https://doi.org/10.1126/science.7256265
[27]  Kamiike, W., Fujikawa, M., Koseki, M., Sumimura, J., Miyata, M., Kawashima, Y., et al. (1989) Different Patterns of Leakage of Cytosolic and Mitochondrial Enzymes. Clinica Chimica Acta, 185, 265-270. https://doi.org/10.1016/0009-8981(89)90216-7
[28]  Gores, G.J., Herman, B. and Lemasters, J.J. (1990) Plasma Membrane Bleb Formation and Rupture: A Common Feature of Hepatocellular Injury. Hepatology, 11, 690-698. https://doi.org/10.1002/hep.1840110425
[29]  Pappas, N.J. (1980) Increased Rat Liver Homogenate, Mitochondrial, and Cytosolic Aspartate Aminotransferase Activity in Acute Carbon Tetrachloride Poisoning. Clinica Chimica Acta, 106, 223-229. https://doi.org/10.1016/0009-8981(80)90175-8
[30]  Pappas, N.J. (1986) Source of Increased Serum Aspartate and Alanine Aminotransferase: Cycloheximide Effect on Carbon Tetrachloride Hepatotoxicity. Clinica Chimica Acta, 154, 181-189. https://doi.org/10.1016/0009-8981(86)90029-X
[31]  Pappas, N.J. (1989) Theoretical Aspects of Enzymes in Diagnosis. Why Do Serum Enzymes Change in Hepatic, Mitochondrial, and Other Diseases? Clinics in Laboratory Medicine, 9, 595-626. https://doi.org/10.1016/S0272-2712(18)30594-8
[32]  Aubert, J., Begriche, K., Delannoy, M., Morel, I., Pajaud, J., Ribault, C., et al. (2012) Differences in Early Acetaminophen Hepatotoxicity between Obese ob/ob and db/db Mice. Journal of Pharmacology and Experimental Therapeutics, 342, 676-687. https://doi.org/10.1124/jpet.112.193813
[33]  Konttinen, A., Murros, J., Ojala, K., Salaspuro, M., Somer, H. and Räsänen, J. (1978) A New Cause of Increased Serum Aspartate Aminotransferase Activity. Clinica Chimica Acta, 84, 145-147. https://doi.org/10.1016/0009-8981(78)90487-4
[34]  Kajita, Y., Majima, T., Yoshimura, M., Hachiya, T., Miyazaki, T., Ijichi, H., et al. (1978) Demonstration of Antibody for Glutamic Pyruvic Transaminase (GPT) in Chronic Hepatic Disorders. Clinica Chimica Acta, 89, 485-492. https://doi.org/10.1016/0009-8981(78)90414-X
[35]  Moriyama, T., Nobuoka, M. and Makino, M. (1990) Incidence and Properties of Aspartate Aminotransferase-Immunoglobulin Complexes in Patients with a High Serum Aspartate to Alanine Aminotransferase Ratio. Clinica Chimica Acta, 190, 47-56. https://doi.org/10.1016/0009-8981(90)90279-2
[36]  Briani, C., Zaninotto, M., Forni, M. and Burra, P. (2003) Macroenzymes: Too Often Overlooked. Journal of Hepatology, 38, 119. https://doi.org/10.1016/S0168-8278(02)00333-1

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