Water Extract of Three Aromatic Plants Mixture Ameliorates Paracetamol-Induced Renal-Hepato Damage in Male Albino Rats
Keywords:
Xylopia aethiopica, Coriandrum sativum, Anethum graveolens, Hepato-Renal Protective Activity, RatsAbstract
Background and Objectives: This study examined the effects of fruit water extracts of mixture from selected three plants (Xylopia aethiopica, Coriandrum sativum and Anethum graveolens) on some indices of liver and kidney function tests in the male albino rats, and also to evaluate the antioxidant power of its water extract and the protective effect against paracetamol-induced hepatic and renal toxicity in male albino rats.
Materials and Methods: Three groups of rats were used (control, paracetamol-treated and protected group), which were supplemented with mixture water extract for four weeks followed by intraperitoneal injection of paracetamol. Levels of ALT, AST, ALP, gamma-glutamyl transferase, CAT, GPx, serum direct bilirubin, serum total bilirubin, serum albumin, serum total globin, total serum urea and serum creatinine, as well as histopathological changes in the liver and kidney were investigated. Quantitative determination of the total phenolic content (TPC) was performed using the Folin-Ciocalteu method, quantitative determination of antioxidant activity was performed according to the ?-carotene bleaching method and Diphenylpicrylhydrazyl (DPPH) free radical scavenging assay. The experiment was conducted for two weeks. Statistical analysis was carried out by analysis of variance.
Results: Oral administration of paracetamol recorded significant decrease in TAC, CAT and GPx compared to normal control rats whereas rats supplemented with water extract and then intoxicated with paracetamol showed a significant increase in TAC, CAT and GPx levels compared with paracetamol intoxicated rats, and compared to normal control. AST, ALT, ALP, GGT, total bilirubin, direct bilirubin and indirect bilirubin levels of rats treated with paracetamol were quite higher than that of control group whereas the rats treated with mixture extract and paracetamol had significant reduction when compared with the paracetamol group. Paracetamol induced significant increase in the concentration of plasma urea and creatinine in intoxicated rats as compared to normal control rats, whreas there was no significant difference between mixtures extract supplemented rats and protected rats as compared with control.
Conclusion: The aqueous extract mixture dose dependably offered potential renal-hepato protection from paracetamol induced hepatic damage, normalizing biochemical parameters in rats.
References
2. Sumit D, Ripunjoy B, Nishant N. A review on immune modulatory effect of some traditional medicinal herbs. Journal of Pharmaceutical Chemical and Biological Science 2014; 2(1): 33-42.
3. Parmar SR, Vashombhai PH, Kabio K. Hepatoprotective activity of some plants extract against paracetamolinduced hepatotoxicity in rats. Journal of Herbal Medicine and Toxicology 2010; 4(2): 101-106.
4. Sharafi S, Rasooli I, Owlia P et al. Protective effects of bioactive phytochemicals from Menthapiperita with multiple health potentials. Pharmocogn Mag 2010; 6(23): 147-153.
5. Abd-Algader NN, EL-Kamali HH, Ramadan MM et al. Xylopiaaethiopica volatile compounds protect against Panadol-induced hepatic and renal toxicity in male rats. World Applied Sciences Journal 2013; 20(2): 78-88.
6. Ramadana MM, Abd-Algaderd NN, El-kamalid HH et al. Volatile compounds and antioxidant activity of the aromatic herb Anethumgraveolens. Journal of Arab Society for Medical Research 2013; 27(1): 10-22.
7. Ramadan MM, Abd Algader NNE, El-Kamali HH et al. Chemopreventive effect of Coriandrum sativum fruits on hepatic toxicity in male rats. World Journal of Medical Sciences 2013; 8(4): 322-333.
8. Omran AME, Abdalla MA, EL-Kamali HH. Biochemical and haematological profiles in male albino rats fed on different percentages of Cardiospermum halicababum mixed with animal diet. Journal of Research in Biochemistry 2012; 1(1): 009-014.
9. EL-Kamali HH, Omran AME, Abdalla MA. Biochemical and haematological assessment of Croton tiglium seeds mixed with animal diet in male albino rats. Annual Research and Review in Biology 2015; 8(4): 1-7.
10. Chew YL, Ling Chan EW, Tan PL et al. Assessment of phytochemical content, polyphenolic composition, antioxidant and antibacterial activities of Leguminosae medicinal plants in Peninsular Malaysia. BMC Complement Altern Med 2011; 11: 12.
11. Matthäus B. Antioxidant activity of extracts obtained from residues of different oilseeds. J Agric Food Chem 2002; 50(12): 3444-2452.
12. Hatano T, Kagawa H, Yasuhara T et al. Two new flavonoids and other constituents in licorice root their relative astringency and radical scavenging effects. Chem Pharm Bull 1988; 36(6): 1090-2097.
13. Ramachandra Setty S, Quereshi AA, Viswanath Swamy AH et al. Hepatoprotective activity of Calotropisprocera flowers against paracetamol-induced hepatic injury in rats. Fitoterapia 2007; 78(7-8): 451-454.
14. Koracevic D, Koracevic G, Djordjevic V et al. Method for the measurement of antioxidant activity in human fluids. J Clin Pathol 2001; 54(5): 356-361.
15. Aebi H. Catalase in vitro. Methods Enzymol 1984; 105: 121-6.
16. Paglia DE, Valentine WN. Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase. J Lab Clin Med 1967; 70(1): 158-169.
17. Gornall AG, Bardawill CJ, David MM. Determination of serum proteins by means of the biuret reaction. J Biol Chem. 1949; 177(2): 751-66.
18. Doumas BT, Watson W, Biggs HG. Albumin standards and the measurement of serum albumin with bromocresol green. Clin Chim Acta 1971; 31(1): 87-96.
19. Reitman S, Frankel S. A colorimetric method for the determination of serum glutamic oxalacetic and glutamic pyruvic transaminases. Am J Clin Pathol 1957; 28(1): 56-63.
20. Belfield A, Goldberg DM. Revised assay for serum phenyl phosphatase activity using 4-amino-antipyrine. Enzyme 1971; 12(5): 561-573.
21. Persijn JP, Van Der Slik W. A new method for the determination of ? glutamyl transferase in serum. J Clin Chem Clin Biochem 1976; 14(9): 421-427.
22. Walters MI, Gerarde HW. An ultra-micro method for the determination of conjugated and total bilirubin in serum or plasma. Microchem J 1970; 15(2): 231-243.
23. Bartles H, Bohmer M, Heirli C. Colorimetric kinetic method for creatinine determination in serum and urine. Clin Chem Acta 1972; 37: 193.
24. Fawcett JK, Scott JE. A rapid and precise method for the determination of urea. J Clin Pathol 1960; 13: 156-159. 25. Drury RAB, Wallington EA. Carleton’s histological technique. 5th ed. Oxford University Press, Oxford. 1980. 188-291.
26. Mazaia D, Brewer P, Alfert M. The cytochemical staining and measurement of protein with mercuric bromophenol blue. Biol Bull 1953; 104: 57-67.
27. McManus JF. Histological demonstration of mucin after periodic acid. Nature 1946; 158: 202.
28. Bailey RA. Association schemes: designed experiments, algebra and combinatorics. Cambridge Studies in Advanced Mathematics, 2004.
29. Azaizh H, Fulder S, Khalil K et al. Ethnobotanical knowledge of local Arab practitioners in the Middle Eastern region. Fitoterapia 2005; 74(1-2): 98-108.
30. Guimarães AG, Oliveira GF, Melo MS, et al. Bioassayguided evaluation of antioxidant and antinociceptive activities of carvacrol. Basic Clin Pharmacol Toxicol 2010; 107(6): 949-957.
31. Moreira JCF, Pasquali MAB, Rabie SMS et al. Antinociceptive activity and redox profile of the monoterpenes (+)-camphene, p-cymene, and geranyl acetate in experimental models. Toxicology 2013: 459530.
32. Coles B, Wilson I, Wardman P et al. The spontaneous and enzymatic reaction of N-acetyl-p-benzo quinonimine with glutathione: a stopped-flow kinetic study. Arch Biochem Biophys 1988; 264(1): 253-260.
33. Dumaswala UJ, Zhuo L, Mahajan S et al. Glutathione protects chemokine-scavenging and antioxidative defense functions in human RBCs. Am J Physiol Cell Physiol 2001; 280: C867-73.
34. Meister A. Metabolism and functions of glutathione. Trends Biochem Sci 1981; 6: 231-4.
35. Suhail M, Ahmad I. In vivo effects of acetaminophen on rat RBC and role of vitamin E. Indian J Exp Biol 1995; 33(4): 269-271.
36. O’Brien PJ, Slaughter MR, Swain A et al. Repeated acetaminophen dosing in rats: adaptation of hepatic antioxidant system. Hum Exp Toxicol 2000; 19(5): 277- 283.
37. Gillette JR. An integrated approach to the study of chemically reactive metabolites of acetaminophen. Arch Intern Med 1981; 141(3): 375-379.
38. Adetoro KO, Bolanle JD, Abdullahi SB et al. In vivo antioxidant effect of aqueous root bark, stem bark and leaves extract of Vitexdoniana in CCl4 induced liver damage rats. Asian Pac J Trop Biomed 2013; 3: 395-400.
39. Yakubu N, Oboh G, Olalekan AA. Antioxidant and hepatoprotective properties of tofu (curdle soymilk) against acetaminophen-induced liver damage in rats. Biotechnol Res Int 2013; 1: 1-7.
40. Sai K, Takagi A, Umemura T et al. Changes of 8-hydroxydeoxyguanosine levels in rat organ DNA during the aging process. J Environ Pathol Toxicol Oncol 1992; 11: 139-114.
41. Pratibha K, Anand U, Agarwal R. Serum adenosine deaminase, 5? nucleotidase and malondialdehyde in acute infective hepatitis. Indian J Clin Biochem 2004; 19(2): 128-131.
42. Guta AK, Misra N. Hepatoprotective activity of aqueous ethanolic extract of chammomile capitula in paracetamol intoxicated albino rats. J Pharmcial Toxical 2010; 1: 17-20.
43. Ravikumar S, Gnanadesigan M, Seshserebiah J et al. Hepatoprotective effect of an Indian salt marsh herb Suaedamonoica Forsk. Ex. Gmel against concanavalin: an induced toxicity in rats. Life Sci Med Res 2010; 2: 1.
44. Da Roch AB, Lopes RM, Schwartsmann G. Natural products in anticancer therapy. Curr Opin Cancer 2001; 1: 364-369.
45. Bents KOR. Commonly used herbal medicines in the united states: a review. Am J Med 2004; 116: 478-485.
46. Ashafa AO, Sunmonu TO, Afolayan AJ. Toxicological evaluation of aqueous leaf and berry extracts of Phytolaccadioical in male Wistar rats. Food Chem Toxicol 2010; 48: 1886-1889.
47. Sureshkumar SV, Mishra SH. Hepatoprotective activity of extracts from Pergulariadaemia Forsk against carbon tetrachloride induced toxicity in rats. Pharmaocogn Mag 2007; 3: 187-191.
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