Phytochemical and biological investigation of the extracts of Nigella sativa L. seed waste
dc.Affiliation | October University for modern sciences and Arts (MSA) | |
dc.contributor.author | Ezzat, Shahira M | |
dc.contributor.author | G. Miche, Camilia | |
dc.contributor.author | S. El-Dine, Nesrine | |
dc.contributor.author | M. Fahmy, Sherifa | |
dc.contributor.author | I. Nesseem, Demiana | |
dc.contributor.author | S. El-Alfy, Taha | |
dc.date.accessioned | 2019-10-29T07:27:17Z | |
dc.date.available | 2019-10-29T07:27:17Z | |
dc.date.issued | 2011 | |
dc.description | MSA Google Scholar | |
dc.description.abstract | Different extracts of Nigella sativa L. seed waste; aqueous (AE) 200 mg/kg, ethanol 70% (EE) 250 mg/kg and hexane (HE) 10 mg/kg, were evaluated for their hepatoprotective activities. They were administered orally, once daily, for 5 consecutive days. On day 5, liver injury was induced in animals by a single i.p. injection of carbon tetrachloride (10 mg/kg b. w. of 0.25% (v/v). Hepatoxicity produced, was evaluated by both biochemical and histopathological investigations. The aqueous extract attenuated the CCl4-induced liver damage likely due to the decrease of proinflammatory cytokines and T-cell proliferation. This was noticed by a significant decreasein both serum and tissue cytokines; tumor necrosis factor-alpha (TNF-α),interferon-gamma (INF-γ ) and interlukin-beta (IL-1β), in themarkers of liver functions; bilirubin and glutamic pyruvic transaminase (GPT) and in the oxidative stress markers; malondialdehyde (MDA) and glutathione content (GSH). Fractionated of this extract was performed and its component, protein, saponin, and polyphenol fractions were evaluated by appropriate analytical procedures. The crude protein of the seed waste reached 36.85% while protein fingerprint showed four bands ranging from 91.97 KD and 29.00 KD. The saponin content was evaluated through the determination of the haemolytic index and reached 15.56 mg/g dry powder. Finally, Folin Ciocalteu method was used for the determination of the total polyphenols. The same biochemical and histopathological studies were again performed on the different fractions of the aqueous extract; protein fraction (PF) 10 mg/kg, saponin fraction (SF) 5 mg/kg and polyphenol fraction (FF) 10 mg/kg. The biochemical changes were improved only by the protein fraction (PF) of the seed waste of Nigella sativa. This was manifested by a significant reduction in both serum and tissue cytokines in the liver markers and in the oxidative stress markers. Moreover, liver histopathology showed that (PF) reduced the incidence of liver lesions including hepatic cells cloudy swelling, lymphocytes infiltration, hepatic necrosis and fibrous connective tissue proliferation induced by CCl4 in mice. From this study, it is concluded that the protein fraction of the aqueous extract of Nigella sativa seed waste exhibited a promising hepatoprotective effect in the management of different liver disorders. Copyright c 2010 John Wiley & Sons, LtdDifferent extracts of Nigella sativa L. seed waste; aqueous (AE) 200 mg/kg, ethanol 70% (EE) 250 mg/kg and hexane (HE) 10 mg/kg, were evaluated for their hepatoprotective activities. They were administered orally, once daily, for 5 consecutive days. On day 5, liver injury was induced in animals by a single i.p. injection of carbon tetrachloride (10 mg/kg b. w. of 0.25% (v/v). Hepatoxicity produced, was evaluated by both biochemical and histopathological investigations. The aqueous extract attenuated the CCl4-induced liver damage likely due to the decrease of proinflammatory cytokines and T-cell proliferation. This was noticed by a significant decreasein both serum and tissue cytokines; tumor necrosis factor-alpha (TNF-α),interferon-gamma (INF-γ ) and interlukin-beta (IL-1β), in themarkers of liver functions; bilirubin and glutamic pyruvic transaminase (GPT) and in the oxidative stress markers; malondialdehyde (MDA) and glutathione content (GSH). Fractionated of this extract was performed and its component, protein, saponin, and polyphenol fractions were evaluated by appropriate analytical procedures. The crude protein of the seed waste reached 36.85% while protein fingerprint showed four bands ranging from 91.97 KD and 29.00 KD. The saponin content was evaluated through the determination of the haemolytic index and reached 15.56 mg/g dry powder. Finally, Folin Ciocalteu method was used for the determination of the total polyphenols. The same biochemical and histopathological studies were again performed on the different fractions of the aqueous extract; protein fraction (PF) 10 mg/kg, saponin fraction (SF) 5 mg/kg and polyphenol fraction (FF) 10 mg/kg. The biochemical changes were improved only by the protein fraction (PF) of the seed waste of Nigella sativa. This was manifested by a significant reduction in both serum and tissue cytokines in the liver markers and in the oxidative stress markers. Moreover, liver histopathology showed that (PF) reduced the incidence of liver lesions including hepatic cells cloudy swelling, lymphocytes infiltration, hepatic necrosis and fibrous connective tissue proliferation induced by CCl4 in mice. From this study, it is concluded that the protein fraction of the aqueous extract of Nigella sativa seed waste exhibited a promising hepatoprotective effect in the management of different liver disorders. Copyright c 2010 John Wiley & Sons, Ltd | en_US |
dc.description.sponsorship | John Wiley & Sons, Ltd. | en_US |
dc.description.uri | https://www.scimagojr.com/journalsearch.php?q=19700174958&tip=sid&clean=0 | |
dc.identifier.citation | [1] B. H. Ali, G. Blunden. Pharmacological and toxicological properties of Nigella sativa. Phytother. Res. 2003, 17, 299. [2] M. L. Salem. Immunomodulatory and therapeutic properties of the Nigella sativa L. seed. Int. Immunopharmacol. 2005, 5, 1749. [3] B. Salih, T. Sipahi, E. O. Donmez. Ancient Nigella seeds from Boyali Hoyuk in North-Central Turkey. J. Ethnopharmacol. 2009, 124, 416. [4] M. A. U. Khan, M. K. Ashfaq, H. S. Zuberi, M. S. Mahmoud, A. H. Gilani. The in-vivo antifungal activity of the aqueous extract from Nigella sativa. Phytother. Res. 2003, 17, 183. [5] T. S. El-Alfy, H. M. El-Fatatry, M. A. Toama. Isolation and Structure Assignment of an Antimicrobial Principle from the Volatile Oil of Nigella sativa L. Seeds. Pharmazie 1975, 30, H2. [6] H. Daba, M. S. Abdel-Rehem. Hepatoprotective activity of thymoquinone in isolated rat hepatocytes. Toxicol. Lett. 1998, 16, 23. [7] M. Ismail, G. Al-Naqeep, K. Wer Chan. Nigella sativa thymoquinonerich fraction greatly improves plasma antioxidant capacity and expression of antioxidant genes in hypercholestermic rats. Free Radical Bio. Med. 2010, 48, 664. [8] S. M. K. Swamy, B. K. H. Tan. Cytotoxic and immunopotentiating effect of ethanolic extract of N. sativa L. seeds. J. Ethnopharmacol. 2000, 70, 1. [9] R. Chopra, S. L. Nayar, I. C. Chopra. Glossary of Indian medicinal plants. Council of Science Industry Research: New Delhi, 1986. [10] P. J. Houghton, R. Zarka, H. B. Delas, J. R. S. Hoult. Fixed oil of Nigella sativa and derived thymoquinone lipid peroxidation. Planta Med. 1995, 61, 33. [11] S. Gallagher, J. A. Smith. In Molecular Biology (Ed: F. Ausubel), Green Pub. and Wiley, Interscience: New York, USA, 1995. [12] C. M. Wilson. Staining of proteins on gels: comparison of dyes and procedures. Method Enzymol. 1983, 91, 236. [13] Y. Birk. Saponins. In Toxic constituents of foodstuffs (Ed: I. E. Liener). Academic Press: New York, 1969, pp. 169–210. [14] R. D. Reichert, J. T. Tatarynovich, R. T. Tyler. Abrasive dehulling of quinoa (Chenopodium quinoa): effect on saponin content as determined by an adopted haemolytic assay. Cereal Chem. 1986, 63, 471. [15] L. C. Miller, M, L, Tainter. An evaluation of toxicity of Taxus baccata Linn. (Talispatra) in experimental animals. P. Soc. Exp. Biol. Med. 1944, 57, 261. [16] M. Uchiyama, M. Mihara. Determination of malondialdehyde precursor in tissues by thiobarbituric acid test. Anal. Biochem. 1978, 86, 271. [17] J. F. Koster, P. Biemond, A. J. G. Swaak. Intracellular and extracellular sulphydryl levels in rheumatoid arthritis. Ann. Rheum. Dis. 1986, 45, 44. [18] A. E. Ahmed, G. L. Hussein, J. Loh, S. Z. Abdel-Rahman. Studies on the mechanism of haloacetonitrile-induced gastrointestinal toxicity: interaction of dibromoacetonitrile with glutathione and glutathione-S-transferase in rats. J. Biochem. Toxicol. 1996, 6, 115. [19] S. Reitman, S. A. Frankel. Colorimetricmethodfor the determination of serum glutamic oxalacetic and glutamic pyruvic transaminases. Am. J. Clin. Pathol. 1957, 28, 56. [20] L. Jendrassik, P. Grof. Spectrophotometric method for the estimation of blood bilirubins. Biochem. Z. 1938, 297, 81. [21] K. Peach, M. V. Tracy. Modern Methods of Plant Analysis, Springer Verlag: Berlin, Gottingen, Heidelberg, 1995. [22] H. Wagner, S. Baldt, Plant Drug Analysis, 2nd Edition, Springer Verlag: Berlin, Heidelberg, New York, 2001. [23] S. Kumazawa, M. Taniguchi, Y. Suzuki, M. Shimura, M. S. Kwan, T. Nakayama. Antioxidant Activity of Polyphenols in Carob pods. J. Agric. Food Chem. 2002, 50, 373. [24] H. Stegemann. In Biology and taxonomy of the Solonaceae (Eds: J. G. Hawkes, R. N. Lester, A. D. Skelding), Academic Press: London, 1979, p. 229. [25] J. B. Harborne, B. L. Turner. PlantChemosystematics, Academic Press: New York, 1984. [26] P. Chauhan, C. Ram, A. Mann, V. Sangwan. Molecular weight analysis of seed proteins of forage sorghum (Sorghum bicolor (L.) Moench). Seed Sci. Technol. 2002, 30, 11. [27] M. Rashed, J. Al-Shaby, A. Atta, M. Sallam, K. Fahmy, S. Abdel Aziz. Assessment of genetic diversity for some Egyptian and Yamenian Sorghum cultivars (Sorghum bicolor L.) using different molecular genetic analysis, Proceedings of the Third International Conference of Biological Sciences (ICBS), 28–29 April 2004. [28] A. Badr, H. H. El-Shazly, M. Abou El-Enain. Seed protein diversity and its implication on the relationships in the genus Lathyrus L. (Fabaceae). Proceedings of the First International Conference of Biological Sciences (ICBS), Tanta University, Egypt, 27–28 April 2002. [29] S. Y. Gui, W. Wei, H. Wang, L. Wu, W. Y. Sun, C. Y. Wu. Protective effect of fufanghuangqiduogan against acute liver injury in mice. World J. Gastroentero. 2005, 11, 2984. [30] M. Lee, S. K. Lee, M. Son, S. W. Cho, S. Park H. I. Kim. Expression of Th1 and Th2 type cytokines responding to HBsAg and HBxAg in chronic hepatitis B patients. J. Korean Med. Sci. 1999, 14, 175. [31] N. Hyodo, M. Tajimi, T. Ugajin, I. Nakamura, M. Imawari. Frequencies of interferon-gamma and interleukin-1 secreting cells in peripheral blood mononuclear cells and liver infiltrating lymphocytes in chronic hepatitis B virus infection. Hepatol. Res. 2003, 27, 109. [32] J. Wang, S. A. Gujar, L. Cova, T. I. Michalak. Bicistronic woodchuck hepatitis virus core and gamma interferon DNA vaccine can protect from hepatitis but does not elicit sterilizing antiviral immunity. J. Virol. 2007, 81, 903. [33] K. L. W. Kovalovich, R. DeAngelis, L. E. Greenbaum, G. Ciliberto, R. Taub. Interleukin-6 protects against Fas-mediated death by establishing a critical level of anti-apoptotic hepatic proteins FLIP, Bcl-2, and Bcl-xL. J. Biol. Chem. 2001, 276, 26605. [34] T. Kondo, T. Suda, H. Fukuyama, M. Adachi, S. Nagata. Essential roles of the Fas ligand in the development of hepatitis. Nat. Med. 1997, 3, 409. [35] B. A. Mico,L. R. Pohl, Reductive oxygenation of carbon tetrachloride: trichloromethylperoxyl radical as a possible intermediate in the conversion of carbon tetrachloride to electrophilic chlorine, Arch. Biochem. Biophys. 1983, 225, 596. [36] T. Castillo, D. R. Koop, S. Kamimura, G. Triadafilopoulos, H. Tsukamoto. Role of cytochrome P-450 2E1 in ethanol-, carbon tetrachloride- and iron-dependent microsomal lipid peroxidation. Hepatology 1992, 16, 992. [37] H. Ishiyama, M. Sato, K. Matsumura, M. Sento, K. Ogino, T. Hobara. Proliferation of hepatocytes and attenuation from carbon tetrachloride hepatotoxicity by gadolinium chloride in rats. Pharmacol. Toxicol. 1995, 77, 293. [38] S. P. Srivastava, N. Q. Chen, J. L. Holtzman. The in vitro NADPH dependent inhibition by CCl4 of the ATP-dependent calcium uptake of hepatic microsomes from male rats. Studies on the mechanism of the inactivation of the hepatic microsomal calcium pump by the CCl 3 radical. J. Biol. Chem. 1990, 265, 8392. | en_US |
dc.identifier.doi | https://doi.org/10.1002/dta.225 | |
dc.identifier.other | https://doi.org/10.1002/dta.225 | |
dc.identifier.uri | https://cutt.ly/xtwhyia | |
dc.language.iso | en | en_US |
dc.publisher | John Wiley & Sons, Ltd | en_US |
dc.relation.ispartofseries | Drug Testing and Analysis;3, 4, 245-254 | |
dc.subject | Nigella sativa seed waste | en_US |
dc.subject | immunostimulant aqueous extract | en_US |
dc.title | Phytochemical and biological investigation of the extracts of Nigella sativa L. seed waste | en_US |
dc.type | Article | en_US |
Files
Original bundle
1 - 1 of 1
Loading...
- Name:
- avatar_scholar_256.png
- Size:
- 6.31 KB
- Format:
- Portable Network Graphics
- Description: