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Nutrients 2014, 6(6), 2376-2386; doi:10.3390/nu6062376
Abstract: We investigated the effect of extra virgin (EV) olive oil and genetically modified (GM) soybean on DNA, cytogenicity and some antioxidant enzymes in rodents. Forty adult male albino rats were used in this study and divided into four groups. The control group of rodents was fed basal ration only. The second group was given basal ration mixed with EV olive oil (30%). The third group was fed basal ration mixed with GM (15%), and the fourth group survived on a combination of EV olive oil, GM and the basal ration for 65 consecutive days. On day 65, blood samples were collected from each rat for antioxidant enzyme analysis. In the group fed on basal ration mixed with GM soyabean (15%), there was a significant increase in serum level of lipid peroxidation, while glutathione transferase decreased significantly. Interestingly, GM soyabean increased not only the percentage of micronucleated polychromatic erythrocytes (MPCE), but also the ratio of polychromatic erythrocytes to normochromatic erythrocytes (PEC/NEC); however, the amount of DNA and NCE were significantly decreased. Importantly, the combination of EV olive oil and GM soyabean significantly altered the tested parameters towards normal levels. This may suggest an important role for EV olive oil on rodents’ organs and warrants further investigation in humans.
Plant food represents a major source of nutrients for humans. As well as performing a protective role against chronic diseases such as coronary heart disease, diabetes mellitus and cancer ; plants are a good source of omega-3 fatty acids, they are rich in antioxidant vitamins (such as alphatocopherol, ascorbic acid and beta-carotene), glutathione, proteins and advantageously they can be grown in many environments including arid climates .
Extra virgin (EV) olive oil is a vegetable oil obtained from olive trees (oleaeuropaea); a traditional tree crop of the Mediterranean Basin. It has many applications including cooking, cosmetics, pharmaceutical preparations and soaps. Olive oil is considered a healthy product because of its constituents, which include oleic acid, palmitic acid and other fatty acids; in addition to traces of squalence and sterols. There is considerable data demonstrating that the consumption of olive oil is beneficial to cardiovascular health; specifically it has a favorable effect on cholesterol regulation and LDL cholesterol oxidation. It has also been shown to have anti-inflammatory, antithrombotic, antihypertensive and vasodilatory effects in both animals and humans .
Soyabean is considered to be one of the most important crops worldwide. It is generally considered to be a protein concentrate as this represents 42% of its make up . Industrially, it is an essential food component for humans and for a wide range of animals .
Ram et al.  found that soyabean contains large amounts of protein and fiber, while Li et al.  reported hypersensitivity type reactions in weaned pigs and in some cases death when fed soyabean meal only. Importantly, Fatma  reported an increased percentage of death and fetal abnormalities associated with soybean consumption in rats. Furthermore, genetically modified (GM) soya bean may also induce damage to DNA in rats, resulting in an acute hepatitis picture that resembles human viral hepatitis [8,9].
The primary aim of this study was to elucidate any potential hepato-protective role that may be performed by natural products such as GM soyabean and whole EV olive oil. To accomplish this we examined their anti-oxidative effects, both individually and in combination, by investigating their effects on damage to DNA in rats. Interestingly, we found a possible protective role when animals are fed with a mixture of EV olive oil and GM soya bean and we believe this outcome represents an important opportunity to examine the potential benefits of these valuable natural products further.
2. Material and Methods
Forty adult white albino rats (Sprague Dawley strain) with an average weight of (150 to 180 g), were used in this study. They were obtained from the laboratory animal house of the ophthalmic research institute, Giza, Egypt. The rats were acclimatised to laboratory condition before the experiment began. They were fed according to the experimental design detailed later in the manuscript and supply was given ad-libitum. All experiments were conducted according to the University’s ethical protocols.
2.2. Plant Material
Soyabean: Soyabean grind was purchased from a local market in Cairo, Egypt. It was freshly prepared and mixed with basal ration for rats, at a concentration of 15% .
Extra virgin olive oil: was purchased from a local market in Cairo, Egypt. It was freshly prepared and mixed with basal ration for rats, at concentration of 30% . The chemical composition of these is detailed in Table 1.
|Group 1||The negative control group was fed basal ration diet only.|
|Group 2||Fed basal ration diet mixed with EV olive oil (30%).|
|Group 3||Fed basal diet mixed with GM soyabean (15%).|
|Group 4||Fed basal diet mixed with EV olive oil (30%) and GM soyabean (15%).|
2.3. Experimental Design
Forty adult rats were divided into four groups of ten. The experiment was conducted over 65 consecutive days. The feeding structure for each group is detailed in Table 1.
2.4.1. Serum Samples
Blood samples were obtained from each animal group from their orbital plexuses and received into a clean, dry tube. Samples were left to clot at room temperature for 2 h, stored overnight in a refrigerator at 4 °C and centrifuged at 3000 revolutions per minute (rpm) for 15 min. Serum samples were then drawn in clean, dry capped bottles and kept in deep freeze at 4 °C for antioxidant enzyme studies. (The animals were fasted for 12 h prior to the sacrificing).
2.4.2. Antioxidant Enzymes Estimation
2.4.3. Determination of DNA
The isolation of DNA from spleen of rats was performed according to the following protocol: first, the tissue was homogenized in isotonic saline buffered with sodium citrate (pH 7.0); protein was then removed by treatment with a chloroform/amyl alcohol mixture and the DNA precipitated with ethanol according to protocols established by Schwander et al. . Estimation of isolated DNA was carried out using diphenylamine reagent and read at 595 nm on spectrophotometer according to the method described by Dische et al. .
The micronucleus test was performed to detect chromosomal damage associated with treatment. Micronuclei were identified as dark blue staining bodies in the cytoplasm of the polychromatic erythrocytes (PCEs) according to the protocol mentioned by Salamon et al. . The polychromatic erythrocytes (PCEs, 1000/animal) were screened for micronuclei and the changes in the mitotic activity were assessed on the basis of the ratio of polychromatic to normochromatic erythrocytes (PCE/NCE ratio) [17,18].
2.5. Statistical Analysis
This study was carried out to investigate the effects of EV olive oil and GM soybean on DNA cytogenicity, as well as looking into its antioxidant role. To address these questions male albino rats were fed one concentration of each plant alone, or combined, for 65 days. We examined the antioxidant enzymes analyses and investigated in order to determine the DNA damage in the spleens and its cytogenicity, in rats.
Diet effects on antioxidant enzymes: Feeding on ration mixed with GM soyabean at concentration 15% caused significant increase in serum level of lipid peroxidation, while the level of glutathione dehydrogenase was significantly reduced (Table 2).
Ration mixed with EV olive oil and GM soyabean significantly altered the serum level of antioxidant enzymes. This change was in the direction of the normal value when compared with the group fed on soyabean only (Table 3).
|EV Olive oil|
|Vitamin E||14 mg|
|Group||Conc.||Lipid peroxidation mmol/L||Glutathione transferase mg/mL|
|Control -ve (negative)||-||4.379 ± 0.156 a, c||14.7 ± 0.78 a, c|
|GM soyabean||15%||5.04 ± 0.128 a||12.846 ± 0.115 a|
|EV olive oil||30%||4.398 ± 0.132 a, c||14.604 ± 0.44 a, c|
|GM soyabean + EV olive oil||15% + 30%||4.64 ± 0.35 a, c||13.546 ± 0.115 a, c|
Diet effects on DNA: Maintaining rats on EV olive oil at concentration 30% for 65 days revealed a significant increase in the amount of DNA (ng/g of spleen) when compared with the control group. The amount of DNA (ng/g of spleen) significantly decreased when feeding rats GM soyabean (15%), while it increased significantly in rats fed EV olive oil (30%) and GM soyabean (15%) (Table 4).
|Control -ve||-||0.35 ± 0.04 a|
|GM soyabean||15%||11.57 ± 0.58 d|
|EV olive oil||30%||4.10 ± 0.22 b|
|GM soyabean + EV olive oil||15% + 30%||5.74 ± 0.23 c|
Diet effects on cytogenicity: Feeding rats GM soyabean only caused a significant increase in micronucleated polychromatic erythrocytes (MPCEs) and the ratio of polychromatic to normochromatic erythrocytes (PCE/NCE). However, maintaining rats on ration mixed with EV olive oil and GM soyabean, instigated significant decrease of MPCEs and the ratio of PCE/NCE, though normochromatic erythrocytes (NCE) increased significantly when compared to the group fed soyabean only (Table 5).
|Control -ve||-||5000||5.60 ± 0.26 a||2183 ± 31.89 g||2.33 ± 0.4 a|
|GM soyabean||15%||5000||4.45 ± 0.79 a||1419 ± 36.05 d||2.57 ± 0.22 a|
|EV olive oil||30%||5000||9.11 ± 0.09 d||829.5 ± 32.17 a||6.18 ± 0.32 d|
|GM soyabean + EV olive oil||15% + 30%||5000||8.00 ± 0.6 c||1071 ± 19.76 c||4.83 ± 0.3c|
EV olive oil is known to have a wide variety of benefits on many different body systems. This study was carried out to examine the effects of EV olive and G.M. soybean oil on DNA, as well as serum antioxidant enzymes.
In our study, rats were fed EV olive oil, GM soya bean, or a combination of the two, at concentrations (30%) or (15%). The study was conducted over 65 consecutive days.
We report a significant decrease in the level of lipid peroxidation and a significant increase in the level of glutathione dehydrogenase, when comparing the EV olive oil and GM soyabean combined group with GM soyabean fed animals only. These results may be attributed to the presence of antioxidants in EV olive oil, which has shown a number of positive effects on liver regeneration [21,22,23].
Our data illustrates that the group of rats fed a mixed ration with EV olive oil for 65 successive days, showed a significant increase in the amount of DNA ng/g of spleen, when compared with the group maintained on soyabean alone.
On the other hand, tests on the rats fed GM soyabean alone revealed a significant decrease in the amount of DNA ng/g of spleen; while the group that was fed a mixed ration of EV olive oil and GM soyabean showed a significant increase in the amount of DNA ng/g of spleen; with these changes in parameters appearing to fall into the normal ranges.
The mechanism for the decrease in the amount of DNA was discussed by Zhou et al.  who reported on hepatocellular degeneration, necrosis, DNA damage and the lesions of the extracellular matrix induced by CCl4. Moreover, Morishita et al. , Amel et al.  and Vanitha et al.  showed that CCl4 could cause liver toxicity due to DNA strand breaks in hepatocytes.
Our results are in agreement with Salvini et al. , Jacomclli et al.  and Quiles et al.  who reported that a diet enriched with olive oil phenolic compound has a protective effect against DNA damage. This is in line with Fabiani et al.  who stated that olive phenolic compounds showed DNA oxidative preventive activity.
Fabiani et al.  suggested that EV olive oil has a protective activity against cancer cells. He described how cell proliferation can become arrested during the cell cycle phases with a role for apoptosis in tumor cells and hydroxytyrosol also being demonstrated. This may suggest that EV olive oil does have some anticancer properties. In this regard Salvini et al.  reported a reduction of DNA damage caused by consumption of an EV olive oil rich in phenols, particularly hydroxytyrosol. Interestingly, Machowetz et al.  and Fabiani et al.  described that high consumption of olive oil in the Mediterranean diet protected DNA against oxidative damage and reduced cancer incidence.
The mechanism for the increase in DNA was explained by Lopez et al.  who illustrated that minor compounds from EV olive oil (mainly phenolics) were antioxidants, and that these performed a radical scavenging role. These minimized the amount of reactive oxygen species generated by fatty acidperoxidation; hence the DNA damage can be reduced with a lower lipid peroxidation.
Jeffery , Jee-Youn et al. , Aiad , Khataibeh et al.  and Tudisco et al.  showed that a GM soya bean diet could lead to liver and/or DNA damage in rats. Our investigation revealed that feeding rats on ration mixed with EV olive oil showed significant increase in normochromatic erythrocytes (NCE). On the other hand, ratio of polychromatic to normochromatic erythrocytes (PCE/NCE) did not induce changes compared to the control group.
Sekene et al.  concluded that the protective effect of EV olive oil and sage against acrylamide mutagenicity may be due to the inclusion of antioxidant compounds and may be useful when added as a food additive when cooking at higher temperatures.
Rats fed a mixed ration with GM soybean showed a significant increase in MPCEs and in the ratio of PCE/NCE; while a significant decrease in NCE was observed. Feeding EV olive oil in combination with GM soyabean to rats, instigated a significant decrease in MPCEs and in the ratio of PCE/NCE and this helped to normalise their values. Suzuki et al.  described that a significant increase in PCE/NCE ratio and enhancement of mitotic activity of bone marrow cells could be considered as a sign of toxicity and/or damage of some organs of the body.
Hanan et al.  reported that the administration of soyabean extract resulted in a dose and time related increase in some blood biochemical parameters and in particular an increase in the percentage of MPECs and the ratio of PCE/NCE.
The mechanism of reducing MPCEs and the ratio of PCE/NCE were explained by Tang et al.  who concluded the oleanolic acid has protective effects on liver mitochondria and the mechanisms underlying its protection may be related to its inhibition to the Ca2+ induced mitochondrial swelling, mitochondrial membrane depolarization and intra-mitochondrial Ca2+ release on mitochondrial permeability transition (MPT). Moreover Sivikova et al.  described that an insufficient confirmation of the genitoxicity of CCl4 and the protective effect of the antioxidants, respectively were seen in cultures with metabolic activation.
We can conclude that adding EV olive oil to the diet of rats appears effective in inhibiting oxidative damage and may act as a protective agent against chronic diseases such as liver fibrosis, hyperlipidemia and diabetes. In addition, EV olive oil may also have a protective function against carcinogenic processes. Further clinical studies are therefore required to determine whether the observations observed in our study translate to human conditions and illnesses.
This Project was funded by Deanship of Scientific Research (DSR), King Abdulaziz University, Jeddah, under grant no (13-34-RG). The authors, therefore, acknowledge with thanks DSR technical and financial support.
Thanaa A. El-Kholy, Hatim Ali Al-Abbadi Abdulhalim Salim Serafi, Ahmad K. Al-Ghamdi and Hanan M. Sobhy, experimental design, implementation and initial write up. Mohammad Abu Hilal and John R. C. Richardson write up.
Conflicts of Interest
The authors declare no conflict of interest.
- Henkel, J. Soy: Health claims for soy protein, questions about other components. FDA Consum.; 2000; 34, pp. 13–15, 18–20. [Google Scholar]
- Simopoulos, A.P. The Mediterranean diets: What is so special about the diet of Greece? The Scientific Evidence. J. Nutr. 2001, 131, 3065S–3073S. [Google Scholar]
- Covas, M.I. Olive oil and cardiovascular system. Pharmacol. Res. 2007, 55, 175–186. [Google Scholar] [CrossRef]
- Raj, P.; Stuffed, S. From Farm to Fork the Hidden Battle for the World Food System; Portabello Books LTD: London, UK, 2008; pp. 169–173. [Google Scholar]
- Ram, J.; Sibgh Randall, L.; Nelson, A.; Gyuhwa, G. Genetic resources chromosome engineering and crop improvement. Am. J. Bot. 2006, 3, 15. [Google Scholar]
- Li, D.F.; Nelssen, J.L.; Reddy, P.G.; Blecha, F.; Hancock, J.D.; Allee, G.L.; Goodband, R.D.; Klemm, R.D. Transient hypersensitivity to soybean meal in the early-weaned pig. J. Anim. Sci. 1990, 68, 1790–1799. [Google Scholar]
- Fatma, A.E.H. Effect of Soyabean and Some Products on Fetal Development and Biochemical Analysis in Rats. Master’s Thesis, Faculty of Home Economic, Al-Azhar University, Cairo, Egypt, 2011. [Google Scholar]
- Beddowes, E.J.; Faux, S.P.; Chipman, J.K. Chloroform, carbon tetrachloride and glutathione depletion induce secondary genotoxicity in liver cells via oxidative stress. Toxicology 2003, 187, 101–115. [Google Scholar] [CrossRef]
- Vanitha, A.; Murthy, K.N.; Kumar, V.; Sakthivelu, G.; Veigas, J.M.; Saibaba, P.; Ravishanker, G.A. Effect of the toxicity in rats. Int. J. Toxicol. 2007, 26, 159–167. [Google Scholar] [CrossRef]
- Olusola, A.A.; Emmannuel, O.S.; Ibidun, J.O.; Waaheed, A.S.; Gbaded, E.A.; Olasupo, S.A. Effects of soyabeans supplements on fertility in male wister rats. Maced. J. Med. Sci. 2001, 4, 54059. [Google Scholar]
- Nabila, Y.M. Nutritional Effect of Olive Oil and Barley on DNA Damage and Cytogenicity in Rats. Ph.D. Thesis, Faculty of Howe Economics, Al-Azhar University, Cairo, Egypt, 2008. [Google Scholar]
- Ohkawa, H.; Ohishi, W.; Yagi, K. Assay for lipid peroxides in animal tissues by thiobarbitutric acid reaction. Anal. Biochem. 1979, 95, 351. [Google Scholar] [CrossRef]
- Habig, W.H.; Pabst, M.J. Glutathion-S-transferees the first enzymatic step in mercapturic acid formation. Biol. Chem. 1974, 249, 7130–7139. [Google Scholar]
- Schwander, H.; Singer, R. Extraction of DNA with strong salt solution. Helv. Clin. Acta 1950, 33, 1521. [Google Scholar] [CrossRef]
- Dische, Z.; Schwarz, U.K. Mikromethode zur Bestimmung verschiedener Pentosen nebeneinander bei Gegenwart von Hexosen. Microchim. Acta 1973, 2, 13–19. (in German). [Google Scholar] [CrossRef]
- Salamon, M.; Hedddle, J.; Stuart, E.; Katz, M. Towards an improved micronucleus test. Studies on 3 model agents, mitomycinc, cycolophosphamed and dimethyl benzanthracene. Mutat. Res. 1980, 74, 347–356. [Google Scholar]
- Hart, J.W.; Engberg-Pederson, H. Statistics of the mouse bone marrow micronucleus test country distribution and evaluation of results. Mutat. Res. 1983, 111, 195–207. [Google Scholar]
- Al-Bekairi, A.M.; Qureshi, S.; Chaudhry, M.A.; Shah, A.H. Uric acid as an inhibitor of cyclophosphamide-induced micronuclei in mice. Mutat. Res. 1991, 262, 115–118. [Google Scholar]
- Duncan, D.B. Multiple range test and multiple F tests. Biometrics 1955, 1191, 1–42. [Google Scholar]
- Spss 14: “Statistical Package for Social Science. SPSS for Windows Release 188.8.131.52 June, 2006”; SPSS Inc.: Chicago, IL, USA.
- Syed, H.O. Oleuropein in olive oil and its pharmacological effects. Sci. Pharm. 2010, 78, 133–154. [Google Scholar] [CrossRef]
- Qing, L.; Huiyuan, Y. Antioxidant activities of olive oil. Food Chem. 2007, 102, 732–737. [Google Scholar] [CrossRef]
- Amel, N.; Wafa, T.; Abir, G.; Manel, I.; Samia, D.; Issam, G.; Meriem, E.; Abdelhed, M.; Mohamed, H. Effect of olive oil and its fraction oxidative stress and the livers fatty acid composition in 2,4-dichlorophenoxyaccetic treated rats. Nutr. Metab. 2010, 7, 80. [Google Scholar] [CrossRef]
- Ok, E.; Yilmaz, Z.; Karaküçük, I.; Akgü, H.; Sahin, H. Use of olive oil based emulsions as an alternative to soybean oil based emulsions in total parenteral nutrition and their effects on liver regeneration following hepatic resection in rats. Ann. Nutr. Metab. 2003, 47, 221–227. [Google Scholar] [CrossRef]
- Tibor, J.; Gabriella, S.; Krisztina, R.; Otto, V.; Emill, P. Comparative study of frost tolerance and antioxidant activity in cereals. Plant Sci. 2003, 164, 301–306. [Google Scholar] [CrossRef]
- Cano, N.J.; Saingera, Y.; Dupuy, A.M.; Loree, M.; Penet, A.M.; Portugal, H.; Leverve, X.M. Intradialytic parenteral nutrition: Comparison of olive oil verussoyabean oil based lipid emulsions. Br. J. Nutr. 2006, 95, 152–159. [Google Scholar]
- Zhou, J.; Zhou, J.; Zhong, X.; Chen, L.; Yang, X. Abnormal expressions of hepatocellular proteins and extra cellular matrix in CCl4-induced liver injury in rats. Chin. Med. J. 1996, 109, 366–371. [Google Scholar]
- Morrishita, K.; Mizukawa, Y.; Kasahara, T.; Okuyama, M.; Takashima, K.; Toritsuka, N.; Miyagishima, T.; Nagao, T.; Urushidani, T. Gene expression profile in liver of differing ages of rats after single oral administration of acetaminophen. J. Toxicol. Sci. 2006, 31, 491–507. [Google Scholar] [CrossRef]
- Salvini, S.; Sera, F.; Caruso, D.; Giovannelli, L.; Visioli, F.; Saieva, C.; Masal, G.; Ceroti, M.; Giovacchini, V.; Pitozzi, V.; et al. Daily consumption of a high-phenol extra-virgin olive oil reduces oxidative DNA damage in postmenopausal women. Br. J. Nutr. 2006, 95, 742–751. [Google Scholar] [CrossRef]
- Jacomelli, M.; Pitozzi, V.; Zaid, M.; Larrosa, M.; Tonini, M.; Martini, A.; Urbani, S.; Taticchi, A.; Servili, M.; Dolara, P.; et al. Dietary extra-virgin olive oil rich in phenolic antioxidants and the aging process: Long-term effects in the rat. J. Nutr. Biochem. 2010, 21, 290–296. [Google Scholar] [CrossRef]
- Quiles, J.L.; Farquharson, A.J.; Simpson, D.K.; Gran, I.; Wahle, K.W. Olive oilphenolics: Effects on DNA oxidation and redox enzyme mRNA in prostate cell. Br. J. Nutr. 2002, 88, 225–234. [Google Scholar] [CrossRef]
- Fabiani, R.; Rosignoli, P.; DeBartolomeo, A.; Fuccell, R.; Servilli, M.; Montedoro, G.F.; Morozzi, G. Oxidative DNA damage is prevented by extracts of olive oil, hydroxylyrosol and other olive phenoliccompoundss in human blood mononuclear cells and HL60 cells. J. Nutr. 2002, 138, 1411–1416. [Google Scholar]
- Machowetz, A.; Poulsen, H.E.; Gruendel, S.; Weimann, A.; Fito, M.; Marrugat, J.; Torre-dela, R.; Salonen, J.T.; Nyyssönen, K.; Mursu, J.; et al. Effect of olive oils on biomarkers of oxidative DNA stress in Northen and Southern Europeans. FASEB J. 2007, 21, 45–52. [Google Scholar]
- Lopez, S.; Pacheco, Y.M.; Bermudez, B.; Abia, R.; Munriana, F. Olive Oil and Cancer; Grasas-Y-Acertes: Sevilla, Spain, 2004; Volume 55, pp. 31–33. [Google Scholar]
- Jeffery, M. Smith Genetic Roulette: The Documented Health Riskes of Genetically Engineered Food; Yesl Book: Fairfield, IA, USA, 2007. [Google Scholar]
- Jee-Youn, S.; Yoo, J.K.; Hye-Sung, L. Effects of soyabeanisoflavones extract on the plasma lipid profiles and antioxidant enzyme activity in streptozotocin-induced diabetic rats. Nutr. Res. Pract. 2008, 2, 218–226. [Google Scholar] [CrossRef]
- Aiad, F.; El-Gamal, B.; Al-Meer, J.; El-Kerdasy, Z.; Zakhary, N.; El-Aaser, A. Protective effect of soyabean against hepatoprotocarcinogenesis induced by dl-ethionine. J. Biochem. Mol. Biol. 2004, 37, 370–375. [Google Scholar]
- Khataibeh, M.; Abu-alruz, K.; Al-widyan, O.; Abu-samak, M.; Al-Qudah, J. Combined supplementation of soy and garlic modulate biochemical parameters of 7,12-dimethylbenz (alpha) anthracene induced mammary cancer in female albino rats. Pak. J. Biol. Sci. 2007, 10, 2308–2313. [Google Scholar] [CrossRef]
- Tudisco, R.; Mastellone, V.; Cutrigelli, M.I.; Lombardi, P.; Bovera, F.; Mirabella, N.; Piccolo, G.; Calabro, S.; Avallone, L.; Infascelli, F. Fate of transgenic DNA and evaluation of metabolic effects in goats fed genetically modified soyabean and their offspring’s. Animal 2010, 4, 1662–1671. [Google Scholar] [CrossRef]
- Abd El-Aziem, S.H.; Abdel-Wahab, M.A.; Mahmoud, A.M.; Hassan, A.M.; Mahrous, K.F. Chemoprevention of olive oil and sage against acrylamide induced genotoxic, biochemical and histopathological alterations in rats. Egypt. J. Hosp. Med. 2004, 15, 40–56. [Google Scholar]
- Suzuki, H.; Hirrano, N.; Watanbe, C.; Tarumoto, Y. Carbon tetrachloride does not induced micronucleus in either mouse bone marrow or peripheral blood. Mutat. Res. 1997, 394, 1662–1671. [Google Scholar]
- Hanan, M.S.; Hanaa, A.O.; Gamal, E.S.; Gehan, J.S.; Gehan, A.H. Pharmacological, cytogenetic and pathological effect of longterm administration of soyabean extract in rats. Egypt. J. Comp. Pathol. Clin. Pathol. 1995, 8, 87–100. [Google Scholar]
- Tang, X.H.; Gao, J.; Fang, F.; Chen, J.; Xu, Z.; Zhao, N.; Xu, Q. Hepatoprotection of oleanolic acid is related to its inhibition on mitochondrial permeability transition. Am. J. Chin. Med. 2005, 33, 627–637. [Google Scholar] [CrossRef]
- Sivikova, K.; Piesova, E.; Dianovshy, J. The protection of vitamin E and selenium against carbon tetrachloride-induced genotoxicity in ovine peripheral blood lymphocytes. Mutat. Res. 2001, 494, 135–142. [Google Scholar] [CrossRef]
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