Skip to content

Advertisement

  • Research article
  • Open Access

Selected spices and their combination modulate hypercholesterolemia-induced oxidative stress in experimental rats

  • †1, 3,
  • †2,
  • †2 and
  • †1Email author
†Contributed equally
Biological Research201447:5

https://doi.org/10.1186/0717-6287-47-5

©  Otunola et al.; licensee BioMed Central Ltd. 2014

  • Received: 24 September 2013
  • Accepted: 9 December 2013
  • Published:

Abstract

Background

Effect of aqueous extracts of Allium sativum (garlic), Zingiber officinale (ginger), Capsicum fructensces (cayenne pepper) and their mixture on oxidative stress in rats fed high Cholesterol/high fat diet was investigated. Rats were randomly distributed into six groups (n = 6) and given different dietary/spice treatments. Group 1 standard rat chow (control), group 2, hypercholesterolemic diet plus water, and groups 3, 4, 5, 6, hypercholesterolemic diet with 0.5 ml 200 mg · kg-1 aqueous extracts of garlic, ginger, cayenne pepper or their mixture respectively daily for 4 weeks.

Results

Pronounced oxidative stress in the hypercholesterolemic rats evidenced by significant (p < 0.05) increase in MDA levels, and suppression of the antioxidant enzymes system in rat’s liver, kidney, heart and brain tissues was observed. Extracts of spices singly or combined administered at 200 mg.kg-1 body weight significantly (p < 0.05) reduced MDA levels and restored activities of antioxidant enzymes.

Conclusions

It is concluded that consumption of garlic, ginger, pepper, or their mixture may help to modulate oxidative stress caused by hypercholesterolemia in rats.

Keywords

  • Lipid peroxidation
  • Oxidative stress
  • Spices
  • Hypercholesterolemia
  • ROS

Backgroud

Hypercholesterolemia is a lipoprotein metabolic disorder characterized by high serum levels of low density lipoprotein (LDL-C) and blood cholesterol. Alteration in cholesterol and triglycerides metabolism as a result of hypercholesterolemia has been shown to negatively affect oxidative stress biomarkers and promotes production of reactive oxygen species (ROS) by various mechanisms, that leads to increased lipid peroxidation [1].

Oxidative stress is derivate from an imbalance between the generation of ROS and the endogenous antioxidant systems so that the latter is overwhelmed [2]. It has been reported to lead to increased lipid peroxidation, which in turn is involved in the aetiology of several chronic diseases [3]. The significant role of ROS in the pathogenesis of certain human diseases such as cardiovascular disease, cancer, arthritis and post-ischemic re-oxygenation injury is increasingly being recognized [4]. ROS are highly reactive molecules derived from normal essential metabolic processes in the human body. They could also come from external sources such as exposure to X-rays, ozone, cigarette smoking, alcohol and industrial chemicals [5].

According to several reports, controlling ROS is believed to be more effective in preventing cardiovascular diseases with more potential for success than restrictive fat and cholesterol diets [6–9]. The significant role of ROS in the induction of oxidative damage to biomolecules is increasingly being reported [4, 10]. Oxidative damage of cell membranes, DNA, and proteins induced by ROS has been implicated in the aetiology of several degenerative diseases like aging, cancer and cardiovascular diseases [11].

There is a growing interest in the mechanism of antioxidants in relation to damage caused by aggressive oxygen species and thiyl radicals. The main work of antioxidants seems to be scavenging these ROS and converting them to inactive substances [12]. Antioxidants are therefore crucial to the body’s multilevel defense against free radicals. Lines of defense include enzymes (glutathione reductase, glutathione peroxidase, catalase, superoxide dismutase), vitamins (C, E and carotenoids), polyphenolics and other bioactive compounds, [13–15].

Spices are reported to contain natural chemicals like vitamins, phytonutrients, mineral elements, alkaloids, flavonoids, terpenoids and sesquisterpenes, [16]. These chemicals confer on spices, excellent antioxidant properties that help to neutralize free radicals in the body and prevent lipid peroxidation and mutation of DNA and healthy cells into cancerous cells, [17].

Garlic (Allium sativum), ginger (Zingiber officinale) and cayenne pepper (Capsicum fructensces) are common culinary spices that have been reported to possess antioxidant properties. The prophylactic and therapeutic effects of dietary garlic, ginger and pepper in reducing the risks of cardiovascular diseases, atherosclerosis, bacterial infections, inflammation, as well as vasodilator, anti-diabetic, anti-ulcer and hypocholesterolemic agents amongst others have been reviewed [16, 18–21]. These spices are either used singly or combined in most cuisines all over the world. It is believed that when multiple antioxidants are used in combination, they prevent vulnerability to other agents and synergistically pool their antioxidant properties.

This study was therefore undertaken to assess the individual and combined additive or synergistic effects of the three spices- garlic, ginger and pepper on oxidative injury caused by dietary hypercholesterolemia in order to establish if combining the three will be more effective therapeutically using rat models.

Results and discussion

In this study, control rats fed normal diet were used as the reference point for each variable measured. Lipid peroxidation in the cardiac, hepatic, renal and brain tissues are presented in Figure 1. There was pronounced oxidative stress in the hypercholesterolemic rats as evidenced by significant (p < 0.05) increase in MDA levels in the liver, heart, kidney and brain tissues compared with the control group. MDA in all the tissues of hypercholesterolemic rats was significantly (p < 0.05) elevated compared to control. However, rats administered with 200 mg/kg body weight extract of any of the spices or their mixture exhibited significant (p < 0.05) decrease in MDA levels when compared with the hypercholesterolemic rats, with the mixture extract showing the best modulatory action.
Figure 1
Figure 1

Effect of extracts of spices on malondialdehyde content in hypercholesterolemia-induced oxidative stress in rat tissues. aValues are means ± SD (n=6). bBars with different superscripts within the same tissues are significantly different at p<0.05. cMalondialdehyde is expressed per milligram of protein. dGrp 1- control, Grp 2- hypercholesterolemic diet, Grp 3- hypercholesterolemic diet + garlic, Grp 4- hypercholesterolemic diet + ginger, Grp 5- hypercholesterolemic diet + pepper, Grp 6- hypercholesterolemic diet + mixture.

Figures 2, 3 and 4 depicts the altered activities of antioxidant enzymes namely SOD, GPex and GRed in the cardiac, hepatic, renal and brain tissues of rats. Compared to the control, the hypercholesterolemic rats showed a significant (p < 0.05) depression in SOD, GPex and GRed activities. Hypercholesterolemic rats treated with 200 mg.kg-1 body weight of the spice extracts exhibited a significant (p < 0.05) elevation of enzymes activities in all the tissues.
Figure 2
Figure 2

Effect of extracts of spices on superoxide dismutase activity in hypercholesterolemia-induced oxidative stress in rat tissues.aValues are means ± SEM (n=6, p<0.05). bBars with the same colour but different letters are significantly different. cGrp1-control, Grp 2- hypercholesterolemic diet, Grp 3- hypercholesterolemic diet + garlic, Grp 4- hypercholesterolemic diet + ginger, Grp 5- hypercholesterolemic diet + pepper, Grp 6- hypercholesterolemic diet + mixture of spices.

Figure 3
Figure 3

Effect of extracts of spices on glutathione peroxidase activity in hypercholesterolemia-induced oxidative stress in rat tissues.aValues are means ±SEM (n=6) (p<0.05). bBars with the same colour but different letters are significantly different. cGrp1- control, Grp 2- hypercholesterolemic diet, Grp 3- hypercholesterolemic diet + garlic, Grp 4- hypercholesterolemic diet + ginger, Grp 5- hypercholesterolemic diet + pepper, Grp 6- hypercholesterolemic diet + mixture of spices.

Figure 4
Figure 4

Effect of extracts of spices on glutathione reductase activity in hypercholesterolemia-induced oxidative stress in rat tissues. aValues are means ± SEM (n=6), (p<0.05). bBars with the same colour but different letters are significantly different. cGrp1-control, Grp 2-hypercholesterolemic diet, Grp 3-hypercholesterolemic diet + garlic, Grp 4- hypercholesterolemic diet + ginger, Grp 5-hypercholesterolemic diet + pepper, Grp 6- hypercholesterolemic diet + mixture of spices.

Hypercholesterolemic rats treated with extract of the mixture gave the best response for SOD and GRed indicating an additive effect of the three spices, while for GPex it was those treated with pepper extract that gave the best result.

Lipid peroxidation is a process associated with the pathogenesis of many chronic diseases such as atherosclerosis, cancer and diabetes. In this study, elevated cardiac, hepatic, renal and brain lipid peroxidation status in untreated hypercholesterolemic rats indicate increased oxidative injury and is consistent with reports from similar studies that showed that hypercholesterolemia leads to increased lipid peroxidation [22–24]. This effect was ameliorated following administration of 200 mg/kg body weight extract of the garlic, ginger, pepper and their mixture as evidenced by the reduced level of MDA. Ability of the spice extracts singly and combined to inhibit lipid peroxidation in vivo could be attributed to the free radical scavenging activities of their components especially phenols, flavonoids, and antilipidemic agents [25]. Similar observations were made by [26, 27] on the effect of cinnamon/garlic extracts and phenolic compounds from rosemary respectively on hypercholesterolemia induced oxidative stress in rats. Garlic, ginger and pepper have been reported to possess antioxidants especially flavonoids and phenolics which could account for their antioxidant activity [28–30].

Antioxidant enzymes such as SOD, GPex, and GRed catalyse the conversion of reactive oxygen species to harmless species. In this study, the reduced activities of hepatic, renal, cardiac and brain antioxidant enzymes in rats fed a hypercholesterolemic diet could be as a result of increased demand for these enzymes in deactivating the high influx of ROS generated by the high cholesterol diet, insufficiency of the enzymes, or failure of the antioxidant defence system to overcome the influx of reactive oxygen species [31, 32]. Administration of 200 mg/kg extracts of garlic, ginger, pepper or their mixture significantly improved the antioxidant enzymes activities by restoring them almost to normal levels in the rats treated. These findings agree with earlier reports by other investigators on modulation of hypercholesterolemia induced oxidative stress in rats using Bacopa monniera, ascorbic acid, rutin and mushrooms respectively [1, 31, 32].

Conclusions

Findings of this study suggest that extracts of garlic, ginger and pepper singly or combined possess antioxidant activity. Administration of a 200 mg/kg body weight aqueous extract of any of the spices significantly reduced lipid peroxidation and modulated effect of hypercholesterolemia induced oxidative stress, as well as improved the antioxidant defence system.

The results here therefore suggest that dietary consumption of these spices may provide benefits for patients with hypercholesterolemia-induced oxidative stress. The health implications of these findings may however be limited by the small group of rats used and the fact that these results may not be extrapolated to human populations. More detailed clinical studies involving human models may therefore be necessary.

Methods

Preparation of spice extracts

Garlic (Allium sativum), ginger (Zingiber officinale) and pepper (Capsicum fructensces) obtained from the local market in Ilorin, Nigeria, were individually sorted to remove grits and dirt, washed, thinly sliced, then oven-dried at 60°C for 72 h. The dried spices were milled into fine powder, packed into airtight plastic bottles and stored in a cold room at -20°C until needed. From the powdered samples, 50 g of each spice was extracted with 1 L of distilled water and boiled for 10 min at 100°C. It was allowed to cool, filtered and freeze-dried (Vir Tis bench top K, Vir Tis, Gardiner, New York, USA) for 48 h. To prepare a mixture of the spices, equal amounts of each spice (50:50:50 g), were weighed and thoroughly mixed together by passing through a coffee grinder of a home blender set. From the mixture, 50 g was taken and extracted in like manner as described above. The freeze-dried samples were stored in airtight plastic bottles at 4°C.

Dose equivalent to 200 mg of each spice and their combination extract per kg body weight of rat was calculated and reconstituted in distilled water. These dose is consistent with reports from previous studies [33–36].

Housing and management of animals

Thirty six (36) male rats of Wistar strain weighing 168 ± 10 g were randomly distributed into six groups, with six animals (n = 6) in each group after one week of acclimatization. They were exposed to a 12 h light/dark cycle, constant temperature (22°C ± 2°C) and humidity (70% ± 4%) with water and feed made available ad libitum. The animals were handled according to the guidelines of the National Research Council Guide for the Care and Use of Laboratory Animals [37] and the study was approved by the Animal Ethics Committee, University of Fort Hare, Alice, South Africa.

Experimental protocols

Two diets, namely standard rat chow and hypercholesterolemic diet (1% cholesterol and 25% soybean oil) that has been established to induce hypercholesterolemia [38, 39] were used. The diets were kept refrigerated and used within 1 week of preparation. Rats in group 1 (positive control), were fed the standard rat chow with water ad libitum. Group 2 (negative control) were fed the hypercholesterolemic diet and water, while groups 3, 4, 5, and 6 rats were fed the hypercholesterolemic diet and administered daily with aqueous extracts of garlic, ginger, pepper or their mixture at a dose equivalent to 200 mg/kg body weight of rats respectively.

At the end of 4 weeks, all the animals were fasted overnight and anaesthetized by intraperitoneal injection of pentobarbital sodium (45 mg/kg). Blood samples were collected by cardiac puncture into vacutainers (CE Sterile R 456018P, greiner.bio.one, United Kingdom) for various biochemical analyses. The rats were finally euthanized and the heart, liver and kidney excised and rinsed in ice-cold saline to maintain physiologic status.

Determination of lipid peroxidation and antioxidant enzymes activities in liver, kidney, heart and brain of rats

Lipid peroxidation in the organs was determined by estimating levels of malondialdehyde (MDA) as described by [40]. This method was used to measure spectrophotometrically the color produced by the reaction of TBA with malondialdehyde at 532 nm using a Randox chemical assay kit. Tissue supernatants (50 μl) were added to test tubes containing 2 μl of butylated hydroxytoluene (BHT) in methanol. Next, 50 μl of acid reagent (1 M phosphoric acid) was added and finally 50 μl of TBA solution was added. The tubes were mixed vigorously and incubated for 60 min at 60°C. The mixture was centrifuged at 10,000 × g for 3 min. The supernatant was put into microplate wells in aliquots of 75 μl, and absorbance was measured with a microplate reader at 532 nm. TBARS levels were expressed as nmol/mg protein in various organs (brain, liver, heart and kidney).

Activities of superoxide dismutase (SOD), glutathione peroxidase (GPex) and glutathione reductase (GRed) were assayed in the liver, heart, kidney and brain of experimental rats.

SOD accelerates the dismutation of the toxic superoxide radical (O2.) produced during oxidative energy processes to hydrogen peroxide and molecular oxygen. SOD was determined using Randox kits as described by [41]. The method uses xanthine and xanthine oxidase to generate superoxide radicals which reacts with 2-(4-iodophenyl)-3-(4-nitrophenol)-5-phenyltetrazolium chloride (I.N.T) to form a red formazan dye which absorbs at 505 nm. A 30 μl of sample was pipetted into a cuvette with 1000 μl of buffer (reagent 1) R1, and mixed well. To this mixture, 150 μl of xanthine oxidase, (reagent 2) R2 was added and mixed, absorbance was read at 505 nm.

Gpex activity was determined using Randox assay kit as described by the manufacturer based on the method of [42]. Glutathione peroxidase catalyses oxidation of glutathione by cumene hydroperoxide. In the presence of glutathione reductase and NADPH, the oxidized glutathione (GSSG) is immediately converted to the reduced form with a concomitant oxidation of NADPH to NADP+. An aliquot (10 μl) of the sample was added to 500 μl of reagent 1 (R1) and mixed. To this mixture was added 20 μl of cumene (R2 reagent 2). A blank was set up using 10 μl of distilled water and absorbance was read at 340 nm.

GRed activity was determined as described by [43] using Randox kits. Glutathione reductase catalyses the reduction of glutathione (GSSG) in the presence of NADPH, which is oxidized to NADP+. The decrease in absorbance of the sample is measured at 340 nm. 10 μl of tissue sample was mixed with 250 μl of substrate R1 (reagent 1) after which 50 μl of R2 (reagent 2) was added, mixed and the timer started. Initial absorbance was read at1 min, read again after 2, 3, 4, and 5 min.

Statistical analysis

Data were expressed as means ± SEM from 6 determinations. Both descriptive and inferential statistical methods were used for data analysis. When the data were subjected to prior investigations before analysis, parametric assumptions including homoscedasticity, normality and independence of observations were satisfied. Hence, a parametric test (analysis of variance, ANOVA) was used to test for statistical significance among the treatment means. Differences among treatment means were considered significant at P < 0.05. Means that were significantly different from each other were segregated using Duncan’s Multiple Range Test. All analyses were done using MINITAB (Student Version 12 for Windows) Software.

Notes

Declarations

Acknowledgements

This study was supported by Govan Mbeki Research Development Council, University of Fort Hare, South Africa.

Authors’ Affiliations

(1)
Current address Medicinal Plant and Economic Development Research Centre, Department of Botany, University of Fort Hare, Alice 5700, South Africa
(2)
Department of Biochemistry, University of Ilorin, Ilorin, Nigeria
(3)
Department of Home Economics and Food Science, University of Ilorin, Ilorin, Nigeria

References

  1. Abuohashish HM, Aleisa AM, Ahmed MM, Alkhamees OA, Al-Rejaie SS, Alroujayee AS: Ameliorative effects of rutin and ascorbic acid combination on hypercholesterolemia-induced hepatotoxicity in female rats. Afr J Pharm Pharmacol 2013, 7(6):280-288. 10.5897/AJPP12.745View ArticleGoogle Scholar
  2. Ahmad A, Singhal U, Hossain MM, Islam N, Rizvil I: The role of endogenous antioxidant enzymes and malondialdehyde in essential hypertension. J Clin Diaggnostic Res 2013, 7(6):987-990.Google Scholar
  3. Kasdallah-Grissa A, Nakbi A, Koubaa N, El Fazaa S, Gharbi N, Kamoun A, Hammani M: Dietary virgin olive oil protects against lipid peroxidation and improves antioxidant status in the liver of rats chronically exposed to ethanol. Nutr Res 2008, 28: 477-419.View ArticleGoogle Scholar
  4. Halliwell B, Gutteridge JMC: ROS in biology and medicine. Oxford, UK: Claredon Press; 1989:245-257.Google Scholar
  5. Bagchi K, Puri S: ROS and antioxidants in Health and disease. East Mediterr Health J 1998, 4: 350-360.Google Scholar
  6. Maxwell SRJ, Lip GYH: Free radicals in cardiovascular diseases. Br J Clin Pharmacol 1997, 44(4):307-317.PubMed CentralView ArticlePubMedGoogle Scholar
  7. Mimic-Oka J, Simic DV, Simic TP: Free radicals in cardiovascular diseases. Med Biol 1999, 6(1):11-22.Google Scholar
  8. Kita T, Kune N, Minanim , Hayashida K, Murayana T, Sano H: Role of oxidized LDL in atherosclerosis. Ann N Y Acad Sci 2001, 947: 199-205.View ArticlePubMedGoogle Scholar
  9. Reddy KS, Katan MB: Diet, nutrition and the prevention of hypertension and cardiovascular diseases. Public Health Nutr 2004, 7(1A):167-186.View ArticleGoogle Scholar
  10. Hazra B, Biswas S, Mandal N: Antioxidant and free radical scavenging activity of Spondias pinnata . BMC Compl Alter Med 2008, 8: 63. 10.1186/1472-6882-8-63View ArticleGoogle Scholar
  11. Fang D, Wei-Feng C, Bo Z, Li Y, Zhong-Li L: Antioxidative effects of curcumin and its analogues against the free-radical-induced peroxidation of linoleic acid in micelles. Phytother Res 2009, 23: 1220-1228. 10.1002/ptr.2517View ArticleGoogle Scholar
  12. Stocker R, Frei B: Endogenous antioxidant defences in human blood plasma. In Oxidative stress, oxidants and antioxidants. Edited by: Sies H. London, UK: Academic Press; 1991:213-243.Google Scholar
  13. Reddy ACP, Lokesh BR: Studies on spice principles as antioxidants in the inhibition of lipid peroxidation of rat liver microsomes. Mol Cell Biochem 1992, 111: 117-124.PubMedGoogle Scholar
  14. Reddy ACP, Lokesh BR: Alterations in lipid peroxidation in rat liver by n-3 fatty acids: modulation of anti-oxidant enzymes by curcumin, eugenol and vitamin E. J Nutr Biochem 1994, 5: 181-188. 10.1016/0955-2863(94)90070-1View ArticleGoogle Scholar
  15. Adak SK, Sarkar AK, Bhattacharya P, Marmthu P, Chaudhuri RN, Barnerjee KK: Risk assessment of cardiovascular diseases among bank employees- a biochemical approach. Occup Med 1999, 49: 313-318. 10.1093/occmed/49.5.313View ArticleGoogle Scholar
  16. Srinivasan K: Spices as influencers of body metabolism: An overview of three decades of research. Food Res Int 2005, 38: 77-86. 10.1016/j.foodres.2004.09.001View ArticleGoogle Scholar
  17. Shobana S, Naidu KA: Antioxidant activity of selected Indian spices. J Prostaglandins Leukotrien Essen Fatty acids 2000, 62: 107-110. 10.1054/plef.1999.0128View ArticleGoogle Scholar
  18. Carmichael JK: Treatment of herpes and post herpetic neuralgia. Am Fam Phys 1991, 44: 203-210.Google Scholar
  19. Hoareau L, Dasilva EJ: Medicvinal plants: a re-emerging health aid. E J Biotech 1999, 2(2):56-70.Google Scholar
  20. Owen PL, John T: Antioxidants in Medicines and spices as cardio protective agents in Tibetan Highlanders. Pharm Biol 2002, 40: 346-357. 10.1076/phbi.40.5.346.8461View ArticleGoogle Scholar
  21. Shukla Y, Singh M: Cancer preventive properties of ginger: a brief review. Food Chem Toxicol 2007, 45: 683-690. 10.1016/j.fct.2006.11.002View ArticlePubMedGoogle Scholar
  22. Yang B, Kalimo KO, Kallio SE, Mattila LM, Katajisto JK, Kallio HP, Peltola OJ: Effects of dietary supplementation with seabuckthorn ( Hippophae rhamnoides ) seed and pulp oils on atopic dermatitis. J Nutr Biochem 1999, 10: 622-630. 10.1016/S0955-2863(99)00049-2View ArticlePubMedGoogle Scholar
  23. Dutta K, Bishayi B: Escherichia coli lipopolysaccharide administration alters antioxidant profile during hypercholesterolemia. Ind J Clin Biochem 2009, 24: 179-183. 10.1007/s12291-009-0032-zView ArticleGoogle Scholar
  24. MA J, Qiao Z, Xiang X: Aqueous extract of Astragalus mongholicus ameliorates high cholesterol diet induced oxidative injury in experimental rat models. J Med Plant Res 2011, 5: 855-858.Google Scholar
  25. Oloyede OB, Otunola GA, Oladiji AT, Afolayan AJ: Comparative analysis of the chemical composition of three spices- Allium sativum L., Zingiber officinale Rosc and Capsicum frutescens L. commonly consumed in Nigeria. Afr J Biotech (2010b, 9: 6927-6931.Google Scholar
  26. Noori S, Azmat M, Mahboob T: Study on antioxidant effects of cinnamon and garlic extract in liver, kidney and heart tissue of rat. Biosci Res 2012, 9: 17-22.Google Scholar
  27. Osilva AM, Afonso MS, Carvalho EBT, Barros SBM, Rivelli DP, Rogero MM, Torres RP, Lottenberg AM, Mancini-Fillio J: Phenolic compounds from Rosemary ( Rosmarinus officinalis L.) attenuate oxidative stress and reduce blood cholesterol concentrations in diet-induced hypercholesterolemic rats. Nutr Metab 2013, 10: 19. 10.1186/1743-7075-10-19View ArticleGoogle Scholar
  28. Orekhov AN, Grunwald J: Effects of garlic on atherosclerosis. Nutrition 1997, 13: 656-663. 10.1016/S0899-9007(97)83010-9View ArticlePubMedGoogle Scholar
  29. Nicoll R, Henein MY: Ginger ( Zingiber officinale Roscoe): a hot remedy for cardiovascular disease? Int J Cardiol 2009, 131: 408-409. 10.1016/j.ijcard.2007.07.107View ArticlePubMedGoogle Scholar
  30. Wu CT, Chang NW, Wang SY, Lin CF, PEI RJ: Alpinia pricei Hayata rhizome extracts have suppressive and preventive potencies against hypercholesterolemia. Food Chem Toxicol 2010, 48: 2350-2356. 10.1016/j.fct.2010.05.070View ArticlePubMedGoogle Scholar
  31. Khan MDA, Rahman MM, Tania M, Uddin MDN, Ahmed S: Pleurotus sajor-caju and Pleurotus florida mushrooms improve some extant of the antioxidant systems in the liver of hypercholesterolemic rats. The Open Nutraceut J 2011, 4: 20-24. 10.2174/1876396001104010020View ArticleGoogle Scholar
  32. Kamesh V, Sumathi T: Effect of Bacopa monniera L in attenuating hepatic oxidative stress in hypercholesterolemia induced rats. Asian J Pharm Clin Res 2012, 5: 90-95.Google Scholar
  33. Shanmugam KR, Ramakrishna CH, Mallikarjuna K, Reddy KS: Protective effect of ginger against alcohol-induced renal damage and antioxidant enzymes in male albino rats. Ind J Exper Biol 2010, 48: 143-149.Google Scholar
  34. Nwanjo H, OzE G: Antiarrythmic and antihyperlipidaemic potentials of aqueous garlic extract in hypercholesterolaemic rats. Int J Nutr Wellness 2006, 3: 2.Google Scholar
  35. Ahmadi R, Pishghdaus S, Mollamine F, Manfared MRZ: Comparing the effects of ginger and glinbenclamide on dihydroxybenzene metabolites produced in Stz-induced diabetic rats. Int J Endocrin Metab 2013, 11(4):e10266.View ArticleGoogle Scholar
  36. Abduljawad SH, Hassaneim MA, Heaader EA: Influence of aqueous extract of red chillis pepper as curative for gastric ulcer in albino rats. J Nat Sci Res 2013, 3(4):78-87.Google Scholar
  37. National Research Council: Guide for the Care and Use of Laboratory Animals, Committee on Care and Use of Laboratory Animals of the Institute of Laboratory Animal Resources DHHS Publication No. (NIH). 1985, 85-93.Google Scholar
  38. Paula H, Matos SL, Pedrosa ML, Oliveira EL, Santos RC, Chianca JNRDA, Silva ME: Dietary Models for inducing Hypercholesterolemia in rats. Braz Arch Biol Tech 2005, 48: 203-209.Google Scholar
  39. Otunola GA, Oloyede OB, Oladiji AT, Afolayan AJ: Hypolipidemic effect of aqueous extracts of selected spices and their mixture on diet-induced hypercholesterolemia in Wistar rats. Can J Pure Appl Sci 2012, 6: 2063-2071.Google Scholar
  40. Ohkawa H, Ohisi N, Yagi K: Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Annu Rev Plant Physiol Plant Mol Biol 1979, 95: 351-358.Google Scholar
  41. Wooliams JA, Wiener G, Anderson PH, Mcmurray CH: Variation in the activities of glutathione peroxidase and superoxide dismutase and in the concentration of copper in the blood of various breed crosses of sheep. Res Vet Sci 1983, 34: 69-77.Google Scholar
  42. Paglia DE, Valentine WJN: Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase. Lab Clin Med 1967, 70: 158-169.Google Scholar
  43. Spooner RJ, Goldberg DM: Assay of glutathione reductase. In Methods of enzymatic analysis. 3rd edition. Edited by: Bergmeyen HV. Deerfield Beach (Fla): Verlag Chemie; 1983:258-265.Google Scholar

Copyright

© Otunola et al.; licensee BioMed Central Ltd. 2014

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Advertisement

Biological Research

ISSN: 0717-6287

Contact us