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Research Article | Open Access

Polyphenolic extract of Sorghum bicolor grains enhances reactive oxygen species detoxification in N-nitrosodiethylamine-treated rats

Taofeek O. Ajiboyea( )Yesirat O. KomolafeaOyelola B. OloyedeaSimiat M. OgunbodebMoriam D. AdeoyecIbrahim O. AbdulsalamicQuadri O. Nurudeend
Antioxidants, Free Radicals and Toxicology Research Laboratory, Biochemistry and Nutrition Unit, Department of Chemical Sciences, Fountain University, Osogbo, Nigeria
Nutritional Biochemistry Research Laboratory, Biochemistry and Nutrition Unit, Department of Chemical Sciences, Fountain University, Osogbo, Nigeria
Industrial and Environmental Chemistry Unit, Department of Chemical Sciences, Fountain University, Osogbo, Nigeria
Phytomedicine, Toxicology and Reproductive Biochemistry Research Laboratory, Department of Biochemistry, University of Ilorin, Ilorin, Nigeria

Peer review under responsibility of Beijing Academy of Food Sciences.

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Abstract

Reactive oxygen species detoxification potentials of Sorghum bicolor polyphenolic extract was investigated in the liver of N-nitrosodiethylamine-treated rats. Male rats, weighing (135 ± 5.5) g were completely randomized into 7 groups (A–G) of five rats each. Rats in C, D, E and F were administered orally once daily at 24-h interval for 7 d with 500, 125, 250 and 500 mg/kg body weight of polyphenolic extract of S. bicolor, respectively. Group G was given 100 mg/kg body weight of vitamin C. On the sixth day, groups B, D, E, F and G were administered with 100 mg/kg body weight N-nitrosodiethylamine (NDEA). Group A, which served as the control was treated like the test groups except, that the animals received distilled water only. Reactive oxygen species detoxifying enzymes (superoxide dismutase, catalase, glutathione peroxidase, glutathione reductase and glucose 6-phosphate dehydrogenase) activities were significantly (P < 0.05) induced by S. bicolor. These inductions significantly (P < 0.05) attenuated the NDEA-mediated decrease in reactive oxygen species detoxifying enzymes and compared favourably with vitamin C. NDEA-mediated elevation in the concentrations of oxidative stress biomarkers; malondialdehyde, conjugated dienes, lipid hydroperoxides, protein carbonyl and percentage DNA fragmentation were significantly (P < 0.05) lowered by S. bicolor polyphenolic extract. Overall, the results obtained from this study revealed that the polyphenolic extract of S. bicolor grains enhanced the detoxification of reactive oxygen species in NDEA-treated rats. The polyphenols also prevented the peroxidation of lipid, oxidation of proteins as well as fragmentation of DNA component in the liver of rats and hence gave the evidence of possible prophylactic potentials of S. bicolor grains.

References

[1]

V. Sivaramakrishnan, P.N.M. Shilpa, V.R. Praveen Kumar, et al., Attenuation of N-nitrosodiethylamine-induced hepatocellular carcinogenesis by a novel flavonol-Morin, Chemico-biological Interactions 171 (2008) 79–88.

[2]

C. Gupta, A. Vikram, D.N. Tripathi, et al., Antioxidant and antimutagenic effect of quercetin against DEN induced hepatotoxicity in rat, Phytotherapy Research 24 (2010) 119–128.

[3]

F.P. Guengerich, D.H. Kim, M. Iwasaki, Role of human cytochrome P-450 IIE1 in the oxidation of many low molecular weight cancer suspects, Chemical Research in Toxicology 4 (1991) 168–179.

[4]

O. Teufelhofer, W. Parzefall, E. Kainzbauer, et al., Superoxide generation from Kupffer cells contributes to hepatocarcinogenesis: studies on NADPH oxidase knockout mice, Carcinogenesis 26 (2005) 319–329.

[5]

P.J. Wills, V. Suresh, M. Arun, et al., Antiangiogenic effect of Lygodium flexuosum against N-nitrosodiethylamine-induced hepatotoxicity in rats, Chemico-biological Interactions 164 (2006) 25–38.

[6]

K. Pradeep, C.V.R. Mohan, K. Gobianand, et al., Silymarin modulates the oxidant–antioxidant imbalance during diethylnitrosamine induced oxidative stress in rats, European Journal of Pharmacology 560 (2007) 110–116.

[7]

M. Bains, E.D. Hall, Antioxidant therapies in traumatic brain and spinal cord injury, Biochimica et Biophysica Acta (BBA): Molecular Basis of Disease 1822 (2012) 675–684.

[8]

M. Ushio-Fukai, Y. Nakamura, Reactive oxygen species and angiogenesis: NADPH oxidase as target for cancer therapy, Cancer Letters 266 (2008) 37–52.

[9]

L. Covarrubias, D. Hernández-García, D. Schnabel, et al., Function of reactive oxygen species during animal development: passive or active?, Developmental Biology 320 (2008) 1–11.

[10]

E.R. Stadtman, R.L. Levine, Protein oxidation, Annals of the New York Academy of Sciences 899 (2006) 191–208.

[11]

M. Valko, C.J. Rhodes, J. Moncol, et al., Free radicals, metals and antioxidants in oxidative stress-induced cancer, Chemico-biological Interactions 160 (2006) 1–40.

[12]

J. Chandra, A. Samali, S. Orrenius, Triggering and modulation of apoptosis by oxidative stress, Free Radical Biology and Medicine 29 (2000) 323–333.

[13]

H. Jaeschke, A. Ramachandran, Reactive oxygen species in the normal and acutely injured liver, Journal of Hepatology 55 (2011) 227–228.

[14]

H. Jaeschke, Reactive oxygen and mechanisms of inflammatory liver injury: present concepts, Journal of Gastroenterology and Hepatology 26 (Suppl. 1) (2011) 173–179.

[15]

T.O. Ajiboye, Redox status of the liver and kidney of 2,2-dichlorovinyl dimethyl phosphate (DDVP) treated rats, Chemico-biological Interactions 185 (2010) 202–207.

[16]

T.O. Ajiboye, A.K. Salau, M.T. Yakubu, et al., Acetaminophen perturbed redox homeostasis in Wistar rat liver: protective role of aqueous Pterocarpus osun leaf extract, Drug and Chemical Toxicology 33 (2010) 77–87.

[17]

T.O. Ajboye, M.T. Yakubu, A.K. Salau, et al., Antioxidant and drug detoxification potential of aqueous extract of Annona senegalensis leaves in carbon tetrachloride-induced hepatocellular damage, Pharmaceutical Biology 48 (2010) 1361–1370.

[18]

T.O. Ajiboye, M.T. Yakubu, A.T. Oladiji, Electrophilic, free radical and reactive oxygen species scavenging and detoxification potentials of Lophiraalata stem bark extract, Free Radicals and Antioxidants 1 (2011) 40–47.

[19]

T.O. Ajiboye, In vivo antioxidant potentials of Piliostigma thonningii (Schum) leaves: studies on hepatic marker enzyme, antioxidant system, drug detoxifying enzyme and lipid peroxidation, Human & Experimental Toxicology 30 (2011) 55–62.

[20]

L.F. Dowling, C. Arndt, B.R. Hamaker, Economic viability of high digestibility sorghum as feed for market broilers, Agronomy Journal 94 (2002) 1050.

[21]

C.S. Kwak, S.C. Park, S.J. Lim, et al., Antioxidative and antimutagenic effects of Korean buckwheat, sorghum, millet and Job’s tears, Journal of The Korean Society of Food Science and Nutrition 33 (6) (2004).

[22]

L. Dykes, L.M. Seitz, W.L. Rooney, et al., Flavonoid composition of red sorghum genotypes, Food Chemistry 116 (2009) 313–317.

[23]

T.O. Ajiboye, Y.O. Komolafe, H.O.B. Oloyede, et al., Diethylnitrosamine-induced redox imbalance in rat microsomes: protective role polyphenolic rich extract from Sorghum bicolor grains, Journal of Basic and Clinical Physiology and Pharmacology 24 (1) (2013) 41–49.

[24]

National Research Council, Guide for the Care and Use of Laboratory Animals, 8th ed., National Academies Science Press, 2011, pp. 161–196.

[25]
World Health Organization (WHO), Basic OECD Principles of GLP, World Health Organization, Geneva, Switzerland, 1998, Available at: www.who.int/tdrold/publications/publications/pdf/pr15/info.pdf (access date: 24.08.09).
[26]

M.T. Yakubu, M.A. Akanji, A.T. Oladiji, Aphrodisiac potentials of the aqueous extract of Fadogia agrestis (Schweinf, Ex Hiern) stem in male albino rats, Asian Journal of Andrology 7 (2005) 399–404.

[27]

P.J. Wright, P.D. Leathwood, D.T. Plummer, Enzymes in rat urine. Alkaline phosphatase, Enzymologia 42 (1972) 317–327.

[28]

H.U. Bergmeyer, M. Horder, R. Rej, Approved recommendation on IFCC methods for measurement of catalytical concentration of enzymes. Part 3. IFCC method for alanine aminotransferase, Journal of Clinical Chemistry and Clinical Biochemistry 24 (1986) 481–489.

[29]

H.U. Bergmeyer, M. Horder, R. Rej, Approved recommendation on IFCC methods for measurement of catalytical concentration of enzymes. Part 2. IFCC method for aspartate aminotransferase, Journal of Clinical Chemistry and Clinical Biochemistry 24 (1986) 497–508.

[30]

H.P. Misra, I. Fridovich, The role of superoxide anion in the autoxidation of epinephrine and a simple assay for superoxide dismutase, Journal of Biological Chemistry 247 (1972) 3170–3175.

[31]

R.F. Beers, I.W. Sizer, A spectrophotometric method for measuring the breakdown of hydrogen peroxide by catalase, Journal of Biological Chemistry 195 (1952) 133–140.

[32]

J.T. Rotruck, A.L. Pope, H.F. Ganther, et al., Selenium: biochemical role as a component of glutathione peroxidase, Science 179 (1973) 588–590.

[33]

R.D. Mavis, E. Stellwagen, Purifcation and subunit structure of glutathione reductase from bakers’ yeast, Journal of Biological Chemistry 243 (1968) 809–814.

[34]
A. Kornberg, B.L. Horecker, in: S.D. Colowick, N.O. Kaplan (Eds.), Methods Enzymol, Academic Press, New York, 1955, p. 823.
[35]

R.L. Levine, D. Garland, C.N. Oliver, et al., Oxygen Radicals in Biological Systems. Part B. Oxygen Radicals and Antioxidants, Elsevier, 1990.

[36]
J.S. Bus, L.G. Costa, E. Hodgson, et al. (Eds.), Current Protocols in Toxicology, John Wiley & Sons Inc., Hoboken, NJ, USA, 2001.
[37]

K. Burton, A study of the conditions and mechanism of the diphenylamine reaction for the colorimetric estimation of deoxyribonucleic acid, Biochemical Journal 62 (1956) 315–323.

[38]

M.A. Akanji, O.A. Olagoke, O.B. Oloyede, Effect of chronic consumption of metabisulphite on the integrity of the rat kidney cellular system, Toxicology 81 (1993) 173–179.

[39]

G. Ramakrishnan, H.R.B. Raghavendran, R. Vinodhkumar, et al., Suppression of N-nitrosodiethylamine induced hepatocarcinogenesis by silymarin in rats, Chemico-biological Interactions 161 (2006) 104–114.

[40]

A.S. Yadav, D. Bhatnagar, Modulatory effect of spice extracts on iron-induced lipid peroxidation in rat liver, BioFactors (Oxford, England) 29 (2007) 147–157.

[41]

K. Pradeep, C.V.R. Mohan, K. Gobianand, et al., Silymarin modulates the oxidant–antioxidant imbalance during diethylnitrosamine induced oxidative stress in rats, European Journal of Pharmacology 560 (2007) 110–116.

[42]

E. Kozer, S. Evans, J. Barr, et al., Glutathione, glutathione-dependent enzymes and antioxidant status in erythrocytes from children treated with high-dose paracetamol, British Journal of Clinical Pharmacology 55 (2003) 234–240.

[43]

D. Nakae, Y. Kobayashi, H. Akai, et al., Involvement of 8-hydroxyguanine formation in the initiation of rat liver carcinogenesis by low dose levels of N-nitrosodiethylamine, Cancer Research 57 (1997) 1281–1287.

[44]

Y. Sánchez-Pérez, C. Carrasco-Legleu, C. García-Cuellar, et al., Oxidative stress in carcinogenesis. Correlation between lipid peroxidation and induction of preneoplastic lesions in rat hepatocarcinogenesis, Cancer Letters 217 (2005) 25–32.

[45]

S. Das, Vitamin E in the genesis and prevention of cancer: a review, Acta Oncologica (Stockholm, Sweden) 33 (1994) 615–619.

[46]

M. Chevion, E. Berenshtein, E.R. Stadtman, Human studies related to protein oxidation: protein carbonyl content as a marker of damage, Free Radical Research 33 (Suppl.) (2000) S99-S108.

[47]

I. Dalle-donne, R. Rossi, D. Giustarini, et al., Protein carbonyl groups as biomarkers of oxidative stress, Clinica Chimica Acta 329 (2003) 23–38.

[48]

A. Amin, A.A. Hamza, Oxidative stress mediates drug-induced hepatotoxicity in rats: a possible role of DNA fragmentation, Toxicology 208 (2005) 367–375.

[49]

M.S. Cooke, M.D. Evans, M. Dizdaroglu, et al., Oxidative DNA damage: mechanisms, mutation, and disease, FASEB Journal: Official Publication of the Federation of American Societies for Experimental Biology 17 (2003) 1195–1214.

Food Science and Human Wellness
Pages 39-45
Cite this article:
Ajiboye TO, Komolafe YO, Oloyede OB, et al. Polyphenolic extract of Sorghum bicolor grains enhances reactive oxygen species detoxification in N-nitrosodiethylamine-treated rats. Food Science and Human Wellness, 2013, 2(1): 39-45. https://doi.org/10.1016/j.fshw.2013.02.001

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Received: 07 October 2012
Revised: 24 February 2013
Accepted: 27 February 2013
Published: 14 March 2013
© 2013 Beijing Academy of Food Sciences.
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