The Effects of Aflatoxins on Oxidative Stress in Broiler Chickens

Sixty 1-day-old male Ross-PM3 broiler chickens were used in this study. The chickens were divided into 5 groups, including one control and 4 experimental. The control group was fed commercial broiler feed free from aflatoxin (AF), whereas the experimental groups, namely, groups 2, 3, 4 and 5 were given feed containing, respectively, 0.05 ppm, 0.1 ppm, 0.5 ppm and 1.0 ppm of AF (approximately, 81.30% AF B1, 10.40% AF B2, 5.75% AF G1 and 2.55% AF G2) for 45 days. Blood samples were collected on days 15, 30 and 45 of the study. Superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GSH-Px) and glucose-6-phosphate dehydrogenase (G6PD) activity and malondialdehyde (MDA) levels in erythrocytes were determined. The results of this study revealed a significant decline in comparison to the control group with respect to SOD activity on days 30 and 45 in groups 4 and 5, GSH-Px activity on day 30 in group 5 and day 45 in groups 4 and 5, CAT activity on day 45 in group 5 and G6PD activity on day 45 in group 5, and a significant increase in the level of MDA in group 5. Therefore it was concluded that long-term (30 and 45 days) administration of AF at high doses (0.5-1.0 ppm) caused lipid peroxidation in broiler chickens. Certain significant statistical changes that occurred on day 30 in SOD and GSH-Px activities, and on day 45 in primarily SOD and GSH-Px (for groups 4 and 5) and secondly (for group 5) in all enzyme activities and MDA levels are supportive of this hypothesis. Furthermore, it has been understood that the most sensitive parameters utilised in determination of lipid peroxidation may include SOD, GSH-Px and MDA, and these parameters may prove to be significant with regard to the assessment of the severity of aflatoxicosis in poultry naturally intoxicated with AF, implementation of precautions taken against AF intoxication and the evaluation of such practices with regard to success.

The Effects of Aflatoxins on Oxidative Stress in Broiler Chickens

Sixty 1-day-old male Ross-PM3 broiler chickens were used in this study. The chickens were divided into 5 groups, including one control and 4 experimental. The control group was fed commercial broiler feed free from aflatoxin (AF), whereas the experimental groups, namely, groups 2, 3, 4 and 5 were given feed containing, respectively, 0.05 ppm, 0.1 ppm, 0.5 ppm and 1.0 ppm of AF (approximately, 81.30% AF B1, 10.40% AF B2, 5.75% AF G1 and 2.55% AF G2) for 45 days. Blood samples were collected on days 15, 30 and 45 of the study. Superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GSH-Px) and glucose-6-phosphate dehydrogenase (G6PD) activity and malondialdehyde (MDA) levels in erythrocytes were determined. The results of this study revealed a significant decline in comparison to the control group with respect to SOD activity on days 30 and 45 in groups 4 and 5, GSH-Px activity on day 30 in group 5 and day 45 in groups 4 and 5, CAT activity on day 45 in group 5 and G6PD activity on day 45 in group 5, and a significant increase in the level of MDA in group 5. Therefore it was concluded that long-term (30 and 45 days) administration of AF at high doses (0.5-1.0 ppm) caused lipid peroxidation in broiler chickens. Certain significant statistical changes that occurred on day 30 in SOD and GSH-Px activities, and on day 45 in primarily SOD and GSH-Px (for groups 4 and 5) and secondly (for group 5) in all enzyme activities and MDA levels are supportive of this hypothesis. Furthermore, it has been understood that the most sensitive parameters utilised in determination of lipid peroxidation may include SOD, GSH-Px and MDA, and these parameters may prove to be significant with regard to the assessment of the severity of aflatoxicosis in poultry naturally intoxicated with AF, implementation of precautions taken against AF intoxication and the evaluation of such practices with regard to success.

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  • Shotwell, O.L., Hesseltine, C.W., Stubblefield, R.D., Sorenson, W.G.: Production of aflatoxin on rice. Appl. Microbiol., 1966; 14: 425-428.
  • fianlı, Y., Ceylan, S., Kaya, S.: Karma yemlerde aflatoksin analizi. Ankara Üniv. Vet. Fak. Derg., 1982; 29: 50-70.
  • Roberts, B.A., Patterson, D.S.P.: Detection of twelve mycotoxins in mixed animal feedstuffs, using a novel membrane cleanup procedure. J. Assoc. Off. Anal Chem., 1975; 58: 1178-1181.
  • Nabney, J., Nesbit, B.F.: A spectrophotometric method for determination of the aflatoxins. Analyst, 1965; 3: 155-159.
  • Sun, Y., Oberley, L.W., Li, Y.A.: Simple method for clinical assay of superoxide dismutase. Clin. Chem., 1988; 343: 497-500.
  • Drapper, H.H., Hadley, M.: Malondialdehyde determination as index of lipid peroxidation. Methods Enzymol., 1990; 186: 421- 431.
  • Woolliams, J.A., Wiener, G., Anderson, P.H., McMurray, C.H.: Variation in activities of glutathione peroxidase and superoxide dismutase and in the concentration of copper in the blood in various breed crosses of sheep. Res .Vet. Sci., 1983; 34: 253- 256.
  • Aebi, H.: Catalase in vitro. Methods Enzymol., 1984; 105: 121- 126.
  • Paglia, P.E., Valentine, W.N.: Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase. J. Lab. Clin. Med., 1967; 70: 158-169.
  • Worthington, V.: Worthington Enzyme Manual, Glucose-6- phosphate dehydrogenase, Worthington Biochemical Corporation Frehold, New Jersey, U.S.A. 1993; 189-192.
  • Fairbanks, V.F., Klee, G.G.: Biochemical aspects of hematology. In: Burtis, C.A., Ashwood, E.R. eds. Tietz textbook of clinical chemistry, 3rded, WB Saunders Philadelphia, 1690-1698, 1999.
  • Decoudu, S., Cassand, P., Daubeze, M., Frayssinnet, J., Narbonne, J.F.: Effect of vitamin A dietary intake on in vitro and in vivo activation of aflatoxin B1. Mutat. Res., 1992; 269: 269-278.
  • Comporti, M.: Lipid peroxidation, biophatological significance. Molec. Aspects Med., 1993; 14: 199-207.
  • Kohen, R., Nyska, A.: Oxidation of biological systems: oxidative stress phenomena, antioxidants, redox reactions, and methods for their quantification. Toxicol. Pathol., 2002; 30: 620-650.
  • Gutterridge, J.M.C., Halliwell, B.: The measurement and mechanism of lipid peroxidation in biological systems. Letters, 1990; 15: 129-135.
  • Moore, K., Roberts, L.J.: Measurement of lipid peroxidation. Free Radic. Res., 1998; 28: 659-671.
  • Gözükara, E.M.: Pentoz fosfat metabolik yolu In. Biyokimya, 2. Cilt, Bölüm 20, Ankara, 923-940.
  • Jollow, D.J., McMillan, D.C.: Oxidative stress, glucose-6- phosphate dehydrogenase and the red cell. Adv. Exp. Med. Biol., 2001; 500: 595-605.
  • Keçeci, T., Oğuz, H., Kurtoğlu, V.: Effects of polyvinylpolypyrrolidone, syntetic zeolite and bentonite on serum biochemical and hematological characters of broiler chickens during aflatoxicosis. Br. Poult. Sci., 1998; 39: 452-458.
  • Agil, A., Fuller, C.J., Jialal, I.: Susceptibility of plasma to ferrous iron/hydrogen peroxide-mediated oxidation: demonstration of a possible Fenton reaction. Clin. Chem., 1995; 41: 220-225.
  • Lalor, J.H., Llewellyn, G.C.: Biointeraction of sodium selenite and aflatoxin B1 in the Mongolian gerbil. J. Toxicol. Environ. Health., 1981; 8: 387-400.