Hostname: page-component-586b7cd67f-dlnhk Total loading time: 0 Render date: 2024-11-28T02:36:34.242Z Has data issue: false hasContentIssue false

The role of vitamin E or clay in growing Japanese quail fed diets polluted by cadmium at various levels

Published online by Cambridge University Press:  20 November 2015

D. E. Abou-Kassem
Affiliation:
Poultry Department, Faculty of Agriculture, Zagazig University, Zagazig 44511, Egypt
Kh. M. Mahrose*
Affiliation:
Poultry Department, Faculty of Agriculture, Zagazig University, Zagazig 44511, Egypt
M. Alagawany
Affiliation:
Poultry Department, Faculty of Agriculture, Zagazig University, Zagazig 44511, Egypt
*
Get access

Abstract

This study was conducted to verify whether vitamin (Vit) E or natural clay as feed additives has the potential to modulate the deleterious effects resulting from exposure to cadmium (Cd) in growing Japanese quail. 648 Japanese quail chicks (1 week old) were used to evaluate the effects of dietary Cd (0, 40, 80 and 120 mg/kg diet) and two levels of Vit E (0, 250 mg/kg diet) or two levels of natural clay (0 and 100 mg/kg diet) to study the influences of Cd, Vit E, clay or their different combinations on growth performance, carcass traits, some blood biochemical components and Cd residues in muscles and liver. Live BW and weight gain of quails were linearly decreased with increasing dietary Cd levels. Moreover, feed conversion was significantly worsened with increasing Cd level. Mortality percentage was linearly increased as dietary Cd level increased up to 120 mg/kg diet. Carcass percentage was linearly decreased as dietary Cd level increased. While, giblets percentage were linearly and quadratically differed as dietary Cd level increased. Cd caused significant changes in total plasma protein, albumin, globulin, A/G ratio, creatinine, urea-N and uric acid concentrations as well as ALT, AST and ALP activities. Increasing dietary Cd level was associated with its increase in the muscles and liver. Dietary supplementation with 250 mg of Vit E/kg diet or 100 mg clay/kg improved live BW, BW gain and feed conversion when compared with the un-supplemented diet. Quails fed diet contained 250 mg Vit E/kg and those fed 100 mg clay/kg had the highest percentages of carcass and dressing than those fed the un-supplemented diet. Blood plasma biochemical components studied were better when birds received 250 mg of Vit E/kg diet and those received 100 mg clay/kg. Cd residues in the muscles and liver were significantly less in the birds had 250 mg of Vit E/kg or those received 100 mg clay/kg diet than those un-supplemented with Vit E. Growth performance traits and blood plasma biochemical components studied were significantly affected linearly by the interactions among Cd and each of Vit E and clay levels. In conclusion, the present results indicate that the deleterious effects induced by Cd plays a role in decreasing the performance of Japanese quail and that dietary supplementation with natural clay or Vit E may be useful in partly alleviating the adverse effects of Cd.

Type
Research Article
Copyright
© The Animal Consortium 2015 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Abdel-Wahhab, MA, Nada, SA and Amra, HA 1999. Effect of aluminosilicates and bentonite on aflatoxin-induced developmental toxicity in rat. Journal of Applied Toxicology 19, 199204.3.0.CO;2-D>CrossRefGoogle ScholarPubMed
Abdo, KSA and Abdulla, H 2013. Effect of cadmium in drinking water on growth, some haematological and biochemical parameters of chicken. European Journal of Experimental Biology 3, 287291.Google Scholar
Abou-Kassem, DE 2010. Managerial studies on quail performance under Egyptian Conditions. PhD, Faculty of Agriculture, Zagazig University, Zagazig, Egypt.Google Scholar
Abduljaleel, SA and Shuhaimi-Othman, M 2013. Toxicity of cadmium and lead in Gallus gallus domesticus assessments of body weight and metal content in tissues after metal dietary supplements. Pakistan Journal of Biological Sciences 16, 15511556.CrossRefGoogle ScholarPubMed
Al-Waeli, A, Zoidis, E, Pappas, AC, Demiris, N, Zervas, G and Fegeros, K 2013. The role of organic selenium in cadmium toxicity: effects on broiler performance and health status. Animal 7, 386393.CrossRefGoogle ScholarPubMed
Andronikashvili, TG, Tsereteli, BS, Dolidze, VK and Iremashvili, NG 1994. Zeolite supplements in diets for birds. Zootekhniya 5, 1718.Google Scholar
ATSDR (Agency for Toxic Substances and Disease Registry) 2012. Toxicological Profile for Cadmium. September 2012, US Department of Health and Human Services, Public Health Service, Agency for Toxic Substances and Disease Registry, 1600 Clifton Road NE, Mailstop F-62, Atlanta, Georgia 30333, USA.Google Scholar
Bertin, G and Averbeck, D 2006. Cadmium: cellular effects, modifications of biomolecules, modulation of DNA repair and genotoxic consequences (a review). Biochimie 88, 15491559.CrossRefGoogle ScholarPubMed
Bilal, T and Erçag, E 2003. Retention of cadmium in the tissues of broiler chicks by dietary supplemental microbial phytase. Veterinarni Medicina – Czech 7, 199205.CrossRefGoogle Scholar
Biswas, A, Mohan, J and Sastry, KVH 2010. Effect of vitamin E on productive performance and egg quality traits in Indian nataive Kadaknath hen. Asian Australasian Journal Animal Science 23, 396400.CrossRefGoogle Scholar
Chakraborty, T, Maiti, IB and Biswas, BB 1987. A single form of metallothionin is present in both heavy metal induced and neonatal chicken liver. Journal of Bioscience 11, 379390.CrossRefGoogle Scholar
Chen, L, Liu, L and Huang, S 2008. Cadmium activates the mitogen-activated protein kinase (MAPK) pathway via induction of reactive oxygen species and inhibition of protein phosphatases 2A and 5. Journal of Free Radical Biology and Medicine 45, 10351044.CrossRefGoogle ScholarPubMed
Cinar, M, Yigit, AA, Yalcinkaya, İ, Oruc, E, Duru, O and Arslan, M 2011. Cadmium induced changes on growth performance, some biochemical parameters and tissue in broilers: effects of vitamin C and vitamin E. Asian Journal of Animal and Veterinary Advances 6, 923934.CrossRefGoogle Scholar
Dominy, NJ, Davoust, E and Minekus, M 2004. Adaptive function of soil consumption: an in vitro study modeling the human stomach and small intestine. The Journal of Experimental Biology 207, 319324.CrossRefGoogle Scholar
Duncan 1955. Multiple range and F-tests. vol. 11. Biometrics Longman, New York, NY. pp. 142.Google Scholar
El-Deek, AA, El-Sayed, MA, Kandeel, KM, Al-jasass, FM and Mahmoud, MM 2011. Effect of different levels of cadmium and selenium on 2-Biochemical constituents of broiler chickens. Egyptian Poultry Science Journal 31, 117.Google Scholar
El-Deek, AA, El-Sayed, MA, Kandeel, KM and Mahmoud, MM 2010. Effect of different levels of cadmium and selenium on 1-Performance of broiler chickens. Egyptian Poultry Science Journal 30, 699712.Google Scholar
El-Demerdash, FM, Yousef, MI, Kedwany, FS and Baghdadi, HH 2004. Cadmium induced changes in lipid peroxidation, blood hematology, biochemical parameters and semen quality of male rats: protective role of vitamin E and β-carotene. Food and Chemical Toxicology 42, 15631571.CrossRefGoogle ScholarPubMed
Erdogan, Z, Erdogan, S, Celik, S and Unlu, A 2005. Effects of ascorbic acid on cadmium-induced oxidative stress and performance of broilers. Biological Trace Element Research 104, 1932.CrossRefGoogle ScholarPubMed
Gail, L, Baker, CH and Baker, DH 1982. Tolerance of the chick to excess dietary cadmium as influenced by dietary cysteine and by experimental infection with Eimeria acervulina . Journal of Animal Science 54, 983988.Google Scholar
Gore, AB and Qureshi, MA 1997. Enhancement of humoral and cellular immunity by vitamin E after embryonic exposure. Poultry Science 76, 984991.CrossRefGoogle ScholarPubMed
Hardej, D and Trombetta, LD 2004. Metals. In Clinical toxicology principles and mechanism (ed. FA, Barile), pp. 295316. CRC Press, Boca Raton, Florida, USA.Google Scholar
Hassan, RA, Amin, DM, Rahmy, NA, Hatem, ME and Dessouky, MI 2012. Clinicopathological, histopathological and immunological studies on animals exposed to lead and cadmium under experimental conditions. New York Science Journal 5, 120136.Google Scholar
Hayes, AW ed. 1989. Principles and methods of toxicology, 2nd edition, Chapter 3 and 20. Raven Press Ltd, New York, USA.Google Scholar
Herzig, I, Navratilova, M, Suchy, P, Vecerek, V and Totusek, J 2007. Model trial investigating retention in selected tissues using broiler chickens fed cadmium and humic acid. Veterinarni Medicina 52, 162168.CrossRefGoogle Scholar
IARC (International Agency for Research on Cancer) 1993. Cadmium and cadmium compounds. In Beryllium, cadmium, mercury and exposures in the glass manufacturing industry. IARC monographs on the evaluation of carcinogenic risk of chemicals to humans (ed. Sine nomine), 58, pp. 119–239. IARC, Lyon, France.Google Scholar
Julshman, K 1983. Analysis of major and minor elements in mollusks from Norway. PhD. Institute of Nutrition Direction of Bergen Nygardsangen, Bergen University, Bergen, Norway.Google Scholar
Kanter, M, Aksu, B, Akpolat, M, Tarladacalisir, YT, Aktas, C and Uysal, H 2009. Vitamin E protects against oxidative damage caused by cadmium in the blood of rats. European Journal of General Medicine 6, 154160.Google Scholar
Karmakar, R, Bhattacharya, R and Chatterjee, M 2000. Biochemical, haematological and histopathological study in relation to time related cadmium-induced hepatotoxicity in mice. Biometals 13, 231239.CrossRefGoogle ScholarPubMed
Katsumata, H, Kaneco, S, Inomata, K, Itoh, K, Funasaka, K, Masuyama, K, Suzuki, T and Ohta, K 2003. Removal of heavy metals in rinsing wastewater from plating factory by adsorption with economical viable materials. Journal of Environmental Management 69, 187191.CrossRefGoogle ScholarPubMed
Kour, N, Rahman, S, Azmi, S, Hussain, K, Raghuwanshi, P and Dutta, S 2014. Effect of cadmium toxicity on general growth performance parameters in Wistar rats. Indian Journal of Veterinary and Animal Sciences Research 43, 288297.Google Scholar
Leach, RM, Wang, KW and Baker, DE 1979. Cadmium in the foot chain: the effect of dietary cadmium on tissue composition in chicks and laying hens. Journal of Nutrition 109, 437443.CrossRefGoogle Scholar
Liu, J and Klaassen, CD 1996. Dosage-dependent disposition of cadmium in metallothionein-I transgenic mice. Fundamental and Applied Toxicology 29, 294300.CrossRefGoogle Scholar
Lotfy, SA 2000. Clay minerals as natural sources for detoxification of aflatoxins. MSc. Faculty of Agriculture, Zagazig University, Zagazig, Egypt.Google Scholar
Mahrose, KhM, Sonbol, ShM and Abd El-Hack, ME 2012. Response of laying hens to dietary vitamins A, E and selenium supplementation under Egyptian summer conditions. Egyptian Journal of Animal Production 47 (Suppl), 167181.Google Scholar
Mahrous, KF, Hassan, AM, Radwan, HA and Mahmoud, MA 2015. Inhibition of cadmium-induced genotoxicity and histopathological changes in Nile tilapia fish and Tunisian montmorillonite clay. Ecotoxicology and Environmental Safety 119, 140147.CrossRefGoogle ScholarPubMed
Mahrous, KF, Khalil, WKB and Mahmoud, MA 2006. Assessment of toxicity and clastogenicity of sterigmatocystin in Egyptian Nile tilapia. African Journal of Biotechnology 5, 11801189.Google Scholar
Marai, IFM, Ayyat, MS, Gaber, HA and Abdel-Monem, O 1996. Effect of heat stress and its amelioration on reproductive performance of New Zealand White adult female and male rabbits under Egyptian Conditions. Paper presented at the 6th World Rabbit Congress, 9 to 12 July 1996, Toulous, France, 2, pp. 197–202.Google Scholar
National Research Council (NRC) 1994. Nutrient requirements of poultry 9th edition National Academy of Science, Washington, DC, USA.Google Scholar
Navarro, CM, Montilla, PM, Martin, A, Jimenez, J and Utrilla, PM 1993. Free radicals scavenger and antihepatotoxic activity of rosmarinus. Planta Medica 59, 312314.CrossRefGoogle Scholar
Olgun, O 2015. The effect of dietary cadmium supplementation on performance, egg quality, tibia biomechanical properties, and eggshell and bone mineralization in laying quails. Animal 9, 12981303.CrossRefGoogle Scholar
Phillips, TD 1999. Dietary clay in the chemoprevention of aflatoxin-induced disease. Toxicological Sciences 52, 118126.CrossRefGoogle ScholarPubMed
Rahman, MS, Sasanami, T and Mori, M 2007. Effects of cadmium administration on reproductive performance of Japanese quail (Coturnix japonica). The Journal of Poultry Science 44, 9297.CrossRefGoogle Scholar
Rambeck, WA and Kollmer, WE 1990. Modifying cadmium retention in chickens by dietary supplements. Journal of Animal Physiology and Animal Nutrition 63, 6674.CrossRefGoogle Scholar
Sant’Ana, MG, Moraes, R and Bernardi, MM 2005. Toxicity of cadmium in Japanese quail: evaluation of body weight, hepatic and renal function and cellular immune response. Environmental Research 99, 273277.CrossRefGoogle ScholarPubMed
SAS Institute 2008. SAS stat user’s guide. version 9.2 edition. SAS Institute Inc, Cary, NC.Google Scholar
Sell, JL 1975. Cadmium and the laying hen: apparent absorption, tissue distribution and virtual absence of transfer into eggs. Poultry Science 54, 16741678.CrossRefGoogle ScholarPubMed
Toury, R, Boissonneau, E, Stelly, N, Dupuis, Y, Berville, A and Perasso, R 1985. Mitochondrial alterations in Cd2+ – treated rats: general regression of inner membrane cristae and electron transport. Biology of the Cell 55, 7186.CrossRefGoogle ScholarPubMed
Trckova, M, Matlova, L, Dvorska, L and Pavlik, I 2004. Kaolin, bentonite, and zeolites as feed supplements for animals: health advantages and risks. Veterinary Medicine – Czech 49, 389399.CrossRefGoogle Scholar
Whelton, BD, Peterson, DP, Moretti, ES, Mauser, RW and Bhattacharyya, M 1997a. Kidney changes in multiparous, nulliparous and ovariectomized mice fed either a nutrient-sufficient or – deficient diet containing cadmium. Toxicology 119, 123140.CrossRefGoogle ScholarPubMed
Whelton, BD, Peterson, DP, Moretti, ES, Mauser, RW and Bhattacharyya, M 1997b. Hepatic levels of cadmium, zinc and copper in multiparous, nulliparous and ovariectomized mice fed either a nutrient-sufficient or – deficient diet containing cadmium. Toxicology 119, 141153.CrossRefGoogle ScholarPubMed
Yamani, KAO, Rashwan, AA and Magdy, MM 1997. Effects of copper, zinc and tafla dietary supplementation on broiler performance. Paper presented in the International Conference on Animal, Poultry and Rabbit Production and Health, 2 to 4 September 1997, Egyptian International Centre for Agriculture, Dokki, Cairo, Egypt, pp. 457–463.Google Scholar
Yiin, SJ, Chern, CL, Sheu, JY, Tseng, WC and Lin, TH 1999. Cadmium-induced renal lipid peroxidation in rats and protection by selenium. Journal of Toxicology and Environmental Health 57, 403413.Google ScholarPubMed
Yu, BP 1994. Cellular defense against damage from reactive oxygen species. Physiological Reviews 74, 139162.CrossRefGoogle ScholarPubMed
Zídková, J, Melčová, M, Batošová, K, Šestáková, I, Zídek, V, Száková, J, Miholová, D and Tlustoš, P 2014. Impact of cadmium on the level of hepatic metallothioneins, essential elements, and selected enzymes in the experimental rat model. Czech Journal of Animal Science 59, 548556.CrossRefGoogle Scholar