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Vitamin E in laying hens diets

The Role of Clay or Vitamin E in Silver Montazah Layer Hens Fed on Diets Contaminated by Lead at Various Levels. Performance and Egg Components

Published: December 30, 2011
By: Prof. Dr. Ayyat Mohamed Salah, A. I. Attia (Zagazig University) A. A. Bakir and A. A. El – Zaiat (Animal Production Research Institute, Egypt)
SUMMARY
A total number of 240 laying hens and 24 cocks of Silver Montazah strain at 40 weeks of age were randomly divided into 12 groups (20 hens and 2 cocks / each treatment group). Birds in all treatments were nearly similar in the average initial body weights and average daily egg production A 4 x 3 factorial design experimentwas performed including four levels of supplemented lead (0. 250,500 and 1000 mg/kg diet) and three levels of feed additives (without clay or vitamin E, 3 % Natural clay, tafla, and 200 mg /kg vitamin E). Live body weight change, egg production and egg weight, egg compenents, fertility and hatchability were studied.
Results obtained reveled that lead contaminated feed caused significant live body weight retardation, lower egg production and egg weight, lower egg component and lower fertility and hatchability. On the other hand, the addition of natural clay or vitamin E to the diets for laying hens caused a significant improve in all aforementioned traits. With respect to interaction between lead and the experimental additives the results obtained showed that, within each lead level clay or vitamin E supplementation recorded higher body weight, increased egg production, egg weight and best egg fertility & hatchability.
On the basis of the results obtained in this study, it can be concluded that the consumption of polluted diets with heavy metal such as lead cause rious effects in the productive performance, egg components and reproductive performance of Silver Montazah laying hens, while, dietary addition of natural clay or vitamin E to the diet of laying hens cause beneficial effects on egg components, productive and reproductive performance. Moreover, clay or vitamin E supplementation diminished the toxic effect of lead on all egg quality, productive and reproductive results during treatment period and supported recovering after the lead contamination.
Key words:  Lead, growth performance, egg production, fertility and hatchability 
INTRODUCTION
 The contaminations of poultry feeds with heavy metals especially lead cause a high reduction in growth rate, feed efficiency and egg production, which result finally great economic loss for poultry farmers. Nearly, all potential food ingredients contain some kinds of heavy metals. Lead is considered one of the major environmental pollutants (Jeng et al., 1997) .
The contamination of laying hen s diets or environment with heavy metals remains a problem for poultry meat industry, food safety regulatory agencies and concerned consumers. According to the extensive use of lead in human activities e.g. industrial processes, plant protection, paint industry and motor-engine emission, the possibilities of bird s diet pollution become more evident.
Previous works on poultry have revealed that lead consumption can cause rious affects on growth performance (Youssef et al., 1995 and Abou-Zeid et al., 2000), efficiency of feed utilization (Edens and Melvin, 1989), egg production (Eden and Garlieh, 1983) and reproductive efficiency (Vodela et al., 1997).
Supplementation of poultry diets with natural clays enhances growth rate and egg production. This may be due to improvement in either of feed conversion, digestibility, ability to bind metallic cations and rendering them more available to the bird and nitrogen retention in bird body, in addition to retard the absorption of toxic products of digestion that reduce toxicity. Ability of clays to diminish the harmful effects of radiation may have a role in this respect (Ayyat and Marai, 1997).
Vitamin E has a number of different biological function. One of the most important functions is the role as an intracellular antioxidant. In this capacity Gore and Qureshi (1997) speculated that vitamin E prevents oxidation of unsaturated lipid materials within cells, thus protecting the cell membrane from oxidative damage. Vitamin E sometimes called antisterility vitamin. As reported by Kling and Scares (1980), Japanes quail maintained on a low vitamin E diet for 35 weeks, showed a lower presence of fertile eggs after 20 weeks and hatchability severely depressed probably due to the inadequate deposition of vitamin E in the egg to support embryonic growth
Therefore, the present study was carried out to investigate the efficacy of clay and vitamin E to alleviate severity of lead contamination and its effect on the productive performance, egg quality and reproductive performance of silver Montaza layers.
MATERIALS AND METHODS
This work was carried out at Inshas Poultry Research Farm belonging to Animal Production Research Institute, Agricultural Research Center, Ministry of Agriculture, Cairo, Egypt.
A total number of 240 hens and 24 cocks of Silver Montazah strain at 40  weeks of age were randomly divided into 12 groups (20 hens and 2 cocks / each treatment group). Birds in all treatments were nearly similar in the average initial body weights and average daily egg production. A 4x3 factorial design experiment was performed including four levels of supplemented lead (0.250 500 and 1000 mg/kg diet) and three levels of feed additives (without clay or vitamin E, 3 % Natural clay, tafla, and 200 mg /kg vitamin E). Tafla is a desert clay and analyzed as soluble cations and anions (meq/ 100 g dry matter soil ) were Ca++ 0.75, Mg++ 0.25, Na+ 0.05, K+ 0.10, Cl 0.55, SO4 0.30 and HCO3 0.75. Exchangeable cations (meq/100 g DM soil) were 2.65 and available nutrients (mg/100 g dry matter soil) were P 5.0, K 1.2, Mn 2.4, Zn 0.74, Cu 0.30 and Fe 0.55 mg( Maria et al 1996). The composition and calculated chemical analysis of the experimental laying diet are presented in Table 1. The birds were fed the contaminated diets from 40 to 52 weeks of age, while at period from 52 to 56 weeks of age, birds were fed diets without lead addition.
Birds of all experimental groups were housed in suitable pens during the experimental period and were kept in the same conditions. Feed and water were offered ad libitum and maintained on 16 hours light per day. Body weight was recorded at the start (40 weeks old) then biweekly intervals there after, during the experimental periods. Feed consumption was recorded biweekly, while egg production rate and egg weight were recorded daily.
At 52 and 56 weeks of age ten eggs from each treatment group were randomly selected  to measure egg components. Eggs were individually weighted, broken and albumine, yolk and shell weight were recorded to calculate albumine, yolk and shell percentage values.
During the experimental period eggs were collected from each experimental group, then weighed and stored for one week in refrigerator (at 12 oC and 70 % RH). Eggs were maintained in room temperature for about 12 hours, before incubation. Only sound and normal eggs were fumigated with formaldhyde gas and set in a forced air incubator. Incubation was carried out under recommended conditions for chicks eggs. At the 14th days of incubation period infertile eggs (those no visible embryonic development) and dead embryo were removed and recorded. Fertility was estimated at the end of hatching period as number of fertile eggs / number of eggs set. Hatchability of eggs from each experimental group was also estimated as ratio of number of chicks hatched to number of fertile eggs.
The obtained data were statistically analyzed by using 4x3 factorial design by Snedecor and Cochran (1982). according to the following model: Yijk = μ + Li + Aj + LAij + eijk
where, μ = the overall mean, Li = the fixed effect of ith lead level in diets   (i = 1,.. 4), Aj = the fixed effect of jth feed additives (j = 1,.. 3), LAij = the interaction between the ith lead level and feed additives and eijk = random error. Significant differences were determined by Duncan s Multiple Range test (Duncan, 1955).
RESULTS AND DISCUSSION
Layer performance:
Body weight:
Effect of lead pollution:
Growth inhibition is one sign of overt toxicosis in chickens.In this experiment, significant (P<0.05)  reduction was shown in live body weight with increasing the lead level in the diet, during the whole experimental period when compared with those fed the control diet without lead contamination  (Table 2). At 56 weeks of age, the reduction in growth rate was slightly lower than in the other periods, this may be related to the physiological response of the birds to recover toxicity from the lead.
The reduction in live body weight as affected with the lead pollution may be related either to change in behavior of eating habbit through the inhibition of the hypothalamic appetite center  (Cragg and Ress, 1984) or to alteration in digestive enzyme secretion (Deborah et al., 1980). Beyer et al. (1988) reported that birds of different species exposed to different levels of dietry lead exhibited cases of proventriculi impacted with feed, reduced feed consumption, smaller weight and death. The assent results concerning live body weight retardation may be also related to the diminishing in hemoglobin synthesis and can react with cell membranes, This may cause increased permeability of the cells and damage or even death of those cells. Lead can disppace calcium in bone, deposit there and from softer, lead binds with the sulfhydryl bonds and inactivates the cysteine-containing enzymes, which allows more internal toxicity from free radicals, chemicals, and other heavy metals. Lead is also an immunosuppressant; it lowers host resistance to bacteria and viruses, and thus allows increase infection susceptibility (Hass, 1992).
Decreased body weight was also observed in Japanese quail hens exposed to dietary lead at 500 mg from hatching through reproduction (Edens et al 1976, Edens and Garlich, 1983).A recent study by Vodela et al., (1997) demonstrated a linear relationship between increasing concentration of the lead in feeding diet and a decreasing body weight of broiler breeder hens.
However, many other workers found no growth changes due to lead treatments (Custer et al., 1984; Krishman and Marshall 1988; and Jeng et al., 1997). This could be attributed to different doses of administration, compound nature of lead and / or to the animal species.
Effect of feed additives:
Live body weight did not show any significant improvement by the feed additives (Table 2). Final body weight of hens fed diet supplemented with clay or vitamin E slightly increased than those fed control diet. Karelina (1985) and Gonalez et al. (1996) found that supplementing various sources of natural clay in broiler diets increased body gain and improved feed conversion. On the other hand. Ward et al. (1993) found that growth rate decreased with addition of 0.75% sodium zeolite in chick diets.  Larry (2002) indicated that vitamin E supplementation in the diets improved the growth rate.
Interaction between feed additives and lead pollution:
Live body weight was not significantly affected due to the interaction effects between feed additives and lead contamination (Table 2). At any lead level, clay supplementation in hen diets recorded higher body weight than the other experimental groups then those fed diets supplemented with vitamin E.The results show that lead poisoning can be partially reduced by providing supplementaly vitamin E and natural clay, but the interaction of vitamin E remains to be elucidated.In this respect Larry (2002) reported that vitamin E improves cellular immune function, which potentially lowers the risk of infection. Also, Shalaby and Ayyat (1999) reported that the natural clay addition in chicken diets reduced the toxicity effects of the pesticides (profenofos and monocrotophos).
Egg production and egg weight:
Effect of lead pollution:
Egg production was significantly (P<0.01 or 0.001) dcreased in hens as the concentration of the lead  diets increased at all the experimental periods (Table 3). The presence of lead in the diet could have contributed to impaired egg production through the suppression of calcium metabolism. Dietary lead at 200 mg is known to influence egg production and calcium metabolism (Edens and Garlich, 1983). When lead was added to the diet, highly significant decrease occurred in red blood cell delta amino levulinic acid dehydratase (RBCALAD) activity. The lowered enzyme activity may be related to calcium metabolism and egg production (Stone and Scare 1976). Dcreased egg production was also observed in laying hens exposed to lead concentrations of 200 mg /kg diet for 4 weeks (Edens and Garlich, 1983).
Egg weight significantly (P<0.001) affected with lead contamination in hen feeds at 40-44 and 48-52 weeks of age (Table 3). Egg weight increased slightly with increasing lead level in hen diets at 48-52 weeks of age. These findings may be attributed to the decrease in egg production when hens fed on the diets contaminated with lead. Estrogen plays a rol in controlling egg weights vai changes in fat metabolism and oviductal protein synthesis (Whirtehead et al., 1993). A decreased level of estrogen receptors (58%) was reported in a human breast cancer cell line exposed to cadmium (Morales et al., 1994). A decrease in uterine estradiol receptors was also observed in rats exposed to 200 mg of lead in drinking water for 35 d (Wiebe and Barr, 1988). Exposure to low concentration of lead in drinking water for 10 weeks in broiler breeder hers resulted in dcreased egg weights (Vodela et al. 1997).On the contrary, Whisenhunt and Maurice (1981) reported that feeding chicken hens on diet containing 500 mg lead/kg diet showed no significant effects on egg production and egg weight.
Effect of feed additives:
Clay or vitamin E supplementation significantly(P<0.01 or P< 0.001)  increased egg production and egg weights comparing to hens fed on a diet without supplementation during the whole experimental periods (Table 3) except egg weight during 52-56 weeks of age. Higher values of both egg production and egg weights were also observed by Abd El-Latif (1999) with Japanese quail birds which received vitamin E (25 and 50 mg / kg diet). This observation could explain the important role of vitamin E in female reproductive function (King and Scares 1980). The beneficial effect of vitamin E for egg production was associated with increased plasma concentration of egg yolk precursors, vitellogenin and very low density lipoprotein (Bollengier et al., 1999). According to Elliot and Edwards (1991) natural zeolite a clinoptilolite-bearing rock material, were found to increase egg weight and albumin weight when it was incorporated in the hen s diet at an inclusion rate of less than 10%.
Interaction between feed additives and lead pollution:
The results obtained revealed that egg production  and egg weights were significantly (P<0.05 and P<0.01) affected by the interaction between feed additives and lead contamination during the whole experimental period, except at 52-56 weeks of age (Table 3). Within any lead level, clay or vitamin E supplementation increased egg production  and egg weights when compared with the groups fed diets without feed additives. In general, the results indicated that the use of the cation exchange capability to reduce the uptake, and influence the distribution of these heavy metals in poultry tissues is promising. Evans et al. (1993) concluded that the use of synthetic and natural zeolites limited economic benefit or application for improving the performance and egg shell quality in poultry. On the other hand vitamin E supplementation may have enhanced synthesis of egg yolk precursors, uitelloginin and very low density lipoprotein in the liver by protecting the liver from lipid peroxidation and damage to cell membranes.
Fertility and hatchability:
Effect of lead pollution :
Data in Table 4 showed that increasing lead level in the diets of hens significantly (P<0.001) decreased the fertility and hatchability percentages when compared with those fed the control diet without lead contamination. It is clear that increasing the exposing time to lead contamination the harmful effect on the fertility and hatchability increased (Table 4).At 52-56 weeks of age, the effect of lead toxicity on fertility and hatchability reduced, these findings may relate to the ability of birds to recover during a layer period of lead toxicity. The reduction in fertility rates in the present study may be due to impaired semen characteristics in this study. Abaza et al., (1996) demonstrated that the lead cause dysfunction in the reproductive and physiological systems of cockerels. It is manifested in the decrease in semen volume and relative sperm motility. Edens et al. (1976) reported reproductive dysfunction increasing significantly the age of sexual maturity in Japanese quail fed diet contained 10, 100 or 1000 mg lead.While the reduction in hatchability rates may be due to the eggs laid by hens treated with lead contained high proportion of source element (Jeng et al., 1997).The egg components are the main source nutrients for the developing embryo and the newly hatched chicks absorb in their body approximately 6% of the total egg yolk. This amount of yolk usually is consumed during the first days of life after hatching. This might mean that lead will be exist in the metabolism of the developing embryo as well as during the early days of the hatched chick.
The obtained results are in agreement with the  findings, De Gennaro (1978) who reported that the lead-treated embryos failed to be hatched and the embryos died before 21-day of incubation. Also, Vodela et al. (1997) indicated that the broilers drinking water containing 6.7 mg lead significantly increased the embryonic mortality (68.84%) compared with the control birds (16.16%).
Effect of feed additives :
Fertility and hatchability percentages were insignificantly increased by the clay or vitamin E supplementation feed in the diets during the whole experimental period, except at 48 - 52 weeks of age the egg fertility and  hatchability percentages significantly (P<0.05) increased (Table 4).This finding may be related to the improvement of egg quality with feed additives
Interaction between feed additives and lead pollution:
The interaction between feed additives and lead level in fertility and hatchability percentages were not significant during all the experimental periods (Table 4).
Egg components:
Effect of lead pollution:
Data in Table 5 showed significant (P<0.001) increase in  albumin percentage and significant (P<0.001) decrease in  yolk percentage with increasing lead level in the diet at 52  weeks of age , while egg shell  percentage were not significantly affected .
Effect of feed additives :
Egg components percentages  were not significantly affected by clay or vitamin E supplementation  at 52 weeks of age (Table 5). According to Yannakopoylps et al., (1998) natural zeolite was found to increase both egg weight and albumin weight, while yolk weight was not significantly affected. They also found that the yolk : albumin ratio was lower (more albumin) in eggs laid by hens on zeolite treatments .  Hossain and Sergio (1995) found insignificant effect of vitamin E on egg quality in broiler breeders.
Interaction between feed additives and lead pollution:
There was no significant interaction between the feed additives and lead level in egg components percentages  at 52 weeks of age (Table 5).
On the basis of the results obtained in this study, it can be concluded that the consumption of polluted diets with heavy metal such as lead cause rious effects in the productive performance, egg components and reproductive performance of Silver Montazah laying hens, while, dietary addition of natural clay or vitamin E to the diet of laying hens cause beneficial effects on egg components, productive and reproductive performance. Moreover, clay or vitamin E supplementation diminished the toxic effect of lead on all egg quality, productive and reproductive results during treatment period and supported recovering after the lead contamination.
REFERENCES
Abaza M. Azza El-Sebai and Szalay L.. (1996). Reproductive traits and serum parameters of cockerels exposed to heavy metals. Egyp. J.  Poult. Sci., 16 (III): 689-702.
Abd Eil-Latif, S.A. (1999). Nutritional interrelationships of vitamine E and selenium on laying Japanese quail. Egyp. J. Nutr. and Feeds (Special Issue) 2:711-718.
Abou-Zeid, A. E.; Sorour, J. and El-Habbak, M. M (2000). Magnitude of lead Toxicity in white Pekine duckling. Egyp. J. Poult. Sci., 20:789-815.
Ayyat M.S. and Marai I.F.M. (1997). Use of natural clays in animal production. Proceedings of the International Conference on Animal, Poultry and Rabbit Production and Health, Cairo, Egypt, pp 91 -111.
Beyer, W. N.; Spann, J. W.; Sileo, L. and Franson, J. C. (1988). Lead poisoning in Six Captive avain species. Arch. Environ. Contam. Toxicol., 17 : 121 - 130.
Bollengier, S.; Williams, P.E.V.; and Whithead, C.C. (1999). Optimal dietary concentration of vitamin E for alleviating the effect of heat stress on egg production in laying hens. Brit. Poult. Sci.. 40 : 102 -107.
Cragg, B. and Rees, S. (1984). Increased body: brain weight ratio in developing rats after low exposure to organic lead. Exp. Neural. 86; 113.
Custer, T. W.; Franson, J. C. and Pattee, O. H. (1984). Tissue lead distribution and hematologic effects in Amercan Kestrels fed biological incorporated lead. J. Wildlife Disease., 20 : 39 - 42.
De Gennaro L.D. (1978). The effects of lead nitrate on the central nervous system of the chick embryo. 1. Observations of light and electron microscopy. Growth, 24: 141-155.
Deborah A.; Slechta, C.; Grman, R. H. and Seidman, D. (1980). Lead-induced crop dysfunction in the Pigeon. Toxi. Appli. Pharm.. 52 :462-467.
Duncan D.B. (1955). Multiple Range and Multiple F-test. Biometrics, 11: 1-42.
Edens F.W. and Garlich J.D. (1983). Lead induced egg production decreases in Leghorn and Japanese quail hens. Poult. Sci., 62: 1757-1763.
Edens F.W. and Melvin V.K. (1989). Lead influences on physiological and growth responses in Conturnix Japonica selected for large body weights. Envir. Res., 50: 140-156.
Edens F.W., Emily B., Morgan G.W., Bursian S.J. and Thaxton P. (1976). Effect of dietary lead on reproductive performance in Japanese quail. Tox. Appl. Pharmac., 38: 307-314.
Elliot, M.A. and Edwards H.M. (1991). Comparison of the effects of synthetic and natural zeolite on laying hen. Poul. Sci., 70 (10) : 2115-2130.
Evans M., Farrell D.J. and Farrell D.J. (1993). Are there economic benefits to adding zeolites to poultry diets ; Recent advances in animal nutrition in Australia, Univ. New England, Armidale, Australia, 303-316.
Gonalez L.M., Valdivie M. and Lon-Wo E. (1996) Sacchaina and zeolite in broiler feeding. Cuban Journal of Agric. Sci., 30: 30-313.
Gore, A. B. and Qureshi, M. A. (1997). Enhancement of humoral and cellular immunity by vitamin E after embryonic exposure. Poult. Sci.76 : 984 - 991.
Hass, E. (1992). Staying Healthy with Nutrition, The Complete Guide to Diet and Nutritional Medicine. 10th printing. Celestial Arts (Berkeley, CA), 1168 p. Health World, Health Bookstore - ISBN 0890874816.
Hossain, S.M. and Sergio, L. (1995). Influence of various levels of vitamin E on reproductive performance of broiler breeders. Poult. Sci., 74 (suppl.) : 133.
Jeng S.L., Eec S.J., Eiu Y.F., Yang S.C. and Eiou P.P. (1997). Effect of lead ingestion on concentrations of lead in tissues and eggs of laying Tsaiya ducks in Taiwan. Poult. Sci., 76 (I): 13-16.
Karelina, O. (1985). 2,eolites for feeding broilers. Ptitsevodstvo, 9 : 26.
King, L. J. and Scares, J. H. (1980). Vitamin E deficiency in the Japanese quail. Poult. Sci., 59 : 2352 - 2354.
Klaassen C.D. (1980). Goodman and Gilman s the pharmacological basis of therapeutic. 6th ed., Macmillan Publishing Co. Inc., New York, p. 1616.
Krishnan, K. and Marshall, W. D. (1988). Avian tissues as bioindicators of exposure to Alkylleads : Metabolism of ethyllead salt by Japanese quail. Envir. Sci. Technol., 22 : 1038 - 1043.
Larry J. (2002). The Merck Manual Geriatrics, Section 8: Metabolic and Endocrine Disorders, Chapter 60. Vitamin and Trace Mineral Disorders. Copyright, Merck Co. Inc., 2002, Whitehouse Station, NJ, USA
Maria, I.F.M; Ayyat, M.S.; Gaber, H.A. and Abdel-Momem, U.M. (1996). Effect of heat stress and its amelioration on reproductive performance of New Zeland White adult female and male rabbits under Egyptian conditions, 6 th World Rabbit Congr., Toulous, .).
Morales, G. P.; Sacenda, M.; Kenney, M.; Kim, M.; Solomon, D.; Gottardis, M. M.; Solomon, H. B.; Sholler, P. F.; Jordan, V. C. and Martin, M. B. (1994). Effect of cadmium on estrogen receptor levelsand estrogen- induced responses in human breast cancer cell. J. Biol. Chem.269: 16896-16901.
NRC (1994). Nutrient Requirements of Poultry. 9th Revised Edition, National Academy Press, Wasington, D.C., USA.
Shalaby A.A. and Ayyat M.S. (1999). Effect of natural clay addition of the residues of profenofos and monocrotophos and their effect on some blood components in liens. Egyptian Journal of Applied Science, 14(6): 286-300.
Snedecor, G.W. and Cochran, G.W. (1982). Statistical methods. 6th Ed. The Iowa State University. Press Ames., USA.
Stone C.L. and Scares J.H. (1976). Studies on the metabolism of lead in the Japanese quail. Poult. Sci., 53: 1982.
Van Tienhouven, A (1968). Reproductive Physiology of Vertebrates.  W.B. Saunders, Philadelphia.
Vodela J.K., Leri2; S.D., Renden J.A., Mcelhenney W.H. and Kemppainen B.W. (1997). Drinking water contaminated (arsenic cadmium, lead, benzene and trichloroethylene). 2. Effects on reproductive performance, egg quality and embryo toxicity in broiler breeders. Poult. Sci., 76: 1493-1500.
Ward T.L., Watkins K.L. and Southern L.L. (1993). Interactive effect of sodium zeolite A and Eimeria acervulina infection on growth and tissue minerals in chicks. Poult. Sci., 72 (11): 2172-2175.
Whisenhunt J.E. anc Maurice D.V. (1981). The response of egg shell quality to dietary manganese and lead. Poult. Sci., 60: 1609.
Whitehead, C. C.; Bowman, A. S. and Giffm, H. D. (1993). Regulation of plasma oestrogen by dietary fats in the laying hen relationship with egg weight. Br Poult. Sci., 34 : 999 - 1010.
Wiebe, J. P. and Barr, K. J. (1988). Effect of prenatal and neonatal exposure to lead on the affinity and number of estradiol receptors in uterus. J. Toxicol. Envir Helth., 24: 451 - 460.
Yannakopoylps, A. L., Tserveni - Gousi, A. S. and Christaki, E. (1998). Effect of natural zeolite on yolk: albumine ratio in hen eggs. Brit. Poult. Sci., 39 : 506 - 510.
Youssef, S. A.; El-Miniawy, H. M.; Soliman, G. A. and Brawy, A. M. (1995). Some lexicological and pathological studies on the effect of subchronic lead poisoning in broiler with reference to immune system. Egyp. J.  Comp. - Pathol. and Clin. Pathol. 8 : 93-104.
Table 1. Composition and calculated analysis of the experimental laying diet:
The Role of Clay or Vitamin E in Silver Montazah Layer Hens Fed on Diets Contaminated by Lead at Various Levels. Performance and Egg Components - Image 1
Each kg of premix contain : 5, 000, 000 I. U. Vit. A; 1, 250, 000 I. U. Vit. D3; 2 g Vit. K; 3g Vit B2 ; 15 g nicotinic acid; 4 g calcium D-Pantothenate; 8 g Vit. B12 ; 150 choline chloride ; 80 g D. O. T. (35 Dinitro ortho toluamide); 40 g manganese; 20 g iron; 20 g zinc; 1 g copper; 1 g iodine and 1 g cobalt. 
Table 2. Live body weight , g, mean ±SE, of Silver Montazah hens as affected by lead, feed additives  and their interaction at different experimental ages.
The Role of Clay or Vitamin E in Silver Montazah Layer Hens Fed on Diets Contaminated by Lead at Various Levels. Performance and Egg Components - Image 2
Means in the same column within each classification with different letters, differ significantly (P<0.05).
NS = not significant, * P<0.05 
Table 3. Egg production  (mean ±SE) of Silver Montazah laying hens as affected by lead, feed additives and their interaction during the different experimental periods.
Table 4. Fertility and hatchability (mean + SE) of Silver Montazah laying hens as affected by lead, feed additives and their interaction   during the different experimental periods.

The Role of Clay or Vitamin E in Silver Montazah Layer Hens Fed on Diets Contaminated by Lead at Various Levels. Performance and Egg Components - Image 5
Table 5. Egg components (mean ±SE) of Silver Montazah laying hens as affected by lead, feed additives and their  interaction at 52 weeks of age
The Role of Clay or Vitamin E in Silver Montazah Layer Hens Fed on Diets Contaminated by Lead at Various Levels. Performance and Egg Components - Image 7
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Authors:
Prof. Dr. Ayyat Mohamed Salah
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Maheswar Rath
6 de febrero de 2013

Dear author,
Your target of the experiment is to project how some clay and vitE support contaminated feed on laying hen.
My point is chicken feed should be properly screened before feeding for commercial purpose when layers are in confined rearing program by farmer. In free range rearing birds has selective eating powers.
My worry is what I should remember from such experiment? If i know from test that the feed is contaminated with heavy metal then how it is fed to bird? Unless the feed is free from such heavy metals, toxins, antitoxins then perhaps any additive to remove the impact is a costly proposal. In my opinion let us look to the brighter side of the layers who are to be protected through planning for best nutrition. Nutritionists use bantonite ,vitE all the time as toxin binder and for better resistance power etc.. Pl let me kindly be enlighten on the targets of your experiment? Thank you sir.

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Mahmood Ali Tabassum
6 de febrero de 2013

Informative article related to contaminated feed and its remedy.

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Kunal Goyal
2 de febrero de 2013

Respected Dr.,

Does any Clay based Pellet Binder bind vitamins? My specific query is regarding B Group Vitamins.

Is there any suggested particle size of such clay binders?

Thanks & Sincere Regards

Kunal Goyal

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Prof. Dr. Ayyat Mohamed Salah
19 de enero de 2012
Dr. Jenan Najdat Al-bazzaz Dr. Zahid Hasan Dr. Nitin Suryavanshi Dr. Pardeep Bansal Please visit my websit: www.ayyat.4t.com There are many manuscripts published in scientific journals related to the use on natural clay
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Prof. Dr. Ayyat Mohamed Salah
19 de enero de 2012
In this study we used bentonite. Natural clays are crystalline alumino-silicates characterized by their ably to exchange cations without major changes in structure. Zeolite and bentonite are the most common natural clays wed in animal production. Natural clays can be used as feed binders hi feed manufacturing. Natural clays can adsorb toxic products of digestion and decrease the accumulation of toxic substance in animal tissues, thus decreasing the incidence of internal disorders. Natural clays may stimulate the lining of the intestinal tract that increases the production of antibodies, which could then inhibit the onset of enteritis. Addition of natural clays in animal diets improves growth rate, feed conversion and increases return from body gain and final margin. Nutrient digestibility increases by natural clay supplementation in animal diets, due to its low rate of passage.
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Jenan Najdat Al-bazzaz
19 de enero de 2012

Thank u dr.ayyat for your useful article. I'm a veternerian and get Msc. degree in poultry diseases. My question dear dr. if there is any toxicity with lead in drinking water of chicken can we treated it with clay or vit. E especialy we know that the bird drink double dose when compard with feed intake and how much we must add to the drinking water for poultry especially brioler breed and how long we must added it?

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Pardeep Bansal
19 de enero de 2012

please tell name of clay

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Nitin  Suryavanshi
19 de enero de 2012

A good article about contaminated feed and indicating the efficacy of VIT.E as a potential antioxidant. 
it is also revealed that lead as a contaminant to poultry feed especially in layers is hazardous to human as the meat ,egg .albumen ,liver ,has the potential to absorb these toxic effect ,causing health hazard to humans.

also i wish to know what are the effects on broilers ,and especially the breeders [hatchability % ,embryo deformity ,and subsequent chick performance on farms.]
thanks

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Zahid Hasan
19 de enero de 2012
Thank you again for reply me. My Email: zahidh59@gmail.com . Sir I want to know from you about cobb500 great grand parent related journals,publication,management guide if you kind to me
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Prof. Dr. Ayyat Mohamed Salah
18 de enero de 2012
Mr. Zahid Hasan Dear colleague Please sent your Email, and Thank You for your comment
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PhD, senior director of animal welfare at Tyson Foods
United States
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