Egg Iron Enrichment in Response to Various Levels of Pomegranate by-Product in Laying Hen Diet


Department of Animal Science, Faculty of Agriculture, Bu Ali Sina University, Hamedan, Iran


The present study was conducted to investigate the effects of different levels of pomegranate by- product (PBP) on performance, egg quality and blood parameters in laying hens. A total of 144 Bobze layer hens from 44 to 56 weeks during 12 weeks were randomly assigned into 4 treatments including 0 (control, corn and soy bean meal), 4, 8 and 12% of PBP, with 4 replicates and 9 layers in each. Results have indicated thatthere was a significant increase in egg mass, egg production the decrease in feed intake and feed conversion ratio by 4% PBP in comparison to other treatments (P<0.05). Significantly increased egg weight by inclusion of 8% PBP compared with 0 and 12% PBP. There was no significant effect of PBP levels on external and internal egg characteristics. The lowest cholesterol and the higher high-density lipoprotein and malondialdehyde have shown by 4% PBP (P<0.05). The highest amount of iron in egg yolk was observed respectively by treatments 4 and 12% PBP. It was concluded that egg yolk iron and production rate were increased by 4% PBP supplementation in diet.



Eggs bring up as a good source of the three principal nutritional requirements: energy, protein and essential ancillary factors (vitamins, carotenoids, minerals and certain fatty acids). In terms of this fact eggs are economical feed and near the perfect food (Ramadan et al. 2010). Today nutritionists have close attention to increasing the nutritive value of eggs through altering the nutritional composition of the layer hens diet. Many types of minerals can also be enriched in designer eggs. This could be achieved by the dietary manipulation of hen's diet. These trace minerals are very important for human health because the deficiency of these components are leading to development of certain deficiency disease (Al-Massad et al. 2011). Lack of iron is one of the most prevalent nutritional disorders affecting human health and being recognized as causing 2.4% of the total global burden of diseases (Ezzati et al. 2004; Rodgers et al. 2004). It is well known that the nutritive composition of egg can be changed by the nutritional composition of diet fed (Ambikadevi and Lalithambika, 2000; Paik et al. 2009). Enriched eggs with iron will resulted in eggs with superior biological and nutritional value for human consumption (Park et al. 2004). In humans, iron is an essential component of proteins involved in oxygen transport (Ramadan et al. 2010; Varmaghany et al. 2013). Park et al. (2004) have reported Fe content of egg could be enriched by Fe supplementation and organic forms (Fe-Met or Availa-Fe) are more effective than sulfate form. Researches have demonstrated that iron content of eggs could be increased by organic iron supplemented (Paik et al. 2009). The total pomegranate production in Iran was estimated to be approximately seven hundred thousand (700000) tons annually (FAO, 2009) which accounted for half of the global production (Abbasi et al. 2008; Eikani et al. 2012). Increasing agro-industrial units for producing pomegranate juice has led to increased amounts of by-products including peels and seeds (Shabtay et al. 2008; Oliveira et al. 2010). Annual production of pomegranate by-products (peels and seeds) exceeds one hundred and twenty thousand (120000) tons in Iran (Afshar, 2011; Taher-Maddah et al. 2012). In spite of sufficient knowledge of the biological effects of pomegranate by- product in human and animal health, there is scant information on its nutritive value for poultry (Viuda Martos et al. 2010). Pomegranate peels are characterized by an interior network of membranes comprising almost 26-30% of total fruit weight and are characterized by substantial amounts of phenolic compounds, including flavonoids (anthocyanins, catechins and other complex flavonoids) and hydrolyzable tannins (punicalin, pedunculagin, punicalagin, gallic and ellagic acid). These compounds are concentrated in pomegranate peel and juice, which account for 92% of the antioxidant activity associated with the fruit (Negi et al. 2003; Afaq et al. 2005; Zahin et al. 2010). Iron and magnesium are present in large quantities in the peel as compared with comestible part, the pomegranate contains 47.5 mg/g (Nasr et al. 1996). According to the Iran situation in facing the anemia crisis especially in children, in this study an attempt has been made to enrich egg yolk iron content in respect to different levels of pomegranate by- product (PBP) iron in layers diet.



Animals, management and sample collection

In total 144 Bovans laying hen with an initial age of 44 weeks were in completely randomized design (CRD) allocated into 4 dietary treatments, 4 replicates and 9 birds in each. Four dietary treatments were included: a control diet (without PBP), and 2, 3 and 4 treatments by 4, 8 and 12% PBP levels respectively, during 12 weeks experiment. The experimental composition diets presented in Table 1. Feed intake (FI) was recorded weekly and egg production (EP) and egg weight (EW) were considered daily. Average daily feed intake (ADFI), egg mass (EM) hen-day egg production (HDP) and feed conversion ratio (FCR) were calculated by these information. Egg mass was calculated by multiplying percentage egg production by egg weight for each replicate. Hen-day egg production was computed using following formula given by North (North and Bell, 1990):

Egg production (%)= (number of egg produced on each day/number of hens alive on each day) × 100

At 56 weeks of age, blood samples (5 mL) were collected from the brachial vein and centrifuged for 20 minutes at 3500 rpm to obtain plasma samples. Plasma samples were used for the determination of the cholesterol, triglyceride, high density lipoprotein (HDL), total antioxidant (TA) and malondialdehyde (MDA) contents. Cholesterol, triglyceride and HDL were measured by enzymatic method. Malondialdehyde was tested as an index of lipid peroxidation by the thiobarbituric acid (TBA) method according to Hong et al. (1989). Total antioxidant was assayed by Randox kit according to Miller et al. (1993). Egg internal (albumen and yolk indexes, Haugh unit (HU)) and external (egg shell weight, ratio and breaking strength) quality parameters were determined in four randomly selected eggs in each replicate in every two weeks (16 eggs in treatment in 2 weeks). After weighting eggs individually, they were broken by sheer pressure to measure breaking strength, and then the shells were washed and dried in an oven for determination of shell weight (Harms and Russell, 2001). Also, total lipid present in a homogenized sample of egg yolk were extracted by the method of Folch et al. (1957) and determination of egg yolk cholesterol according to Caston and Leeson (1990) and egg yolk iron according to Kiliç et al. (2002). Albumen and yolk heights and widths were measured for Haugh unit and yolk index respectively in each egg. Then Haugh unit was calculated using the following formula (Eikani et al. 2012):

HU= 100 log (AH+7.57-1.7 EW0.37)


AH: albumen height.

EW: egg weight (g).


Chemical analysis of feed

In order in formulating diet initially dry matter (DM), crude protein (CP), crude fiber (CF), ether extract (EE), ash and gross energy (GE) in feed analysis laboratory system by using AOAC (1990) were determined. Also, the amount of tannin based on the method (Schofield et al. 2001) and iron (AOAC, 2000) were measured by Spectrophotometry (Table 2).


Table 1 Composition and chemical analyses of experimental diets


1 Vitamin premix supplied per kg of diet: vitamin A: 7.2 g; vitamin D3: 7 g; vitamin E: 14.4 g; vitamin K3: 1.6 g; vitamin B1: 0.72 g; vitamin B2: 3.3 g; vitamin B3: 12.16 g; vitamin B5: 12 g; vitamin B6: 6.2 mg; vitamin B12: 0.6 g; Biotin: 0.2 g and Cholin chloride: 440 mg.

2 Mineral premix supplied per kg of diet: Manganese: 64 mg; Iron: 100 mg; Zinc: 44 mg; Copper: 16 mg; Iodine: 0.64 mg and Selenium: 8 mg.


Table 2 Chemical analysis of feed ingredients (as-fed basis, %)


DM: dry matter; CP: crude protein; CF: crude fibre; EE: ether extract and GE: gross energy.


Statistical analyses

Results compared using SAS 9.1 (SAS, 2008) software. For performance data the statistical model was:

Yij= μ + Ti + eij


Yij: observations.

μ: overall mean.

Ti: effect of treatment.

eij: residual error.

Plasma and egg parameters data were compared using the following model:

Yijk= μ + Ti + eij + εijk


Yijk: observations.

μ: overall mean.

Ti: effect of treatment.

eij: random error.

εijk: subsampling error.

Means were separated by Duncan’s multiple range tests. Treatments differences were considered significant at (P<0.05).



The results of laying hens performance were presented in Table 3. There were the highest EM and EP and lowest FCR and FI by treatment 2 (4% PBP). Egg weight were increased by 8% of PBP in comparison to all treatments groups (P<0.05). There were no significant effect of PBP levels on external and internal egg characteristics (Tables 4 and 5). Shell thickness significantly (P<0.05) increased in control and 4% PBP compared to other treatments. Yolk color score was increased significantly (P<0.05) with higher levels of dietary PBP. Plasma cholesterol decrease and plasma HDL increase by 4% PBP in diet compared with other treatments (P<0.05). The lowest levels of LDL were shown in hens feeding by basal diet. No significant differences were observed in triglyceride and total antioxidant among treatments (Table 6). As shown in Table 6, MDA concentration increased significantly by 4% PBP in comparison to other treatments (P<0.05). No differences were found on egg yolk cholesterol in controls and other PBP treatments, Table 7 (P>0.05). Egg yolk iron levels significantly increased by 4 and 8% PBP treatments compared with control (P<0.05). In contrast no significant difference has shown in plasma iron levels by increasing PBP in diet. It was clearly noted that increasing levels PBP in diet, enhance the levels of iron in the diet treatments. The highest amount of iron in egg yolk was observed respectively by treatments 4 and 12% PBP, whereas the control treatment was in the lowest levels of iron (Table 8). The highest EM and EP and lowest FCR and FI were observed by 4% PBP in diet which may be due to palatability of this level of PBP in the diet. Improvement in EW was observed in diet containing 8% of PBP which could be due to increase of FI (Sunder et al. 2013). It was found that with the increased concentration of pomegranate by- product in the hens’ diet, FI was significantly increased that agreement with (Kostogrys et al. 2017) reported the lowest consumption was observed at the highest concentration of pomegranate seed oil. In terms of performance, the results of Saki et al. (2014) on performance was in line with this study. They have shown that body weight gain (BWG), FCR and FI of broiler chickens were not affected by pomegranate peel powder (PPP) treatments. Also these results were disagreement with Rajani et al. (2011) who have shown that BWG, FCR and FI of broiler chickens were not affected by pomegranate peel treatments. However, PPP had significant effects on yolk diameter and shell weight (Yassein et al. 2015). According to Hamady et al. (2015), the improvement in FCR and EP is attributed to the positive effect that plant feed (pomegranate peel extract) additives exert on gastro-intestinal enzymatic activity and thus enhancing nutrients absorption and digestibility. Pomegranate by-products are natural growth promoter attributed to the level of polyphenolic compounds, especially pomegranate peel have ellagitannins, gallagic acid, punicalagin and ellagic acid (Bostami et al. 2015). In addition, some investigations have shown antibiotic activity pomegranate by-products due to phenolic compounds particularly ellagic acid and punicalagin (Hassan et al. 2012; Saeed et al. 2018), which might improve the growth performance with reduce the microbial into the gastrointestinal tract. Consequently, it favors improvement of performance in the present study. Supplementation of PBP levels in diet did not affect the external and internal egg characteristics. Kostogrys et al. (2017) reported that some parameters of egg quality (e.g. shell thickness, shell strength, yolk color, yolk index, egg diameter, Haugh units) were improved when hens were fed diet with pomegranate seed oil. Egg yolk color has always closed attention as an important egg quality characteristic. In this study, yolk color index was significantly increased by increasing the amount of PBP in diet that could be related by pigments in pomegranate peel. The lowest plasma cholesterol and the highest HDL have achieved by 4% PBP. Low density lipoprotein (LDL) has increased with increasing dietary PBP levels. Reduction in plasma cholesterol by 4 and 8% PBP in the diet may be due to its high fiber content. Similar results to ours were reported by Abbas et al. (2017) who found a decrease in serum cholesterol, glucose and triglyceride by PPP, probably due to PPP phenolic compounds (punicalagin, punicalin, gallic acid and particularly elegiac acid). Fiber by binding with bile salt in the intestinal tract, reduces intestinal transit time and increased excretion of sterols (increased secretion of bile) affects cholesterol metabolism and ultimately leads to the lower serum cholesterol levels (Jiménez-Moreno et al. 2009; Mateos et al. 2012). Since, HDL content of plasma was affected by dietary treatments; it probably that low density lipoprotein (LDL) and very low density lipoprotein (VLDL) are reduced in current study (Ramírez et al. 2013).


Table 3 Effects of different dietary levels of pomegranate by-product (PBP) on the performance of laying hen between 44-56 weeks of age


The means within the same row with at least one common letter, do not have significant difference (P>0.05).

SEM: standard error of the means.


Table 4 Effects of different dietary levels of pomegranate by-product (PBP, %) on external egg characteristics (EEC) of laying hen between 44-56 weeks of age


The means within the same row with at least one common letter, do not have significant difference (P>0.05).

SEM: standard error of the means.


Table 5 Effects of different dietary levels of pomegranate by-product (PBP, %) on internal egg characteristics (IEC) of laying hen between 44-56 weeks of age


The means within the same row with at least one common letter, do not have significant difference (P>0.05).

SEM: standard error of the means.


Furthermore, polyphony's of pomegranate may stimulate and promote cholesterol metabolism by modifying cholesterol transport by HDL (Esmaillzadeh et al. 2004). In an earlier experiment conducted by Saki et al. (2014), there were no significant differences between the control and supplementation of pomegranate seed pulp (PSP) in the hematological parameters of laying hens. Decreases in plasma cholesterol, HDL and LDL were shown by PPP supplementation in diets (Yassein et al. 2015). On the other hand, Hossin, (2009) have demonstrated significant decrease in total cholesterol and HDL in hypercholestrolemic rats (positive control) administrated with PPP (5, 10 and 15%) and its extracts (1, 2 and 3%), although there were no significant effect of dietary PBP on plasma triglyceride and TA concentrations in the current study. Some researchers have reported that the pomegranate juice, pomegranate rind powder extract treatment substantially inhibited lipid oxidation in cooked chicken to a much greater extent than butylated hydroxyl toluene (BHT) treatment. Results by Yamasaki et al. (2006) have shown that feeding rats with 0.12 and 1.2% pomegranate oil, led to significant increase of serum triglycerides and phospholipids, but no significant response was found on total serum cholesterol. Higher MDA have shown by 4% PBP in comparison to other treatments. Previous reports (Rajabian et al. 2001; Saki et al. 2014) further have supported these results. Malondialdehyde can generally be used as a biomarker for free radical induced damage and endogenous lipid peroxidation (Singh et al. 2002; Rosenblat et al. 2006; Li et al. 2016).


Table 6 Effect of different dietary levels of pomegranate by-product (PBP, %) on some hematological parameters of laying hens (%)


The means within the same row with at least one common letter, do not have significant difference (P>0.05).

SEM: standard error of the means.


Table 7 Effects of different dietary levels of pomegranate by-product (PBP, %) on egg yolk cholesterol


SEM: standard error of the means.


Table 8 Effects of different dietary levels of pomegranate by-product (PBP, %) on plasma and egg yolk iron contents


The means within the same row with at least one common letter, do not have significant difference (P>0.05).

SEM: standard error of the means.


Most of the cholesterol found in the egg yolk is synthesized in the liver of the hen, and transported by the blood in the form of lipoproteins and deposited in developing follicles. The concentration of plasma cholesterol is closely associated with the egg yolk cholesterol concentration (El-Bagir et al. 2006; Tang et al. 2015). Increased egg yolk iron levels by 4 and 8% PBP in diet could lead to the enrichment of eggs iron. It is well known that diet-origin iron can be incorporated into the egg yolk (Seo et al. 2010; Bess et al. 2012). In contrast decrease egg yolk iron levels were indicated by increasing 8 and 12% PBP in diet. Iron percentage in vegetable sources such as pomegranate pulp have a low absorption rate and this may decreased absorption of the treatments includes 8 and 12% PBP (Cediel et al. 2012; Pizarro et al. 2016). The other factor which could reduce the iron absorption in this respect, may be related to PBP tannins content. Since these tannins could be complications by mineral and lead to mineral decrease absorption (Mahmood et al. 2014; Batonon-Alavo et al. 2015). Decreases cholesterol and triglyceride concentrations in serum and egg-yolk as well as increasing HDL concentration in serum and markedly improving yolk color in all dietary were shown in diet supplemented by PBP.



In conclusion, the supplementation of pomegranate by- product in layer diets under the present study did not appear to cause any adverse effects on egg production and egg quality compared with the control in laying hens. Using of 4% PBP in diet can improve egg production rate and increased iron in egg yolk.

Abbas R.J., Al-Salhie K.C.K. and Al-Hummod S.K. (2017). The effect of using different levels of pomegranate (Punica granatum) peel powder on productive and physiological performance of Japanese quail (Coturnix coturnix Japonica). Livest. Res. Rural Dev. Available at:
Abbasi H., Rezaei K. and Rashidi L. (2008). Extraction of essential oils from the seeds of pomegranate using organic solvents and supercritical CO2. J. Am. Oil. Chem. Soc. 85, 83-89.
Afaq F., Saleem M., Krueger C.G., Reed J.D. and Mukhtar H., (2005). Anthocyanin and hydrolyzable tannin rich pomegranate fruit extract modulates MAPK and NF κB pathways and inhibits skin tumorigenesis in CD 1 mice. Int. J. Cancer. 113, 423-433.
Afshar M. (2011). Evaluating potential nutritive value of pomegranate processing byproducts for ruminants using in vitro gas production pechnique. J. Agric. Biol. Sci. 6, 45-51.
Al-Massad M., Al-Shdefat R. and Khashroum A. (2011). The effect of microbial phytase and dietary calcium level on the performance and eggshell quality in laying hens fed marginal phosphorus diets. Asian-Australasian J. Anim. Sci. 5, 118-126.
Ambikadevi V. and Lalithambika M. (2000). Effect of organic acids on ferric iron removal from iron-stained kaolinite. Appl. Clay Sci. 16, 133-145.
AOAC. (1990). Official Methods of Analysis. Vol. I. 15th Ed. Association of Official Analytical Chemists, Arlington, VA, USA.
AOAC. (2000). Official Methods of Analysis. Vol. I. 17th Ed. Association of Official Analytical Chemists, Arlington, VA, USA.
Batonon-Alavo D., Faruk M.U., Lescoat P., Weber G.M. and Bastianelli D. (2015). Inclusion of sorghum, millet and cottonseed meal in broiler diets: a meta-analysis of effects on performance. Animal. 9, 1120-1130.
Bess F., Vieira S., Favero A., Cruz R. and Nascimento P. (2012). Dietary iron effects on broiler breeder performance and egg iron contents. Anim. Feed Sci. Technol. 178, 67-73.
Bostami A.B.M.R., Ahmed S.T., Islam M.M., Mun H.S., Ko S.S., Kim S. and Yang C.J. (2015). Growth performance, fecal noxious gas emission and economic efficacy in broilers fed fermented pomegranate byproducts as residue of fruit industry. Int. J. Adv. Res. 3(3), 102-114.‏
Caston L. and Leeson S. (1990). Dietary flax and egg composition. Poult. Sci. 69, 1617-1620.
Cediel G., Olivares M., Gaitán D., Flores S., Brito A. and Pizarro F. (2012). Effect of trypsin and mucin on heme iron bioavailability in humans. Biol. Trace Elem. Res. 150, 37-41.
Eikani M.H., Golmohammad F. and Homami S.S. (2012). Extraction of pomegranate (Punica granatum) seed oil using superheated hexane. Food. Bioprod. Process. 90, 32-36.
El-Bagir N.M., Hama A.Y., Hamed R.M., El Rahim A.A. and Beynen A.C. (2006). Lipid composition of egg yolk and serum in laying hens fed diets containing black cumin (Nigella sativa). Int. J. Poult. Sci. 5, 574-578.
Esmaillzadeh A., Tahbaz F. and Gaini I. (2004). Concentrated pomegranate juice improves lipid profiles in diabetic patients with hyperlipidemia. J. Med. Food. 7, 305-308.
Ezzati M., Rodgers A., Lopez A.D., Vander Hoorn S. and Murray C.J. (2004). Comparative Quantification of Health Risks: Global and Regional Burden of Diseases Attributable to Selected Major Risk Factors. World Health Organization Geneva, Geneva, Switzerland.
Folch J., Lees M. and Sloane Stanley G.H. (1957). A simple method for the isolation and purification of total lipides from animal tissues. J. Biol. Chem. 226(1), 497-509.‏
Hamady G.A., Abdel-Moneim M.A., El-Chaghaby G.A., Abd-El-Ghany Z.M. and Hassanin M.S. (2015). Effect of Pomegranate peel extract as natural growth promoter on the productive performance and intestinal microbiota of broiler chickens. African J. Agric. Sci. Technol. 3(12), 514-519.‏
Harms R. and Russell G. (2001). Evaluation of valine requirement of the commercial layer using a corn-soybean meal basal diet. Poult. Scie. 80, 215-218.
Hassan N.A., El-Halwagi A.A. and Sayed H.A. (2012). Phytochemicals, antioxidant and chemical properties of 32 pomegranate accessions growing in Egypt. World Appl. Sci. J. 16(8), 1065-1073.
Hong Y., Li C., Burgess J., Chang M., Salem A., Srikumar K. and Reddy C.C. (1989). The role of selenium-dependent and selenium-independent glutathione peroxidases in the formation of prostaglandin F2 alpha. J. Biochem. Chem. 264, 13793-13800.
Hossin F.L.A. (2009). Effect of pomegranate (Punica granatum) peels and it’s extract on obese hypercholesterolemic rats. Pakistan J. Nutr. 8, 1251-1257.
Jiménez-Moreno E., González-Alvarado J., González-Serrano A., Lázaro R. and Mateos G. (2009). Effect of dietary fiber and fat on performance and digestive traits of broilers from one to twenty-one days of age. Poult. Sci. 88, 2562-2574.
Kiliç Z., Acar O., Ulaşan M. and Ilim M. (2002). Determination of lead, copper, zinc, magnesium, calcium and iron in fresh eggs by atomic absorption spectrometry. Food Chem. 76(1), 107-116.‏
Kostogrys R.B., Filipiak-Florkiewicz A., Dereń K., Drahun A., Czyżyńska-Cichoń I., Cieślik E. and Franczyk-Żarów M. (2017). Effect of dietary pomegranate seed oil on laying hen performance and physicochemical properties of eggs. Food Chem. 221, 1096-1103.‏
Li J., Zhang X., Yuan C., Miao L., Yan H., Dong X., Lu J. and Zou X. (2016). Effects of dietary L-threonine levels on antioxidant capacity, digestive enzyme activities, and antibody production of Xinyang green-shell laying hens. J. Appl. Poult. Res. 25, 422-427.
Mahmood S., Ali H., Ahmad F. and Iqbal Z. (2014). Estimation of tannins in different sorghum varieties and their effects on nutrient digestibility and absorption of some minerals in caged white leghorn layers. Int. J. Agric. Biol. 16(1), 217-221.
Mateos G., Jiménez-Moreno E., Serrano M. and Lázaro R. (2012). Poultry response to high levels of dietary fiber sources varying in physical and chemical characteristics. J. Appl. Poult. Res. 21, 156-174.
Miller N.J., Rice-Evans C., Davies M.J., Gopinathan V. and Milner A. (1993). A novel method for measuring antioxidant capacity and its application to monitoring the antioxidant status in premature neonates. Clin. Sci. 84, 407-412.
Nasr C.B., Ayed N. and Metche M. (1996). Quantitative determination of the polyphenolic content of pomegranate peel. European Food Res. Technol. 203, 374-378.
Negi P., Jayaprakasha G. and Jena B. (2003). Antioxidant and antimutagenic activities of pomegranate peel extracts. Food Chem. 80, 393-397.
North M.O. and Bell D.D. (1990). Commercial Chicken Production Manual. Van Nostrand Reinhold, New York.
Oliveira R., Narciso C., Bisinotto R., Perdomo M., Ballou M., Dreher M. and Santos J. (2010). Effects of feeding polyphenols from pomegranate extract on health, growth, nutrient digestion, and immunocompetence of calves. J. Dairy Sci. 93, 4280-4291.
Paik I., Lee H. and Park S. (2009). Effects of organic iron supplementation on the performance and iron content in the egg yolk of laying hens. J. Poult Sci. 46, 198-202.
Park S., Namkung H., Ahn H. and Paik I. (2004). Production of iron enriched eggs of laying hens. Asian-Australasian J. Anim. Sci. 17, 1725-1728.
Pizarro F., Olivares M., Valenzuela C., Brito A., Weinborn V., Flores S. and Arredondo M. (2016). The effect of proteins from animal source foods on heme iron bioavailability in humans. Food Chem. 196, 733-738.
Rajabian T., Fallah H.H. and Karami M. (2001). Effects of pomegranate juice and seed oil on blood lipid levels and atherosclerosis in rabbits hypercho lestrolemic. J. Med. Plant. 25, 93-104
Rajani J., Torshizi M.K. and Rahimi S. (2011). Control of ascites mortality and improved performance and meat shelf-life in broilers using feed adjuncts with presumed antioxidant activity. Anim. Feed Sci. Technol. 170, 239-245.
Ramadan N.A., Omar A.S., Bahakaim A. and Osman S.M. (2010). Effect of using different levels of iron with zinc and copper in layer’s diet on egg iron enrichment. Int. J. Poult. Sci. 9, 842-850.
Ramírez C.M., Rotllan N., Vlassov A.V., Dávalos A., Li M., Goedeke L., Aranda J.F., Cirera-Salinas D., Araldi E. and Salerno A. (2013). Control of cholesterol metabolism and plasma HDL levels by miRNA-144. Circ. Res. 112, 1592-1601.
Rodgers A., Ezzati M., Vander Hoorn S., Lopez A.D., Lin R.B. and Murray C.J. (2004). Distribution of major health risks: Findings from the global burden of disease study. PLoS Med. 1(1), e27.
Rosenblat M., Volkova N., Coleman R. and Aviram M. (2006). Pomegranate byproduct administration to apolipoprotein e-deficient mice attenuates atherosclerosis development as a result of decreased macrophage oxidative stress and reduced cellular uptake of oxidized low-density lipoprotein. J. Agric. Food Chem. 54, 1928-1935.
Saeed M., Naveed M., Bibi J., Kamboh A.A., Arain M.A., Shah Q.A. and Tiwari R. (2018). The promising pharmacological effects and therapeutic/medicinal applications of Punica granatum (pomegranate) as a functional food in humans and animals. Recent patents on inflammation and allergy drug discovery. Recent Pat. Inflamm. Allergy Drug. Discov. 12(1), 24-38. ‏
Saki A., Rabet M., Zamani P. and Yousefi A. (2014). The effects of different levels of pomegranate seed pulp with multi-enzyme on performance, egg quality and serum antioxidant in laying hens. Iranian J. Appl. Anim. Sci. 4, 803-808.
SAS Institute. (2008). SAS®/STAT Software, Release 9.1. SAS Institute, Inc., Cary, NC. USA.
Schofield P., Mbugua D. and Pell A. (2001). Analysis of condensed tannins: A review. Anim. Feed Sci. Technol. 91, 21-40.
Seo Y., Shin K., Rhee A., Chi Y., Han J. and Paik I. (2010). Effects of dietary Fe-soy proteinate and MgO on egg production and quality of eggshell in laying hens. Asian-Australasian J. Anim. Sci. 23, 1043-1048.
Shabtay A., Eitam H., Tadmor Y., Orlov A., Meir A., Weinberg P., Weinberg Z.G., Chen Y., Brosh A. and Izhaki I. (2008). Nutritive and antioxidative potential of fresh and stored pomegranate industrial byproduct as a novel beef cattle feed. J. Agric. Food. Chem. 56, 10063-10070.
Singh R., Chidambara Murthy K. and Jayaprakasha G. (2002). Studies on the antioxidant activity of pomegranate (Punica granatum) peel and seed extracts using in vitro models. J. Agric. Food Chem. 50, 81-86.
Sunder J., Jeyakumar S., Sujatha T. and Kundu A. (2013). Effect of feeding of morical: A herbal based supplement on production and egg quality in Japanese quail. Adv. Anim. Vet. Sci. 1, 157-160.
Taher-Maddah M., Maheri-Sis N., Salamatdoustnobar R. and Ahmadzadeh A. (2012). Estimating fermentation characteristics and nutritive value of ensiled and dried pomegranate seeds for ruminants using in vitro gas production technique. Open Vet. J. 2, 40-45.
Tang S.G.H., Sieo C.C., Kalavathy R., Saad W.Z., Yong S.T., Wong H.K. and Ho Y.W. (2015). Chemical compositions of egg yolks and egg quality of laying hens fed prebiotic, probiotic, and synbiotic diets. J. Food Sci. 80(8), 1686-1695.
Varmaghany S., Rahimi S., Torshizi M.K., Lotfollahian H. and Hassanzadeh M. (2013). Effect of olive leaves on ascites incidence, hematological parameters and growth performance in broilers reared under standard and cold temperature conditions. Anim. Feed Sci. Technol. 185, 60-69.
Viuda Martos M., Fernández López J. and Pérez Álvarez J. (2010). Pomegranate and its many functional components as related to human health: A review. Compr. Rev. Food Sci. Food Saf. 9, 635-654.
Yamasaki M., Kitagawa T., Koyanagi N., Chujo H., Maeda H., Kohno-Murase J., Imamura J., Tachibana H. and Yamada K. (2006). Dietary effect of pomegranate seed oil on immune function and lipid metabolism in mice. Nutrition. 22, 54-59.
Yassein D.M., Abdallah E., Ismail I.I., Faddle A. (2015). Effect of dietary supplementation of pomegranate peel powder and butylated hydroxy toluene on some productive, physiological and immunological parameters of japanese quail. Egypt J. Anim. Prod. 52, 105-113.
Zahin M., Aqil F. and Ahmad I. (2010). Broad spectrum antimutagenic activity of antioxidant active fraction of Punica granatum peel extracts. Mutat. Res. Genet. Toxicol. Environ. Mutagen. 703, 99-107.
Volume 9, Issue 4
December 2019
Pages 747-754
  • Receive Date: 25 June 2018
  • Revise Date: 28 September 2018
  • Accept Date: 30 January 2019
  • First Publish Date: 01 December 2019