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Omega-3 and Omega-6 Fatty Acids in Poultry Nutrition: Effect on Production Performance and Health

Published: June 25, 2021
By: Mahmoud Alagawany 1, Shaaban S. Elnesr 2, Mayada R. Farag 3, Mohamed E. Abd El-Hack 1, Asmaa F. Khafaga 4, Ayman E. Taha 5, Ruchi Tiwari 6, Mohd. Iqbal Yatoo 7, Prakash Bhatt 8, Sandip Kumar Khurana 9 and Kuldeep Dhama 10.
Summary

Author details:

1 Department of Poultry, Faculty of Agriculture, Zagazig University, Zagazig 44511, Egypt; 2 Department of Poultry Production, Faculty of Agriculture, Fayoum University, Fayoum 63514, Egypt; 3 Forensic Medicine and Toxicology Department, Faculty of Veterinary Medicine, Zagazig University, Zagazig 44511, Egypt; 4 Department of Pathology, Faculty of Veterinary Medicine, Alexandria University, Edfina 22758, Egypt; 5 Department of Animal Husbandry and Animal Wealth Development, Faculty of Veterinary Medicine, Alexandria University, Behira, Rasheed, Edfina 22758, Egypt; 6 Department of Veterinary Microbiology and Immunology, College of Veterinary Sciences, UP Pandit Deen Dayal Upadhayay Pashu Chikitsa Vigyan Vishwavidyalay Evum Go-Anusandhan Sansthan (DUVASU), Mathura 281001, Uttar Pradesh, India; 7 Division of Veterinary Clinical Complex, Faculty of Veterinary Sciences and Animal Husbandry, Jammu and Kashmir, Srinagar 190006, India; 8 Teaching Veterinary Clinical Complex, College of Veterinary and Animal Sciences, Govind Ballabh Pant University of Agriculture and Technology, Pantnagar 263145, (Udham Singh Nagar), Uttarakhand, India; 9 ICAR-Central Institute for Research on Buffaloes, Sirsa Road, Hisar 125 001, Haryana, India; 10 Division of Pathology, ICAR-Indian Veterinary Research Institute, Izatnagar, Bareilly 243122, Uttar Pradesh, India.

Simple Summary: In this review, we discuss previous studies, state-of-the-art technology, and the potential implications of utilizing omega-3 and omega-6 fatty acids in poultry diets, as well as the application of these fatty acids in the poultry industry for improving poultry production and health. Essential roles are played by these fatty acids in development and metabolism, growth and productive performance, immune response and anti-oxidative properties, improving meat quality, bone growth and development, and improving fertility rates and semen quality.

Abstract: Omega-3 (ω-3) and omega-6 (ω-6) fatty acids are important components of cell membranes. They are essential for health and normal physiological functioning of humans. Not all fatty acids can be produced endogenously owing to the absence of certain desaturases; however, they are required in a ratio that is not naturally achieved by the standard diet of industrialized nations. Poultry products have become the primary source of long-chain polyunsaturated fatty acids (LC-PUFA), with one of the most effective solutions being to increase the accretion of PUFAs in chicken products via the adjustment of fatty acids in poultry diets. Several studies have reported the favorable effects of ω-3 PUFA on bone strength, bone mineral content and density, and semen quality. However, other studies concluded negative effects of LC-PUFA on meat quality and palatability, and acceptability by consumers. The present review discussed the practical application of ω-3 and ω-6 fatty acids in poultry diets, and studied the critical effects of these fatty acids on productive performance, blood biochemistry, immunity, carcass traits, bone traits, egg and meat quality, and semen quality in poultry. Future studies are required to determine how poultry products can be produced with higher contents of PUFAs and favorable fatty acid composition, at low cost and without negative effects on palatability and quality.

Keywords: omega-3; omega-6; fatty acid; nutrition; performance; antioxidant; egg and meat quality; fertility; immunity; health.

1. Introduction
Fatty acids, especially essential fatty acids, are gaining importance in poultry feeding systems not only for improving the health and productivity of birds, but also because of our health-conscious society that prefers properly balanced diets to minimize adverse health issues [1–3]. Among various fatty acids, omega-6 (ω-6) and omega-3 (ω-3) fatty acids are proving indispensable in a properly maintained ratio for numerous biological [4,5], physiological [2], developmental [6], reproductive [7], and beneficial health functions [3,8,9]. Adequate supplementation of poultry diets with novel and beneficial feed additives or supplements is gaining importance as it significantly improves overall poultry production and performance as well as safeguards the health of birds [10–13]. In poultry production, the advantages of using oils in diets involves a reduction of feed dust and improvement in hydrolysis and absorption of the lipoproteins that supply fatty acids [14]. In addition, oils are the main source of energy for the birds and have the highest caloric value among all dietary nutrients. They can also enhance the absorption of fat-soluble vitamins, increase diet palatability, and improve the utilization of the consumed energy. Moreover, the rate of food passage through the gastrointestinal tract can be reduced, with subsequent better absorption of all dietary nutrients [15].
In the diets of humans, ω-6 and ω-3 are essential fatty acids. However, considerable modification in dietary patterns has resulted in alterations of the consumption of such fatty acids, with subsequent elevation in the consumption of ω-6fatty acids and a marked decrease in the consumption of ω-3 fatty acids. This modification has led to an imbalance in the ω-6/ω-3 ratio, which at 20:1 now differs considerably from the original ratio (1:1). Therefore, dietary supplements of foodstuffs such as eggs and meat are a clear alternative to increase the daily consumption of ω-3 to meet the recommended doses [16]. Foods that provide ω-6 fatty acids include soybean, palm, sunflower, and rapeseed oils, whereas foods that provide ω-3 fatty acids include certain nuts, and plant and fish oils [17–20]. Omega-9 fatty acids are not essential and are found in olive oil and animal fat [21]. Fish oil (FO) includes two types of ω-3 fatty acids: docosahexaenoic acid (DHA) and eicosapentaenoic acid (EPA). Certain vegetables, nuts, and seed oils include alpha-linolenic acid (ALA), which can be converted to DHA and EPA in the body, with linseed oil containing more than 50% ALA [22].
High doses of omega sources in the diet may have deleterious effects on humans, such as increased bleeding risk and higher levels of low density lipoprotein (LDL) cholesterol. Omega-3 fatty acids may influence heart rates. The consumption of high rates of fatty acids (e.g., ω-6) has been linked with a higher occurrence of health problems, such as type 2 diabetes, obesity, and coronary artery diseases [23]. Maintaining a proper ratio of ω-3 and ω-6 fatty acids not only improves performance, but also prevents these health risks. Devising the correct ratios requires the addition of oils having appropriate ω-3 and ω-6 fatty acid levels [24]. Omega-3 fatty acids EPA and DHA have shown many health benefits; they are helpful in fetal development and cardiovascular function, and prevent Alzheimer’s disease [25]. In addition, they play a role in modulating immunity [26,27]. The ratio of n-6:ω-3 fatty acids also plays an important role in the immune response, production performance of broilers and designing meat enriched with ω-3 polyunsaturated fatty acids (PUFAs) [26,27]. The addition of FO to the poultry diet may yield poultry products (such as eggs and meat) that are enriched with ω-3, such as EPA and DHA. Additionally, FO is more effective than other vegetable oils [28]. However, many aspects of essential fatty acids are still unknown and their diverse functions and importance in health and production should be explored. The objective of the present review is to assess the influence of dietary ω-6 and ω-3 PUFAs on the productive performance, antioxidant properties, immunity, carcass traits, bones, egg and meat quality, and semen quality of poultry, as well as their limitations in the poultry industry.
2. Beneficial Applications of ω-3 and ω-6 Oils in Poultry
Adding ω-3 and ω-6 fatty acids to the diet has become more important recently [3,29]. For at least the past three decades, studies on the beneficial activities of long-chain PUFAs (LC-PUFAs) in biological processes have been conducted. Dietary intervention with ω-3 may influence chicken immunity and lead to the production of poultry products with health benefits for the consumer [30]. Therefore, research on broiler chickens has focused on the functional action of different LC-PUFA forms and their dietary levels on the metabolism of lipids in birds. Other than the LC-PUFA source, high levels of fatty acids, particularly of the ω-3 family, lead to accelerated lipid oxidation when broiler chickens are under oxidative stress because of genetic selection [31].
Using PUFAs in poultry diets significantly reduces the cholesterol and total lipid content in the blood and egg yolk. Several studies have been conducted to minimize the harmful effects of triglycerides and total cholesterol in poultry products (edible parts). Ahmad et al. [32] reported that the cholesterol content of eggs was decreased when birds were fed a diet supplemented with ω-3 fatty acids. Moreover, increasing dietary levels of FO and milled flaxseed improved the concentration of linoleic acid (LA), EPA, and DHA in the yolk, and the fatty acid deposition from FO was found to be two times greater than that from milled flaxseed when fed at the same dietary levels [33].
Designer eggs offer balanced ratios of PUFA: SFA (1:1) or ω-6/ω-3 PUFA (1:1). Omega-3 UFAs are important nutritional factors that modulate immune functions and are of great importance for nervous system development and for lowering blood platelet aggregation and the incidence of thrombosis, hypertension, and atherosclerosis, and have anti-tumor, anti-inflammatory, and cardioprotective effects [34]. The content of ω-3 fatty acids in eggs can be increased by supplementing the diets of laying hens with certain dietary supplements, such as flaxseed, fish oil, safflower oil, linseed, fish meal, or algae. Omega-3 fatty acids can be introduced to the human consumer’s body through these designer eggs; they play an important role in the maintenance of the normal functioning of the body in that they protect the body from cardiovascular problems such as heart attacks. In addition, they can replace fish products in consumer diets [35]. Ebeid et al. [36] stated that hens fed a diet containing different concentrations of ω-3 PUFA showed a linear decrease and increase (p < 0.05) in egg yolk content of ω-6 PUFA and ω-3 PUFA, respectively, compared to the control hen group. The levels of ALA, EPA, DHA, and docosapentaenoic acid (DPA) were higher in the egg yolks of laying hens fed linseed meal and fish oil as dietary supplements than in the un-supplemented hen group [37]. Similarly, ALA was higher in the egg yolk of hens fed diets that contained ω-3 fatty acid dietary supplements than in the control bird group [32]. It has been previously concluded that laying hens can synthesize EPA and DHA from ALA during metabolic processes if ALA is present in adequate quantities [38,39]. However, in mammals, the synthesis rates of DHA from ALA are low compared to the dietary intake and tissue demand, with the estimation of percent conversion of ALA to DHA differing widely, ranging from 0% to 9.2%, supporting the conclusion that DHA synthesis from ingested ALA is not an efficient process in humans [40]. Moreover, metabolization of ALA in vivo is not adequate to improve meat quality in ω-3 LC-PUFA, and direct supplementation of the diet with ω-3 LC-PUFA is a better alternative to modulate an increase in beneficial fatty acids of broiler meat [41]. The efficiency of ALA conversion to ω-3 LC-PUFA derivatives and deposition in peripheral tissues might not be sufficiently high to improve the nutritional value of muscle. Because there is competition among the enzymes involved in the elongation and desaturation of both LA and ALA, high amounts of LA suppress the conversion of ALA to EPA or DHA; therefore, an optimal intake of LA relative to ALA is crucial for normal metabolism [42].
Regarding egg production performances, Buitendach et al. [43] investigated the effects of dietary fatty acid saturation on the production performance of laying hens at end-of-lay (58–74 weeks of age). These authors reported no significant differences in hen-day egg production, egg weight, egg output, feed efficiency, and body weights at end-of-lay. Similar results were reported by Cachaldora et al. [44,45] who concluded that dietary fatty acid saturation had no significant effects on the egg production performance of layer hens. In contrast, Shang et al. [46] stated that body weight gain, rate of egg production, egg weight, and feed efficiency decreased linearly with an increase in dietary fatty acid unsaturation levels during the 8-week experimental period between 40 and 48 weeks of age. Yin et al. [47] reported a decrease in egg and body weights with an increase in dietary UFAs at 50–58 weeks of age. This decrease in the performance parameters of hens as recorded by Shang et al. [46] and Yin et al. [47] is mostly attributed to the fact that these authors used conjugated linoleic acid (CLA) at higher inclusion levels (up to 7.8%) to enhance the UFA profile of their experimental diets. CLA causes weight loss in humans [47]; therefore, it appears that this specific type of unsaturated fatty acid has a similar negative effect on the body weights of laying hens and consequently on egg production and egg size.
3. Improved Growth and Productive Performance
Growth and production performance of poultry are improved by supplementation of fatty acids or their sources. The supplementation of fats and oils (as an omega source) in limited amounts leads to better utilization of feed and energy, with subsequent improvement in growth and performance [48]. The body mass and percentage body mass gain of quails was improved via dietary supplementation of sunflower and soyabean oil for a 12-week period [49]. The feed conversion ratio (FCR) and growth performance of broilers were improved via dietary supplementation with sunflower and canola oil [14]. Smith et al. [50] stated that the supplementation of animal fat, corn oil, fish oil, and a blend of vegetable and animal oils did not affect the feed intake, but positively influenced the body gain and FCR in heat-stressed broilers compared to heat-stressed un-supplemented broilers. Jalali et al. [51] found that the addition of soybean oil (high in ω-3 PUFA) significantly (p < 0.05) improved the FCR and body weight gain of broilers during the total and growth rearing periods. Abdulla et al. [52] found that the supplementation of soybean oil in broiler diets increased the body weight and weight gain at 6 weeks of age compared with the supplementation of LO (p < 0.05).
Fébel et al. [53] noticed that the difference in diets supplemented with sunflower oil (SO) or lard was not significant for the growth performance of broilers. Supplementation of fish oil in poultry diets had no influence on feed consumption, live weight, or weight gain [48] compared with the control diet (without fat). Ebeid et al. [54] reported that dietary ω-3 PUFA in Japanese quail had no adverse effects on the growth performance, such as the final body weight, feed intake, or FCR. Raj Manohar and Edwin [55] declared that dietary ω-3 PUFA in quails had a significant (p < 0.01) influence on body weight gain and non-significant differences in feed intake and feed efficiency. In addition, Qi et al. [56] demonstrated that decreasing dietary ω-6/ω-3 improved FCR, with the best result obtained from the diet with 5:1 ω-6/ω-3. Puthpongsiriporn and Scheideler [57] reported that four dietary ratios (17:1, 8:1, 4:1, and 2:1) of LA to ALA had no significant effect on the body weight of chickens over 16 weeks. However, Ayerza et al. [58] observed a marked reduction in the body weight and FCR of broilers fed on chia and flaxseed (rich in ALA), which may be attributed to one or more of the anti-nutritional factors present in flaxseed. Crespo and Esteve Garcia [59], Newman et al. [60], and Ferrini et al. [61] reported that the digestibility of fat increased with increasing unsaturation; therefore, the effect of the type of fat on feed efficiency could reflect the degree of unsaturation. This is consistent with the improvement of growth performance noted by Zollitsch et al. [62], Huo et al. [63], and Lopez-Ferrer et al. [48] with increasing content of UFA.
Generally, a dietary supplementation of a PUFA-enriching ingredient has an improvement effect on live weight, weight gain, and FCR of poultry. However, no adverse effects on feed intake have been reported in almost all designed studies to date.
4. Improved Immune Response and Anti-Oxidative Properties
Fatty acid supplementation affects both immune and oxidative status in poultry. It can modulate immune system through both cellular and humoral immune responses. Proliferation, maturation,function and cytokine production of lymphocytes, heterophils and splenocytes are influenced by omega fatty acids, besides antibody production like IgM and IgG (Table 1). Similarly, neutralization of oxidants and an increase of antioxidants level directly or indirectly by fatty acids minimizes the risk of oxidative stress. The immune response and oxidative mechanisms are interlinked and affect one another, hence modulation of one can impact the other. The supplementation of natural antioxidants has become a pressing research topic [64–66]. Different studies have confirmed the many favorable effects of dietary ω-3 PUFA, including anti-oxidative properties and lipid peroxidation, as well as immune response effects [36,67]. For instance, dietary ω-3 PUFA can modulate the immune response in poultry [68]. Ebeid et al. [36] found that dietary FO supplementation below a level of 35 g/kg in the diet induced antibody titers in hens. The levels of antibodies were higher in laying hens fed oils (FO or LO) rich in ω-3 PUFAs than those in laying hens fed oil rich in ω-6 PUFAs (maize oil) [69]. Ebeid et al. [54] stated that dietary ω-3 PUFA (FO or LO) had a positive influence on humoral immunity (p ≤ 0.05) at 42 days of age as measured by antibody titers against Newcastle disease virus (NDV) compared to the control diet. Al-Khalifa et al. [70] declared that SO replaced by fish oil at low levels showed no evidence of adverse effects on the immune function of broilers. Jameel et al. [71] showed that chicks fed a diet supplemented with FO had significantly higher (p ≤ 0.05) antibody titers and percentages of spleen and bursa than that of the control group.
 One of the earliest studies on the effects of fatty acid supplementation on immune tissues was by Fritsche et al. [72]. They noted that the supplementation of diets rich in ω-3 fatty acids to chicks decreased levels of arachidonic acid (AA) (C20:4n-6) in the serum and immune tissues by 50–75%. However, the levels of EPA (C20:5n-3) and DHA (C20:6n-3) increased [72], suggesting an influence on the immune system. During the early stages of life, ω-3 and ω-6 fatty acids are more important for immunity in chicks as they play a role in cellular and humoral immunity, and are regulators of inflammation [1,73]. They determine the immunoglobulin G (IgG) content of chicks produced by maternal hens, which are essential for passive immunity [74]. An inflammatory role for these fatty acids in delayed-type hypersensitivity has also been reported [75]. Further, they help in maintaining membrane integrity, thus preventing pathogen entry or infection.
Wang et al. [68] noted that the LA to ALA ratio may influence IgG-receptor activity in yolk sac membranes and thereby influence the maternal-embryo transfer of yolk IgG. Adding fish oil to broiler diets significantly induced antibody titers for the LaSota vaccine at 35 days of age after vaccination against Newcastle disease because of ω-3, which plays a role in the production of immunomodulators (leukotriene and prostaglandin). In addition, fish oil has the capacity to modulate the production of cytokines via signal transduction and lymphocytes in a population of immune cells [76]. Al-Mayah [76] showed that chickens fed a diet supplemented with fish oil at a level of 50 g/kg showed a higher production of antibodies (IgM and IgG) and globulins in the serum and maintained immune function after vaccination compared to the control group.
A moderate intake of ω-3 PUFAs enhances anti-oxidative properties, such as glutathione peroxidase (GSH-Px) activity, in laying hens [36] and decreases lipid peroxidation in abdominal fat and serum [36,67]. Ebeid et al. [54] reported that adding FO and LO at a level of 20 g/kg to Japanese quail diets significantly increased both the total antioxidant capacity and GSH-Px activity, and decreased the thiobarbituric acid reactive substances in the serum compared with the negative control. SO-enriched diets led to a reduction in the deposition of abdominal fat [77]. Additionally, adding SO and LO to the diet of birds led to a greater decrease in abdominal fat deposition than that observed after adding olive oil and tallow [67]. The addition of SO in broiler diets significantly increased (p < 0.05) the relative weight of the abdominal fat pad [51], whereas the abdominal fat of broilers was decreased with fish oil [64,78]. Diets high in ω-3 fatty acids increased the incorporation of these fatty acids into tissue lipids, leading to oxidative stress in cells [30]. A diet enriched in ω-3 PUFA improved the gene expression of lipin-1, which regulates triglyceride synthesis, in chicken abdominal fat [79]. Ibrahim et al. [26] stated that FO and LO supplementation had a low but significant effect (p ≤ 0.05) on the malondialdehyde (MDA) concentration in broilers. Reducing the ratios of ω-6:ω-3 PUFAs were found to be linked to a significant (p ≤ 0.05) induction of glutathione S transferase (GSH-ST). Moreover, superoxide dismutase, GSH-ST, and cardiac GSH-Px activities were augmented in the ω-3 PUFA-rich treatment, and MDA was reduced [79]. Omega-3 PUFAs have shown beneficial immune responses in infectious bursal disease challenged broilers [80]. However, despite the noted improvements, these fatty acids must be evaluated and properly monitored for ratios to prevent adverse effects on immune status [70].
5. Improving Egg Quality and Nutritional Value of Eggs
The nutraceutical value and health benefits of eggs can be enhanced by adapting appropriate feeding strategies in poultry as well as by developing designer eggs [10,12,20]. These improve the quality and quantity of eggs [33]. Eggs are not naturally rich in ω-3 PUFA; therefore, ω-3 PUFA supplementation in poultry rations is required to obtain enriched ω-3 PUFA eggs [81,82]. Designer eggs are enriched in ω-3 fatty acids for beneficial health effects in human nutrition [12,83]. Designer eggs offer balanced ratios of PUFA: SFA (1:1) or ω-6/ω-3 PUFA (1:1) and provide more than 600 mg of ω-3 PUFA [34]. The content of ω-3 fatty acids in eggs can be increased by supplementing the diets of laying hens with certain dietary supplements, such as groundnut oil, fish oil, safflower oil, linseed, fish meal, or algae [15–18,58]. Omega-3 fatty acids include EPA, DPA, DHA, and linolenic acid (LNA), whereas AA and LA are examples of ω-6 fatty acids. Omega-3 fatty acids can be introduced to the body through designer eggs [35]. Omega 3-PUFAs serve as good fats for human health, therefore increasing PUFA contents in the egg yolk helps to decrease the bad cholesterol content [84]. The stability of ω-3 PUFAs can be improved by vitamin E and/or organic selenium, which reduces oxidation in raw eggs; thus, these confer protective effects during the marketing, storage, and cooking of ω-3 enriched eggs [85,86].
Meluzzi et al. [87] reported that the key ω-3 and ω-6 PUFAs are LNA and LA, respectively. LNA is metabolized inside the body to EPA, DHA, and DPA, whereas LA is metabolized to AA. LNA was higher in the egg yolk of hens after feeding them diets that contained ω-3 fatty acid dietary supplements than those of the control birds [88].
Ceylan et al. [89] evaluated the effect of dietary supplementation on two levels (15 g/kg and30 g/kg diet) of SO, rapeseed oil, and LO for 12 weeks in laying hens. They concluded that egg production, egg weight, feed intake, FCR, and live weight were not significantly affected by the treatments. However, hens receiving SO produced less intensively colored egg yolks than those receiving other oils in their diet (p < 0.01). Moreover, the composition of fatty acid in egg yolks was significantly (p < 0.01) affected by the treatment, whereas the cholesterol content was not influenced. There was a significant (p < 0.05) interaction between fat source and the level of inclusion in the diet, and LNA content was increased when hens were fed diets with linseed and rapeseed oil (30 g/kg diet). In contrast, da Silva Filardi et al. [90] studied the effects of the dietary inclusion (for 12 weeks) of different fat sources (cottonseed oil, soybean oil, lard, SO, or canola oil) on egg quality, and egg yolk lipid profiles. The different fat sources did not affect eggshell quality; however, the lipid profile of the egg yolk changed based on dietary fat sources. Optimal changes were considered to be lower levels of SFA and LA, and higher levels of ALA and DHA. Such changes were promoted by the addition of different fat sources, particularly canola oil; however, it did not enhance the egg content of PUFAs.
6. Improving Meat Quality
In human diets, there is a marked reduction in ω-3PUFA and an imbalance in the ratio of ω-6/ω-3 PUFA. Currently, the ratio of ω-6 to ω-3 fatty acids is approximately 10 to 20:1 rather than the recommended ratio (1 to 4:1). The decrease in ω-3PUFA consumption is due to the low intake of sea fish, which are the major source of ω-3 PUFA. An accepted solution for this situation could be based on the production of suitable functional foods with adjusted PUFA content, which is generally accepted to confer nutritional effects and beneficial physiological properties. The enrichment of poultry meat with ω-3 PUFA may provide an excellent alternative source for such acids in the human diet because of their relative availability [87]. Schiavone et al. [91] illustrated that the content of lipids, protein, and moisture in breast meat was not significantly affected by the addition of fish oil to the diet of the Muscovy duck. Additionally, Ebeid et al. [54] reported that adding n-3 PUFA to Japanese quail diets had no significant influence on the content of crude protein, ash, and dry matter in the meat, whereas the addition of ether extract significantly influenced these parameters. Additionally, the physical traits of the meat except for the water-holding capacity were not significantly influenced when ω-3PUFA was added to the diet. Though the fatty acid composition of meat is influenced by ω-3 PUFA supplementation or their sources in diet, meat quality parameters like meat pH, tenderness, grilling loss, toughness, and juiciness are not affected [48,54,87,91]. This can be exploited for designing functional foods with adjusted PUFA and having no differences in palatability.
In broiler diets, replacing soybean oil with LO along with the addition of pomegranate peel extract enriched muscle meat with antioxidants and ω-3 and improved broiler immunity and their serum lipid profile [92]. Also, natural antioxidants, especially those extracted from herbal plants, have greater potential for increasing the stability, palatability, and shelf-life of meat products [93,94]. The meat quality of broilers improved with fish oil supplementation in the diet [78]. Inclusion of fish oil (FO) and different fat sources [linseed oil (LO), rapeseed oil (RO), sunflower oil (SO)] for providing different PUFA (ω-3 and ω-6 PUFA) in diets and their deposition into the eggs’ fat revealed that smaller proportions of FO resulted in lower values of saturated and higher values of ω-6 FA contents. Replacing FO with LO showed the lowest turn down of its derivatives by elongation and desaturation and an increase in the total ω-3 FA in the form of linolenic acid [95]. The use of LO as ground or whole flaxseed before slaughter is recommended to broiler breeders and producers as a feeding strategy to optimize ω-3 enrichment, without compromising poultry performance [96]. The fat and cholesterol content in poultry meat may decrease because of dietary supplements, such as ω-3 PUFA, and high PUFA concentrations in the diet (addition of vegetable oils) decrease the storage stability of meat [97].
A proper ratio of ω-6:ω-3 fatty acids is essential for maintaining health, oxidative balance and quality of meat. Recently, Konieczka et al. [8] found that feeding birds with a diet containing a PUFA ω-6:ω-3 ratio exceeding the recommended levels resulted in damage to the intestinal epithelial cells. Further, low PUFA ω-6:ω-3 ratio diets increased MDA in tissues including the meat. This can affect meat quality owing to peroxidative changes [8]. Hence, these authors recommended balanced supplementation to prevent oxidative damage and loss of meat quality. Similarly, Kalakuntla et al. [6] noted that the supplementation of ω-3 PUFA-rich oil sources in the broiler diet during starter and finisher phases can affect fatty acid composition, quality, and organoleptic characters of broiler chicken meat. At 2% and 3% addition levels, mustard oil, fish oil, and LO improved ω-3 PUFA levels and sensory attributes such as the appearance, flavor, juiciness, tenderness, and overall acceptability of meat; however, due to an increase of thiobarbituric acid-reacting substances, the meat quality might be compromised as it might cause oxidative damage to meat.
The content of ω-3 fatty acids in poultry meat, especially as EPA and DHA, can be readily improved by increasing the levels of ω-3 PUFA in poultry diets via the inclusion of oily fish by-products [98]. Qi et al. [56] concluded that substituting ω-3 for ω-6 in the diets of chickens resulted in a significant effect on the subcutaneous and intramuscular fat content and on meat quality (color and tenderness).
Unfortunately, although poultry meat is considered one of the main potential sources of ω-3 LC-PUFA for humans, particularly in developed countries [99,100], there are some disadvantages related to meat oxidative stability. LC-PUFAs are very susceptible to oxidation, producing off-flavors and odors in meat that are often associated with a fishy flavor [101]. This oxidative instability can influence meat quality and, consequently, reduce acceptability to consumers [41,102,103]. Oken et al. [104] concluded that the supplementation of chicken diets with fish-derived products led to unacceptable odors in the product, which has restricted the adoption of this strategy [105]. Vegetable sources such as LO may clearly increase the ω-3 PUFA content in the form of ALA, which is the precursor of the entire ω-3 family [42].
Conclusively, dietary supplementation of ω-3 fatty acids in poultry diet, particularly in the form of EPA and DHA, can improve various parameters of meat quality. However, LC-PUFAs are extremely susceptible to oxidative deterioration, resulting in off-flavors and odors, which adversely affect acceptability to consumers, especially when fish-derived products are used.
7. Effects of Dietary ω-3 and ω-6 Fatty Acids on Bones
The ω-3 and ω-6 fatty acids or their sources like fish oil, linseed oil, soybean oil and palm oil have bearing effects on mineral metabolism and hence promote bone formation, growth and development. Fat supplementation in the diet influences mineral metabolism, especially calcium, zinc, and magnesium [106], because of insoluble soap formation between these minerals and fatty acids during digestion, which makes them unavailable [107]. This can affect mineral retention, and influence bone and eggshell quality in birds. Dietary lipids play a remarkable role in the growth, development, and formation of bones [106–108]. Sun et al. [108] reported that dietary fish oil supplementation led to significantly higher bone mineral density in the proximal tibia and distal femur than supplementation with maize oil. Some studies have reported non-significant correlations between fatty acid supplementation and bone characteristics. Baird et al. [109] reported that feeding laying chickens a diet high in ω-3 PUFA did not have a significant effect on bone morphological characteristics, bone mineral content, or bone mineral density. However, there are many studies that can prove interrelation of fatty acid supplementation and bone growth and development. Ebeid et al. [36] declared that using ω-3 PUFA in Japanese quail diets improved the tibia bone and morphological characteristics and, in quails fed diets supplemented with FO and LO at a level of 20 g/kg diet, there was increased tibia bone wall thickness, tibia diameter, and the percentage of tibia ash and tibia bone breaking strength compared with that in quails fed the control diet. Abdulla et al. [52] clarified that chicks fed a diet supplemented with LO had non-significantly higher ash percentage, tibia weight, and bone-breaking strength than those fed diets supplemented with SO and palm oil. In addition, ω-3 PUFA may improve bone health by inducing calcium absorption in the gut and inducing osteoblast activity and differentiation, decreasing osteoclast activity, and stimulating the deposition of minerals in developing bones [110]. Reproducible and consistent beneficial effects of ω-3 fatty acids have been observed for bone/joint diseases and bone metabolism [111]. Recently, the importance of yolk as a mineral source for chicks and possible alterations via interventions strategies for future usage has been analyzed [112]. The amount of minerals in yolk reflects that the uptake content and enrichment can have beneficial effects [113]. In-ovo supplementation of minerals has improved bone properties and development in hatchlings and mature broilers [113–115].
8. Improved Fertility Rates and Semen Quality
Fatty acid supplementation, especially of ω-3 and ω-6, helps in improving fertility, semen quality and quantity. Kelso et al. [114] found that dietary fish oil or corn oil supplementation to chickens at a level of 50 g/kg in their diet led to significantly higher (96%) fertility rates than the rates prior to supplementation (89%). Kelso et al. [115] noticed that the supplementation of ALA in male diets led to higher fertility at 39 weeks of age because of the increased ω-3 fatty acid proportion in the phospholipids of sperm. Cerolini et al. [116] reported that dietary FA supplementation can influence spermatozoa traits. Hudson and Wilson [117] stated that the supplementation of menhaden oil at 30 g/kg in the diets of male broiler breeders improved the quality of semen and increased fertility and hatchability. Bongalhardo et al. [118] reported that supplementing cockerel diets with fish oil improved fertility, which was attributed to the lower fatty acid ratio (ω-6:ω-3) in the membrane of spermatozoa that may change the membrane resistance to peroxidative damage or its physical characteristics [119].
Fertility and quality of sperms both have been found to be affected during cryopreservation, and fatty acids act as protectants for sperms. Cryopreservation of semen affects survivability, which to a greater extent is dependent on lipid content in spermatozoa [119]. Blesbois et al. [119] noted a decrease in cholesterol/phospholipid ratio in poultry sperms following cryopreservation and a relation with fluidity, hence affecting survivability. Fatty acids can prevent damage to sperms, whether it be physical (cryopreservation) or chemical (oxidative). Zaniboni and Cerolini [120] stated that the dietary ω-3 LC-PUFA treatment of turkey prevented the negative influence of sperm storage on sperm sensitivity and quality and promoted in-vitro peroxidation and sperm death. Additionally, dietary maize oil supplementation decreased the spermatozoa number per ejaculate by 50% between 26 and 60 weeks of age. Al-Daraji et al. [121] noticed that dietary fish oil supplementation produced the best results for sperm concentration (p < 0.05) based on the ejaculate volume, live sperm, total sperm count, and sperm quality factors, followed by flax oil; however, the worst results for these traits were found with treatments of corn oil and SO. Al-Daraji [122] determined that the correlation between the spermatozoa number and glucose concentration in the seminal plasma was highly significant and negative, indicating that the spermatozoa utilized glucose. Additionally, Al-Daraji [123] noticed that spermatozoa used glucose in the seminal plasma for metabolism. Al-Daraji et al. [121] also clarified that dietary SO or corn oil supplementation had a significant effect (p < 0.05) on the semen glucose content, alanine aminotransferase activity, and semen protein content, followed by the results for flax oil and fish oil.
A diet supplemented with a moderate ratio of ω-3:ω-6 fatty acids increased DHA and ω-3PUFAs and decreased docosatetraenoic acid and AA in rooster sperm [124]. Sperm motility, progressive motility, membrane functionality, and viability were significantly improved; the testosterone concentration increased; and a higher fertility rate was noted [125]. Feng et al. [7] reported no significant effect on the testis index; however, the spermatogonial development and germ cell layers and gonadotropin-releasing hormone, luteinizing hormone (LH), follicle-stimulating hormone (FSH), and testosterone hormone levels increased. Further, they reported that PUFAs regulate the expression of hormone receptors and steroid acute regulator protein (StAR). PUFAs significantly increased the mRNA levels of all hormone-related genes (GnRHR, FSHR, LHR, and StAR mRNA levels).
An overview of different dietary manipulations for improving nutritional quality of poultry products (egg and meat) is presented in Table 1.
9. Conclusions and Future Perspectives
The present review revealed that ω-3 and ω-6 fatty acids could be successfully utilized in poultry feeds to promote immune responses and improve the nutritional value of eggs, meat quality and growth in poultry. Omega-3 fatty acids have anti-inflammatory or inflammation-reducing properties because they can reduce the liberation of cytokines. Omega-6 fatty acids at high levels are associated with an increased prevalence of severe conditions, such as depression and heart disease. However, these fatty acids have a tremendous range of health benefits, including improved cholesterol levels and a reduced occurrence of coronary heart disease. Numerous studies have reported the favorable effects of ω-3 PUFA on bone strength, bone mineral content, and bone mineral density. Furthermore, the content of ω-3 fatty acids in eggs can be increased by supplementing the diets of laying hens with certain dietary supplements, such as groundnut oil, fish oil, safflower oil, linseed, fish meal, or algae. Dietary supplementation with different sources of ω-3 or ω-6 to cockerels improved the semen quality and increased fertility and hatchability. In the present review, we proposed that supplementing poultry diets with different sources of ω-3 and ω-6 fatty acids represented a potential strategy for poultry produced for human consumption. However, some disadvantages were related to meat oxidative stability, where LC-PUFAs were very susceptible to oxidation, resulting in off-flavors and odors in poultry meat, which negatively influence meat quality and acceptability by consumers. Therefore, future studies should investigate how we can produce poultry products with higher contents of PUFAs and favorable fatty acid composition, with low cost and without negative effects on palatability and quality, and subsequently on acceptability by consumers.
 
 
This article was originally published in Animals 2019, 9, 573; doi:10.3390/ani9080573. This is an Open Access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).

1. Cherian, G. Nutrition and metabolism in poultry: Role of lipids in early diet. J. Anim. Sci. Biotechnol. 2015, 6,
28. [CrossRef] [PubMed]
2. Simopoulos, A.P. An increase in the omega-6/omega-3 fatty acid ratio increases the risk for obesity. Nutrients
2016, 8, 128. [CrossRef] [PubMed]
3. Lee, S.A.; Whenham, N.; Bedford, M.R. Review on docosahexaenoic acid in poultry and swine nutrition:
Consequence of enriched animal products on performance and health characteristics. Anim. Nutr. 2019, 5,
11–21. [CrossRef] [PubMed]
4. Cherian, G.; Gopalakrishnan, N.; Akiba, Y.; Sim, J.S. Effect of maternal dietary n-3 fatty acids on the accretion of long-chain polyunsaturated fatty acids in the tissues of developing chick embryo. Biolo. Neonate. 1997, 72,
165–174. [CrossRef] [PubMed]
5. Simopoulos, A.P. Importance of the omega-6/omega-3 balance in health and disease: Evolutionary aspects of diet. World Rev. Nutr. Diet. 2011, 102, 10–21.
6. Kalakuntla, S.; Nagireddy, N.K.; Panda, A.K.; Jatoth, N.; Thirunahari, R.; Vangoor, R.R. Effect of dietary incorporation of n-3 polyunsaturated fatty acids rich oil sources on fatty acid profile, keeping quality and sensory attributes of broiler chicken meat. Anim. Nutr. 2017, 3, 386–391. [CrossRef]
7. Feng, Y.; Ding, Y.; Liu, J.; Tian, Y.; Yang, Y.; Guan, S.; Zhang, C. Effects of dietary omega-3/omega-6 fatty acid ratios on reproduction in the young breeder rooster. BMC Vet. Res. 2015, 11, 73. [CrossRef]
8. Konieczka, P.; Barszcz, M.; Choct, M.; Smulikowska, S. The interactive effect of dietary n-6:N-3 fatty acid ratio and vitamin E level on tissue lipid peroxidation, DNA damage in intestinal epithelial cells, and gut morphology in chickens of different ages. Poult. Sci. 2017, 97, 149–158. [CrossRef]
9. Arias-Rico, J.; Cerón-Sandoval, M.I.; Sandoval-Gallegos, E.M.; Ramírez-Moreno, E.; Fernández-Cortés, T.L.;
Jaimez-Ordaz, J.; Contreras-López, E.; Añorve-Morga, J. Evaluation of consumption of poultry products enriched with omega-3 fatty acids in anthropometric, biochemical, and cardiovascular parameters.
J. Food Quality 2018, 2018, e9620104. [CrossRef]
10. Dhama, K.; Tiwari, R.; Khan, R.U.; Chakraborty, S.; Gopi, M.; Karthik, K.; Saminathan, M.; Desingu, P.A.;
Sunkara, L.T. Growth promoters and novel feed additives improving poultry production and health, bioactive principles and beneficial applications: The trends and advances—A review. Int. J. Pharmacol. 2014, 10,
129–159. [CrossRef]
11. Dhama, K.; Latheef, S.K.; Mani, S.; Samad, H.A.; Karthik, K.; Tiwari, T.; Khan, R.U.; Alagawany, M.;
Farag, M.R.; Alam, G.M.; et al. Multiple beneficial applications and modes of action of herbs in poultry health and production—A review. Int. J. Pharmacol. 2015, 11, 152–176. [CrossRef]
12. Laudadio, V.; Lorusso, V.; Lastella, N.M.B.; Dhama, K.; Karthik, K.; Tiwari, R.; Alam, G.A.; Tufarelli, V.
Enhancement of nutraceutical value of table eggs through poultry feeding strategies. Int. J. Pharmacol. 2015,
11, 201–212.
13. Yadav, A.S.; Kolluri, G.; Gopi, M.; Karthik, K.; Malik, Y.S.; Dhama, K. Exploring alternatives to antibiotics as health promoting agents in poultry—A review. J. Exp. Biol. Agri Sci. 2016, 4, 368–383.
14. Nobakht, A.; Tabatbaei, S.; Khodaei, S. Effects of different sources and levels of vegetable oils on performance, carcass traits and accumulation of vitamin in breast meat of broilers. Cur. Res. J. Biolo. Sci. 2011, 3, 601–605.
15. Poorghasemi, M.; Seidavi, A.; Qotbi, A.A.; Laudadio, V.; Tufarelli, V. Influence of dietary fat source on growth performance responses and carcass traits of broiler chicks. Asian Australas. J Anim Sci. 2013, 26, 705–710.
[CrossRef] [PubMed]
16. Baiao, N.C.; Lara, L.J.C. Oil and fat in broiler nutrition. Braz. J. Poul. Sci. 2005, 7, 129–141. [CrossRef]
17. Gómez, C.C.; Bermejo, L.L.M.; Loria, K.V. Importance of a balanced omega 6/omega 3 ratio for the maintenance of health. Nutritional recommendations. Nutr. Hosp. 2011, 26, 323–329.
18. Samman, S.; Kung, F.P.; Carter, L.M.; Foster, M.J.; Ahmad, Z.I.; Phuyal, J.L.; Petocz, P. Fatty acid composition of certified organic, conventional and omega-3 eggs. Food Chem. 2009, 116, 911–914. [CrossRef]
19. Kassis, N.; Drake, S.R.; Beamer, S.K.; Matak, K.E.; Jaczynski, J. Development of nutraceutical egg products with omega-3-rich oils. Food Sci. Technol. 2010, 43, 777–783. [CrossRef]
20. Sujatha, T.; Narahari, D. Effect of designer diets on egg yolk composition of ‘White Leghorn’ hens. J. Food
Sci. Technol. 2011, 48, 494–497. [CrossRef]
21. Alagawany, M.; Farag, M.R.; Abd El-Hack, M.E.; Dhama, K. The practical application of sunflower meal in poultry nutrition. Adv. Anim. Vet. Sci. 2015, 3, 634–648. [CrossRef]
22. Shiels, M.I. Fatty acids and early human development. Early Hum. Develop. 2007, 83, 761–766.
23. Richardson, A.J. Omega-3 fatty acids in ADHD and related neurodevelopmental disorders. Int. Rev. Psychiatry
2006, 18, 155–172. [CrossRef] [PubMed]
24. Simopoulos, A.P. Essential fatty acids in health and chronic disease. Am. J. Clin. Nutr. 1999, 70, 560–569.
[CrossRef] [PubMed]
25. DiNicolantonio, J.J.; O’Keefe, J.H. Importance of maintaining a low omega-6/omega-3 ratio for reducing inflammation. Open Heart 2018, 5, e000946. [CrossRef] [PubMed]
26. Swanson, D.; Block, R.; Mousa, S.A. Omega-3 fatty acids EPA and DHA: Health benefits throughout life.
Adv. Nutr. 2012, 3, 1–7. [CrossRef] [PubMed]
27. Ibrahim, D.; El-Sayed, R.; Khater, S.I.; Said, E.N.; El-Mandrawy, S.A.M. Changing dietary n-6: n-3 ratio using different oil sources affects performance, behavior, cytokines mRNA expression and meat fatty acid profile of broiler chickens. Anim. Nutr. 2018, 4, 44–51. [CrossRef] [PubMed]
28. Al-Zuhairy, M.A.; Jameel, Y.J. Effect of ND vaccine, multivitamins AD3E, and omega-3 on performance and immune response of broilers. Mirror Res. Vet Sci. Anim. 2014, 3, 42–50.
29. Irving, G.F.; Freund-Levi, Y.; Eriksdotter-Jonhagen, M.; Basun, H.; Brismar, K.; Hjorth, E.; Palmblad, J.;
Vessby, B.; Vedin, I.; Wahlund, L.O.; et al. Omega-3 fatty acid supplementation effects on weight and appetite in patients with Alzheimer’s disease: The omega-3 Alzheimer’s disease study. J. Am. Geriatr. Soc. 2009, 57,
11–17. [CrossRef]
30. Mousa, S.A.; Abdel-Raheem, S.M.; Abdel-Raheem, H.A.; Sadeek, A.L.S. Effect of dietary fat sources and antioxidant types on growth performance and carcass quality of Japanese quails. Int. J. Poult. Sci. 2017, 16,
443–450.
31. Wu, Y.B.; Li, L.; Wen, Z.G.; Yan, H.J.; Yang, P.L.; Tang, J.; Xie, M.; Hou, S.S. Dual functions of eicosapentaenoic acid-rich microalgae: Enrichment of yolk with n-3 polyunsaturated fatty acids and partial replacement for soybean meal in diet of laying hens. Poult. Sci. 2019, 98, 350–357. [CrossRef] [PubMed]
32. Konieczka, P.; Czauderna, M.; Smulikowska, S. The enrichment of chicken meat with omega-3 fatty acids by dietary fish oil or its mixture with rapeseed or flaxseed—Effect of feeding duration dietary fish oil, flaxseed, and rapeseed and n-3 enriched broiler meat. Anim. Feed Sci. Technol. 2017, 223, 42–52. [CrossRef]
33. Sihvo, H.K.; Immonen, K.; Puolanne, E. Myodegeneration with fibrosis and regeneration in the pectoralis major muscle of broilers. Vet. Path. 2014, 51, 619–623. [CrossRef] [PubMed]
34. Ahmad, S.A.; Yousaf, M.; Sabri, M.A.; Kamran, Z. Response of laying hens to omega-3 fatty acids for performance and egg quality. Avian Biol. Res. 2012, 5, 1–10. [CrossRef]
35. Ehr, I.J.; Persia, M.E.; Bobeck, E.A. Comparative omega-3 fatty acid enrichment of egg yolks from first-cycle laying hens fed flaxseed oil or ground flaxseed. Poult. Sci. 2017, 96, 1791–1799. [CrossRef] [PubMed]
36. Hamosh, M. Fatty acids and growth and development. In Fatty Acids in Foods and Their Implications;
Chow, C.K., Ed.; CRC Press: Boca Raton, FL, USA, 2008; pp. 899–933.
37. Horrocks, L.; Yeo, Y. Health benefits of docosahexaenoic acid (DHA). Pharmacol. Res. 1999, 40, 211–225.
[CrossRef] [PubMed]
38. Ebeid, T.; Eid, Y.; Saleh, A.; Abd El-Hamid, H. Ovarian follicular development, lipid peroxidation, antioxidative status and immune response in laying hens fed fish oil-supplemented diets to produce n-3-enriched eggs. Animal 2008, 2, 84–91. [CrossRef]
39. Yalcin, H.; Unal, M.K. The enrichment of hen eggs with ω-3 fatty acids. J. Med. Food 2010, 13, 610–614.
[CrossRef]
40. Cherian, G. Egg quality and yolk polyunsaturated fatty acid status in relation to broiler breeder hen age and dietary n-3 oils. Poult. Sci. 2008, 87, 1131–1137. [CrossRef]
41. Kralik, G.; Škrti´c, Z.; Suchý, P.; Straková, E.; Gajˇcevi´c, Z. Feeding fish oil and linseed oil to laying hens to increase the n-3 PUFA of egg yolk. Acta Veterinaria Brno 2008, 77, 561–568. [CrossRef]
42. Domenichiello, A.F.; Kitson, A.P.; Bazinet, R.P. Is docosahexaenoic acid synthesis from α-linolenic acid sufficient to supply the adult brain? Prog. Lipid Res. 2015, 59, 54–66. [CrossRef] [PubMed]
43. Ribeiro, T.; Lordelo, M.M.; Alves, S.P.; Bessa, R.J.B.; Costa, P.; Lemos, J.P.C.; Ferreira, L.M.A.; Fontes, C.M.G.A.;
Prates, J.A.M. Direct supplementation of diet is the most efficient way of enriching broiler meat with n-3 long-chain polyunsaturated fatty acids. Br. Poult. Sci. 2013, 54, 753–765. [CrossRef] [PubMed]
44. Lopez-Ferrer, S.; Baucells, M.D.; Barroeta, A.C.; Grashorn, M.A. n-3 enrichment of chicken meat. 2. Use of precursors of long-chain polyunsaturated fatty acids: Linseed Oil. Poult. Sci. 2001, 80, 753–761. [PubMed]
45. Buitendach, G.C.; De Witt, F.H.; Hugo, A.; Van Der Merwe, H.J.; Fair, M.D. Effect of dietary fatty acid saturation on egg production at end-of-lay. S. Afr. J. Anim. Sci. 2013, 43, 126–131.
46. Cachaldora, P.; Garcia-Rebollar, P.; Alvarez, C.; De Blas, J.C.; Mendez, J. Effect of type and level of fish oil supplementation on yolk fat composition and n-3 fatty acid retention efficiency in laying hens. Br. Poult. Sci.
2006, 47, 43–49. [CrossRef] [PubMed]
47. Cachaldora, P.; Garcia-Rebollar, P.; Alvarez, C.; De Blas, J.C.; Mendez, J. Effect of type and level of basal fat and level of fish oil supplementation on yolk fat composition and n-3 fatty acids deposition efficiency in laying hens. Anim. Feed Sci. Technol. 2008, 141, 104–114. [CrossRef]
48. Shang, X.G.; Wang, F.L.; Li, D.F.; Yin, J.D.; Li, J.Y. Effects of dietary conjugated linoleic acid on the productivity of laying hens and egg quality during refrigerated storage. Poult. Sci. 2004, 83, 1688–1695. [CrossRef]
49. Yin, J.D.; Shang, X.G.; Li, D.F.; Wang, F.L.; Guan, Y.F.; Wang, Z.Y. Effects of dietary conjugated linoleic acid on the fatty acid profile and cholesterol content of egg yolks from different breeds of layers. Poult. Sci. 2008, 87,
284–290. [CrossRef]
50. López-Ferrer, S.; Baucells, M.D.; Barroeta, A.C.; Grashorn, M.A. n-3 enrichment of chicken meat. 1. Use of very long-chain fatty acids in chicken diets and their influence on meat quality: Fish oil. Poult. Sci. 2001, 80,
741–752. [CrossRef]
51. Donaldson, J.; Madziva, M.T.; Erlwanger, K.H. The effects of high-fat diets composed of different animal and vegetable fat sources on the health status and tissue lipid profiles of male Japanese quail (Coturnix coturnix japonica). Asian Australas. J. Anim. Sci. 2017, 30, 700–711. [CrossRef]
52. Smith, M.; Soisuvan, K.; Miller, L. Evaluation of dietary calcium level and fat source on growth performance and mineral utilization of heat-distressed broilers. Poult. Sci. 2003, 2, 32–37.
53. Jalali, S.M.A.; Rabiei, R.; Kheiri, F. Effects of dietary soybean and sunflower oils with and without
L-carnitine supplementation on growth performance and blood biochemical parameters of broiler chicks.
Arch. Anim. Breed. 2015, 58, 387–394. [CrossRef]
54. Abdulla, N.R.; Loh, T.C.; Akit, H.; Sazili, A.Q.; Foo, H.L.; Kareem, K.Y.; Mohamad, R.; Rahim, R.A. Effects of dietary oil sources, calcium and phosphorus levels on growth performance, carcass characteristics and bone quality of broiler chickens. J. App. Anim. Res. 2017, 45, 423–429. [CrossRef]
55. Fébel, H.; Mezes, M.; Palfy, T.; Herman, A.; Gundel, J.; Lugasi, A.; Balogh, K.; Kocsis, I.; Blazovics, A. Effect of dietary fatty acid pattern on growth, body fat composition and antioxidant parameters in broilers. J. Anim.
Physiol. Anim. Nutr. 2008, 92, 369–376. [CrossRef] [PubMed]
56. Ebeid, T.; Fayoud, A.; Abou El-Soud, S.; Eid, Y.; El-Habbak, M. The effect of omega-3 enriched meat production on lipid peroxidation, antioxidative status, immune response and tibia bone characteristics in
Japanese quail. Czech J. Anim. Sci. 2011, 56, 314–324. [CrossRef]
57. Raj Manohar, G.; Edwin, S.C. Effect of dietary omega-3 PUFA rich sources on growth performance of Japanese quail. Int. J. Sci. Env. Technol. 2015, 4, 393–399.
58. Qi, K.K.; Chen, J.L.; Zhao, G.P.; Zheng, M.Q.; Wen, J. Effect of dietary ω6/ω3 on growth performance, carcass traits, meat quality and fatty acid profiles of Beijing-you chicken. J. Anim. Physiol. Anim. Nutr. 2010, 94,
474–485. [CrossRef]
59. Puthpongsiriporn, U.; Scheideler, S.E. Effects of dietary ratio of linoleic to linolenic acid on performance, antibody production, and in vitro lymphocyte proliferation in two strains of leghorn pullet chicks. Poult. Sci.
2005, 84, 846–857. [CrossRef]
60. Ayerza, R.; Coates, W. Omega-3 enriched eggs: The influence of dietary alpha-linolenic fatty acid source on egg production and composition. Can. J. Anim. Sci. 2001, 81, 355–362. [CrossRef]
61. Crespo, N.; Esteve-Garcia, E. Dietary polyunsaturated fatty acids decrease fat deposition in separable fat depots but not in the remainder carcass. Poult. Sci. 2002, 81, 512–518. [CrossRef]
62. Newman, R.E.; Bryden, W.L.; Fleck, E.; Ashes, J.R.; Buttemer, W.A.; Storlien, L.H.; Downing, J.A. Dietary n-3 and n-6 fatty acids alter avian metabolism: Metabolism and abdominal fat deposition. Br. J. Nutr. 2002, 88,
11–18. [CrossRef] [PubMed]
63. Ferrini, G.; Baucells, M.D.; Esteve-Garcia, E.; Barroeta, A.C. Dietary polyunsaturated fat reduces skin fat as well as abdominal fat in broiler chickens. Poult. Sci. 2008, 87, 528–535. [CrossRef] [PubMed]
64. Zollitsch, W.; Knaus, W.; Aichinger, F.; Lettner, F. Effects of different dietary fat sources on performance and carcass characteristics of broilers. Anim. Feed Sci. Technol. 1997, 66, 63–73. [CrossRef]
65. Huo, W.; Li, M.; Wang, J.; Wang, Z.; Huang, Y.; Chen, W. On growth performance, nutrient digestibility, blood
T lymphocyte subsets, and cardiac antioxidant status of broilers. Anim. Nutr. 2019, 5, 68–73. [CrossRef]
[PubMed]
66. Elwan, H.A.; Elnesr, S.S.; Mohany, M.; Al-Rejaie, S.S. The effects of dietary tomato powder (Solanum lycopersicum L.) supplementation on the haematological, immunological, serum biochemical and antioxidant parameters of growing rabbits. J. Anim. Physiol. Anim. Nutr. 2019, 103, 534–546. [CrossRef] [PubMed]
67. Velmurugan, N.; Kalpana, D.; Cho, J.Y.; Lee, Y.S. Chemical composition and antioxidant capacity of the aqueous extract of Phellodendronamurense. J. Forest. Res. 2018, 29, 1041–1048. [CrossRef]
68. Changxing, L.; Dongfang, D.; Lixue, Z.; Saeed, M.; Alagawany, M.; Farag, M.R.; Chenling, M.; Jianhua, L.
Heracleum persicum: Chemical composition, biological activities and potential uses in poultry nutrition.
World. Poult. Sci. J. 2019, 75, 207–217. [CrossRef]
69. Shen, Y.; Wang, D.; Zhao, J.; Chen, X. Fish red blood cells express immune genes and responses. Aquac. Fish
2018, 3, 14–21. [CrossRef]
70. Wang, Y.W.; Field, C.J.; Sim, J.S. Dietary polyunsaturated fatty acids alter lymphocyte subset proportion and proliferation, serum IgG concentration and immune tissue development in chicks. Poult. Sci. 2000, 80,
1741–1748. [CrossRef]
71. Yuming, G.; Chen, S.; Xia, Z.; Yuan, J. Effects of different types of polyunsaturated fatty acids on immune function and PGE2 synthesis by peripheral blood leukocytes of laying hens. Anim. Feed Sci. Technol. 2004,
116, 249–257.
72. Al-Khalifa, H.; Givens, D.; Rymer, C.; Yaqoob, P. Effect of n-3 fatty acids on immune function in broiler chickens. Poult. Sci. 2012, 91, 74–88. [CrossRef]
73. Jameel, Y.J.; Sahib, A.M.; Husain, M.A. Effect of dietary omega-3 fatty acid on antibody production against
Newcastle disease in broilers. Int. J. Sci. Nat. 2015, 6, 23–27.
74. Fritsche, K.L.; Cassity, N.A.; Huang, S.C. Effect of dietary fats on the fatty acid compositions of serum and immune tissues in chickens. Poult. Sci. 1991, 70, 1213–1222. [CrossRef]
75. Cherian, G. Essential fatty acids and early life programming in meat-type birds. World Poult. Sci. 2011, 67,
599–614. [CrossRef]
76. Wang, Y.W.; Sunwoo, H.; Cherian, G.; Sim, J.S. Maternal dietary ratio of linoleic acid to alpha-linolenic acid affects the passive immunity of hatching chicks. Poult. Sci. 2004, 83, 2039–2043. [CrossRef]
77. Wang, Y.W.; Ajuyah, A.O.; Sunwoo, H.H.; Cherian, G.; Sim, J.S. Maternal dietary n-3 fatty acids alter the spleen fatty acid composition and bovine serum albumin-induced wing web swelling in broilers. Poult. Sci.
2002, 81, 1722–1727. [CrossRef]
78. Al-Mayah, A.A.S. Effect of fish oil on humoral immunity of broiler chicks. Basrah J. Vet. Res. 2009, 8, 23–32.
[CrossRef]
79. Fouad, A.M.; El-Senousey, H.K. Nutritional factors affecting abdominal fat deposition in poultry: A review.
Asian Australas. J. Anim. Sci. 2014, 27, 1057–1068. [CrossRef]
80. Yang, X.; Zhang, B.; Guo, Y.; Jiao, P.; Long, F. Effects of dietary lipids and Clostridium butyricum on fat deposition and meat quality of broiler chickens. Poult. Sci. 2010, 89, 254–260. [CrossRef]
81. Chen, W.; Wang, J.P.; Huang, Y.Q. Effects of dietary n-6: n-3 polyunsaturated fatty acid ratio on cardiac antioxidative status, T-cell and cytokine mRNA expression in the thymus, and blood T lymphocyte subsets of broilers. Livest. Sci. 2012, 150, 114–120. [CrossRef]
82. Maroufyan, E.; Kasim, A.; Ebrahimi, M.; Loh, T.C.; Bejo, M.H.; Zerihun, H.; Hosseni, F.; Goh, Y.M.; Farjam, A.S.
Omega-3 polyunsaturated fatty acids enrichment alters performance and immune response in infectious bursal disease challenged broilers. Lipids Health Dis. 2012, 25, 15. [CrossRef]
83. Kassis, N.M.; Gigliotti, J.C.; Beamer, S.K.; Tou, J.C.; Jaczynski, J. Characterisation of lipids and antioxidant capacity of novel nutraceutical egg products developed with omega-3-rich oils. J. Sci. Food Agric. 2012, 92,
66–73. [CrossRef]
84. Fraeye, I.; Bruneel, C.; Lemahieu, C.; Buyse, J.; Muylaert, K.; Foubert, I. Dietary enrichment of eggs with omega-3 fatty acids: A review. Food Res. Int. 2012, 48, 961–969. [CrossRef]
85. Alagawany, M.; Farag, M.R.; Dhama, K.; Patra, A. Nutritional significance and health benefits of designer eggs. World’s Poult. Sci. J. 2018, 74, 317–330. [CrossRef]
86. Juturu, V. Omega-3 fatty acids and the cardiometabolic syndrome. J. Cardiometab. Syndr. 2008, 3, 244–253.
[CrossRef]
87. Galobart, J.; Barroeta, A.C.; Baucells, M.D.; Guardiola, F. Lipid oxidation in fresh and spray-dried eggs enriched with omega-3 and omega-6 polyunsaturated fatty acids during storage as affected by dietary vitamin E and canthaxanthin supplementation. Poult. Sci. 2001, 80, 327–337. [CrossRef]
88. Ren, Y.; Perez, T.I.; Zuidhof, M.J.; Renema, R.A.; Wu, J. Oxidative stability of omega-3 polyunsaturated fatty acids enriched eggs. J. Agri. Food Chem. 2013, 61, 11595–11602. [CrossRef]
89. Schneiderová, D.; Zelenka, J.; Mrkvicová, E. Poultry meat production as a functional food with a voluntary n-6 and n-3 polyunsaturated fatty acids ratio. Czech J. Anim. Sci. 2007, 52, 203–213. [CrossRef]
90. Ahmad, S.; Yousaf, M.; Kamran, Z.; Sohail, M.U. Production of n-3 pufa enriched eggs by feeding various dietary ratios of n-6 to n-3 fatty acids and vitamin a levels to the laying hens in hot climate. J. Poult. Sci. 2014,
51, 213–219.
91. Ceylan, N.; Ciftçi, I.; Mızrak, C.; Kahraman, Z.; Efil, H. Influence of different dietary oil sources on performance and fatty acid profile of egg yolk in laying hens. J. Anim. Feed Sci. 2011, 20, 71–83. [CrossRef]
92. Da Silva Filardi, R.; Junqueira, O.M.; de Laurentiz, A.C.; Casartelli, E.M.; Aparecida Rodrigues, E.; Francelino
Araujo, L. Influence of different fat sources on the performance, egg quality, and lipid profile of egg yolks of commercial layers in the second laying cycle. J. Appl. Poult. Res. 2005, 258, 264. [CrossRef]
93. Schiavone, A.; Marzoni, M.; Castillo, A.; Nery, J.; Romboli, I. Dietary lipid sources and vitamin E affect fatty acid composition or lipid stability of breast meat from Muscovy duck. Can. J. Anim. Sci. 2010, 90, 371–378.
[CrossRef]
94. Kishawy, A.T.; Amer, S.A.; Abd El-Hack, M.E.; Saadeldin, I.M.; Swelum, A.A. The impact of dietary linseed oil and pomegranate peel extract on broiler growth, carcass traits, serum lipid profile, and meat fatty acid, phenol, and flavonoid contents. Asian Australas. J. Anim. Sci. 2019, 32, 1161–1171. [CrossRef]
95. Jung, S.; Choe, J.H.; Kim, B.; Yun, H.; Kruk, Z.A.; Jo, C. Effect of dietary mixture of gallic acid and linoleic acid on antioxidative potential and quality of breast meat from broilers. Meat Sci. 2010, 86, 520–526. [CrossRef]
96. Mohamed, L.A.; El-Hindawy, M.M.; Alagawany, M.; Salah, A.S.; El-Sayed, S.A. Effect of low- or high-CP diet with cold-pressed oil supplementation on growth, immunity and antioxidant indices of growing quail.
J. Anim. Physiol. Anim. Nutr. 2019, 1–8. [CrossRef]
97. Baucells, M.D.; Crespo, N.A.C.; Barroeta, S.; Ferrer, L.; Grashorn, M.A. Incorporation of different polyunsaturated fatty acids into eggs. Poult. Sci. 2000, 79, 51–59. [CrossRef]
98. Shunthwal, J.; Sheoran, N. Influence of linseed oil feeding on performance and fatty acid composition of muscles in broiler chicks. Pharma Innov. J. 2017, 6, 268–273.
99. Zsédely, E.; Tóth, T.; Eiban, C.S.; Virág, G.Y.; Fábián, J.; Schmidt, J. Effect of dietary vegetable oil (sunflower, linseed) and vitamin E supplementation on the fatty acids composition, oxidative stability and quality of rabbit meat. In Proceedings of the 9th World Rabbit Congress, Verona, Italy, 10–13 June 2008; pp. 1473–1477.
100. Hulan, H.W.; Ackman, R.G.; Ratnayake, W.M.N.; Proudfoot, F.G. n-3 fatty acid levels and performance of broilers chickens fed redfish meal or redfish oil. Can. J. Anim. Sci. 1988, 68, 533–547. [CrossRef]
101. Rymer, C.; Givens, D. n−3 fatty acid enrichment of edible tissue of poultry: A review. Lipids 2005, 40, 121–130.
[CrossRef]
102. Givens, D.; Gibbs, R.A. Current intakes of EPA and DHA in European populations and the potential of animalderived foods to increase them. Proc. Nutr. Soc. 2008, 67, 273–280. [CrossRef]
103. Wood, J.D.; Enser, M.; Fisher, A.V.; Nute, G.R.; Sheard, P.R.; Richardson, R.I.; Hughes, S.I.; Whittington, F.M.
Fat deposition, fatty acid composition and meat quality: A review. Meat Sci. 2008, 78, 343–358. [CrossRef]
104. Amaral, A.B.; Silva, M.V.D.; Lannes, S.C.D.S. Lipid oxidation in meat: Mechanisms and protective factors–a review. Food Sci. Technol. 2018, 38, 1–15. [CrossRef]
105. Ribeiro, T.; Lordelo, M.M.; Costa, P.; Alves, S.P.; Benevides, W.S.; Bessa, R.J.B.; Lemos, J.P.C.; Pinto, R.M.A.;
Ferreira, L.M.A.; Fontes, C.M.G.A.; et al. Effect of reduced dietary protein and supplementation with a docosahexaenoic acid product on broiler performance and meat quality. Br. Poult. Sci. 2014, 55, 752–765.
[CrossRef]
106. Oken, E.; Kleinman, K.P.; Olsen, S.F.; Rich-Edwards, J.W.; Gillman, M.W. Associations of seafood and elongated n-3 fatty acid intake with fetal growth and length of gestation: Results from a us pregnancy cohort.
Am. J. Epidemiol. 2004, 160, 774–783. [CrossRef]
107. Gonzalez-Esquerra, R.; Leeson, S. Effects of menhaden oil and flaxseed in broiler diets on sensory quality and lipid composition of poultry meat. Br. Poult. Sci. 2000, 41, 481–488. [CrossRef]
108. Leeson, S.; Atteh, J. Utilization of fats and fatty acids by turkey poults. Poult. Sci. 1995, 74, 2003–2010.
[CrossRef]
109. Leeson, S.; Summers, J. Commercial Poultry Production; University Books: Guelph, ON, Canada, 2005.
110. Sun, D.; Krishnan, A.; Zaman, K.; Lawrence, R.; Bhattacharya, A.; Fernandes, G. Dietary n-3 fatty acids decrease osteoclastogenesis and loss of bone mass in ovariectomized rats. J. Bone Min. Res. 2003, 18, 1206–1216.
[CrossRef]
111. Baird, H.T.; Eggett, D.L.; Fullmer, S. Varying ratios of omega-6: Omega-3 fatty acids on the pre-and postmortem bone mineral density, bone ash, and bone breaking strength of laying chickens. Poult. Sci. 2008,
87, 323–328. [CrossRef]
112. Lau, B.Y.Y.; Cohen, D.J.A.; Ward, W.E.; Ma, D.W.L. Investigating the role of polyunsaturated fatty acids in bone development using animal models. Molecules 2013, 18, 14203–14227. [CrossRef]
113. Yair, R.; Shahar, R.; Uni, Z. In ovo feeding with minerals and vitamin D3 improves bone properties in hatchlings and mature broilers. Poult. Sci. 2015, 94, 2695–2707. [CrossRef]
114. Hopcroft, R.L.; Cowieson, A.J.; Muir, W.I.; Groves, P.J. Changes to mineral levels in the yolk of meat chicken embryos during incubation. Poult. Sci. 2018, 98, 1511–1516. [CrossRef]
115. Yair, R.; Uni, Z. Content and uptake of minerals in the yolk of broiler embryos during incubation and effect of nutrient enrichment. Poult. Sci. 2011, 90, 1523–1531. [CrossRef]
116. Kelso, K.A.; Cerolini, S.; Noble, R.C.; Sparks, N.H.C.; Speake, B.K. Lipid and antioxidant changes in semen of broiler fowl from 25 to 60 weeks of age. J. Rep. 1996, 106, 201–206. [CrossRef]
117. Kelso, K.A.; Cerolini, S.; Speake, B.K.; Gavalchini, L.G.; Noble, R.C. Effects of dietary supplementation with alpha-linolenic acid on the phospholipids fatty acid composition and quality of spermatozoa in cockerel from 24–72 weeks of age. J. Rep. 1997, 110, 53–59. [CrossRef]
118. Cerolini, S.; Surai, P.; Ggavalchini, L.G.M.; Noble, R.C. Effect of n3 and n6 fatty acid supplemented diet and vitamin E level on semen quality in cockerels. Br. Poult. Sci. 2000, 41, 8–10. [CrossRef]
119. Hudson, P.; Wilson, J. Effects of dietary menhaden oil on fertility and sperm quality of broiler breeder males.
J. App. Poult. Res. 2003, 12, 341–347. [CrossRef]
120. Bongalhardo, D.C.; Leeson, S.; Buhr, M.M. Dietary lipids differentially affect membranes from different areas of rooster sperm. Poult. Sci. 2009, 88, 1060–1069. [CrossRef]
121. Blesbois, E.; Grasseau, I.; Seigneurin, F. Membrane fluidity and the ability of domestic bird spermatozoa to survive cryopreservation. Reproduction 2005, 129, 371–378. [CrossRef]
122. Waterhouse, K.E.; Hofmo, P.O.; Tverdal, A.; Miller, R.R. Within and between breed differences in freezing tolerance and plasma membrane fatty acid composition of boar sperm. Reproduction 2006, 131, 887–894.
[CrossRef]
123. Zaniboni, L.; Cerolini, S. Liquid storage of turkey semen: Changes in quality parameters, lipid composition and susceptibility to induced in vitro peroxidation in control, n-3 fatty acids and alpha tocopherol rich spermatozoa. Anim. Reprod. Sci. 2009, 112, 51–65. [CrossRef]
124. Al-Daraji, H.J.; Al-Mashadani, H.A.; Al-Hayani, W.K.; Al-Hassani, A.S.; Mirza, H.A. Effect of n-3 and n-6 fatty acid supplemented diets on semen quality in Japanese quail (Coturnix coturnix japonica). Int. J. Poult. Sci.
2010, 9, 656–663. [CrossRef]
125. Al-Daraji, H.J. Sperm-egg penetration in laying breeder flocks: A technique for the prediction of fertility.
Br. Poult. Sci. 2001, 42, 266–270. [CrossRef]
126. Al-Daraji, H.J. Studies of the semen characteristics of certain breeds of Iraqi cocks. Iraqi J. Agric. Sci. 2002, 33,
257–262.
127. Swi ˛atkiewicz, S.; Arczewska-Włosek, A.; Krawczyk, J.; Szczurek, W.; Puchała, M.; J ´ ózefiak, D. Effect of selected feed additives on egg performance and eggshell quality in laying hens fed a diet with standard or decreased calcium content. Ann. Anim. Sci. 2018, 18, 167–183. [CrossRef]
128. Gakhar, N.; Goldberg, E.; Jing, M.; Gibson, R.; House, J.D. Effect of feeding hemp seed and hemp seed oil on laying hen performance and egg yolk fatty acid content: Evidence of their safety and efficacy for laying hen diets. Poult. Sci. 2012, 91, 701–711. [CrossRef]
129. Shahid, S.; Chand, N.; Khan, R.U.; Suhail, S.M.; Khan, N.A. Alternations in cholesterol and fatty acids composition in egg yolk of Rhode Island Red x Fyoumi Hens fed with hemp seeds (Cannabis sativa L.).
J. Chem. 2015, 2015, 6. [CrossRef]
130. Neijat, M.; Suh, M.; Neufeld, J.; House, J.D. Hempseed products fed to hens effectively increased n 3 polyunsaturated fatty acids in total lipids, triacylglycerol and phospholipid of egg yolk. Lipids 2016, 51,
601–614. [CrossRef]
131. Mattioli, S.; Dal Bosco, A.; Martino, M.; Ruggeri, S.; Marconi, O.; Sileoni, V.; Falcinelli, B.; Castellini, C.;
Benincasa, P. Alfalfa and flax sprouts supplementation enriches the content of bioactive compounds and lowers the cholesterol in hen egg. J. Funct. Foods. 2016, 22, 454–462. [CrossRef]
132. Park, N.; Lee, T.K.; Nguyen, T.T.H.; An, E.B.; Kim, N.M.; You, Y.H.; Park, T.S.; Kim, D. The effect of fermented buckwheat on producing l-carnitine-and γ-aminobutyric acid (GABA)-enriched designer eggs.
J. Sci. Food Agric. 2017, 97, 2891–2897. [CrossRef]
133. Lokhande, A.; Ingale, S.L.; Lee, S.H.; Sen, S.; Khong, C.; Chae, B.J.; Kwon, I.K. Effects of dietary supplementation with Gynuraprocumbens (Merr.) on egg yolk cholesterol, excreta microflora and laying hen performance. Br. Poult. Sci. 2014, 55, 524–531. [CrossRef]
134. Elkin, R.G.; Ying, Y.; Harvatine, K.J. Feeding laying hens stearidonic acid-enriched soybean oil, as compared to flaxseed oil, more efficiently enriches eggs with very long-chain n-3 polyunsaturated fatty acids. J. Agric.
Food Chem. 2015, 63, 2789–2797. [CrossRef]
135. Petrovic, M.; Gacic, M.; Karacic, V.; Gottsteinc, Z.; Mazijac, H.; Medic, H. Enrichment of eggs in n-3 poly unsaturated fatty acids by feeding hens with different amount of linseed oil in diet. Food Chem. 2012, 135,
1563–1568. [CrossRef]
136. Herzallah, S. Enrichment of conjugated linoleic acid (CLA) in hen eggs and broiler chickens meat by lactic acid bacteria. Br. Poult. Sci. 2013, 54, 747–752. [CrossRef]
137. Kostogrys, R.B.; Filipiak-Florkiewicz, A.; Dere ´n, K.; Drahun, A.; Czy˙zy ´nska-Cicho ´n, I.; Cie´slik, E.;
Szymczyk, B.; Franczyk-Zar ˙ ów, M. Effect of dietary pomegranate seed oil on laying hen performance and physicochemical properties of eggs. Food Chem. 2017, 221, 1096–1103. [CrossRef]
138. Park, J.H.; Upadhaya, S.D.; Kim, I.H. Effect of dietary marine microalgae (Schizochytrium) powder on egg production, blood lipid profiles, egg quality, and fatty acid composition of egg yolk in layers. Asian Australas.
J. Anim. Sci. 2015, 28, 391–397. [CrossRef]
139. El-Katcha, M.I.; El-Kholy, M.E.; Soltan, M.A.; El-Gayar, A.H. Effect of dietary omega-3 to omega-6 ratio on growth performance, immune response, carcass traits and meat fatty acids profile of broiler chickens.
J. Poult. Sci. 2014, 2, 71–94.
140. Lemahieu, C.; Bruneel, C.; Ryckebosch, E.; Muylaert, K.; Buyse, J.; Foubert, I. Impact of different omega-3 polyunsaturated fatty acid (n-3 PUFA) sources (flaxseed, Isochrysisgalbana, fish oil and DHA Gold) on n-3
LC-PUFA enrichment (efficiency) in the egg yolk. J. Funct. Foods 2015, 19, 821–827. [CrossRef]
141. Lemahieu, C.; Bruneel, C.; Termote-Verhalle, R.; Muylaert, K.; Buyse, J.; Foubert, I. Impact of feed supplementation with different omega-3 rich microalgae species on enrichment of eggs of laying hens.
Food Chem. 2013, 14, 4051–4059. [CrossRef]
142. Scollan, N.D.; Price, E.M.; Morgan, S.A.; Huws, S.A.; Shingfield, K.J. Can we improve the nutritional quality of meat? Proc. Nutr. Soc. 2017, 76, 603–618. [CrossRef]
143. Saeed, M.; Yatao, X.; Hassan, F.U.; Arain, M.A.; Abd El-Hack, M.E.; Noreldin, A.E.; Sun, C. Influence of graded levels of l-theanine dietary supplementation on growth performance, carcass traits, meat quality, organs histomorphometry, blood chemistry and immune response of broiler chickens. Int. J. Mol. Sci. 2018,
19, 462. [CrossRef]
144. Zhang, P.; Tang, C.; Ding, Z.; Huang, H.; Sun, Y. Effects of simultaneous supplementation of laying hens with
α-linolenic acid and eicosapentaenoic acid/docosahexaenoic acid resources on egg quality and n-3 fatty acid profile. Asian Australas. J. Anim. Sci. 2017, 30, 973–978. [CrossRef]

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Authors:
Dr. Mahmoud Alagawany
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Shaaban El-Nesr
Fayoum University
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Sandip Khurana
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