Go to Top Go to Bottom
Anim Biosci > Volume 34(3); 2021 Special Issue > Article
Ismail, Alagawany, Taha, Puvača, Laudadio, and Tufarelli: Effect of dietary supplementation of garlic powder and phenyl acetic acid on productive performance, blood haematology, immunity and antioxidant status of broiler chickens

Abstract

Objective

The effect of garlic powder (GP) and phenyl acetic (PA) acid throughout the fattening period of broiler chickens on performance, blood parameters, immune, and antioxidant parameters as well as carcass traits was evaluated.

Methods

A total of 210 day-old Cobb broiler chicks were randomly distributed into seven dietary treatments having five replications with six chicks per replicate. The first group (control) fed a basal diet without supplements, whereas the 2nd, 3rd, and 4th group were fed basal diet plus 0.25, 0.50, and 0.75 g GP/kg diet, respectively and the group 5th, 6th, and 7th were fed on the basal diet plus 0.25, 0.50, and 0.75 g PA/kg diet.

Results

Broiler body weight and gain at 21 and 42 days were increased (p<0.05) with diets supplemented with GP and PA. Red blood cells and hemoglobin were improved in chickens fed diets enriched with GP. Broiler chickens received diets containing either GP or PA recorded the higher values (p<0.05) of total protein, globulin, high-density lipoprotein, immunoglobulin M (IgM), and IgG, superoxide dismutase and total antioxidant capacity; while, blood total cholesterol, low-density lipoprotein, aspartate-aminotransferase, and malondialdehyde were lowered (p<0.05) compared to control-diet. Liver and immune-related organs weight were improved (p<0.05) in broilers fed diet supplemented with GP and PA.

Conclusion

Feeding of GP or PA in diet had positive effects on performance traits and immunological, antioxidant and physiological status of broilers. Thus, the use of tested feed additives as an eco-friendly alternative to antibiotics produced a positive effect on animal health.

INTRODUCTION

In the recent years broiler production was spread on the large scale in many countries to provide the requirements of animal protein for human. The usage of antibiotics as growth promoters in broiler diet has been forbid because the anxiety of their residues in poultry tissues which lead to the inducement of new strains of microorganism resistant of antibiotic [1]. Poultry meat and egg production, still pain from great losses due to food contamination with harmful bacteria and their influences also on the poultry performance, such as decrease weight and increase of mortality rate [2]. The use of natural feed additives and growth promoters from different sources in animal feeds is an effective way to enhance nutrient utilization and to reduce the antibiotic residues. Phytogenic supplements are plant-derived products used in feeding poultry to maintain performance of livestock species [3]. Among a large number of herbs, garlic has been considered as an effective plant having antioxidant and antimicrobial activities along with multiple beneficial uses [4]. It was reported that phytogenic feed additives improving body weight, feed efficiency ratio, and increased viability of chickens [5]. Garlic (Allium sativum) has a lot of beneficial bioactive substances [6]. In a study, Ziarlarimi et al [7] stated that garlic powder (GP) included many organosulfur compounds such as allicin, alliin, ajoene, diallylsulfide, dithiin, and S-allylcysteine, so that garlic as a natural plant-derived feed additives may be successfully used to improve broiler growth. Further, garlic has been widely used as feed additives or growth promoter substance since antiquity [8] and it has been also identified as a medicinal plant in prevention and treatment of many heart, intestinal and metabolic diseases, such as atherosclerosis, thrombosis, dementia, cancer, and diabetes [9]. Several studies reported that garlic has many beneficial properties such as antimicrobial, antioxidative, antithrombotic, antiplatelet aggregator, and antihypertensive in broilers [10,11].
Organic acids or their salts are used as dietary supplement due to their ability on inhibiting microbial growth in nutrients and then maintain the microbial equilibrium in digestive system. Also, they can convert intestinal pH improving consequently feed ingredients solubility, digestion and their absorption [12]. Actually, organic acids celebrated as non-antibiotic growth promoters in poultry nutrition [13]. Acetic acid is one of organic acids which used to inhibit harmful microbial content in gut, modifying pH level and enhancing feed efficiency [14]. Viveros et al [15] reported that organic acids improve digestion and absorption of feed ingredients and modulate positively immunity mucosa layer in broiler chickens. Thus, there is a need to use more effective feeding strategies and economic alternatives for improving health status and performance of poultry.
Therefore, this study was carried out to examine the effects of GP and phenyl acetic (PA) acid on broiler performance, carcass traits and blood haematology, as well as some immune and antioxidant parameters.

MATERIALS AND METHODS

This study was designed and carried out at the Poultry Department, Faculty of Agriculture, Zagazig University, Zagazig, Egypt. The protocol was approved by the experimentation rules of the Internal Commission for Environmental and Ethics of Zagazig University.

Experimental design

A total of 210 day-old Cobb broiler chickens were obtained from a commercial hatchery. Chicks were split randomly to seven dietary treatments having five replicates of six birds each. Birds were kept in floor pens supplied with wood shavings. The first group (control) fed a basal diet without supplements, whereas the group 2nd, 3rd, and 4th were fed basal diet plus 0.25, 0.50, and 0.75 g GP/kg diet, respectively; and the group 5th, 6th, and 7th were fed on the basal diet plus 0.25, 0.50, and 0.75 g PA/kg diet. Birds were reared under the same environmental conditions. Room temperature was 33°C at initial experiment, then decreased gradually to reach 25°C at 15 days of age and kept constant. The basal starter diet (1 to 21 days of age) consisted of 23% crude protein (CP) and 3,000 ME kcal/kg, while the finisher diet (22 to 42 days of age) of 20% CP and 3,150 ME kcal/kg, as recommended by NRC [16]. The experimental diets were prepared by blending the basal diet with 0.25, 0.50, and 0.75 g/kg diet of GP or PA acid. The GP was purchased from a local market in Zagazig City (Sharkia, Egypt) and phenylacetic acid (PA; C8H8O2) from El Gomhouria Co., GOMAC (Zagazig, Egypt), then added to diets. Feed and water were offered ad libitum.

Body weight, carcass traits, and blood sampling

Birds of all groups were individually weighed after arriving to the farm. Body weight (BW) and gain were recorded and calculated at 21 and 42 days of age. Birds (four subjects per replicate) were weighed individually and slaughtered after blood samples collection, by neck cut and allowed to bleed. The Bursa of Fabricius, thymus, spleen, liver, heart and empty small intestine were removed and weighed, then calculated the relative weight to live BW. Small intestine length, width and cecum length were also recorded [17].
From the same chickens, blood samples were taken from the wing vein using a sterile syringe into tubes containing ethylenediaminetetraacetic acid to obtain whole blood and plasma to determine blood hematology and biochemical components. Blood heamatology, including red blood cells (RBC) count, hemoglobin (Hb) concentration, packed cell volume (PCV) by standard procedures [18]. Total white blood cells (WBC) count, percentage of heterocytes, percentage of monocytes, and percentage of lymphocytes were analyzed [19].

Plasma biochemistry and antioxidant status

Blood samples were centrifugated at 3,000 g×20 min to obtain the plasma, then stored at −20°C for analysis. The plasma samples were analyzed to determine total protein (TP), albumin (Alb), globulin (Glb), alanine-aminotransferase (ALT) and aspartate-aminotransferase (AST), total cholesterol (TC), triglycerides, high- and low-density lipoprotein (HDL and LDL), superoxide dismutase (SOD), total antioxidant capacity (TAC), malondialdehyde (MDA), immunoglobulins (IgG and IgM) spectrophotometrically using commercial kits.

Statistical analysis

Data were analyzed using SAS (SAS Software, Inst. Inc., Cary, NC, USA) according to completely randomized design. Differences among groups were separated by Duncan’s multiple range test. The level of significance was pre-set at p<0.05, following the model: Yij = μ+Ti+eijk; where: Yij = individual observation, μ = the overall mean, Ti = effect of treatment (i = 1, 2, 3,…7), and eijk = random error.

RESULTS

Growth and carcass traits

The effect of different levels of GP or PA on broiler’s performance as BW and daily gain is shown in Table 1. Broiler BW at 21 and 42 days of age and BW gain during 1 to 21, 21 to 42, and 1 to 42 days of age were significantly (p<0.05) improved in groups fed diet supplemented with GP or PA. Feeding of 0.75 g GP/kg led to heaviest (p<0.05) final BW and gain compared to the other diets.
Relative weight of liver was significantly increased (p< 0.01) when broilers fed different levels of GP and PA compared to control (Table 2). Conversely, post-slaughter weight, heart percentage, and cecum length were not affected by treatments. However, dietary additives recorded the highest values of small intestine length width compared to control (Table 2). In particular, the higher liver relative weight of 2.93% was observed in broilers fed 0.75 g GP/kg diet, whereas the highest small intestine length of 196.35 mm was detected when fed 0.75 g PA/kg compared to the other groups including control-diet.

Blood hematology and biochemical parameters

The effect of treatments on blood hematology is reported in Table 3. The RBC and Hb were significantly (p<0.01) increased in chicks fed GP, when compared to those treated with 0.50 and 0.75 g/kg of PA and control-diet. Further, chicks fed diet containing 0.75 g GP/kg diet had the highest value of Hb (13.46 g/dL) compared with the other groups. Lymphocytes and heterocytes levels were increased (p<0.05) with GP and PA supplementation than control. However, GP or PA treatments did not elicit a significant alteration in PCV and WBCs among groups (Table 3).
Data in Table 4 show that chickens fed diets containing different levels of either GP or PA (0.25, 0.50, and 0.75 g/kg) had higher (p<0.05) values of TP and Glb than those in control. Also, broilers supplemented with GP or PA had lower (p<0.01) LDL, TC, and AST than control. Conversely, HDL was increased (p<0.01) in all treated groups than control. No significant differences were detected in Alb, triglycerides and ALT levels in birds receiving feed additives.

Immunity and antioxidant parameters

As reported in Table 5, dietary supplementation of GP and PA increased significantly the broiler immunological parameters (IgM and IgG) and immune organs (relative weight of thymus, Bursa of Fabricius and spleen), in particular when birds fed enriched diets with 0.75 g GP or PA/kg. Compared to control-diet, antioxidant status in terms of SOD and TAC was improved in birds fed GP or PA; where, broiler supplemented with 0.50 and 0.75 g/kg of GP or PA achieved the highest values of SOD and TAC (p<0.05; Table 6). Also, MDA value was significantly (p<0.0021) reduced in groups receiving feed additives (lowest value recorded in 0.75 g GP/kg) compared to control.

DISCUSSION

Additing of GP and PA in broiler diets enhanced BW and BW gain at 21 and 42 days of age. The obtained results are in agreement with the findings of Khan et al [6] who observed that broiler treated with GP had significantly higher live weight and gain than unsupplemented group. The same trend was also found by Suriya et al [20] who used 0.5% GP in broiler diet. The better effect of garlic as natural feed additives might be due to increased enzymes activity of pancreas, which offer a better environment for digestion and absorption of nutrients. Our results corroborated those of Nourmohammadi and Khosravinia [21] who showed that addition of 30 g citric acid/kg diet significantly improved broiler BW gain. The improvement in BW and gain achieved when broilers fed GP and PA may be due to dialkylpolysulphide as antibacterial compound which in garlic and playing axial role in broiler weight gain [22]. Furthermore, our observations agreed with those obtained by Dibner and Buttin [23] who illustrated that addition of acetic acid to drinking water of chicks almost increased BW and it may be due to improved digestion of protein, energy and retention by reduced microbial competition for nutrients.
In the current study, results showed that supplementing diet with PA or GP improved the relative weight of liver. Similar trend was previously observed with Ashayerizadeh et al [24] who showed that addition of garlic at 1 kg/ton in broiler diet enhanced carcass yield when compared with control. Conversely, Raeesi et al [25] reported that feeding of 0.5%, 1.0%, and 3% garlic decreased only broiler heart weight. On the other hand, Sohail et al [26] postulated that addition of organic acids in chicken diets did not affect carcass traits such as dressing percentage, liver, heart and spleen weights. Small intestine length and average width were higher in broilers received diet supplemented with both feed additives than control group. In parallel, Denli et al [27] observed that intestinal weight and length were significantly affected by administration of a mixture of organic acids (propionic and formic acid salts) in chickens. Moreover, broilers fed diet supplemented with organic acids increased intestinal weight and length at slaughter age of 42 days, enhancing also growth performance and carcass yield [28].
Values of RBC, Hb, lymphocytes and heterocytes in chickens fed either GP- or PA- enriched diets were higher than those in control-diet. In line with our findings, Askar [29] who found that RBCs, Hb and PCV% increased in broiler fed diet supplemented with PA. The same Author observed also an increase of WBCs in PA supplemented groups. In a study, Rehman et al [30] stated that inclusion dietary acetic acid led to an increase only of lymphocytes count and H/L ratio in broiler chickens. Further, Wang et al [31] when supplemented broiler diet with PA found an increase in WBC and lymphocyte being in agreement with our findings. It was reported by Haque et al [32] that the lymphoid organs content of lymphocytes improved with addition citric acid in diet due to enhanced non-specific immunity. Our results are partially in agreement with previous findings observing that Hb and PCV were not affected by dietary GP in broilers [12]. Also, Elagib et al [33] found that no effect of diets containing 3% and 5% GP on broiler RBC, PCV, and WBC. The hemolytic bioactive and their metabolites in garlic may be responsible of these effects. The improvement in RBC with GP supplementation could be due to the end-product produced from garlic metabolism possible stimulates formation and secretion of erythropoietin of the kidney directly to cause erythrocyte synthesis [34]. Dorhoi et al [35] demonstrated that garlic extract addition to laying hens diet tended to enhance spleen RBCs uptake.
Findings of our study showed that supplementing diets with GP and PA decreased blood TC and LDL, and increased TP, Glb, and HDL. These results are partially in agreement with Rahimi et al [36] who found in broilers that blood triglycerides, TC, and LDL concentrations were decreased, while HDL increased when fed enriched-diet with 0.1% GP. At this regard, Issa and Omar [37] showed that addition of GP at 0.2% and 0.4% reduced significantly concentrations of triglycerides, cholesterol, LDL in Cobb broiler, increasing the level of HDL compared to control. On the contrary, it was reported no differences in serum biochemical parameters (TP, Alb, Glb, cholesterol, triglycerides, ALT, and AST) of broilers fed diet enriched with garlic [6]. The potential effect of garlic products may be due to depressing the lipogenic and cholesterogenic activity of liver enzymes such as fatty acid synthase, glucose-6-phosphatase dehydrogenase, malic enzyme, and 3-hydroxy-3-methylglutaryl-CoA reductase, consequently, the mechanism of hypocholesterol and hypolipid syntheses [38].
In a study, Rehman et al [30] reported that broilers fed diet supplemented with acetic acid had the highest value of TP and Glb comparing to control diet. Previously, Askar [29] observed that birds receiving 0.075%, 0.150%, and 0.225% PA had lower value of cholesterol than control group. The increase in Glb led to improved immunity, and Rahmani and Speer [39] demonstrated that dietary inclusion of organic acid increased concentration of serum Glb and induced better immune response in broilers. Our dietary treatments decreased ALT levels in comparison to control, and this result partially agreed those of Askar [29] who found that addition of PA reduced significantly ALT than control. The same trend was obtained by Salgado-Tránsito et al [40] who found that 50 g/kg citric acid in broiler diet decreased ALT activity; however, increased serum AST concentration. Further, Nourmohammadi and Khosravinia [21] showed that citric acid supplemented into diet at 60 g/kg significantly reduced concentrations of HDL and AST than control birds.
A significant increase was observed in the broiler serum IgG and IgM and weights of thymus, Bursa of Fabricius and spleen when fed GP and PA. These improvements in immunological parameters may be due to the bioactive molecules in GP and PA. In agreement with our results, Rahimi et al [36] found that dietary supplementation of garlic improved the relative weight of Bursa of Fabricius than non-treated birds. Conversely, Raeesi et al [25] reported that chicks fed diet with 0.5%, 1.0%, and 3% garlic had lower weights of bursa and spleen. The same trend of our study was also found by Hossain et al [41] who reported that L. mesenteroides-fermented garlic did not affect Bursa Fabricius. Hanieh et al [28] observed that dietary garlic supplementation increased IgG concentration. In the same trend, Askar [29] showed that relative weight of Bursa of Fabricius and spleen significantly increased in broiler treated with PA, whereas, Sohail et al [26] reported that organic acids addition did not affect spleen weight of broilers.
In the GP- and PA-treated groups, the levels of TAC and SOD were significantly increased at 0.75 g/kg; while, the highest concentration of MDA was recorded in control group. Our results agreed those obtained by Pourali et al [42] who indicated that adding garlic to broiler diet decreased of MDA concentrations by 30% compared to birds fed basal-diet, without affecting SOD. Recently, Nasiroleslami et al [43] showed that broiler fed diet supplemented with guanidinoacetic acid significantly improved glutathione peroxidase activity in broiler liver and decreased serum MDA. Furthermore, Alagawany et al [44] demonstrated that dietary supplementation of garlic in diet had positive impact on SOD and TAC activities.
In conclusion, based on our findings, both GP and PA acid, as natural feed additives in diet, had antioxidant and immune effects in broilers, having also influence on their growth performance and blood parameters and lipid peroxidation. In particular, both natural feed additives resulted more effective when supplemented at the rate of 0.50 or 0.75 g/kg diet.

Notes

CONFLICT OF INTEREST

We certify that there is no conflict of interest with any financial organization regarding the material discussed in the manuscript.

ACKNOWLEDGMENTS

Authors extend thanks to their respected institutes and universities.

Table 1
Live body weight and body weight gain of broiler chicks as affected by dietary garlic powder and phenyl acetic acid supplementation
Treatment Live BW (g/bird) Daily BW gain (g/d/bird)


21 days 42 days 1–21 days 21–42 days 1–42 days
Control 928.1c 1,986.3d 41.64c 50.38d 46.93c
GP (g/kg)
 0.25 945.5c 2,035.2c 42.26c 51.91d 47.53c
 0.50 1,033.3a 2,175.2b 47.11a 54.18b 52.62b
 0.75 1,052.7a 2,245.1a 47.85a 56.81a 55.42a
PA (g/kg)
 0.25 985.6b 2,159.6b 45.85b 55.32b 48.21c
 0.50 993.9b 2,190.4b 45.37b 57.21a 51.28a
 0.75 943.6c 2,065.1c 42.14c 53.42c 47.74c
SEM 18.75 23.01 8.173 1.513 4.074
Pr>f 0.0124 0.0087 0.0279 0.0193 0.00126

BW, body weight; GP, garlic powder; PA, phenyl acetic; SEM, standard error of the mean.

a–d Means within the same column with different common superscripts differ.

Table 2
Carcass traits of broiler chicks as affected by dietary garlic powder and phenyl acetic acid supplementation
Treatment Post-slaughter weight (g) Liver (%) Heart (%) Cecum length (cm) Small intestine measurements

Width (mm) Length (mm) Weight (g)
Control 1,876.6 1.61c 0.456 14.67 8.67b 154.67c 114.34
GP (g/kg)
 0.25 1,954.1 2.36ab 0.597 17.96 10.61a 183.99b 135.01
 0.50 1,943.3 2.57ab 0.603 19.21 11.21a 150.34c 122.35
 0.75 1,871.5 2.93a 0.671 21.63 10.64a 180.67b 115.43
PA (g/kg)
 0.25 1,859.6 2.18b 0.572 20.43 7.85b 179.35b 114.12
 0.50 1,828.3 2.64ab 0.569 17.82 8.13b 150.41c 130.67
 0.75 1,885.1 2.81a 0.655 17.37 10.42a 196.35a 122.36
SEM 48.57 0.668 0.086 1.523 4.018 5.493 8.175
Pr>f 0.1870 0.0017 0.0680 0.1007 0.0004 0.0001 0.0583

GP, garlic powder; PA, phenyl acetic; SEM, standard error of the mean.

a–c Means within the same column with different common superscripts differ.

Table 3
Blood hematology of broiler chicks as affected by dietary garlic powder and phenyl acetic acid supplementation
Treatment RBC (×106/mL) PCV (%) Hb (g/dL) WBC (×103/mL) Monocytes (%) Lymphocytes (%) Heterophils (%)
Control 2.84ab 38.03 9.27c 22.27 4.87 33.08b 42.13d
GP (g/kg)
 0.25 2.96ab 40.66 11.93ab 23.89 5.46 45.23a 51.38bc
 0.50 3.28a 38.84 12.71ab 24.18 5.31 47.51a 57.68ab
 0.75 3.16a 42.22 13.46a 26.21 4.97 52.42a 59.62ab
PA (g/kg)
 0.25 3.01ab 43.95 11.34ab 23.44 5.73 48.13a 62.28a
 0.50 2.89bc 39.01 10.52bc 21.97 4.81 47.32a 47.01cd
 0.75 2.61bc 38.93 10.11bc 23.65 5.62 46.78a 58.53ab
SEM 1.328 4.007 1.881 3.075 2.609 4.915 4.063
Pr>f 0.0081 0.1290 0.0100 0.1800 0.084 0.0490 0.0015

RBC, red blood cells; PCV, packed cell volume; Hb, hemoglobin; WBC, red blood cells; GP, garlic powder; PA, phenyl acetic; SEM, standard error of the mean.

a–d Means within the same column with different common superscripts differ.

Table 4
Blood biochemistry parameters of broiler chicks as affected by dietary garlic powder and phenyl acetic acid supplementation
Treatment TP (g/dL) Alb (g/dL) Glb (g/dL) TC (mg/dL) HDL (mg/dL) LDL (mg/dL) Triglycerides (g/dL) AST (μ/L) ALT (μ/L)
Control 3.01b 1.78 1.23b 95.64a 17.84c 42.41a 72.76 246.81a 12.63
GP (g/kg)
 0.25 4.06b 2.55 1.51ab 72.51bc 26.67bc 26.71b 58.37 196.63b 9.96
 0.50 4.51ab 2.58 1.93a 64.75bc 28.79ab 24.23b 50.18 170.55bc 7.82
 0.75 4.87a 2.76 2.11a 58.87c 38.24a 21.97b 48.71 138.94c 6.91
PA (g/kg)
 0.25 4.22b 2.31 1.91a 71.63bc 21.44bc 30.76b 55.42 186.88c 8.24
 0.50 4.21b 2.49 1.72a 63.21bc 21.36bc 27.65b 61.78 201.07b 10.63
 0.75 3.96b 2.19 1.77a 81.17ab 27.04bc 24.91b 58.21 172.34bc 9.98
SEM 1.549 0.546 0.164 14.758 5.589 13.954 21.134 38.619 3.765
Pr>f 0.002 0.198 0.029 0.006 0.008 0.004 0.149 0.005 0.221

TP, total protein; Alb, albumin; Glb, globulin; TC, total cholesterol; HDL, high-density lipoprotein; LDL, low-density lipoprotein; AST, aspartate-aminotransferase; ALT, alanine-aminotransferase; GP, garlic powder; PA, phenyl acetic; SEM, standard error of the mean.

a–c Means within the same column with different common superscripts differ.

Table 5
Immune parameters of broiler chicks as affected by dietary garlic powder and phenyl acetic acid supplementation
Treatment Relative weight of immune organs IgM (mg/dL) IgG (mg/dL)

Bursa Fabricius (%) Thymus (%) Spleen (%)
Control 0.092b 0.395b 0.068c 71.81d 195.32b
GP (g/kg)
 0.25 0.161ab 0.578ab 0.121ab 100.67cd 295.65ab
 0.50 0.167a 0.719a 0.128ab 112.92bc 298.87ab
 0.75 0.183a 0.753a 0.151a 149.89a 335.85a
PA (g/kg)
 0.25 0.162ab 0.548ab 0.112b 96.68cd 317.35ab
 0.50 0.173a 0.681a 0.127ab 111.92bc 328.95ab
 0.75 0.163ab 0.756a 0.137ab 130.87ab 357.44a
SEM 0.0362 0.1308 0.0134 20.161 154.112
Pr>f 0.0367 0.0134 0.0095 0.0010 0.0310

Ig, immunoglobulin; GP, garlic powder; PA, phenyl acetic; SEM, standard error of the mean.

a–d Means within the same column with different common superscripts differ.

Table 6
Antioxidant status of broiler chicks as affected by dietary garlic powder and phenyl acetic acid supplementation
Treatment SOD (nmol/mL) TAC (nmol/mL) MDA (nmol/mL)
Control 0.036c 0.116d 0.285a
GP (g/kg)
 0.25 0.181abc 0.212abc 0.158b
 0.50 0.189ab 0.231abc 0.104b
 0.75 0.254a 0.281a 0.098b
PA (g/kg)
 0.25 0.131bc 0.163cd 0165b
 0.50 0.147bc 0.206bc 0.161b
 0.75 0.224ab 0.247ab 0.146b
SEM 0.053 0.054 0.070
Pr>f 0.0240 0.0027 0.0021

SOD, superoxide dismutase; TAC, total antioxidant capacity; MDA, malondialdehyde; GP, garlic powder; PA, phenyl acetic; SEM, standard error of the mean.

a–d Means within the same column with different common superscripts differ (p<0.05) or (p<0.01).

REFERENCES

1. Saleha AA, Myaing TT, Ganapathy KK, Zulkifli I, Raha R, Arifah K. Possible effect of antibiotic-supplemented feed and environment on the occurrence of multiple antibiotic resistant Escherichia coli in chickens. Int J Poult Sci 2009;8:28–31. https://doi.org/10.3923/ijps.2009.28.31
crossref
2. Khoobani M, Hasheminezhad SH, Javandel F, et al. Effects of dietary chicory (Chicorium intybus L.) and probiotic blend as natural feed additives on performance traits, blood biochemistry, and gut microbiota of broiler chickens. Antibiotics 2020;9:5. https://doi.org/10.3390/antibiotics9010005
crossref
3. Dhama K, Latheef SK, Mani S, et al. Multiple beneficial applications and modes of action of herbs in poultry health and production-a review. Int J Pharmacol 2015;11:152–76. https://doi.org/10.3923/ijp.2015.152.176
crossref
4. Puvača N, Kostadinovic L, Popovic S, et al. Proximate composition, cholesterol concentration and lipid oxidation of meat from chickens fed dietary spice addition (Allium sativum, Piper nigrum, Capsicum annuum). Anim Prod Sci 2016;56:1920–7. https://doi.org/10.1071/AN15115
crossref
5. Javandel F, Navidshad B, Seifdavati J, Pourrahimi GH, Baniyaghoub S. The favorite dosage of garlic meal as a feed additive in broiler chickens ratios. Pak J Biol Sci 2008;11:1746–9. https://doi.org/10.3923/pjbs.2008.1746.1749
crossref pmid
6. Khan RU, Nikousefat Z, Tufarelli V, Naz S, Javdani M, Laudadio V. Garlic (Allium sativum) supplementation in poultry diets: effect on production and physiology. Worlds Poult Sci J 2012;68:417–24. https://doi.org/10.1017/S0043933912000530
crossref
7. Ziarlarimi A, Irani M, Gharahveysi S, Rahmani Z. Investigation of antibacterial effects of garlic (Allium sativum), mint (Menthe spp.) and onion (Allium cepa) herbal extracts on Escherichia coli isolated from broiler chickens. Afr J Biotechnol 2011;10:10320–2. https://doi.org/10.5897/AJB10.2513
crossref
8. Teshika JD, Zakariyyah AM, Zaynab T, et al. Traditional and modern uses of onion bulb (Allium cepa L.): a systematic review. Crit Rev Food Sci Nutr 2019;59:Suppl 1S39–70. https://doi.org/10.1080/10408398.2018.1499074
crossref pmid
9. Kim YJ, Jin SK, Yang HS. Effect of dietary garlic bulb and husk on the physicochemical properties of chicken meat. Poult Sci 2009;88:398–405. https://doi.org/10.3382/ps.2008-00179
crossref pmid
10. Stanaćev V, Glamočić D, Milošević N, Puvača N, Stanaćev V, Plavša N. Effect of garlic (Allium sativum L.) in fattening chicks nutrition. Afr J Agric Res 2011;6:943–8. https://doi.org/10.5897/AJAR10.908
crossref
11. Ur Rahman S, Khan S, Chand N, Sadique U, Khan RU. In vivo effects of Allium cepa L. on the selected gut microflora and intestinal histomorphology in broiler. Acta Histochem 2017;119:446–50. https://doi.org/10.1016/j.acthis.2017.04.004
crossref pmid
12. Adams C. Poultry and dietary acids. Feed Int 1999;20:1370–2.

13. Dhama K, Tiwari R, Khan RU, et al. 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;10:129–59. https://doi.org/10.3923/ijp.2014.129.159
crossref
14. Cooksley J. Acetic acid supplementation reduces the effects of heat stress in poultry. Anitox Solution for Safer Feed and Food USA 2011.

15. Viveros A, Brenes A, Arija I, Centeno C. Effects of microbial phytase supplementation on mineral utilization and serum enzyme activities in broiler chicks fed different levels of phosphorus. Poult Sci 2002;81:1172–83. https://doi.org/10.1093/ps/81.8.1172
crossref pmid
16. NRC. Nutrient requirements of poultry. 9th rev edWashington, DC, USA: National Academies Press; 1994.

17. Ebrahimi A, Qotbi AAA, Seidavi A, Laudadio V, Tufarelli V. Effect of different levels of dried sweet orange (Citrus sinensis) peel on broiler chickens growth performance Abbas. Arch Anim Breed 2013;56:11–7. https://doi.org/10.7482/0003-9438-56-002
crossref
18. Lamberg SL, Rothstein R. Laboratory manual of hematology and urinalysis. West Port, CT, USA: Avid Publishing Company, Inc; 1978.

19. Campbell TW. Avian hematology and cytology. Ames, IA, USA: Iowa State University Press; 1988. p. 3–17.

20. Suriya R, Zulkifli I, Alimon AR. The effect of dietary inclusion of herbs as growth promoter in broiler chickens. J Anim Vet Adv 2012;11:346–50. http://dx.doi.org/10.3923/javaa.2012.346.350
crossref
21. Nourmohammadi R, Khosravinia H. Acidic stress caused by dietary administration of citric acid in broiler chickens. Arch Anim Breed 2015;58:309–15. https://doi.org/10.5194/aab-58-309-2015
crossref
22. Ross ZM, O’Gara EA, Hill DJ, Sleightholme HV, Maslin DJ. Antimicrobial properties of garlic oil against human enteric bacteria: evaluation of methodologies and comparisons with garlic oil sulfides and garlic powder. Appl Environ Microbiol 2001;67:475–80. https://doi.org/10.1128/AEM.67.1.475-480.2001
crossref pmid pmc
23. Dibner JJ, Buttin P. Use of organic acids as a model to study the impact of gut microflora on nutrition and metabolism. J Appl Poult Res 2002;11:453–63. https://doi.org/10.1093/japr/11.4.453
crossref
24. Ashayerizadeh O, Dastar B, Shargh MS, Ashayerizadeh A, Rahmatnejad E, Hossaini SMR. Use of garlic (Allium sativum), black cumin seeds (Nigella sativa L.) and wild mint (Mentha longifolia) in broiler chickens diets. J Anim Vet Adv 2009;8:1860–3.

25. Raeesi M, Hoseini-Aliabad SA, Roofchaee A, Zare Shahneh A, Pirali S. Effect of periodically use of garlic (Allium sativum) powder on performance and carcass characteristics in broiler chickens. World Acad Sci Eng Technol 2010;4:1388–94.

26. Sohail R, Saeed M, Chao S, et al. Comparative effect of different organic acids (benzoic, acetic and formic) on growth performance, immune response and carcass traits of broilers. J Anim Prod Adv 2015;5:757–64.
crossref
27. Denli M, Okan F, Celik K. Effect of dietary probiotic, organic acid and antibiotic supplementation to diets on broiler performance and carcass yield. Pak J Nutr 2003;2:89–91. https://doi.org/10.3923/pjn.2003.89.91
crossref
28. Hanieh H, Narabara K, Piao M, Gerile C, ABE A, Kondo Y. Modulatory effects of two levels of dietary Alliums on immune response and certain immunological variables, following immunization, in White Leghorn chickens. Anim Sci J 2010;81:673–80. https://doi.org/10.1111/j.1740-0929.2010.00798.x
crossref pmid
29. Askar AA. Some physiological and immunological effects of phenyllactic acid in broiler chicks. Egypt J Anim Prod 2012;49:87–93.
crossref
30. Rehman Z, Haq A, Akram N, et al. Growth performance, intestinal histomorphology, blood hematology and serum metabolites of broilers chickens fed diet supplemented with graded levels of acetic acid. Int J Pharmacol 2016;12:874–83. http://dx.doi.org/10.3923/ijp.2016.874.883
crossref
31. Wang JP, Yoo JS, Lee JH, et al. Effects of phenyllactic acid on production performance, egg quality parameters, and blood characteristics in laying hens. J Appl Poult Res 2009;18:203–9. https://doi.org/10.3382/japr.2008-00071
crossref
32. Haque MN, Islam KMS, Akbar MA, et al. Effect of dietary citric acid, flavomycin and their combination on the performance, tibia ash and immune status of broiler. Can J Anim Sci 2010;90:57–63. https://doi.org/10.4141/CJAS09048
crossref
33. Elagib HAA, El-Amin WIA, Elamin KM, Malik HEE. Effect of dietary garlic (Allium sativum) supplementation as feed additive on broiler performance and blood profile. J Anim Sci Adv 2013;3:58–64.
crossref
34. Rehman ZU, Munir MT. Effect of garlic on the health and performance of broilers. Veterinaria 2015;3:32–9.

35. Dorhoi A, Dobrean V, Zahan M, Virag P. Modulatory effects of several herbal extracts on avian peripheral blood cell immune responses. Phytother Res 2006;20:352–8. https://doi.org/10.1002/ptr.1859
crossref pmid
36. Rahimi S, Teymouri Zadeh Z, Karimi Torshizi MA, Omidbaigi R, Rokni H. Effect of the three herbal extracts on growth performance, immune system, blood factors and intestinal selected bacterial population in broiler chickens. J Agric Sci Technol 2011;13:527–39.

37. Issa KJ, Omar JMA. Effect of garlic powder on performance and lipid profile of broilers. Open J Anim Sci 2012;2:62–8. https://doi.org/10.4236/ojas.2012.22010
crossref
38. Mahmoud KZ, Gharaibeh SM, Zakaria HA, Qatramiz AM. Garlic (Allium sativum) supplementation: influence on egg production, quality, and yolk cholesterol level in layer hens. Asian-Australas J Anim Sci 2010;23:1503–9. https://doi.org/10.5713/ajas.2010.10124
crossref
39. Rahmani HR, Speer W. Natural additives influence the performance and humoral immunity of broilers. Int J Poult Sci 2005;4:713–7. https://doi.org/10.3923/ijps.2005.713.717
crossref
40. Salgado-Tránsito L, Del Río-García JC, Arjona-Román JL, Moreno-Martinez E, Mendez-Albores A. Effect of citric acid supplemented diets on aflatoxin degradation, growth performance and serum parameters in broiler chickens. Arch Med Vet 2011;43:215–22. https://doi.org/10.4067/S0301-732X2011000300003
crossref
41. Hossain MM, Lee SI, Kim IH. Effect of dietary Korean aged garlic extract by Leukonostoc citreum SK2556 on production, hematological status, meat quality, relative organ weight, targeted Escherichia coli colony and excreta gas emission in broilers. Anim Feed Sci Technol 2014;198:333–40. https://doi.org/10.1016/j.anifeedsci.2014.09.015
crossref
42. Pourali M, Kermanshahi H, Golian A, Razmi GR, Soukhtanloo M. Antioxidant and anticoccidial effects of garlic powder and sulfur amino acids on Eimeria-infected and uninfected broiler chickens. Iran J Vet Res 2014;15:227–32. https://doi.org/10.22099/ijvr.2014.2531
crossref
43. Nasiroleslami M, Torki M, Saki AA, Abdolmohammadi AR. Effects of dietary guanidinoacetic acid and betaine supplementation on performance, blood biochemical parameters and antioxidant status of broilers subjected to cold stress. J Appl Anim Res 2018;46:1016–22. https://doi.org/10.1080/09712119.2018.1450751
crossref
44. Alagawany M, Ashour E, Reda FM. Effect of dietary supplementation of garlic (Allium sativum) and turmeric (Curcuma longa) on growth performance, carcass traits, blood profile and oxidative status in growing rabbits. Ann Anim Sci 2016;16:489–505. https://doi.org/10.1515/aoas-2015-0079
crossref


Editorial Office
Asian-Australasian Association of Animal Production Societies(AAAP)
Room 708 Sammo Sporex, 23, Sillim-ro 59-gil, Gwanak-gu, Seoul 08776, Korea   
TEL : +82-2-888-6558    FAX : +82-2-888-6559   
E-mail : editor@animbiosci.org               

Copyright © 2024 by Asian-Australasian Association of Animal Production Societies.

Developed in M2PI

Close layer
prev next