Spanish Journal of Agricultural Research 22 (3)
ISSN-L: 1695-971X, eISSN: 2171-9292
https://doi.org/https://doi.org/10.5424/sjar/2024223-20936

The effect of diets containing different amounts of chasteberry seed on performance, carcass, meat quality and stress parameters of Japanese quails

 

Introduction

 

Chasteberry (Vitex agnus-castus L.) is a small deciduous shrub, belonging to the Lamiaceae family and is native to the European, Mediterranean, and Central Asian countries (Zahid et al., 2016ZahidH, RizwaniGH, IshaqeS, 2016. Phytopharmacological review on Vitex agnus-castus: a potential medicinal plant. Chin Herb Med8(1): 24-29. 10.1016/s1674-6384(16)60004-7; Niroumand et al., 2018NiroumandMC, HeydarpourF, FarzaeiMH, 2018. Pharmacological and therapeutic effects of Vitex agnus castus L.: A review. Phcog Rev12(23): 103-114. 10.4103/phrev.phrev_22_17; Souto et al., 2020SoutoEB, DurazzoA, NazhandA, LucariniM, ZaccardelliM, SoutoSB, SilvaAM, SeverinoP, NovellinoE, SantiniA, 2020. Vitex agnus-castus L.: Main features and nutraceutical perspectives. Forests11: 761-776. 10.3390/f11070761). Fruits, flowers, and leaves of chasteberry contain diverse bioactive compounds, such as phenolic acids and their derivatives, volatile oils (limonene, pinene, and sabinene), essential fatty acids (oleic, linolenic, palmitic, and stearic acids), flavonoids, tannins, iridoids and diterpenoids (Niroumand et al., 2018NiroumandMC, HeydarpourF, FarzaeiMH, 2018. Pharmacological and therapeutic effects of Vitex agnus castus L.: A review. Phcog Rev12(23): 103-114. 10.4103/phrev.phrev_22_17; Souto et al., 2020SoutoEB, DurazzoA, NazhandA, LucariniM, ZaccardelliM, SoutoSB, SilvaAM, SeverinoP, NovellinoE, SantiniA, 2020. Vitex agnus-castus L.: Main features and nutraceutical perspectives. Forests11: 761-776. 10.3390/f11070761; Alamoudi & Bakrshoom, 2021AlamoudiMO, BakrshoomYF, 2021. Vitex agnus cactus and some female disorders: A review. Agric Rev42(2): 209-214. 10.18805/ag.r-170; Zhelev et al., 2022ZhelevI, PetkovaZ, KostovaI, DamyanovaS, StoyanovaA, Dimitrova-DyulgerovaI, AntovaG, ErcisliS, AssouguemA, KaraM, et al. , 2022. Chemical composition and antimicrobial activity of essential oil of fruits from Vitex agnus-castus L., growing in two regions in Bulgaria. Plants11: 896. 10.3390/plants11070896.; Boujbiha et al., 2023BoujbihaMA, ChahdouraH, AdouniK, ZianiBEC, SnoussiM, ChakrounY, Ciudad-MuleroM, Fernández-RuizV, AchourL, SelmiB, et al.2023. Wild Vitex agnus-castus L.: phytochemical characterization, acute toxicity, and bioactive properties. Molecules28: 5096. 10.3390/molecules28135096). The relative proportions of the essential oil components vary depending on the place of growth, phenotypic characteristics, and the duration of the distillation process used to obtain the oil, however, the main components have been identified as sabinene (16.4%-44.1%), 1,8-cineole (8.4%-15.2%), β-caryophyllene (2.1%-5.0%) and trans-β-farnesene (5.0%-11.7%) (Adamov et al., 2022AdamovGV, RendyukTD, SaybelOL, DargaevaTD, TsitsilinAN, BokovDO, 2022. Vitex agnus-castus: Botanical features and area, chemical composition of fruit, pharmacological properties, and medicinal uses. J Appl Pharm Sci12(03): 034-044. 10.7324/japs.2022.120304).

Thanks to their various therapeutic effects, including antioxidant, anti-inflammatory, anticarcinogenic, antifungal, antibacterial, antidiabetic, and hepatoprotective properties, these bioactive components have found extensive use in diverse fields such as pharmacology, agricultural practices, and the food industry (Shaaban et al., 2012ShaabanHAE, El-GhorabAH, ShibamotoT, 2012. Bioactivity of essential oils and their volatile aroma components: Review. J Essent Oil Res24(2): 203-212. 10.1080/10412905.2012.659528; Gonçalves et al., 2017GonçalvesR, AyresVFS, CarvalhoCE, SouzaMGM, GuımarãesAC, CorrêaGM, MartinsCHG, TakearaR, SilvaEO, CrottiAEM, 2017. Chemical composition and antibacterial activity of the essential oil of Vitex agnus-castus L. (Lamiaceae). An Acad Bras Cienc89(4): 2825-2832. 10.1590/0001-3765201720170428; El-Nawasany, 2019El-NawasanyLI, 2019. The Use of Vitex agnus-castus to Produce Functional Stirred Yoghurt, J of Food and Dairy Sci10(9): 297-301. 10.21608/jfds.2019.54517; Alamoudi & Bakrshoom, 2021AlamoudiMO, BakrshoomYF, 2021. Vitex agnus cactus and some female disorders: A review. Agric Rev42(2): 209-214. 10.18805/ag.r-170; Al-Otibi et al., 2022Al-OtibiFO, AlrumaizanGI, AlharbiRI, 2022. Evaluation of anticandidal activities and phytochemical examination of extracts prepared from Vitex agnus‑castus: a possible alternative in treating candidiasis infections. BMC Complement Med Ther22: 69. 10.1186/s12906-022-03552-x; Kamal et al., 2022KamalN, Mio AsniNS, RozlanINA, Mohd AzmiMAH, MazlanNW, MedianiA, BaharumSN, LatipJ, AssawS, Edrada-EbelRA, 2022. Traditional medicinal uses, phytochemistry, biological properties, and health applications of Vitex sp.Plants11: 1944. 10.3390/plants11151944). While limited studies are available regarding the effects of chasteberry on poultry performance and product quality, several studies have been conducted specifically on laying hens. In these studies, it was reported that the addition of chasteberry seeds (CS) to the diets of laying hens increased egg production and egg quality (Salary et al., 2016SalaryJ, Matin HematiHR, HajatiH, 2016. The Effect of a dietary innovative multi-material on sex hormones and molting period of canaries and laying-hens. Iran J Appl Anim Sci6(4): 937-942.; Saleh et al., 2019SalehAA, AhmedEAM, EbeidTA, 2019. The impact of phytoestrogen source supplementation on reproductive performance, plasma profile, yolk fatty acids and antioxidative status in aged laying hens. Reprod Dom Anim54: 846-854. 10.1111/rda.13432). However, there are no studies investigating the effects of CS addition on broiler chickens or quail performance. In addition to the effects of chasteberry seed on performance parameters, although there are no studies showing that chasteberry eliminates oxygen radicals in poultry, it has been suggested that CS has antioxidant activity due to its flavonoid, diterpenoid and ecdysteroid content and may provide bioactive mechanisms in the treatment and prevention of many diseases associated with oxidative stress (Ahangarpour et al., 2016AhangarpourA, NajimiSA, FarboodY, 2016. Effects of Vitex agnus-castus fruit on sex hormones and antioxidant indices in a d-galactose-induced aging female mouse model. J Chin Med Assoc79(11): 589-596. 10.1016/j.jcma.2016.05.006; Boujbiha et al., 2023BoujbihaMA, ChahdouraH, AdouniK, ZianiBEC, SnoussiM, ChakrounY, Ciudad-MuleroM, Fernández-RuizV, AchourL, SelmiB, et al.2023. Wild Vitex agnus-castus L.: phytochemical characterization, acute toxicity, and bioactive properties. Molecules28: 5096. 10.3390/molecules28135096).

Therefore, it is important to explore the possibilities of incorporating diets containing CS or their leaves into poultry nutrition, as well as investigating their effects on meat quality and oxidative-antioxidant parameters. This study aims to determine the effects of diets containing different levels of CS on growing performance, slaughter characteristics, meat quality, as well as oxidative and antioxidant parameters of breast meat in quails.

Material and methods

 

Experimental design

 

All experimental procedures using animals were conducted following the European Guidelines for Care and Use of Animals for Research Purpose, and they were approved by the Local Ethics Committee for Animal Testing of the Aydın Adnan Menderes University (64583101/2019/048).

A total of two hundred and forty, one-day-old mixed-sex Japanese quail (Coturnix coturnix japonica) chicks with an average body weight of 9.38 ± 0.02 g were divided into three groups, each consisting of four replicates with 20 chicks each cage. CS were ground during the preparation of the diets and mixed into the diets with other feeds. Three isocaloric and iso-nitrogenous experimental diets containing control, 25 g/kg chasteberry seeds (CS25), and 50 g/kg chasteberry seeds (CS50) were formulated according to the NRC (1994NRC, 1994. Nutrient requirements of poultry. 9th rev. ed. National Academy Press, National Research Council. Washington, D.C.) (Table 1). The chemical analysis of the diets was carried out by standard methods described by AOAC (2005AOAC, 2005. Official Methods of Analysis of AOAC International (17th ed.). Association of the Official Analytical Chemists. Gaithersburg. MD. USA. 10.1093/9780197610145.003.1380). The ambient temperature was set at 32 °C for the first three days. After that, the temperature was decreased by 3 °C each week until it reached 21 °C and it remained until the end of study. The lighting schedule was set to 24 hours a day for the first three days of the study. After that, it was reduced to 23 hours a day until the trial was over. During the 35-day experiment period, the water and feed requirements of the animals were provided ad libitum.

Table 1 The ingredients and nutrient composition of the experimental diets. 
CS0CS25CS50
Ingredients, g/kg
Corn471.00426.7385.70
Soybean meal459.00465.00468.1
Vegetable oil38.4053.566.30
Chasteberry seed0.025.0050.00
Dicalcium phosphate 15.5015.6015.70
Calcium carbonate 10.008.008.00
Salt3.003.003.00
DL-Methionine0.600.700.72
Vitamin-Mineral Premix[1]2.502.502.50
Nutrient composition[2]
Dry matter, g/kg876.9857.0837.0
Crude protein, g/kg240239.2237.2
Ether extract, g/kg62.876.187.2
Crude fiber, g/kg42.742.241.4
Ash, g/kg63.161.060.8
Calcium, g/kg9.38.58.5
Available phosphorus, g/kg4.54.54.5
Methionine, g/kg4.24.34.2
Lysine, g/kg13.413.413.4
Metabolizable energy, kcal/kg289328932878
 

CS0: Control, CS25: 25 g/kg chasteberry seed, CS50: 50 g/kg chasteberry seed.

[1] 

Vitamin-mineral premix per kg of diet: retinol acetate 5160 µg, cholecalciferol 50 mg, D-alpha-tocopherol 50 mg, ascorbic acid 50 mg, niacin 55 mg, menadione nicotinamide bisulfite 5 mg, riboflavin 6 mg, thiamin 3 mg, pyridoxine 5 mg, cobalamin 30 µg, biotin 100 µg, folic acid 1 mg, Ca-D-pantothenate 12 mg, choline chloride 300 mg, manganese 80 mg, iron 60 mg, zinc 60 mg, copper 5 mg, iodine 2 mg, selenium 150 µg, cobalt 300 µg.

[2] 

Determined according to AOAC (2005AOAC, 2005. Official Methods of Analysis of AOAC International (17th ed.). Association of the Official Analytical Chemists. Gaithersburg. MD. USA. 10.1093/9780197610145.003.1380).

Growth performance

 

The body weight (BW), and feed intake (FI) of quail were recorded weekly throughout the experiment. Body weight gain (BWG) and feed conversion ratio (FCR) were calculated at 0-21, 21-35 and 0-35 days.

Carcass and organ weights

 

At the end of the experiment, 12 male and 12 female quails were randomly selected from each group for carcass traits and analysis. A total of 72 quails were slaughtered. Before slaughtering, the body weight of quails was determined. After weighing, quails were slaughtered, de-feathered, processed (removal of head and feet), and eviscerated (removal of the gastrointestinal tract) one by one. The weight of the hot carcass, liver, heart, gizzard, and proventriculus was separately determined. The relative weight of the liver, heart, gizzard, and proventriculus was calculated as percentages of body weight (g/100 g body weight).

Meat quality

 

Right breast samples were taken from the carcasses of 72 birds to determine the water-holding capacity (WHC), cooking loss (CL), drip loss (DL), shear force (SF), and color. The samples were frozen and stored in a freezer at –20 °C until further analyses.

Water holding capacity

 

A 3-gram sample of meat was put on Whatman No. 1 filter paper, which had been dried and weighed, together with two thin plastic films. The filter paper and plastic films containing the meat sample were then placed between Plexiglas plates. For five minutes, a 2.5 kg load was applied. Wet filter paper and plastic films were promptly weighed following the exact removal of the compressed meat. The WHC percentage was calculated as follows (Joo, 2018JooST, 2018. Determination of water-holding capacity of porcine musculature based on released water method using optimal load. Korean J Food Sci Anim Resour38(4): 823-828.):

WHC % = damp filter paper and plastic film weights – filter paper and plastic film weights/meat sample weight × 100.

Cooking loss

 

To evaluate CL, each breast meat sample was weighed, placed into a sealed polyethylene bag, and cooked in a water bath at 80 °C until the sample core temperature reached 75oC. After allowing the cooked meat samples to cool down to room temperature in tap water, they were reweighed (Honikel, 1998Honikel, KO, 1998. Reference methods for the assessment of physical characteristics of meat. Meat Sci. 49(4): 447-457. 10.1016/s0309-1740(98)00034-5). Using the following formula, CL was determined:

CL % = raw weight – cooked weight/ raw weight ×100

Drip loss

 

To calculate the DL, the method described by Honikel (1998Honikel, KO, 1998. Reference methods for the assessment of physical characteristics of meat. Meat Sci. 49(4): 447-457. 10.1016/s0309-1740(98)00034-5) was used. In order to avoid any contact between the sample and the bag, each sample was first weighed and then suspended in an inflated plastic container at 4 °C for 24 hours. Subsequently, the samples were re-weighed. Then the DL was calculated as the percentage of weight loss:

DL % = [(initial weight–final weight)/initial weight] × 100

Shear force

 

Cooked meat samples were tested for SF. Two strips of meat, each measuring 2.5 × 1.0 × 1.0 cm3, were sliced parallel to the muscle fibers. The Zwick Testing Machine Model Z2.5/TN1S (Zwick GmbH and Co, Germany) was used to measure the maximum SF of the meat samples, using a Warner-Bratzler shear. The meat samples were cut perpendicular to the fiber direction at a test speed of 2 mm/s. The maximum SF was measured in Newton force (N) (dos Santos et al., 2020Dos SantosTC, GatesRS, TinôcoIFF, EstradaMM, Chizzotti, ML, 2020. Meta quality traits of European quails reared under different conditions of temperatures and air velocity. Poult Sci99: 848-856.10.1016/j.psj.2019.10.037).

Meat color

 

A colorimeter (Color Flex EZ, Hunterlab, USA) was used to determine the meat color equipped with a standard D65 illuminant and a “2” position of the standard observer, along with a pulse xenon lamp and an 8-mm reading surface area. Before taking the measurements, the device was calibrated using a black-and-white standard plate. Three measurements per sample were taken of the surface area of breast meat, and L*, a*, and b* values were recorded. The hue angle and chroma (saturation index) values were calculated using the a* and b* values using the following formulas (AMSA, 2012AMSA, 2012. Meat color measurement guidelines. American Meat Science Association. Illinois, USA.):

Chroma = (a*2 +b*2)1/2

Hue angle (º) = arctan (b*/a*)

Oxidant and antioxidant parameters

 

To determine the oxidant and antioxidant parameters breast samples were taken from the left breast of 12 male quails. Tissue samples were weighed and placed in 50 mM potassium phosphate buffer (pH 7.4). Samples were cooled in an ice bath and homogenized for 20 s. The homogenate was cooled in an ice bath for 30 seconds and subjected to sonication. It was then centrifuged at 10,000 × g at 4°C for 15 min. Superoxide dismutase (SOD), catalase (CAT), glutathione (GSH) and malondialdehyde (MDA) experiments were carried out in supernatants.

The content of SOD was determined by method of Sun et al. (1988SunY, OberleyLW, LiY, 1988. A simple method for clinical assay of superoxide dismutase. Clin Chem, 34(3), 497-500. 10.1093/clinchem/34.3.497). CAT activity was measured according to Aebi (1984AebiH, 1984. Catalase in vitro. Methods Enzymol105: 121-126.) method. GSH content was determined using the method developed by Sedlak and Lindsay (1968SedlakJ, LindsayRH, 1968. Estimation of total, protein-bound, and non-protein sulfhydryls groups in tissue with Ellman’s reagent. Anal Biochem25:192-205. 10.1016/0003-2697(68)90092-4). MDA levels were determined by the double heating method of Draper & Hadley (1990DraperHH, HadleyM, 1990. Malondialdehyde determination as index of lipid peroxidation. Methods Enzymol186: 421-431. 10.1016/0076-6879(90)86135-i).

Economic analysis

 

The economic effectiveness of CS supplementation was calculated using the following formulae as described by Shehata et al. (2021ShehataSF, SallamEA, AzamAE, SolimanMM, MohammedLS, 2021. Effect of different dietary inclusion levels of mulberry leaves on productive traits, economic indices, and immunity of white and brown Japanese quail. AJVS70(2): 63-75. 10.5455/ajvs.115295).

Total feed cost (TFC) = total feed intake per bird per gram × cost of one gram diet

Feed cost/kg BWG (average cost of each kg BWG from the feed) = feed conversion × cost of one kg diet.

Economic efficiency index (EEI) = (lowest cost of kg BWG from feed/ average cost of kg BWG from the feed) × 100

Total return (TR) = live body weight × price of each gram

Net profit = TR-TFC.

Statistical analyses

 

The experiment was conducted as a completely randomized design with three treatments of four replicates each. All data were analyzed by one-way ANOVA using the GLM procedure with SAS software (SAS, 1999SAS, 1999. SAS user’s guide: Statistics, Version 8 Edition. SAS Inst., Inc., Cary, NC.). The differences among the means were tested using Duncan multiple-range tests. All statements of significance were based on a probability of p < 0.05.

Results

 

Growth performance

 

The growing performances of quails fed diets containing different levels of ground CS are given in Table 2.

Table 2 Effects of different levels of chasteberry seed on growth performance of quails [1]
Treatment
CS0CS25CS50p value
Body weight, g/bird
Initial weight9.36±0.019.39±0.029.38±0.020.274
21 days old110.87±1.95a106.07±2.36b99.47±1.60c<0.001
35 days old188.67±3.22a186.63±2.03a181.76±3.07b0.026
Body weight gain, g/bird
0-21 days101.51±1.96a96.43±2.07b88.66±2.55c<0.001
21-35 days77.23±3.3379.49±3.6081.67±2.240.229
0-35days178.74±3.19a176.61±2.02a171.75±3.02b0.024
Feed intake, g/bird
0-21 days255.72±5.01a245.66±8.36a229.63±3.09b0.001
21-35 days332.85±2.92332.34±8.27322.71±5.670.100
0-35days588.57±2.13a578.00±16.38a552.34±7.43b0.006
Feed conversion ratio, g feed intake/g body weight gain
0-21 days2.48±0.032.48±0.032.56±0.090.154
21-35 days4.27±0.174.09±0.223.91±0.150.084
0-35days3.29±0.063.27±0.133.22±0.0670.555
 

CS0: Control, CS25: 25 g/kg chasteberry seed, CS50: 50 g/kg chasteberry seed.

[1] 

Data are expressed as mean ± SD.

a,b] 

Means within the same row in each group with different superscript are significantly different (p< 0.05).

On the 21st day of the study, it was determined that the BW and BWG of the quails decreased as the level of CS in the diets increased (p<0.001). As well as, on the 35th day of the experiment, the BW of the quails in the CS50 group were lower than in the other groups (p<0.05). Although the BWG of quails on days 21-35 were not statistically affected by increasing levels of CS, there was a tendency for an increase in the BWG of quails compared to the control group. During the overall period of the study (0-35 days of age), it was observed that BWG of quails in the CS50 group was lower than that of the other groups (p<0.05).

Feed intake of quails on days 21-35 was not affected by the addition of CS. However, during days 0-21 and 0-35, it was observed that the FI of the CS50 group was lower than that of the other groups. Diets containing different levels of CS did not statistically affect the FCR.

Carcass and organ weights

 

The effects of diets containing different levels of CS on carcass and some internal organ weights of male and female quails are given in Table 3.

Table 3 Effects of different levels of chasteberry seed on carcass and internal organ weights of male and female quails[1]
ParametersCS0CS25CS50p value
Male
Slaughter weight, g172.32±12.20169.67±20.80175.59±10.560.647
Warm carcass weight, g126.04±9.27122.07±15.29126.12±8.730.641
Warm carcass yield, %73.15±1.6871.94±1.5471.80±1.420.119
Liver weight, g/100 g BW3.40±0.583.72±0.753.96±0.560.158
Gizzard weight, g/100 g BW3.56±0.363.58±0.584.03±0.510.058
Heart weight, g/100 g BW1.54±0.161.49±0.231.63±0.180.239
Female
Slaughter weight, g207.40±22.16206.26±25.57187.89±19.500.086
Warm carcass weight, g144.78±16.95141.34±14.73132.63±14.000.172
Warm carcass yield, %69.77±2.2668.72±3.0370.64±3.400.306
Liver weight, g/100 g BW5.42±1.336.16±2.174.96±1.790.283
Gizzard weight, g/100 g BW4.54±0.614.37±0.494.56±0.690.702
Heart weight, g/100 g BW1.71±0.271.73±0.211.62±0.310.581
 

CS0: Control, CS25: 25 g/kg chasteberry seed, CS50: 50 g/kg chasteberry seed.

[1] 

Data are expressed as mean ± SD.

a,b 

Means within the same row in each group with different superscript are significantly different (p< 0.05).

It was observed that adding CS had no effect on the slaughter weight, warm carcass weight, warm carcass yield, and relative organ weights (liver, gizzard, and heart) in male and female quails.

Meat quality

 

When the effects of different levels of CS addition on meat quality were analyzed (Table 4), no effect of CS addition was observed in breast meat of male animals (p>0.05).

Table 4 The effect of different levels of chasteberry seeds on breast meat quality characteristics of male and female quail [1]
ParametersCS0CS25CS50p value
Male
Water holding capacity, %8.37±1.047.97±1.008.55±1.290.446
Cooking loss, %28.00±6.0124.18±6.1023.74±1.870.128
Drip loss, %6.96±2.766.70±5.155.55±3.090.666
Shear force, N207.67±41.78201.53±59.41192.67±42.070.781
L*47.68±3.1946.67±2.7645.18±1.690.094
a*8.78±1.118.64±0.779.20±0.420.211
b*11.73±1.2111.03±1.3110.87±0.990.237
Croma14.67±1.3914.04±1.2014.26±0.690.431
Hue angle53.21±3.5051.77±3.8449.64±3.320.085
Female
Water holding capacity, %8.10±0.86b9.17±1.08a9.25±0.91a0.022
Cooking loss, %26.15±3.9023.13±2.8324.66±3.900.169
Drip loss, %8.60±1.537.84±3.125.96±2.720.071
Shear force, N199.78±59.46184.40±75.86192.36±63.750.874
L*48.82±2.32a48.49±2.64a45.54±3.45b0.021
a*8.63±0.79b8.59±0.92b9.50±0.99a0.038
b*11.87±1.1012.15±0.4811.44±0.900.134
Croma14.69±1.1014.90±0.6014.89±1.030.848
Hue angle53.92±3.08a54.79±3.22a50.32±3.26b0.005
 

CS0: Control, CS25: 25 g/kg chasteberry seed, CS50: 50 g/kg chasteberry seed.

[1] 

Data are expressed as mean ± SD.

a,b 

Means within the same row in each sex with different superscript are significantly different (p< 0.05).

In female animals, a statistically significant difference was found in WHC, L*, a*, and hue angle values in breast meat (p<0.05). The highest WHC and a* values were observed in the CS50 group, while the lowest L* and hue angle values were also found in the CS50 group. However, the difference between the Control and CS25 groups was not significant, especially in terms of color parameters (p>0.05).

Oxidant and antioxidant parameters

 

The effects of diets containing different levels of CS on breast meat oxidant and antioxidant parameters of male quails are given in Table 5. It was observed that the addition of different levels of chasteberry seed increased the antioxidant parameters (SOD, CAT, GSH), and decreased the oxidant parameter (MDA) compared to the control group in the current study (p<0.05).

Table 5 Effects of chasteberry seed on oxidant and antioxidant parameters[1]
ParametersCS0CS25CS50p value
SOD, mmol/m/mg0.185±0.007a0.229±0.008b0.274±0.009c0.022
CAT, mmol/m/mg1418±0.071a1633±0.087b1712±0.098c0.018
GSH, nmol/g0.244±0.019a0.286±0.022b0.302±0.035c0.034
MDA, nmol/g tissue1.601±0.063a1.447±0.051b1.378±0.046c0.016
 

CS0: Control, CS25: 25 g/kg chasteberry seed, CS50: 50 g/kg chasteberry seed, SOD: superoxide dismutase, CAT: catalase, GSH: glutathione, MDA: malondialdehyde.

[1] 

Data are expressed as mean ± SD.

a,b 

Means within the same row in each group with different superscript are significantly different (p< 0.05).

Economic analysis

 

The results of economic efficiency metrics are displayed in Table 6. There was a statistically significant difference between the groups in terms of feed cost, and the lowest feed cost was obtained in the CS50 group (p<0.05). CS50 group was followed by CS25 and control group, respectively. Feed cost/BW, feed cost/BWG and EEI values did not differ between the groups (p>0.05). Although the lowest TR was observed in the CS50 group (p<0.05), there was no significant difference between the groups in net profit values (p>0.05).

Table 6 Effects of chasteberry seed on economic efficiency parameters[1]
ParametersCS0CS25CS50p value
Feed cost, $/bird0.52 ± 0.002a0.51 ± 0.014b0.48 ± 0.007c0.010
Feed cost/BW2.73 ± 0.0502.72 ± 0.1032.68 ± 0.0540.596
Feed cost/BWG2.88 ± 0.0562.87 ± 0.1122.83 ± 0.0590.692
EE index95.34 ±1.85995.75 ± 3.69997.04 ± 1.9970.649
Total return2.65 ± 0.045a2.63 ± 0.029a2.56 ± 0.043b0.026
Net profit2.14 ± 0.0462.12 ± 0.0412.07 ± 0.0430.153
 

CS0: Control, CS25: 25 g/kg chasteberry seed, CS50: 50 g/kg chasteberry seed, EE index: economic efficiency index.

[1] 

Data are expressed as mean ± SD.

a,b 

Means within the same row in each group with different superscript are significantly different (p< 0.05).

Discussion

 

Growth performance

 

In the current study, although the addition of 50 g/kg chasteberry seeds had negative effects on the BW of the animals, it was observed that the BWG of the CS25 and CS50 groups tended to increase at 21-35 days. In addition, it was observed that chasteberry seed supplementation had positive effects on FCR by decreasing FI. It was thought that the decrease in body weight with the addition of chaste seed may be due to the decrease in protein and nutrient efficiency due to the interaction of hydroxyl groups of phenolic compounds such as polyphenols and oxalates, which are considered as anti-nutritional factors, with protein carbonyl groups, as well as having negative metabolic effects related to the inhibition of digestive enzymes (Vargas-Sánchez et al., 2019Vargas-SánchezRD, Ibarra-AriasFJ, Torres-MartínezBDM, Sánchez-EscalanteA, Torrescano-UrrutiaGR, 2019. Use of natural ingredients in Japanese quail diet and their effect on carcass and meat quality - A review. Asian-Australas J Anim Sci32(11): 1641-1656. 10.5713/ajas.18.0800; Samtiya et al., 2020SamtiyaM, AlukoRE, DhewaT, 2020. Plant food anti-nutritional factors and their reduction strategies: an overview. Food Prod Process Nutr2(6): 1-14. 10.1186/s43014-020-0020-5; Popescu et al., 2021PopescuRG, VoicuSN, PircalabioruGG, GharbiaS, HermeneanA, GeorgescuSE, PanaiteTD, TurcuRP, 2021. Impact of dietary supplementation of flaxseed meal on intestinal morphology, specific enzymatic activity, and cecal microbiome in broiler chickens. Appl Sci11: 6714. 10.3390/app11156714).

While previous studies on diets containing CS and their impact on the growth performance of poultry are not readily available, various studies have examined the effects of CS supplementation on the performance of laying hens. El-Saadany et al. (2022El-SaadanyAS, HanafyMM, ElkomyAE, 2022. Flaxseed and Agnus-castus on vitex as a source of phytoestrogens and their impact on productive performance, some blood constituents, and blood oestradiol profile of aged laying hens. Ital J Anim Sci21(1): 821-830. 10.1080/1828051x.2022.2066578) reported that the addition of 2.5 and 5 g/kg of CS to the diets of laying hens at 58 weeks of age improved feed conversion ratio, egg production, egg weight, egg mass, eggshell thickness, and yolk color and weight. However, in another study conducted by Nazari et al. (2023NazariM, GhorbaniMR, NassiriMTB, FathimoghadamN, SabahiR, MosaviST, 2023. The effects of Chaste-berry fruits on hypothalamic-pituitary-ovarian markers gene expression and immune response of laying hens: Phytoestrogens in Chaste-berry are ERβ-selective. IVJ19(1): 61-71.), it was reported that the addition of 1% and 2% CS to the diets of laying hens at 72 weeks of age had no effect on the performance and egg quality of the animals. Similarly, it was reported that supplementation of flaxseed, which is a phytoestrogen source, such as chasteberry, in the diets of older laying hens increased egg production and egg quality (Salary et al., 2016SalaryJ, Matin HematiHR, HajatiH, 2016. The Effect of a dietary innovative multi-material on sex hormones and molting period of canaries and laying-hens. Iran J Appl Anim Sci6(4): 937-942.; Saleh et al., 2019SalehAA, AhmedEAM, EbeidTA, 2019. The impact of phytoestrogen source supplementation on reproductive performance, plasma profile, yolk fatty acids and antioxidative status in aged laying hens. Reprod Dom Anim54: 846-854. 10.1111/rda.13432). However, Popescu et al. (2021PopescuRG, VoicuSN, PircalabioruGG, GharbiaS, HermeneanA, GeorgescuSE, PanaiteTD, TurcuRP, 2021. Impact of dietary supplementation of flaxseed meal on intestinal morphology, specific enzymatic activity, and cecal microbiome in broiler chickens. Appl Sci11: 6714. 10.3390/app11156714) reported that broiler chickens fed a flaxseed diet had negative effects on the performance parameters due to anti-nutritional factors compared to laying hens. As a result of various studies conducted, it has been reported that there is a decrease in the performance parameters of broiler chickens fed with different levels of flaxseed ranging from 2-20% (Mridula et al., 2015MridulaD, KaurD, NagraSS, BarnwalP, GurumayumS, SinghKK, 2015. Growth performance and quality characteristics of flaxseed-fed broiler chicks. J Appl Anim Res43(3): 345-351. 10.1080/09712119.2014.978773; Beheshti Moghadam et al., 2017Beheshti MoghadamMH, RezaeiM, BehgarM, KermanshahiH, 2017. Effects of irradiated flaxseed on performance, carcass characteristics, blood parameters, and nutrient digestibility in broiler chickens. Poult Sci J5(2): 153-163; Zhaleh et al., 2019ZhalehS, GolianA, ZerehdaranS, 2019. Effect of rolled or extruded flaxseeds in finisher diet on pellet quality, performance, and n-3 fatty acids in breast and thigh muscles of broiler chickens. Poult Sci J7(1): 63-75.; El-Bahr et al., 2021El-BahrSM, ShoushaS, AlfattahMA, Al-SultanS, KhattabW, SabeqII, Ahmed-FaridO, El-GarhyO, AlbusadahKA, AlhojailyS, et al.2021. Enrichment of broiler chickens’ meat with dietary linseed oil and lysine mixtures: Influence on nutritional value, carcass characteristics and oxidative stress biomarkers. Foods10: 618. 10.3390/foods10030618; Kumar et al., 2021KumarF, TyagiPK, MirNA, DevK, BegumJ, TyagiPK, BiswasA, SahuB, DinaniOP, SharmaD, 2021. Growth pattern, lipid composition, oxidation status, and serum biochemical profile of broiler chicken fed flaxseed meal for different durations. Lett Anim Biol01(01): 08-18. 10.62310/liab.v1i1.54). Tamasgen et al. (2021TamasgenN, UrgeM, GirmaM, NurfetaA, 2021. Effect of dietary replacement of soybean meal with linseed meal on feed intake, growth performance and carcass quality of broilers. Heliyon7: e08297. 10.1016/j.heliyon.2021.e08297) reported that different processing methods can reduce the anti-nutritional factor content of the seed, thus reducing its negative effects. Research has shown that the negative effects of flaxseed can be reduced by irradiation and seed extrusion (Beheshti Moghadam et al., 2017Beheshti MoghadamMH, RezaeiM, BehgarM, KermanshahiH, 2017. Effects of irradiated flaxseed on performance, carcass characteristics, blood parameters, and nutrient digestibility in broiler chickens. Poult Sci J5(2): 153-163; Gheorghe et al., 2020GheorgheA, LefterNA, IdriceanuL, RopotăM, HăbeanuM, 2020. Effects of dietary extruded linseed and Lactobacillus acidophilus on growth performance, carcass traits, plasma lipoprotein response, and caecal bacterial populations in broiler chicks. Ital J Anim Sci19(1): 822-832. 10.1080/1828051x.2020.1801359; Zhaleh et al., 2020ZhalehS, GolianA, ZerehdaranS, 2020. Effects of one week feeding finisher diets containing rolled and extruded flaxseed on performance, lipid peroxidation and omega-3 fatty acids in breast and thigh meat of broiler chickens.. Poult Sci J8(1): 83-94.).

Carcass and organ weights

 

In the current study, CS supplementation had no effect on the carcass and internal organ weights of male and female animals. Carcass and internal organ results of the current study are consistent with the results of Zadeh et al. (2020ZhelevI, PetkovaZ, KostovaI, DamyanovaS, StoyanovaA, Dimitrova-DyulgerovaI, AntovaG, ErcisliS, AssouguemA, KaraM, et al. , 2022. Chemical composition and antimicrobial activity of essential oil of fruits from Vitex agnus-castus L., growing in two regions in Bulgaria. Plants11: 896. 10.3390/plants11070896.) who reported that there was no significant effect on the relative weight of the carcass of broilers fed the finisher diet for one week with different levels of flaxseed compared to the control diet. Similarly, Gheorghe et al. (2020GheorgheA, LefterNA, IdriceanuL, RopotăM, HăbeanuM, 2020. Effects of dietary extruded linseed and Lactobacillus acidophilus on growth performance, carcass traits, plasma lipoprotein response, and caecal bacterial populations in broiler chicks. Ital J Anim Sci19(1): 822-832. 10.1080/1828051x.2020.1801359) also reported that the addition of flaxseed in the broiler diet up to %12 had no effect on carcass yield and internal organ weights. However, in contrast to the findings of the current study, Mridula et al. (2015MridulaD, KaurD, NagraSS, BarnwalP, GurumayumS, SinghKK, 2015. Growth performance and quality characteristics of flaxseed-fed broiler chicks. J Appl Anim Res43(3): 345-351. 10.1080/09712119.2014.978773) reported a significant decrease in carcass yield with the addition of flaxseed. Additionally, Tamasgen et al. (2021TamasgenN, UrgeM, GirmaM, NurfetaA, 2021. Effect of dietary replacement of soybean meal with linseed meal on feed intake, growth performance and carcass quality of broilers. Heliyon7: e08297. 10.1016/j.heliyon.2021.e08297) did not determine any difference in carcass weights of broilers as a result of replacing 25% and 50% of soybean meal with flaxseed, but they observed an increase in small intestine weight and length. It is reported that this reduction in carcass characteristics and edible portions may be due to the development of the digestive tract and increased length and weight of the small intestine, together with the interference of phytogenic with phenolic compounds and phenolic groups on digestion and availability of dietary protein and essential amino acids (Ghazaghi et al., 2014GhazaghiM, MehriM, Bagherzadeh-KasmaniF, 2014. Effects of dietary Mentha spicata on performance, blood metabolites, meat quality and microbial ecosystem of small intestine in growing Japanese quail. Anim Feed Sci Technol194: 89-98. 10.1016/j.anifeedsci.2014.04.014; Mehri et al., 2015Mehri, M., Sabaghi, V., Bagherzadeh-Kasmani, F., 2015. Mentha piperita (peppermint) in growing Japanese quails diet: Performance, carcass attributes, morphology and microbial populations of intestine. Anim Feed Sci Technol207: 104-111. 10.1016/j.anifeedsci.2015.05.021).

Meat quality

 

The addition of different amounts of CS did not affect the breast meat quality of males. With the addition of 50 g/kg chasteberry seed, the L* and hue angle values of the breast meat of females decreased, while the WHC and a* values increased. However, Mapiye et al. (2011MapiyeC, ChimonyoM, DzamaK, HugoA, StrydomPE, MuchenjeV, 2011. Fatty acid composition of beef from Nguni steers supplemented with Acacia karroo leaf-meal. J Food Comp Anal24: 523-528. 10.1016/j.jfca.2011.01.018) reported that phytogenic plants may promote lighter meat color. Although studies specifically focusing on CS were not found, when examining research on various phytogenic plants, there are studies reporting that plants such as mint, thyme, cumin, flaxseed, hemp, black cumin, and fever tea have an effect on meat quality (Mnisi et al., 2017MnisiCM, MatshogoTB, van NiekerkR, MlamboV, 2017. Growth performance, haemo-biochemical parameters and meat quality characteristics of male Japanese quails fed a Lippia javanica-based diet. S Afr J Anim Sci47: 661-671. 10.4314/sajas.v47i5.9; Yalçın et al., 2017ZahidH, RizwaniGH, IshaqeS, 2016. Phytopharmacological review on Vitex agnus-castus: a potential medicinal plant. Chin Herb Med8(1): 24-29. 10.1016/s1674-6384(16)60004-7; Singh et al., 2018SinghJ, SharmaM, MehtaN, SinghND, KaurP, SethiAPS, SikkaSS, 2018. Influence of supplementation of black pepper powder through feed in broiler chickens on their growth performance, blood profile, meat sensory qualities and duodenum morphology. Indian J Anim Sci88(2): 215-221. 10.56093/ijans.v88i2.79346; Tashla et al., 2019TashlaT, PuvačaN, Ljubojević PelićD, ProdanovićR, IgnjatijevićS, BoškovićJ, IvaniševićD, JahićM, MahmoudM, GiannenasI, LevićJ, 2019. Dietary medicinal plants enhance the chemical composition and quality of broiler chicken meat. J Hellenic Vet Med Soc70(4): 1823-1832. 10.12681/jhvms.22229; Vargas-Sánchez et al., 2019Vargas-SánchezRD, Ibarra-AriasFJ, Torres-MartínezBDM, Sánchez-EscalanteA, Torrescano-UrrutiaGR, 2019. Use of natural ingredients in Japanese quail diet and their effect on carcass and meat quality - A review. Asian-Australas J Anim Sci32(11): 1641-1656. 10.5713/ajas.18.0800; El-Bahr et al. 2021El-BahrSM, ShoushaS, AlfattahMA, Al-SultanS, KhattabW, SabeqII, Ahmed-FaridO, El-GarhyO, AlbusadahKA, AlhojailyS, et al.2021. Enrichment of broiler chickens’ meat with dietary linseed oil and lysine mixtures: Influence on nutritional value, carcass characteristics and oxidative stress biomarkers. Foods10: 618. 10.3390/foods10030618). Mnisi et al. (2017MnisiCM, MatshogoTB, van NiekerkR, MlamboV, 2017. Growth performance, haemo-biochemical parameters and meat quality characteristics of male Japanese quails fed a Lippia javanica-based diet. S Afr J Anim Sci47: 661-671. 10.4314/sajas.v47i5.9) reported an increase in L* and a* values of breast meat and no difference in CL and SF with the addition of 25g/kg fever tea to quail diets. Similarly, it was reported that the addition of hemp seeds to quail diets increased L* and a* values of breast meat and decreased CL, while there was no difference in thawing loss (Yalcin et al., 2017YalcinH, KoncaY, DurmuscelebiF, 2017. Effect of dietary supplementation of hemp seed (Cannabis sativa L.) on meat quality and egg fatty acid composition of Japanese quail (Coturnix coturnix japonica). J Anim Physiol Anim Nutr102: 131-141. 10.1111/jpn.12670). In another study, it was reported that diets containing 0, 1 or 2% black cumin seeds did not affect the CL and WHC of quail breast meat (Karadağoğlu et al., 2019KaradağoğluÖ, ŞahinT, ÖlmezM, AhsanU, ÖzsoyB, 2019. Fatty acid composition of liver and breast meat of quails fed diets containing black cumin (Nigella sativa L.) and/or coriander (Coriandrum sativum L.) seeds as unsaturated fatty acid sources. Livest Sci223: 164-171. 10.1016/j.livsci.2019.03.015). Vargas-Sánchez et al. (2019Vargas-SánchezRD, Ibarra-AriasFJ, Torres-MartínezBDM, Sánchez-EscalanteA, Torrescano-UrrutiaGR, 2019. Use of natural ingredients in Japanese quail diet and their effect on carcass and meat quality - A review. Asian-Australas J Anim Sci32(11): 1641-1656. 10.5713/ajas.18.0800), reported that adding natural ingredients like medicinal plants to poultry diets can help improve the quality of their carcasses and meat by reducing oxidative stress, but this effect depends on the concentration of the ingredients and the type and/or structure of the compounds present. Although it was also reported that high concentrations of some natural ingredients in the diet may have negative effects on poultry carcasses and meat.

Oxidant and antioxidant parameters

 

Chasteberry plant has been among the medicinal plants utilized by humans throughout history (Zahid et al., 2016ZahidH, RizwaniGH, IshaqeS, 2016. Phytopharmacological review on Vitex agnus-castus: a potential medicinal plant. Chin Herb Med8(1): 24-29. 10.1016/s1674-6384(16)60004-7; Niroumand et al., 2018NiroumandMC, HeydarpourF, FarzaeiMH, 2018. Pharmacological and therapeutic effects of Vitex agnus castus L.: A review. Phcog Rev12(23): 103-114. 10.4103/phrev.phrev_22_17; Kamal et al., 2022KamalN, Mio AsniNS, RozlanINA, Mohd AzmiMAH, MazlanNW, MedianiA, BaharumSN, LatipJ, AssawS, Edrada-EbelRA, 2022. Traditional medicinal uses, phytochemistry, biological properties, and health applications of Vitex sp.Plants11: 1944. 10.3390/plants11151944). In vitro studies on the biological effects of chasteberry have indicated that this plant has antioxidant properties. It has been reported that these biological effects are mostly due to ketosteroids, diterpenoids, flavonoids and iridoids in the composition of chasteberry (Ahangarpour et al., 2016AhangarpourA, NajimiSA, FarboodY, 2016. Effects of Vitex agnus-castus fruit on sex hormones and antioxidant indices in a d-galactose-induced aging female mouse model. J Chin Med Assoc79(11): 589-596. 10.1016/j.jcma.2016.05.006; Souto et al., 2020SoutoEB, DurazzoA, NazhandA, LucariniM, ZaccardelliM, SoutoSB, SilvaAM, SeverinoP, NovellinoE, SantiniA, 2020. Vitex agnus-castus L.: Main features and nutraceutical perspectives. Forests11: 761-776. 10.3390/f11070761; Özderin, 2021ÖzderinS, 2021. Determination of phenolic components of Vitex agnus-castus L. (Verbenaceae) from Muğla-Ula region in Turkey. MKU J Agri Sci26(3): 692-699. 10.37908/mkutbd.937814; Adamov et al., 2022AdamovGV, RendyukTD, SaybelOL, DargaevaTD, TsitsilinAN, BokovDO, 2022. Vitex agnus-castus: Botanical features and area, chemical composition of fruit, pharmacological properties, and medicinal uses. J Appl Pharm Sci12(03): 034-044. 10.7324/japs.2022.120304; Zhelev et al., 2022ZhelevI, PetkovaZ, KostovaI, DamyanovaS, StoyanovaA, Dimitrova-DyulgerovaI, AntovaG, ErcisliS, AssouguemA, KaraM, et al. , 2022. Chemical composition and antimicrobial activity of essential oil of fruits from Vitex agnus-castus L., growing in two regions in Bulgaria. Plants11: 896. 10.3390/plants11070896.; Boujbiha et al., 2023BoujbihaMA, ChahdouraH, AdouniK, ZianiBEC, SnoussiM, ChakrounY, Ciudad-MuleroM, Fernández-RuizV, AchourL, SelmiB, et al.2023. Wild Vitex agnus-castus L.: phytochemical characterization, acute toxicity, and bioactive properties. Molecules28: 5096. 10.3390/molecules28135096). In this study, an increase in SOD, CAT, GSH values was observed in parallel with the increasing amount of chasteberry seeds, while a decrease in MDA value was observed. These results show that CS25 and CS50 diets increase antioxidant capacity and decrease oxidant capacity in quails. No study was found to investigate the antioxidant properties of CS on poultry. However, as a result of studies conducted with flaxseed, another plant with phytoestrogenic properties, it was reported that the addition of flaxseed increased antioxidant capacity similar to this study (Anjum et al., 2013AnjumFM, HaiderMF, KhanMI, SohaibM, ArshadMS, 2013. Impact of extruded flaxseed meal supplemented diet on growth performance, oxidative stability and quality of broiler meat and meat products. Lipids Health Dis12: 13. 10.1186/1476-511x-12-13; Saleh et al., 2019SalehAA, AhmedEAM, EbeidTA, 2019. The impact of phytoestrogen source supplementation on reproductive performance, plasma profile, yolk fatty acids and antioxidative status in aged laying hens. Reprod Dom Anim54: 846-854. 10.1111/rda.13432; Kumar et al., 2021KumarF, TyagiPK, MirNA, DevK, BegumJ, TyagiPK, BiswasA, SahuB, DinaniOP, SharmaD, 2021. Growth pattern, lipid composition, oxidation status, and serum biochemical profile of broiler chicken fed flaxseed meal for different durations. Lett Anim Biol01(01): 08-18. 10.62310/liab.v1i1.54).

Economic analysis

 

In the current study, it was found that the inclusion of CS in the feeds led to a decrease in feed costs. The lowest feed cost was observed in the CS50 group. As the amount of chasteberry seed in the feed increased, the reduction in feed intake was correlated with a decrease in feed costs. The results of this study were in agreement with Simol et al. (2012SimolCF, TuenAA, KhanHHA, ChuboJK, KingPJH, OngKH, 2012. Performance of chicken broilers fed with diets substituted with mulberry leaf powder. Afr J Biotechnol11: 16106-16111. 10.5897/ajb12.1622), who reported that supplementing the diet with mulberry leaves decreased the cost per kilogram of feed. In a similar study, Al-Khalaifah et al. (2020Al-KhalaifahHS, ShahinSE, OmarAE, MohammedHA, MahmoudHI, IbrahimD, 2020. Effects of graded levels of microbial fermented or enzymatically treated dried brewer’s grains on growth, digestive and nutrient transporter genes expression and cost effectiveness in broiler chickens. BMC Vet Res16: 424. 10.1186/s12917-020-02603-0) reported that the addition of microbial fermented or enzymatically treated dried brewer’s grains to broiler diets reduced feed costs. Although there was no difference between the groups in feed cost/BWG values, the lowest value was observed in the CS50 group, which seems to be related to the fact that the best feed conversion was observed in this group (Al-Khalaifah et al., 2020Al-KhalaifahHS, ShahinSE, OmarAE, MohammedHA, MahmoudHI, IbrahimD, 2020. Effects of graded levels of microbial fermented or enzymatically treated dried brewer’s grains on growth, digestive and nutrient transporter genes expression and cost effectiveness in broiler chickens. BMC Vet Res16: 424. 10.1186/s12917-020-02603-0). The highest TR values were found in the control and CS25 groups. These results are related to the high live weight. Although the lowest value in terms of values was found in the CS50 group, there was no difference between the groups in terms of net profit values. Similarly, Shehata et al. (2021ShehataSF, SallamEA, AzamAE, SolimanMM, MohammedLS, 2021. Effect of different dietary inclusion levels of mulberry leaves on productive traits, economic indices, and immunity of white and brown Japanese quail. AJVS70(2): 63-75. 10.5455/ajvs.115295) also reported that the addition of 4% and 8% mulberry leaves to Japanese quails had no negative effect on net profit. Therefore, from an economic point of view, it is understood that especially the addition of 25 g/kg chasteberry seed can be used easily.

Conclusion

 

This study revealed that the supplementation of 25 g/kg chasteberry seeds did not adversely affect the performance, slaughter, carcass parameters, or economic indices compared to the control group; however, it positively changed the antioxidant parameters. These results suggest that chasteberry seed can be safely added up to 25 g/kg in quail diets. Nevertheless, for a better understanding of the mode of action of chasteberry seeds, further studies investigating their effects on both the growth performance and antioxidant parameters of poultry are needed.

Acknowledgements

 

The author would like to thank Mürsel Özdoğan, İlker Yıldırım, and Kazım Eryılmaz for their support in this study.

Competing interests

 

The author has declared that no competing interests exist.

Authors’ contributions

 

Ahmet Onder Ustundag: Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Project administration, Supervision, Visualization, Writing – original draft, Writing – review & editing.

Funding

 

The author received no specific funding for this work.

Abbreviations used

 

BW

body weight

BWG

body weight gain

L*

lightness

a*

redness

b*

yellowness

CAT

catalase

CL

cooking loss

CS

chasteberry seed

DL

drip loss

FI

feed intake

FCR

feed conversion ratio

GSH

glutathione

MDA

malondialdehyde

SF

shear force

SOD

superoxide dismutase

WHC

water holding capacity

TFC

total feed cost

EEI

economic efficiency index

TR

total return

References

 

1 

AdamovGV, RendyukTD, SaybelOL, DargaevaTD, TsitsilinAN, BokovDO, 2022. Vitex agnus-castus: Botanical features and area, chemical composition of fruit, pharmacological properties, and medicinal uses. J Appl Pharm Sci12(03): 034-044. https://doi.org/10.7324/japs.2022.120304

2 

AebiH, 1984. Catalase in vitro. Methods Enzymol105: 121-126.

3 

AhangarpourA, NajimiSA, FarboodY, 2016. Effects of Vitex agnus-castus fruit on sex hormones and antioxidant indices in a d-galactose-induced aging female mouse model. J Chin Med Assoc79(11): 589-596. https://doi.org/10.1016/j.jcma.2016.05.006

4 

AlamoudiMO, BakrshoomYF, 2021. Vitex agnus cactus and some female disorders: A review. Agric Rev42(2): 209-214. https://doi.org/10.18805/ag.r-170

5 

Al-KhalaifahHS, ShahinSE, OmarAE, MohammedHA, MahmoudHI, IbrahimD, 2020. Effects of graded levels of microbial fermented or enzymatically treated dried brewer’s grains on growth, digestive and nutrient transporter genes expression and cost effectiveness in broiler chickens. BMC Vet Res16: 424. https://doi.org/10.1186/s12917-020-02603-0

6 

Al-OtibiFO, AlrumaizanGI, AlharbiRI, 2022. Evaluation of anticandidal activities and phytochemical examination of extracts prepared from Vitex agnus‑castus: a possible alternative in treating candidiasis infections. BMC Complement Med Ther22: 69. https://doi.org/10.1186/s12906-022-03552-x

7 

AMSA, 2012. Meat color measurement guidelines. American Meat Science Association. Illinois, USA.

8 

AnjumFM, HaiderMF, KhanMI, SohaibM, ArshadMS, 2013. Impact of extruded flaxseed meal supplemented diet on growth performance, oxidative stability and quality of broiler meat and meat products. Lipids Health Dis12: 13. https://doi.org/10.1186/1476-511x-12-13

9 

AOAC, 2005. Official Methods of Analysis of AOAC International (17th ed.). Association of the Official Analytical Chemists. Gaithersburg. MD. USA. https://doi.org/10.1093/9780197610145.003.1380

10 

Beheshti MoghadamMH, RezaeiM, BehgarM, KermanshahiH, 2017. Effects of irradiated flaxseed on performance, carcass characteristics, blood parameters, and nutrient digestibility in broiler chickens. Poult Sci J5(2): 153-163

11 

BoujbihaMA, ChahdouraH, AdouniK, ZianiBEC, SnoussiM, ChakrounY, Ciudad-MuleroM, Fernández-RuizV, AchourL, SelmiB, et al.2023. Wild Vitex agnus-castus L.: phytochemical characterization, acute toxicity, and bioactive properties. Molecules28: 5096. https://doi.org/10.3390/molecules28135096

12 

Dos SantosTC, GatesRS, TinôcoIFF, EstradaMM, Chizzotti, ML, 2020. Meta quality traits of European quails reared under different conditions of temperatures and air velocity. Poult Sci99: 848-856.https://doi.org/10.1016/j.psj.2019.10.037

13 

DraperHH, HadleyM, 1990. Malondialdehyde determination as index of lipid peroxidation. Methods Enzymol186: 421-431. https://doi.org/10.1016/0076-6879(90)86135-i

14 

El-BahrSM, ShoushaS, AlfattahMA, Al-SultanS, KhattabW, SabeqII, Ahmed-FaridO, El-GarhyO, AlbusadahKA, AlhojailyS, et al.2021. Enrichment of broiler chickens’ meat with dietary linseed oil and lysine mixtures: Influence on nutritional value, carcass characteristics and oxidative stress biomarkers. Foods10: 618. https://doi.org/10.3390/foods10030618

15 

El-NawasanyLI, 2019. The Use of Vitex agnus-castus to Produce Functional Stirred Yoghurt, J of Food and Dairy Sci10(9): 297-301. https://doi.org/10.21608/jfds.2019.54517

16 

El-SaadanyAS, HanafyMM, ElkomyAE, 2022. Flaxseed and Agnus-castus on vitex as a source of phytoestrogens and their impact on productive performance, some blood constituents, and blood oestradiol profile of aged laying hens. Ital J Anim Sci21(1): 821-830. https://doi.org/10.1080/1828051x.2022.2066578

17 

GhazaghiM, MehriM, Bagherzadeh-KasmaniF, 2014. Effects of dietary Mentha spicata on performance, blood metabolites, meat quality and microbial ecosystem of small intestine in growing Japanese quail. Anim Feed Sci Technol194: 89-98. https://doi.org/10.1016/j.anifeedsci.2014.04.014

18 

GheorgheA, LefterNA, IdriceanuL, RopotăM, HăbeanuM, 2020. Effects of dietary extruded linseed and Lactobacillus acidophilus on growth performance, carcass traits, plasma lipoprotein response, and caecal bacterial populations in broiler chicks. Ital J Anim Sci19(1): 822-832. https://doi.org/10.1080/1828051x.2020.1801359

19 

GonçalvesR, AyresVFS, CarvalhoCE, SouzaMGM, GuımarãesAC, CorrêaGM, MartinsCHG, TakearaR, SilvaEO, CrottiAEM, 2017. Chemical composition and antibacterial activity of the essential oil of Vitex agnus-castus L. (Lamiaceae). An Acad Bras Cienc89(4): 2825-2832. https://doi.org/10.1590/0001-3765201720170428

20 

Honikel, KO, 1998. Reference methods for the assessment of physical characteristics of meat. Meat Sci. 49(4): 447-457. https://doi.org/10.1016/s0309-1740(98)00034-5

21 

JooST, 2018. Determination of water-holding capacity of porcine musculature based on released water method using optimal load. Korean J Food Sci Anim Resour38(4): 823-828.

22 

KamalN, Mio AsniNS, RozlanINA, Mohd AzmiMAH, MazlanNW, MedianiA, BaharumSN, LatipJ, AssawS, Edrada-EbelRA, 2022. Traditional medicinal uses, phytochemistry, biological properties, and health applications of Vitex sp.Plants11: 1944. https://doi.org/10.3390/plants11151944

23 

KaradağoğluÖ, ŞahinT, ÖlmezM, AhsanU, ÖzsoyB, 2019. Fatty acid composition of liver and breast meat of quails fed diets containing black cumin (Nigella sativa L.) and/or coriander (Coriandrum sativum L.) seeds as unsaturated fatty acid sources. Livest Sci223: 164-171. https://doi.org/10.1016/j.livsci.2019.03.015

24 

KumarF, TyagiPK, MirNA, DevK, BegumJ, TyagiPK, BiswasA, SahuB, DinaniOP, SharmaD, 2021. Growth pattern, lipid composition, oxidation status, and serum biochemical profile of broiler chicken fed flaxseed meal for different durations. Lett Anim Biol01(01): 08-18. https://doi.org/10.62310/liab.v1i1.54

25 

MapiyeC, ChimonyoM, DzamaK, HugoA, StrydomPE, MuchenjeV, 2011. Fatty acid composition of beef from Nguni steers supplemented with Acacia karroo leaf-meal. J Food Comp Anal24: 523-528. https://doi.org/10.1016/j.jfca.2011.01.018

26 

Mehri, M., Sabaghi, V., Bagherzadeh-Kasmani, F., 2015. Mentha piperita (peppermint) in growing Japanese quails diet: Performance, carcass attributes, morphology and microbial populations of intestine. Anim Feed Sci Technol207: 104-111. https://doi.org/10.1016/j.anifeedsci.2015.05.021

27 

MnisiCM, MatshogoTB, van NiekerkR, MlamboV, 2017. Growth performance, haemo-biochemical parameters and meat quality characteristics of male Japanese quails fed a Lippia javanica-based diet. S Afr J Anim Sci47: 661-671. https://doi.org/10.4314/sajas.v47i5.9

28 

MridulaD, KaurD, NagraSS, BarnwalP, GurumayumS, SinghKK, 2015. Growth performance and quality characteristics of flaxseed-fed broiler chicks. J Appl Anim Res43(3): 345-351. https://doi.org/10.1080/09712119.2014.978773

29 

NazariM, GhorbaniMR, NassiriMTB, FathimoghadamN, SabahiR, MosaviST, 2023. The effects of Chaste-berry fruits on hypothalamic-pituitary-ovarian markers gene expression and immune response of laying hens: Phytoestrogens in Chaste-berry are ERβ-selective. IVJ19(1): 61-71.

30 

NiroumandMC, HeydarpourF, FarzaeiMH, 2018. Pharmacological and therapeutic effects of Vitex agnus castus L.: A review. Phcog Rev12(23): 103-114. https://doi.org/10.4103/phrev.phrev_22_17

31 

NRC, 1994. Nutrient requirements of poultry. 9th rev. ed. National Academy Press, National Research Council. Washington, D.C.

32 

ÖzderinS, 2021. Determination of phenolic components of Vitex agnus-castus L. (Verbenaceae) from Muğla-Ula region in Turkey. MKU J Agri Sci26(3): 692-699. https://doi.org/10.37908/mkutbd.937814

33 

PopescuRG, VoicuSN, PircalabioruGG, GharbiaS, HermeneanA, GeorgescuSE, PanaiteTD, TurcuRP, 2021. Impact of dietary supplementation of flaxseed meal on intestinal morphology, specific enzymatic activity, and cecal microbiome in broiler chickens. Appl Sci11: 6714. https://doi.org/10.3390/app11156714

34 

SalaryJ, Matin HematiHR, HajatiH, 2016. The Effect of a dietary innovative multi-material on sex hormones and molting period of canaries and laying-hens. Iran J Appl Anim Sci6(4): 937-942.

35 

SalehAA, AhmedEAM, EbeidTA, 2019. The impact of phytoestrogen source supplementation on reproductive performance, plasma profile, yolk fatty acids and antioxidative status in aged laying hens. Reprod Dom Anim54: 846-854. https://doi.org/10.1111/rda.13432

36 

SamtiyaM, AlukoRE, DhewaT, 2020. Plant food anti-nutritional factors and their reduction strategies: an overview. Food Prod Process Nutr2(6): 1-14. https://doi.org/10.1186/s43014-020-0020-5

37 

SAS, 1999. SAS user’s guide: Statistics, Version 8 Edition. SAS Inst., Inc., Cary, NC.

38 

SedlakJ, LindsayRH, 1968. Estimation of total, protein-bound, and non-protein sulfhydryls groups in tissue with Ellman’s reagent. Anal Biochem25:192-205. https://doi.org/10.1016/0003-2697(68)90092-4

39 

ShaabanHAE, El-GhorabAH, ShibamotoT, 2012. Bioactivity of essential oils and their volatile aroma components: Review. J Essent Oil Res24(2): 203-212. https://doi.org/10.1080/10412905.2012.659528

40 

ShehataSF, SallamEA, AzamAE, SolimanMM, MohammedLS, 2021. Effect of different dietary inclusion levels of mulberry leaves on productive traits, economic indices, and immunity of white and brown Japanese quail. AJVS70(2): 63-75. https://doi.org/10.5455/ajvs.115295

41 

SimolCF, TuenAA, KhanHHA, ChuboJK, KingPJH, OngKH, 2012. Performance of chicken broilers fed with diets substituted with mulberry leaf powder. Afr J Biotechnol11: 16106-16111. https://doi.org/10.5897/ajb12.1622

42 

SinghJ, SharmaM, MehtaN, SinghND, KaurP, SethiAPS, SikkaSS, 2018. Influence of supplementation of black pepper powder through feed in broiler chickens on their growth performance, blood profile, meat sensory qualities and duodenum morphology. Indian J Anim Sci88(2): 215-221. https://doi.org/10.56093/ijans.v88i2.79346

43 

SoutoEB, DurazzoA, NazhandA, LucariniM, ZaccardelliM, SoutoSB, SilvaAM, SeverinoP, NovellinoE, SantiniA, 2020. Vitex agnus-castus L.: Main features and nutraceutical perspectives. Forests11: 761-776. https://doi.org/10.3390/f11070761

44 

SunY, OberleyLW, LiY, 1988. A simple method for clinical assay of superoxide dismutase. Clin Chem, 34(3), 497-500. https://doi.org/10.1093/clinchem/34.3.497

45 

TamasgenN, UrgeM, GirmaM, NurfetaA, 2021. Effect of dietary replacement of soybean meal with linseed meal on feed intake, growth performance and carcass quality of broilers. Heliyon7: e08297. https://doi.org/10.1016/j.heliyon.2021.e08297

46 

TashlaT, PuvačaN, Ljubojević PelićD, ProdanovićR, IgnjatijevićS, BoškovićJ, IvaniševićD, JahićM, MahmoudM, GiannenasI, LevićJ, 2019. Dietary medicinal plants enhance the chemical composition and quality of broiler chicken meat. J Hellenic Vet Med Soc70(4): 1823-1832. https://doi.org/10.12681/jhvms.22229

47 

Vargas-SánchezRD, Ibarra-AriasFJ, Torres-MartínezBDM, Sánchez-EscalanteA, Torrescano-UrrutiaGR, 2019. Use of natural ingredients in Japanese quail diet and their effect on carcass and meat quality - A review. Asian-Australas J Anim Sci32(11): 1641-1656. https://doi.org/10.5713/ajas.18.0800

48 

YalcinH, KoncaY, DurmuscelebiF, 2017. Effect of dietary supplementation of hemp seed (Cannabis sativa L.) on meat quality and egg fatty acid composition of Japanese quail (Coturnix coturnix japonica). J Anim Physiol Anim Nutr102: 131-141. https://doi.org/10.1111/jpn.12670

49 

ZahidH, RizwaniGH, IshaqeS, 2016. Phytopharmacological review on Vitex agnus-castus: a potential medicinal plant. Chin Herb Med8(1): 24-29. https://doi.org/10.1016/s1674-6384(16)60004-7

50 

ZhalehS, GolianA, ZerehdaranS, 2019. Effect of rolled or extruded flaxseeds in finisher diet on pellet quality, performance, and n-3 fatty acids in breast and thigh muscles of broiler chickens. Poult Sci J7(1): 63-75.

51 

ZhalehS, GolianA, ZerehdaranS, 2020. Effects of one week feeding finisher diets containing rolled and extruded flaxseed on performance, lipid peroxidation and omega-3 fatty acids in breast and thigh meat of broiler chickens.. Poult Sci J8(1): 83-94.

52 

ZhelevI, PetkovaZ, KostovaI, DamyanovaS, StoyanovaA, Dimitrova-DyulgerovaI, AntovaG, ErcisliS, AssouguemA, KaraM, et al. , 2022. Chemical composition and antimicrobial activity of essential oil of fruits from Vitex agnus-castus L., growing in two regions in Bulgaria. Plants11: 896. https://doi.org/10.3390/plants11070896.