ArticlePDF Available

Effect of different levels of honey on physiological, growth and carcass traits of broiler chickens during dry season

Authors:

Abstract and Figures

p> The objective of this trial was to investigate the effect of different levels of honey in drinking water on the responses of broiler chickens during dry season in hot humid tropics. Three hundred Oba Marshall broiler chicks were used for this study. The day-old chicks were randomly assigned to five treatment groups with each treatment having four replicates of 15 birds. The first 4 treatment groups were daily supplied drinking water without honey (0H), with 20 ml (20H), 40 ml (40H) and 60 ml (60H) of honey per liter of water. The fifth group received drinking water supplemented with 500 mg vitamin C per liter of water (C). Records on daily weight gain (WG) and feed intake (FI) were taken. Feed conversion ratio (FCR) was calculated as the ratio of gain to feed consumed. The supplementation of honey in the drinking water for broiler chickens in 60H during hot dry season in the hot humid tropics improved some stress indices, body weight gain and relative spleen weight. </p
Content may be subject to copyright.
Acta argiculturae Slovenica, 108/1, 45–53, Ljubljana 2016
doi:10.14720/aas.2016.108.1.5 COBISS: 1.01
Agris category code: L02, L51
EFFECT OF DIFFERENT LEVELS OF HONEY ON PHYSIOLOGI
CAL, GROWTH AND CARCASS TRAITS OF BROILER CHICKENS
DURING DRY SEASON
Oyegunle Emmanuel OKE 1, 2, Faith O. SORUNGBE 1, Monsuru Oladimeji ABIOJA 1, Oluwad-
amilola OYETUNJI 1, Anuoluwapo Olamide ONABAJO 1
Received January 13, 2016; accepted May 17, 2016.
Delo je prispelo 13. januarja 2016, sprejeto 17. maja 2016.
1 Federal University of Agriculture, Department of Animal Physiology, PMB 2240, Abeokuta, Nigeria
2 Corresponding author, e-mail: emaoke7@yahoo.co.uk
Eect of dierent levels of honey on physiological, growth and
carcass traits of broiler chickens during dry season
e objective of this trial was to investigate the eect of
dierent levels of honey in drinking water on the responses of
broiler chickens during dry season in hot humid tropics. ree
hundred Oba Marshall broiler chicks were used for this study.
e day-old chicks were randomly assigned to ve treatment
groups with each treatment having four replicates of 15 birds.
e rst 4 treatment groups were daily supplied drinking water
without honey (0H), with 20 ml (20H), 40 ml (40H) and 60
ml (60H) of honey per liter of water. e h group received
drinking water supplemented with 500 mg vitamin C per liter
of water (C). Records on daily weight gain (WG) and feed in-
take (FI) were taken. Feed conversion ratio (FCR) was calcu-
lated as the ratio of gain to feed consumed. e supplementa-
tion of honey in the drinking water for broiler chickens in 60H
during hot dry season in the hot humid tropics improved some
stress indices, body weight gain and relative spleen weight.
Key words: poultry; broiler chickens; animal nutrition;
honey; growth; physiological traits; carcass traits; hot dry sea-
son
Učinek dodajanja različnih količin medu na ziološke, rastne
in klavne lastnosti pitovnih piščancev v sušnih razmerah
Cilj raziskave je bil proučiti vpliv dodajanja različnih ko-
ličin medu v pitno vodo pitovnih piščancev med vročim in su-
him obdobjem v vročih in vlažnih tropih. Za to študijo smo
uporabili 300 pitovnih piščancev provenience Oba Marshall.
Enodnevni piščanci so bili naključno razporejeni v pet posku-
snih skupin, s štirimi ponovitvami s po 15 piščanci v vsaki sku-
pini. V prvih štirih skupinah so piščanci dobivali pitno vodo
brez medu (0H), z 20 ml (20H), 40 ml (40H) in 60 ml (60H)
medu na liter vode. Peta skupina je dobivala pitno vodo, dopol-
njeno s 500 mg vitamina C na liter vode (C). Merili smo dnevne
priraste (WG) in količino zaužite krme (FI). Izkoriščanje krme
(FCR) smo izračunali kot razmerje med prirastom in porabo
krme. Dodatek medu v pitni vodi za pitovne piščance v skupini
60H v vročem in sušnem obdobju v vročih in vlažnih tropih je
izboljšal nekatere pokazatelje stresa, pitovne lastnosti in pove-
čal relativno maso vranice.
Ključne besede: perutnina; pitovni piščanci; prehrana ži-
vali; med; rast; zološke lastnosti; klavne lastnosti; vroče sušno
obdobje
bient temperature and high humidity which have been
reported to aect the productive performance of chick-
ens (Ahmad et al., 2005; Daghir, 2008). Great losses are
being encountered in broiler production in Nigeria every
year due to the eect of heat-stress. e loss is attributed
to the fact that the birds have rapid metabolism, high
body temperature and no sweat gland (Abioja, 2010).
In South Western Nigeria, environmental tempera-
ture is oen higher than the recommended temperature
of 18–21 °C (Charles et al., 2002) for optimal productiv-
ity of growing broiler chickens particularly during the
1 INTRODUCTION
Broiler chicken production plays a vital role in food
security for the fast increasing human population in Ni-
geria due to the short production cycle, high feed e-
ciency and growth rate of the birds. e birds are how-
ever faced with the challenges of coping with the ever
changing elements of weather, especially the ambient
temperature typically during growing-nishing phase in
the tropics. is is partly due to the fact that the tropics
and sub-tropics are faced with the challenge of high am-
Acta agriculturae Slovenica, 108/1 – 2016
46
O. E. OKE et al.
dry season which usually occurs between the month of
November and March. As a result of this peculiarity, a
passable and appropriate measures that can ameliorate
the adverse eect of the environmental factors to the bar-
est minimum to ensure optimum broiler production in
the hot dry season are essential.
Some of the methods recommended to alleviate
the adverse eects of high ambient temperature includ-
ing housing, ventilation, air conditioning and cooling
systems are now issues that are probably applicable on a
regional basis (Armstrong et al., 1999; Yalcin et al., 2001).
However, some of these methods cannot be applied in
developing countries including Nigeria because of their
impracticability and high cost. Instead, nutritional ma-
nipulation with its low cost is a common approach in
poultry production (Austic, 1985; Leeson, 1986; Shane,
1988). Results from various studies (Sayed and Shoeib,
1996; Yahav and McMurty, 2001; Curca et al., 2004; Ara-
das et al., 2005; Gonzalez-Esquerra and Leeson, 2006;
Ramnath et al., 2008; Zhang et al., 2009; Abioja et al.,
2011) on several measures taken to abridge the eect of
heat stress in poultry with the use of several therapeutic
agents remain inconclusive. Moreover, several natural
substances that are rich in antioxidants have also been
used on heat-stressed chickens. ese include bee pollen
(Wang et al., 2005), ginger root (Zhang et al., 2009), etc.
e use of honey has however received a meagre atten-
tion.
Honey is a complex product and contains natural
anti-oxidants. Antioxidants play a major role in the pro-
tection of cells from reactive oxygen species (ROS) by
reducing chemical radicals and preventing the process
of lipid peroxidation (Yu, 1994). When compared to
synthetic vitamin C that is conventionally used, honey
is more readily available while vitamin C may not be
readily available especially to the local farmers. Honey
is a good example of natural substance that contains
phytochemicals such as vitamin C, thiamine, riboavin,
pyridoxine, pantothenic acid, nicotinic acid, phenolic
compounds, and enzymes glucose oxidase, catalase, and
peroxidise. Honey has been used by man for several pur-
poses especially as an antioxidant. However, there is a
dearth of reports on the use of h oney in poultry produc-
tion. Our previous study (Abioja et al., 2010) on the in-
clusion levels of honey (0, 10, 20 ml) in drinking water of
broiler chickens neither aected the growth nor reduced
the body temperature while there was no change in the
physiological responses and haematology on adding 0
and 10 ml of honey but slight change in physiological re-
sponses occurs on adding 20 ml of honey. erefore this
trial was carried out to determine if an increase in the in-
clusion levels of honey (20, 40, 60 mls) in drinking water
of broiler chickens from day-old to 8weeks old would in-
uence more changes in the physiological responses and
also bring about the possibility of better performance of
broiler chickens. is study therefore aimed at determin-
ing the eect of dierent levels of honey on the physio-
logical response of broiler chicken during hot-dry season
2 MATERIALS AND METHODS
2.1 EXPERIMENTAL SITE
e experiment was carried out at the poultry unit
of Directorate of University Farms (DUFARMS) and the
laboratory, Federal University of Agriculture, Abeokuta
(FUNAAB). e University is located on latitude 7°10’N,
longitude 3°2’E and altitude 76 m above sea level. It lies
between South-Western part of Nigeria with a prevailing
tropical climate with a mean annual rainfall of 1,037 mm,
and annual mean temperature and relative humidty of
34 °C and 82 %, respectively (Amujoyegbe et al., 2008).
e vegetation in the University represents the inter-
phase between the tropical rain forest and the derived sa-
vannah. e average maximum and minimum tempera-
ture during the period of the experiment was 35.5 °C and
23.8 °C, respectively while relative humidity was 92 %.
2.2 EXPERIMENTAL ANIMALS AND PROCE
DURE
ree hundred Oba Marshall broiler day-old chicks
purchased from a reputable hatchery at one day of age
were used for this study. e brooding temperature was
maintained at 35 °C for the rst two days then decreased
gradually until 21 days of age. e light regime was 23L:
1D. e vaccination schedule for commercial broiler
chickens was followed. e chicks were randomly as-
signed to ve treatment groups with each treatment hav-
ing four replicates of 15 birds in a completely randomized
design at day 21. e rst 4 treatment groups were daily
supplied drinking water without honey (0H), with 20 ml
(20H), 40 ml (40H) and 60 ml (60H) of honey per liter
of water. e h group received drinking water supple-
mented with 500 mg vitamin C per liter of water (C).
e birds were kept on deep-litter oor in an open-
sided poultry house. e birds were oor-brooded for
three weeks on wood-shavings. Additional sources of
heat were provided during the brooding period. e
chicks were fed ad libitum with standard starter mash
and thereaer with nisher mash. Water at ambient tem-
perature was supplied ad libitum throughout the period
of the experiment. e composition of the diet is shown
in Table 1.
Acta agriculturae Slovenica, 108/1 – 2016 47
EFFECT OF DIFFERENT LEVELS OF HONEY ON PHYSIOLOGICAL, GROWTH ... OF BROILER CHICKENS DURING DRY SEASON
2.3 DATA COLLECTION
2.3.1 GROWTH PERFORMANCE
Bodyweight of the birds in each replicate were mon-
itored using a sensitive scale every week during the ex-
periment. Records on daily weight gain (WG) and feed
intake (FI) were taken. Feed conversion ratio (FCR) was
calculated as the ratio of gain to feed consumed.
2.3.2 RELATIVE WEIGHTS OF ORGANS
At 56 days of age, 2 birds per replicate were slaugh-
tered. e birds were dissected and the weights of liver,
kidney, lungs, spleen, breast meat, gizzard, drum stick,
shank, thigh, tibia, small intestine, proventriculus, ab-
dominal fat pad, gastrointestinal tract, bursa of Fabricius,
thymus, heart were taken and relative weights were de-
termined as a percentage of birds bodyweights.
2.3.3 HAEMATOLOGY AND SERUM ANALYSIS
Blood samples were collected from two randomly
picked birds from each replicate once a week via brachial
vein into ethylene diamine tetra acetic acid (EDTA) an-
ticoagulant and immediately mixed gently to avoid clot-
ting. Blood samples were analysed for haemoglobin (Hb),
Packed Cell Volume (PCV), Total Erythrocyte Count
(TEC), Total Leukocyte Count (TLC) and Dierential
Leukocyte Count (DLC). Hb estimation was determined
by cyanmethaemoglobin method and PCV by microhe-
matocrit method (Bernard et al., 2000). TEC and TLC
were determined using Neubaurs hemocytometer and To-
luidine blue (0.015 %) saline as diluent (Brar et al., 2002).
e blood lms stained with Wright’s stain (Benjamin,
1985) was studied for DLC. Mean cell volume (MCV),
mean corpuscular hemoglobin (MCH), and mean corpus-
cular hemoglobin concentration (MCHC) were calculated
(Stockham and Scott, 2002).
e blood samples were also analyzed for serum me-
tabolites including serum total protein, albumin, globu-
lin and creatinine. Serum glucose was determined col-
orimetrically using the method described by Braham and
Trinder (1969). e total serum protein was determined
according to the method of Colowick and Kaplan (1955)
while serum albumin and globulin was determined using
bromocresol purple method of Varley et al., (1980). Serum
corticosterone was determined using radio immunoassay
(RIA) technique as described by Darras et al. (1992).
2.4 STATISTICAL ANALYSIS
All data collected were subjected to analysis of vari-
ance using the procedure of SAS (1999). Signicantly
dierent means were compared using Duncan Multiple
Range Test.
3 RESULTS
3.1 SERUM CHEMISTRY
e eect of dierent levels of honey on serum pa-
rameters in broiler chickens at nisher phase during hot-
dry season is shown in Table 2. e blood glucose level
in 0H and 60H treatment groups were similar but higher
than those birds in 40H, 20H and C treatment groups.
Ingredient Starter phase Finisher phase
Maize 46.00 50.00
Soybean meal 18.50 12.00
Groundnut cake 15.00 11.00
Fish meal 2.00 2.00
Wheat oal 12.45 19.05
Bone meal 2.00 2.00
Oyster shell 3.00 3.00
Salt 0.25 0.25
Premix 0.25 0.25
Methionine 0.30 0.25
Lysine 0.25 0.20
100 100
Calculated
Crude protein (%) 23.05 19.91
M.E (Kcal/kg) 2816 2809.6
Ether extract (%) 3.93 3.89
Crude ber (%) 3.67 3.79
Calcium (%) 1.75 1.74
Phosphorus (%) 0.43 0.41
Table 1: Composition of diets for broiler (starter and nisher
phases)
Preglednica 1: Sestava popolne krmne mešanice za pitovne
piščance (začetna in končna faza pitanja)
* 1 kg of premix contains: Vitamin A – 10,000,000 IU; Vitamin
D3 – 2,000,000; Vitamin E – 20,000 IU; Vitamin K – 2,250 mg;
iamine B1 – 1,750 mg; Riboavin B2 – 5,000 mg; Pyridoxine
B6 – 2,750 mg; Niacin – 27,500 mg; Vitamin B12 – 15 mg; Panto-
thenic acid – 7,500 mg; Folic acid – 7,500 mg; Biotin – 50 mg; Choline
chloride – 400 g; Antioxidant – 125 g; Magnesium – 80 g; Zinc –
50 mg; Iron – 20 g; Copper – 5 g; Iodine – 1.2 g; Selenium – 200 mg;
Cobalt – 200 mg
Acta agriculturae Slovenica, 108/1 – 2016
48
O. E. OKE et al.
Moreover, birds on 40H, 20H and C had also similar blood
glucose levels. e level of total protein in the birds in C
and 60H treatment groups were similar but signicantly
higher (p < 0.05) than in birds in 20H and 0H treatments
while those of 40H, 20H and 0H were similar. e triglyc-
eride level of 60H was signicantly higher than those of
other treatment groups. Birds in 40H, 0H, 20H treatment
groups had similar level of triglyceride but lower than that
of C treatment group. Birds in 0H and C treatment group
were similar but higher in aspartate amino-transferase lev-
el than those of the birds in 20H. Birds in C and 60H treat-
ment group were higher in alanine amino-transferase level
than those of 40H treatment group. Also 0H 20H, 60H
and C treatment groups were similar in alanine amino-
transferase levels. Creatine kinase level in 40H was signi-
cantly higher than those of other treatment groups apart
from the birds in 0H which had similar levels. Birds in C
treatment group had similar level of creatine kinase than
those in 20H but lower than the birds in the other treat-
ment groups. Birds in 0H had a signicantly higher level
of creatinine kinase than those of 20H and C treatment
groups. Birds in 0H had higher (p < 0.05) level of serum
corticosterone than those of the other treatment groups.
e level of serum corticosterone recorded in the birds in
20H treatment group was lower (p < 0.05) than those of
0H, 60H, 40H and C treatment group.
Parameters 0H 20H 40H 60H Vit C SEM
Glucose (mg/dl) 124.65a101.90b107.95b125.9a95.8b5.13
Total Protein(g/l) 52.45b52.70b58.55ab 61.15a63.65a1.62
Albumin (g/l) 36.05 34.55 39.45 39.05 41.10 1.20
Globulin (g/l) 16.40 18.15 19.10 21.60 22.55 0.99
Triglyceride(mg/dl) 145.80c123.20c148.25c226.80a185.70b12.50
AST (IU/l) 145.80a112.45b135.60ab 130.85ab 140.40a4.40
ALT (IU/l) 36.70ab 36.40ab 21.85b45.75a57.45a4.38
Creatine kinase (IU/l) 129.15ab 107.90cd 136.15a119.35bc 100.00d4.63
Corticosterone (ng/mL) 237.50a157.00c198.50b203.50b189.50b8.75
Table 2: Eect of dierent levels of honey on serum parameters of broiler chickens at nisher phase
Preglednica 2: Učinek različnih ravni dodajanja medu na parametre krvnega seruma pitovnih piščancev v končnem obdobju pitanja
a, b, c Means within a row with dierent superscripts dier signicantly (p < 0.05). AST – Aspartate amino-transferase; ALT – Alanine amino-transferase
Parameters
Level of honey and vitamin C
SEM0H 20H 40H 60H Vit C
PCV (%) 30.50 27.50 32.00 32.50 37.00 1.57
Haemoglobin (G/Dl) 9.85 8.80 10.55 10.20 11.35 0.44
Red blood cell 2.60 2.30 2.75 2.80 3.15 0.15
White blood cell 10.85 10.20 11.20 10.00 9.80 0.29
Heterophil 30.00 32.00 36.50 30.50 35.50 1.80
Lymphocyte (%) 70.00 66.00 63.50 68.50 63.50 1.85
Eosinophil (%) 0.00 0.50 0.00 0.00 0.50 0.13
Basophil (%) 0.00 0.50 0.00 0.00 0.00 0.10
Monocyte (%) 0.00 1.00 0.00 1.00 0.50 0.27
HL 0.43 0.51 0.58 0.45 0.56 0.04
MCH (µµG) 38.03 38.18 38.26 37.13 36.32 0.95
MCV (µ3) 117.85 119.31 116.39 117.25 118.21 2.64
MCHC (%) 32.33 32.00 32.87 31.61 30.70 0.35
Table 3: Eect of dierent levels of honey on haematological parameters of broiler chickens at nisher phase during hot-dry season
Preglednica 3: Učinek dodajanja medu na hematološke parametre pitovnih piščancev v končni fazi pitanja v vročem in suhem obdobju
MCV – Mean corpuscular volume, MCH – Mean corpuscular haemoglobin, MCHC – Mean Corpuscular haemoglobin concentration,
HL – Heterophil : lymphocyte ratio, PCV – Packed cell volume
Acta agriculturae Slovenica, 108/1 – 2016 49
EFFECT OF DIFFERENT LEVELS OF HONEY ON PHYSIOLOGICAL, GROWTH ... OF BROILER CHICKENS DURING DRY SEASON
Table 3 shows the eect of dierent levels of honey on
haematological parameters of broiler chickens at nisher
phase during the hot-dry season. ere was no signicant
eect of dierent levels of honey on the haematological
parameters of the birds among the treatment groups at the
nisher phase.
3.2 GROWTH PERFORMANCE
Eect of dierent levels of honey on the perfor-
mance of broiler chickens is presented in Table 4. e
weight gain of the birds in 60H treatment group was
higher than those of the birds in the other treatment
groups. e birds in 20H treatment group had similar-
weight gains as those of 40H and C groups. e weight
gain in 0H was lower than those of the other treatment
groups. Also the feed intake of the birds in 0H was lower
than those of the other treatment groups whose values
were similar. e feed conversion ratio was similar across
the treatment groups (p > 0.05).
3.3 RELATIVE WEIGHTS OF ORGANS
Eect of dierent levels of honey on the relative
weights of organs of broiler chickens is presented in Ta-
ble 5. e body weights of the birds in 20H and 40H were
signicantly higher (p < 0.05) than that of OH group. e
weights of the birds in 60H and C group were similar but
higher than the weights recorded in the other treatment
groups. e relative weights of liver in broiler chickens in
0H group were signicantly higher (p < 0.05) than those
of other treatment groups. e liver relative weights of
the birds in 40H goup were higher than those of 20H,
60H and C group. e relative weights of kidney of the
birds in 40H, 60H and C group were similar but signi-
cantly higher (p < 0.05) than those of 0H and 20H. e
relative weight of the lungs of the birds in 0H was sig-
nicantly higher than those of other treatment groups.
e heart weights of the birds in 0H group were signi-
cantly higher (p < 0.05) than those of the other treatment
groups. e relative weight of small intestine in broiler
chicken of 0H group was signicantly higher (p < 0.05)
than those of the other treatment groups. e birds in
40H group had a signicantly higher (p < 0.05) weights
than those of 60H and C treatment groups. e relative
weight of proventriculus of the birds in 0H group was
signicantly higher (p < 0.05) than those of the other
treatment groups. e relative weights of empty gizzard
in 60H and C group were similar but signicantly higher
(p < 0.05) than that of 40H group whose value was also
higher than that of 20H group. e relative weights of
breast meat of the birds in 20H and 40H group were sim-
ilar but signicantly higher (p < 0.05) than those of 0H,
60H and C treatment groups whose values were similar.
e relative weight of thigh in 0H group was signi-
cantly higher (p < 0.05) than those of the other treatment
groups. e values recorded for the birds in 40H were
higher than those of the birds in 60H and C treatment
groups whose values were similar. e shank relative
weight recorded in the birds in 60H was higher than in
those of the other treatments. e drum stick weight was
also higher in the birds in 60H than the birds in the other
treatment groups. e value for 40H was also higher than
those of 0H and C treatment groups. e GIT relative
weights recorded in the birds in 60H were higher than
those of the other treatment groups. e values in 20H
and 40H were comparable but higher than those of 0H
and C treatment groups.
e relative weights of tibia in 40H were comparable
to those of 60H and C treatment groups but signicantly
higher (p < 0.05) than those of 0H and 20H groups, which
were similar to those of 60H and C treatment groups.
Eect of dierent levels of honey on the relative
weights of lymphoid organs of broiler chickens at nisher
phase during hot-dry season is presented in Table 6. e
relative weight of thymus of the birds in 40H was similar
Parameters
Levels of inclusion honey
Vit C SEM0H 20H 40H 60H
Initial body weight at 4wks (g) 590.52 588.28 586.69 585.41 587.96 2.04
Final body weight (g) 1785.10d1839.44c1855.45b1887.62a1828.36c7.89
Weight gain (g) 1194.59d1251.16bc 1268.76b1302.21a1240.42c8.59
Feed intake (g) 2783.10b2992.05a2973.93a3028.06a2963.39a26.00
Feed conversion ratio 2.32 2.39 2.34 2.32 2.39 0.01
Mortality 00000
Table 4: Eect of dierent levels of honey on performance of broiler chickens at nisher phase
Preglednica 4: Učinek različnih ravni dodanega medu na proizvodne lastnosti pitovnih piščancev v končni fazi pitanja
a, b, c, d Means within rows with dierent superscripts dier signicantly (p < 0.05)
Acta agriculturae Slovenica, 108/1 – 2016
50
O. E. OKE et al.
to that of 60H but signicantly higher than those of 20H,
0H and C treatment groups. However the relative weights
of thymus in broiler chicken of 0H, 20H and C treatment
groups were similar. e relative weights of spleen of the
birds in 40H, 60H and C group were similar but signi-
cantly higher (p < 0.05) than that of 0H and 20H. e
weights recorded in the birds in 20H were signicantly
higher (p < 0.05) than that of 0H.
4 DISCUSSION
Enhanced levels of serum ALT, AST and LDH are
used as indicators of liver damage (Ozaki et al., 1995). In
the present study, the activity of AST and ALT enzymes
did not follow a consistent trend with the inclusion of
honey in the drinking water of broilers during stress. is
supports the ndings of Hosseini-Vashan et al. (2012)
who reported that turmeric powder depressed AST in
heat stressed broiler due to the antioxidant curcumin
which is a component of the additive. e similarity in
levels of serum albumin and globulin in the birds oered
dierent levels of honey and ascorbic acid in the present
study diers from the ndings of Al-Shanti (2005) who
found that supplementing heat stressed broilers with 1 g
vitamin C/l drinking water had no eect on blood albu-
min and globulin
e present study showed that inclusion of honey at
Parameters
Level of honey and vitamin C
SEM0H 20H 40H 60H Vit C
Body weight (kg) 1.70c2.03b2.05b2.25a2.35a0.077
Liver (%) 2.60a2.03c2.27b2.11c2.05c0.072
Kidney (%) 0.12b0.14b0.16a0.16a0.16a0.006
Lungs (%) 0.54a0.51b0.49bc 0.48cd 0.46d0.010
Heart (%) 0.72a0.42b0.43b0.46b0.46b0.038
Small intestine (%) 3.08a2.73bc 2.87b2.66cd 2.55d0.062
Proventriculus (%) 2.66a2.39b2.44b2.25c2.17c0.058
Empty gizzard (%) 0.25d2.14c2.31b2.44a2.43a0.280
Abdominal fat (%) 1.62 1.58 1.69 1.63 1.58 0.018
Breast meat (%) 17.76b19.10a19.15a17.61b16.95b0.312
igh (%) 18.88a9.15d12.23b11.17c10.72c1.129
Shank (%) 2.73b2.74b2.95b5.08a2.648b0.312
Drum stick (%) 4.53cd 4.74bc 4.93b5.65a4.35d0.153
Tibia (%) 0.788b0.803b0.94a0.88ab 0.87ab 0.020
GIT (%) 15.505c16.66b16.92b18.85a14.93c0.463
Table 5: Eect of dierent levels of honey on the relative weight of organs of broiler chickens at nisher phase during hot-dry season
Preglednica 5: Učinek dodajanja različnih količin medu na relativno maso organov pitovnih piščancev v končni fazi pitanja v vročem in
suhem obdobju
a, b, c Means within a row with dierent superscripts dier signicantly (p < 0.05)
Parameters
Level of honey and vitamin C
SEM0H 20H 40H 60H Vit C
Spleen (%) 0.017c0.029b0.038a0.383a0.039a0.075
ymus (%) 3.082bc 3.867b4.019a3.882ab 3.831b0.035
Bursa (%) 0.560 0.545 0.576 0.562 0.553 0.005
Table 6: Eect of dierent levels of honey on the relative weight of lymphoid organs of broiler chickens at nisher phase during hot-dry
season
Preglednica 6: Učinek dodajanja različnih količin medu na relativno maso limfatičnih organov pitovnih piščancev v končni fazi pitanja
v vročem in suhem obdobju
a, b, c Means within a row with dierent superscripts dier signicantly (p < 0.05)
Acta agriculturae Slovenica, 108/1 – 2016 51
EFFECT OF DIFFERENT LEVELS OF HONEY ON PHYSIOLOGICAL, GROWTH ... OF BROILER CHICKENS DURING DRY SEASON
60 ml/l improved the total serum protein. Similar reports
were obtained by Giurgea et al. (1981) who indicated
that daily administration of propolis extract to chickens
had a signicant eect on the serum. On the contrary,
Al-Shanti (2005) reported that supplementing vitamin C
to the heat-stressed broilers had no eect on blood total
protein. is may be due to the dierence in the strains
of the birds used for the experiment. e decrease in the
serum glucose levels of the birds oered honey at 20 and
40 ml/l and vitamin Cin this trial corroborates the nd-
ings of Hazim et al. (2001) who reported an improve-
ment in the blood glucose level of broiler birds whose
diets were supplemented with ascorbic acid (at 0, 150,
300 and 450 mg / kg diet) during summer months.
e creatine kinase levels of the birds oered honey
was not elevated comapred with the birds oered ordi-
nary water in this study. e lower levels observed in the
birds oered 20 ml/l and vitamin C in the present study
may indicate that honey supplementation did not impair
the function of the kidney. Also the corticosterone lev-
els of broiler chickens supplemented with honey were
lower than in the 0H group. is suggests that addition
of honey up to 60H helped in ameliorating heat stress in
broiler chickens compared to 0H group. is is in agree-
ment with previous studies (Mckee and Hurrison, 1995;
Mahmoud et al., 2004) which reported that the improved
performance resulting from the use of ascorbic acid was
associated with the suppressed stress response indicated
by reduction in plasma corticosterone level. Stressors
such as high environmental temperature induce a cascade
of neural and hormonal events, beginning with hypotha-
lamic stimulation and the production of corticotrophin-
releasing factor, which stimulates the anterior pituitary to
produce adrenocorticotropic hormone, and ending with
stimulation of adrenal cortical tissue by adrenocortico-
tropic hormone to increase the production and release of
corticosteroids, primarily corticosterone in birds (Siegel,
1995). e reduction in the levels of serum corticoster-
one in birds oered varying levels of honey in this study,
implies that addition of honey in the drinking water of
broiler chickens had an ameliorative eect on the birds
and they were able to cope with the hot dry season and to
perform better than the birds in the control group.
e higher body weights recorded in the birds in
60H in the present study are in conformity with the re-
port of Gross (1988) who reported that dietary vitamin
C improved growth performance in broilers. e higher
weights of birds associated with higher dosage of honey
beyond 20 ml in this study suggest that this level con-
tained potent antioxidant which was benecial to the
birds during stress. e present observation is an im-
provement on our previous ndings (Abioja et al., 2010)
where it was reported that there was no signicant dier-
ence in the weights of broiler chickens oered honey up
to 20 ml/l in drinking water. is could therefore be ex-
plained by the fact the doses of honey (20 ml/l of water)
administered in the previous study was not high enough
to cause a positive eect. e higher feed intake observed
in the birds oered dietary vitamin C and honey in the
present study corresponds to the report of Bonomi et al.
(1976) who found an increase in feed intake when propo-
lis was fed to laying hens.
Addition of honey to the drinking water of heat-
stressed birds had no signicant eect on PCV, RBC,
WBC, heterophil, lymphocyte, eosinophil, monocyte,
basophil, MCH, MCV, MCHC, haemoglobin and HL.
e PCV values of all the experimental birds were within
the normal range for chickens (24.9–45.2 %) as reported
by Mitruka et al. (1997). Also all HB, MCV, MCH and
MCHC values of all experimental birds were within the
normal range for chickens (7–13, 90–140, 33–47 and
26–35, respectively).
is study has shown that relative weights of tibia
were improved by addition of honey to the drinking
water of broiler chickens especially at high dose (40H).
is might be adduced to the improvement in calcium
metabolism of the birds. e higher relative weight of
the tibiae is concurrent with the ndings of Abioja et al.
(2012) who observed that addition of honey up to 20 ml/l
of water for broiler chickens improved tibiae weight. e
present study has further validated the fact that a dose
higher than 20 ml/l is benecial to the birds during hot
dry season in Nigeria.
e relative weight of thymus was increased by the
addition of 40 ml honey/l of water. Heat stress has been
reported to inhibit immune functions in chickens (Curca
et al. (2003); Mashaly et al. (2004). Surgical removal of
thymus has been used to demonstrate its immunologic
role (Panigraphi et al., 1971). Ecacy of Sb-Asper-C, a
combined ascorbic acid and acetylsalicylic acid treat-
ment in reducing the eects of heat stress was tested in
broilers by Anwar et al. (2004). e authors reported
that the treatment increased the ratio of thymus to body
weight. e thymus of heat-stressed chickens not supple-
mented with Sb-Asper-C was atrophied. e increase in
the thymus in the present study supports the ndings of
Abioja et al. (2012) that honey up to 20 ml per liter of
water reduces the eect of heat stress on thymus.
Increased liver weight has been regarded as one of
the indices of stress conditions (Puvadolpirod and ax-
ton, 2000). e reduced liver relative weights observed
in the birds oered honey in the present study points to
the fact that the antioxidant content in the honey used in
this study was potent enough to cause change in stress
resistancy. e similarity in the relative liver weights of
Acta agriculturae Slovenica, 108/1 – 2016
52
O. E. OKE et al.
the birds oered vitamin C and honey is an indication
that the use of honey can replace vitamin C during stress.
e gastrointestinal tract is responsive to stressors
(Collins et al., 2012; Dinan and Cryan, 2012). e higher
gastrointestinal relative weights of the birds that were of-
fered honey in this study suggests that inclusion of honey
in the water of the birds ameliorated the eects of heat
stress on birds. is is in accordance with the ndings
of Mitchell and Carlisle (1992) who reported that heat
stress lowered the wet and dry weight of small intestine.
Moreover, Hu et al. (2010) also reported that adminis-
tration of corticosterone lowered small intestinal weight
and shortened small intestinal length in broiler chickens.
5 CONCLUSIONS
Addition of 20H/l of drinking water for broilers may
be useful in ameliorating eects of heat stress as it im-
proved some stress indices (serum glucose, corticoster-
one and creatine kinase), feed intake, body weight gain
and mass of lymphoid organ (spleen). e present study
has also shown that the use of honey may serve as an an-
tioxidant for the replacement of vitamin C during stress
conditions.
6 REFERENCES
Abioja, M. O., Osinowo O. A., Smith O. F., Eruvbetine, D., &
Abiona J. A. (2011). Evaluation of cold water and vitamin C
on broiler growth during hot-dry season in south-western
Nigeria. Archivos De Zootecnia, 60, 1095–1103. doi:10.4321/
S0004-05922011000400025
Abioja, M. O. (2010). Monthly fertility and hatchability of
breeder hens and eects of vitamin C and chilled water
on broiler growth, panting and rectal temperature. esis,
144–145.
Abioja, O. M., Ogundimu, K. B., Akibo, T. E., Odukoya, K.
E., Ajiboye, O. O., Abiona, J. A., Williams, T. J., Oke, O.
E., & Osionowo, A. O. (2012). Growth, Mineral Deposi-
tion, and Physiological Responses of Broiler Chickens Of-
fered Honey in Drinking Water during Hot-Dry Season.
International Journal of zoology, Article ID 403502, pp. 6.
doi:10.1155/2012/403502
Ahmad, T., Sarwar M., Un-Nisa M., Ul-Haq A., & Ul-Hasa, Z.
(2005). Inuence of varying sources of dietary electrolytes
on the performance of broilers reared in a high temperature
environment. Animal Feed Science Technology, 20, 277–298.
doi:10.1016/j.anifeedsci.2005.02.028
Al-Shanti, H. A. (2005). e eect of adding vitamin C, potas-
sium chloride and sodium bicarbonate to the water on the
performance of broiler chicks under Palestinian summer
conditions. Agricultural Science, 17, 63–73.
Amujoyegbe, B. J., Bamire, A. S., & Elemo, K. O. (2008). Agro-
nomic Analysis of Fertilizer Eect on Maize/Cowpea Inter-
crop in Ile-Ife and Abeokuta, South-Western Nigeria. Asset,
Series A, 8, 62–72.
Anwar B., Khan S. A., Maqbool, A., & Khan K. A. (2004). Ef-
fects ofascorbic acid and acetylsalicylic acid supplementa-
tion on the performance of broiler chicks exposed to heat
stress. PakistanVeterinary Journal, 24, 109–111.
Aradas, M. E. C., Naas, I. A., & Salgado, D. D. (2005). Com-
paring thermal environment in broiler housing using two
bird’s densities under tropical conditions. Agricultural En-
gineeringInternational, 7, 1–9.
Armstrong, D. V., Hillman, P. E., Meyer, M. J., Smith, J. F.,
Stokes, S. R., & Harner, J. P. (1999). Heat stress manage-
ment in freestall barns in the western U. S. In Proc. West.
Dairy Manage. Conf., Las Vegas, NV (pp. 87–98). Kansas
State University Agricultural Experiment Station and Co-
operative Extension Service, Manhattan.
Austic, R. E. (1985). Feeding poultry in hot and cold climates.
In M. K. Yousef (Ed.), Stress Physiology in Livestock (Vol. 3.,
pp. 123–136). Boca Raton, FL: CRC Press.
Benjamin, M. M. (1985). Outline of veterinary clinical pathology
(3rd ed.). Ames: e Iowa State Uni. Press.
Bernard, F. F., Joseph, G. Z., & Jain, N. C. (2000). Schalm’s Vet-
erinary Hematology (5th ed.). Philadelphia: Lippincott Wil-
liems and Wilkins.
Bonomi, A., Morletto, F., & Binachi, M. (1976). Propolis in
feeds for laying hens. Avicoltura, 54, 43–54.
Brar, R. S., Sandhu, H. S., & Singh, A. (2002) Veterinary clini-
cal diagnosis by laboratory methods (1st ed.). New Delhi:
Kalyani Publishers.
Charles, D. R. (2002). Responses to the thermal environment.
In D. A. Charles, & A. W. Walker (Eds.), Poultry environ-
ment problems, a guide to solutions (pp. 1–16). Nottingham,
U. K.: Nottingham Univ. Press.
Collins, S. M., Surette, M., & Bercik, P. (2012). e interplay
between the intestinal microbiota and the brain. Nature Re-
views Microbiology, 10, 735–742. doi:10.1038/nrmicro2876
Colowick, S. P., & Kaplan, N. O. (1995). Method of enzymology
(2nd ed., p. 104). New York: Academic press.
Curca, D., Andronie, V., Andronie I. C., & Pop, A. (2004). e
inuence of feed supplementation with acid ascorbic and
sodium ascorbate on broilers, under thermal stress. Book
of abstracts of XXII World’s Poult. Congress WPSA, Istanbul,
Tur key , 290.
Daghir, N. J. (2008). Poultry Production in Hot Climates (2nd ed.,
p. 387). Wallinford, Oxfordshire, UK: CAB International.
doi:10.1079/9781845932589.0000
Darras, V. M., Visser, T. J., Berghman, L. R., & Kuhn, E. R.
(1992). Ontogeny of type I and type III deiodinase activi-
ties in embryonic and posthatch chicken: relationship with
changes in plasma triiodothyronine and growth hormone
levels. Comparative Biochemistry and Physiology, 103A,
131–136. doi:10.1016/0300-9629(92)90252-L
Dinan, T. G. & Cryan, J. F. (2012). Regulation of the stress re-
sponse by the gut microbiota: Implications for psychoneu-
roendocrinology. Psychoneuroendocrinology, 37(9), 1369–
1378. doi:10.1016/j.psyneuen.2012.03.007
Duncan, D. B. (1995). Multiple Range and F tests. Biometrics,
11, 1–42. doi:10.2307/3001478
Giurgea, R. Toma, V., Popesv, H., & Polinicencv, C. (1981). Ef-
Acta agriculturae Slovenica, 108/1 – 2016 53
EFFECT OF DIFFERENT LEVELS OF HONEY ON PHYSIOLOGICAL, GROWTH ... OF BROILER CHICKENS DURING DRY SEASON
fect of standardized propolis extracts on certain blood con-
stituents in chickens. Glujul Med, 54, 151–4.
Gonzalez-Esquerra, R., & Leeson, S. (2006). Physiological and
metabolic responses of broilers to heat implications for
protein and amino acid nutrition. World’s poultry Science
Journal, 62, 282–295. doi:10.1079/WPS200597
Gross, W. B. (1988). Eects of ascorbic acid on the mortality of
leghorn-type chickens due to over-heating. Avian Diseases,
32, 561–562. doi:10.2307/1590930
Hazim, J., Al-Daraji, Al-Mashhadani, E. H., & Al-Athari, A. K.
(2001). Eect of ascorbic acid supplementation in the diets
on haematological traits of Fawbro broiler breeders reared
under hot climate. Indian Journal of Animal Science, 71(9),
857–859.
Hosseini-Vashan, S. J., Golian, A., Yaghobfar, A., Zarban, A.
Afzali, N., & Esmaeilinasab, P. (2012). Antioxidant status,
immune system, blood metabolites and carcass characteris-
tic of broiler chickens fed turmeric rhizome powder under
heat stress. African Journal of Biotechnology, 11, 16118–
16125. doi:10.5897/AJB12.1986
Hu, X. F., Guo, Y. M., Huang, B. Y., Zhang, L. B., Bun, S., Liu,
D., ... Jiao, P. (2010). Eect of Corticosterone Administra-
tion on Small Intestinal Weight and Expression of Small
Intestinal Nutrient Transporter mRNA of Broiler Chick-
ens. Asian-Australian Journal Animal Science, 23, 175–181.
doi:10.5713/ajas.2010.90281
Leeson, S. (1986). Nutritional considerations of poultry dur-
ing heat stress. World’s Poultry Science Journal, 42, 69–81.
doi:10.1079/WPS19860007
Mahmoud, K. Z., Edens, F. W., Eisen, E. J., & Havenstein, G.
B. (2004). Ascorbic acid decreases heat shock protein 70
and plasma corticosterone response in broilers (Gallus
domesticus) subjected to cyclic heat stress. Comparative
Biochemistry and Physiology B, 137, 35–42. doi:10.1016/j.
cbpc.2003.09.013
Mckee, J. S., & Hurrison, P. C. (1995). Eects of supplemental
ascorbic acid on the performance of broiler chickens ex-
posed to multiple concurrent stressors. Poultry Science, 74,
1772–1785. doi:10.3382/ps.0741772
Mitchell, M. A., & Carlisle, A, J. (1992). e eect of chronic ex-
posure to elevated environmental temperature on intestinal
morphology and nutrient absorption in the domestic fowl
(Gullus domesticus). Comparative Biochemistry and Physiol-
ogy, 101A, 137–142. doi:10.1016/0300-9629(92)90641-3
Mitruka, B. M., Rawnsley, H. M., & Vadehra, B. V. (1997). Clini-
cal, biochemical and haematological reference values in nor-
mal experimental animals (p. 272). Masson Publishing USA
Inc.
Ozaki, M., Fuchinoue, S., Teraoda, S., & Ota K. (1995). e in
vivo cytoprotection of ascorbic acid against ischemia/re-
oxygenation injury of rat liver. Archive of Biochemistry and
Biophysis, 318, 439–445. doi:10.1006/abbi.1995.1252
Puvadolpirod, S., & axton, J. P. (2000). Model of physiologi-
cal stress in chickens 1. Response parameters. Poultry Sci-
ence, 79, 363–369. doi:10.1093/ps/79.3.363
Ramnath V., Rekha P. S., & Sujatha, K. S. (2008). Amelioration
of heat stress induced disturbances of antioxidant defense
system in chicken by Brahma Rasayana. Evidence-Based
Complementary and Alternative Medicine, 5(1), 77–84.
doi:10.1093/ecam/nel116
Richards, M. P., Poch, S. M., Coon, C. N., Rosebrough, R. W.,
Ashwell, C. M., & Mcmurtry, J. P. (2003). Feed restriction
signicantly alters lipogenic gene expression in broiler
breeder chickens. Journal of Nutrition, 133, 707–715.
Sayed, A. N., Shoeib, H. A. (1996). Rapid two weeks evaluation
of vitamin C and B-complex and sodium chloride for heat
stressed-stressed broilers. Assiut Veterinary Medical Jour-
nal, 34, 37–42.
Shane, S. M. (1988). Factors inuencing health and perfor-
mance of poultry in hot climates. Crit. Rev. Poultry Biolol-
ogy, 1, 247–267.
Siegel, H. S. (1995). Stress, strains and resistance. British Poultry
Science, 36, 3–22. doi:10.1080/00071669508417748
Stockham, S. L., & Scott, M. A. (2002). Fundamentals of veteri-
nary clinical pathology. Iowa: Iowa State Press, A Blackwell
Publishing Company.
Trinder, P. (1969). Determination of glucose in blood us-
ing glucose oxidase with an alternative oxygen ac-
ceptor. Annals of Clinical Biochemistry, 6, 24–27.
doi:10.1177/000456326900600108
Varley, H., Gowelock, A. H., & Bells, M. (1980). Detemination
of serum urea using the acetyl monoxide method. Practical
biochemistry (5th ed.). London: William Heinemann Medi-
cal Books Ltd.
Wang, J., Jin, G. M., Zheng, Y. M., Li, S. H., & Wang, H. (2005).
Eect of bee pollen on development of immune organ of
animal. Zhongguo Zhong Yao Za Zhi, 30, 1532–1536.
Yahav, S. Mcmurtry, J. P. (2001). ermotolerance acquisition
in broiler chickens by temperature conditioning early in life
– the eect of timing and ambient temperature. Poultry Sci-
ence, 80, 1662–1666. doi:10.1093/ps/80.12.1662
Yalcin, S., Ozkan, S., Turkmut, L., & Siegel P. B. (2001). Re-
sponses to heat stress in commercial and local broiler
stocks. 1. Performance traits. British Poultry Science, 42,
149–152. doi:10.1080/00071660120048375
Yu, B. P. (1994). Cellular defence against damage from reactive
oxygen species. Physiological Review, 74, 139–162.
Zhang G. F., Yang Z. B., Wang Y., Yang W. R., Jiang S. Z., & Gai
G. S. (2009). Eects of ginger root (Zingiber ocinale) pro-
cessed to dierent particle sizes on growth performance,
antioxidant status, and serum metabolites of broiler chick-
ens. Poultry Science, 88, 2159–2166. doi:10.3382/ps.2009-
00165
... One of the most reliable and efficient strategies to close the gap in animal consumption for underdeveloped nations is through poultry farming [5,6]. Poultry products are among the best animal protein sources for feeding the world's population because of their high nutritional content, short production cycle and reasonably low cost of production [7,8]. Animal protein demand and supply gap among Nigerians has continued to widen, resulting in sub-optimal animal protein intake and consequently predisposing the people to animal protein malnutrition [9]. ...
... Natural antioxidants can be found in honey, which makes it a complex substance. Antioxidants are important because they lower free radicals and stop lipid peroxidation which shield cells from reactive oxygen species (ROS) [22,8]. When compared to the conventional synthetic vitamin C, honey is more widely available, particularly for farmers in the rural areas. ...
... An excellent example of a naturally occurring item that contains phytochemicals is honey. It also contains enzymes, glucose oxidase, catalase, pantothenic acid, thiamine, riboflavin, pyridoxine and peroxidase [8]. Although research has been done on the utilization of vitamin C and honey, there is still a dearth of knowledge regarding the use of vitamin C and honey in Awka, Anambra State, for raising broilers and preventing extreme heat exhaustion. ...
Article
Full-text available
Most African countries experience the challenge of food shortage, primarily protein from animal origin. The current research was conducted to examine the effect of honey and vitamin C on the growth performance of broiler chickens. This study employed sixty broiler chickens that were four weeks old which were assigned to four dietary treatments.Treatment 1 was assigned to broilers in cage A which contained no honey and no vitamin C (Control) in their drinking water. Treatment 2 was assigned to broilers in cage B which contained only 5 ml of honey (H). Treatment 3 was assigned to broilers in cage C which contained only 100 mg of vitamin C (C). Treatment 4 was assigned to broilers in cage D which contained 5 ml of honey and 100 mg of vitamin C (HC). This study lasted for 10 weeks and the following parameters were monitored: weight gain and feed intake. The data collected were subjected to analysis of variance at 5% significant level. The result of this study revealed that the highest feed intake (P<0.05) was recorded in the broilers on Treatment 4 (4182.67 g) followed by those in Treatment 3 (4044.33 g), while the least feed intake was recorded in Treatment 1 (2096.67 g). Broilers on Treatment 4 gained the most weight (2013.333g), whereas those on Treatment 1 gained the least (1422.00g). The broilers in Treatment 4 had the highest specific growth rate (10.84g%/day), whereas Treatment 1 had the lowest (10.33g%/day). The highest feed conversion ratio was recorded in the broilers on Treatment 1 (1.49) while the least was recorded in Treatment 3 (2.50). There was significant difference (P<0.05) among the feed conversion ratio of broiler chicks given the four treatments after 10 weeks. It was concluded that it is better to use a combination of 5 ml honey and 100 mg vitamin C than using honey and vitamin C separately to improve the growth performance of broiler chickens.
... Following digestion, samples were allowed to cool at room temperature. Contents of calcium (Ca), magnesium (Mg), sodium (Na), zinc (Zn), iron (Fe), potassium (K) and phosphorus (P) in the digested samples were determined as described by Oyegunle et al. (2016) using atomic absorption spectrophotometry. All data obtained were statistically analysed by the General Linear Model procedures of SAS (2002) and means, where significant, were separated using Duncan Multiple Range Test. ...
Article
This study was carried out to evaluate the effect of supplemental threonine on the performance, physiological response, bone morphometry and bone minerals of Arbor Acres broiler chickens. One hundred and sixty (160) unsexed birds were randomly divided into four treatments. Each treatment had 4 replicates with each replicate having 10 birds. Thr1 (0 mg/kg), Thr2 (250 mg/kg), Thr3 (500 mg/kg) and Thr4 (750 mg/kg). Growth performance, physiological and bone health parameters were collected using standard protocols. Thr3 resulted in higher (P<0.05) final weight (2397.56g) compared to Thr1 (2322.08g), Thr2 (2327.04g) and Thr4 (2302.93g). Rectal temperature in Thr1 (42.76 0C) was significantly elevated (P<0.05) compared to Thr2 (42.58 0C), Thr3 (42.55 0C) and Thr4 (42.58 0C). Elevated respiratory rate (101.94 breaths/minute) and heart rate (216.92 beats/minute) were observed in Thr4. All bone minerals were significantly elevated (P<0.05) in Thr3. Density of the right femur in Thr2 (1.05) was higher (p<0.05) than that of Thr1 (0.09). Seedor index was also higher (p<0.05) in Thr1 (0.21) compared to Thr2 (0.18), Thr3 (0.17) and Thr4 (0.19). Thickness of left posterior epiphysis was significantly reduced (p<0.05) in Thr2 (11.10mm) compared to Thr3 (14.62mm) and Thr4 (15.04mm). The right anterior epiphysis was also influenced (p<0.05), Thr3 (13.00mm) and Thr4 (12.82mm) were thicker than Thr1 (8.46mm). The right posterior epiphysis had it width thicker (p<0.05) in Thr3 (16.07mm) compared to Thr1 (12.24mm). The study concluded that supplementing threonine at 500mg in diet of broilers improved the physiological status of the birds which in turn enhanced growth, thermo-response and bone health.
... Moreover, in ovo feeding of chickens with extracts from numerous plant products has enhanced their defenses against the contagious bursal virus, avian influenza virus, and fowl pox virus (Sood et al., 2013;Nyandoro et al., 2014) The antioxidant level of the chicken embryo may be enhanced by in ovo injection of antioxidants because they have an effective defense against free radicals (Salary et al., 2014). Recently, attention has been shifted to the use of herbal additives as growth promoters and antioxidant components from herbs, spices, and their products (Oke et al., 2016;Oke et al., 2017;Oke, 2018;Voemesse et al., 2019;Tokofai et al., 2020;Kpomasse et al., 2021;Adjei-Mensah et al., 2022;Kpomasse et al., 2023). ...
... Sustainable feed sourcing and formulations can help minimize the environmental impact of broiler production (Ajayi et al., 2022;Oke et al., 2016;Oke et al., 2017;Oke et al., 2021b;Tallentire et al., 2018). Incorporating locally available feed ingredients, such as insect meal, algae and by-products, can reduce the dependence on resourceintensive feed ingredients and promote circular economy practices . ...
Article
Full-text available
Climate change has emerged as a significant occurrence that adversely affects broiler production, especially in tropical climates. Broiler chickens, bred for rapid growth and high meat production, rely heavily on optimal environmental conditions to achieve their genetic potential. However, climate change disrupts these conditions and poses numerous challenges for broiler production. One of the primary impacts of climate change on broiler production is the decreased ability of birds to attain their genetic potential for faster growth. Broilers are bred to possess specific genetic traits that enable them to grow rapidly and efficiently convert feed into meat. However, in tropical climates affected by climate change, the consequent rise in daily temperatures, increased humidity and altered precipitation patterns create an unfavourable environment for broilers. These conditions impede their growth and development, preventing them from reaching their maximum genetic influence, which is crucial for achieving desirable production outcomes. Furthermore, climate change exacerbates the existing challenges faced by broiler production systems. Higher feed costs impact the industry's economic viability and limit the availability of quality nutrition for the birds, further hampering their growth potential. In addition to feed scarcity, climate change also predisposes broiler chickens to thermal stress. This review collates existing information on climate change and its impact on broiler production, including nutrition, immune function, health and disease susceptibility. It also summarizes the challenges of broiler production under hot and humid climate conditions with different approaches to ameliorating the effects of harsh climatic conditions in poultry.
... Lempuyang mengandung minyak atsiri yang meningkatkan penyerapan nutrisi dan sistem kekebalan tubuh ayam pedaging (Risa et al., 2014;Alfian et al., 2015). Madu memiliki aktivitas antibakteri dan antioksidan (Oke et al., 2016). Oleh karena itu, diperlukan penelitian untuk mengetahui konsentrasi efektif jamu kombinasi jahe, temulawak, lempuyang, dan madu yang mampu memperbaiki performa tanpa mengubah profil organ dan organoleptik daging ayam. ...
Article
Penggunaan antibiotic growth promoters (AGP) dapat menyebabkan residu antibiotik dan resistansi mikroorganisme sehingga dilarang oleh pemerintah. Jamu adalah ramuan herbal Indonesia yang dapat digunakan sebagai upaya alternatif dalam mengatasi masalah tersebut. Penelitian ini bertujuan untuk menentukan konsentrasi efektif jamu kombinasi jahe, temulawak, lempuyang, dan madu dalam memperbaiki performa dan profil organ ayam pedaging/broiler tanpa mengubah organoleptik daging. Penelitian menggunakan 36 ekor day old chick (DOC) strain Cobb yang dipelihara sampai umur 32 hari. Penelitian menggunakan rancangan acak lengkap dengan perlakuan penambahan jamu kombinasi dalam air minum sebanyak 0% (kontrol), 1,25% (P1), 2,5% (P2), dan 5% (P3). Peubah yang diamati meliputi performa (konsumsi pakan dan air minum, pertambahan bobot badan, bobot akhir, bobot karkas, bobot lemak abdominal, feed conversion ratio (FCR), indeks performa (IP), mortalitas) dan profil organ (bobot hati, jantung, paru-paru, limpa, serta bobot dan panjang duodenum, jejunum, ileum) ayam pedaging yang diikuti dengan uji organoleptik terhadap daging ayam. Hasil penelitian menunjukkan bahwa P1, P2, dan P3 secara nyata (p<0.05) dapat meningkatkan bobot akhir dan pertambahan bobot badan. Bobot karkas, bobot lemak abdominal, FCR, IP, mortalitas, serta profil organ tidak memperlihatkan perbedaan nyata (p>0.05) antar ayam perlakuan dan kontrol. Penelitian menunjukkan bahwa jamu kombinasi jahe, temulawak, lempuyang, dan madu dengan konsentrasi 5% dapat memperbaiki performa tanpa merubah profil organ ayam pedaging dan organoleptik daging ayam.
... The antioxidant level of the chicken embryo may be enhanced by in ovo injection of antioxidants because they have an effective defense against free radicals (Salary et al., 2 Akosile et al. 2014). Recently, attention has been shifted to the use of herbal additives as growth promoters and antioxidant components from herbs, spices, and their products due to their benefits (Oke et al., 2016(Oke et al., , 2017Oke, 2018;Voemesse et al., 2019;Tokofai et al., 2020;Kpomasse et al., 2021Kpomasse et al., , 2023Adjei-Mensah et al., 2022). With the growing interest in the use of in ovo phytobiotics, it is crucial to have a thorough understanding of the potential of in ovo feeding of phytobiotics as a method of nutrient delivery during the crucial stages of incubation, hatching events, and posthatch performance and the challenges associated with it to use the technique in poultry production effectively and efficiently and advance research in this area. ...
Article
Full-text available
Hatchery’s goals include maximizing revenue by achieving high hatchability with day-old birds of excellent quality. The advancement of technology has benefited the poultry sector since breeding and genetics technology have increased the rates of meat maturation in developing birds in a short period of time. Excessive use of in-feed antibiotics has been shown in studies to increase the chance of resistance to human infections. Bacterial resistance and antibiotic residues in animal products raised concerns about using antibiotics as growth promoters, eventually leading to a prohibition on using in-feed antibiotics in most industrialized nations. In ovo technology is a novel method for delivering bioactive chemicals to developing avian embryos. In ovo feeding technologies may provide additional nutrients to the embryos before hatching. The introduction of bioactive compounds has the potential to assist in decreasing and eventually eliminating the problems associated with traditional antibiotic delivery in chicken production. Phytobiotics were advocated as an alternative by researchers and dietitians. So far, several studies have been conducted on the use of phytogenic feed additives in poultry and swine feeding. They have primarily demonstrated that phytobiotics possess antibacterial, antioxidant, anti-inflammatory, and growth-stimulating properties. The antioxidant effect of phytobiotics can improve the stability of animal feed and increase the quality and storage duration of animal products. In general, the existing documentation indicates that phytobiotics improve poultry performance. To effectively and efficiently use the in ovo technique in poultry production and advance research in this area, it is important to have a thorough understanding of its potential as a means of nutrient delivery during the critical stage of incubation, its effects on hatching events and posthatch performance, and the challenges associated with its use. Overall, this review suggests that in ovo feeding of phytobiotics has the potential to improve the antioxidant status and performance of chickens.
... To ameliorate the negative impact of thermal stress, promote consumer health and save the environment, researchers have been inspired to investigate a number of PFA that could be employed in poultry diets Bouassi et al., 2021). These additives comprise PFA, immunomodulators, enzymes, phytoncides and organic acids (Bouassi et al., 2021;El-Saadony, Alagawany, et al., 2021;Oke et al., 2016Oke et al., , 2017Tokofai et al., 2020Tokofai et al., , 2021Voemesse et al., 2019), essential oils , herbal extracts (Oke, 2018;Oke, Uyanga, et al., 2021), bioactive medicinal plants , bioactive peptides (El-Saadony, Abd , probiotics , natural pigments , green synthesized nanoparticles (El-Saadony, Abd El-Hack, et al., 2021b), amino acids (Abou-Kassem et al., 2021), prebiotics (Abd El-Hack, El-Saadony, Shafi, et al., 2022 and phytogenic compounds . Various plants' extract, including herbs, spices and others, are being investigated as potential synthetic antioxidant substitutes. ...
Article
Full-text available
The increase in global temperature and consumers' welfare has increased the use of phytogenic feed additives (PFA) to mitigate the negative effects of heat stress on chickens in recent years. Various bioactive compounds capable of improving the thermotolerance of broiler chickens during exposure to thermal challenges have been identified in different plant species and parts. This review is an overview of the roles of bioactive compounds of different PFA, such as polyphenols and flavonoids, antioxidants, growth-promoting and immune-modulating agents, in heat stress management in broiler chickens. Common PFA in use, particularly in tropical environments, are also discussed. An understanding of the roles of the PFA in chickens' thermotolerance could further stimulate interest in their use, thereby improving the birds' productivity and addressing consumers' concerns. This review collates the existing data on the roles of herbs in mitigating heat stress on chickens and highlights future research perspectives.
... Chemically, it is composed of simple sugars (fructose, glucose), minerals (calcium, phosphorus), vitamins (ascorbic acid, riboflavin), enzymes, organic acids (gluconic, butyric), and flavonoids as well as other phenolic and aromatic substances (Alvarez-Suarez 2017). Due to its nutritional and therapeutic properties, honey is considered as an important drinking water additive for poultry (Abioja et al. 2012;Babaei et al. 2016;Oyegunle et al. 2016). The supplementation with honey into the drinking water (20-60 g. ...
Article
The quality and safety attributes of poultry products have been attracting increasing attention and interest from the scientific communities as well as the public worldwide. Recently, nutraceuticals, as natural and safe alternatives to synthetic and artificial chemical drugs such as antibiotics, are used in several poultry farms (˃65%) for producing organic products (0% drugs). Nutraceuticals, such as organic acids (amino acids and fatty acids), herbal products (black cumin and fenugreek), and honeybee products (bee pollen and bee venom), are natural substances. They were added to poultry diets (1–3%) as a source of nutrition and to provide health benefits for birds. In addition, they have several biological functions in the bird’s body and may help birds to enhance their well-being. These supplements can increase the body weight of broilers and the egg production of hens by approximately 7% and 10%, respectively, as well as, enhance meat and eggs quality (˃30%). Moreover, they can improve the semen quality of roosters (ejaculate volume, advanced motility, live sperms, concentrate per ejaculate) by an average of 25%. Previous literature on the main biological activities performed by nutraceuticals has shown that most studies have only focused on the concept of using nutraceuticals as growth promoters, anti-inflammatory and anti-bacterial agents. In the current review, critical effects/functions of the use of nutraceuticals, as natural and safe alternative feed additives in poultry farms, such as antioxidants, sexual-stimulants, immuno-stimulants, and for producing healthy products were discussed.
Article
Full-text available
Oxidative stress (OS) is a major concern that impacts the overall health of chickens in modern production systems. It is characterized by an imbalance between antioxidant defence mechanisms and the production of reactive oxygen species (ROS). This literature review aims to provide a comprehensive overview of oxidative stress in poultry production, with an emphasis on its effects on growth performance, immune responses, and reproductive outcomes. This review highlights the intricate mechanisms underlying OS and discusses how various factors, including dietary components, genetic predispositions, and environmental stressors can exacerbate the production of ROS. Additionally, the impact of oxidative stress on the production performance and physiological systems of poultry is examined. The study also emphasizes the relationship between oxidative stress and poultry diseases, highlighting how impaired antioxidant defenses increase bird's susceptibility to infections. The review assesses the existing approaches to reducing oxidative stress in chickens in response to these challenges. This includes managing techniques to lower stress in the production environment, antioxidant supplements, and nutritional interventions. The effectiveness of naturally occurring antioxidants, including plant extracts, minerals, and vitamins to improve poultry resistance to oxidative damage is also examined. To improve the antioxidant defenses of poultry under stress conditions, the activation of cellular homeostatic networks termed vitagenes, such as Nuclear Factor Erythroid 2-Related Factor 2 (Nrf2) is necessary for the synthesis of protective factors that can counteract the increased production of ROS and RNS. Future studies into novel strategies for managing oxidative stress in chicken production would build on these research advances and the knowledge gaps identified in this review.
Article
Full-text available
Heat stress is a threat that can lead to significant financial losses in the production of poultry in the world’s tropical and arid regions. The degree of heat stress (mild, moderate, severe) experienced by poultry depends mainly on thermal radiation, humidity, the animal’s thermoregulatory ability, metabolic rate, age, intensity, and duration of the heat stress. Contemporary commercial broiler chickens have a rapid metabolism, which makes them produce higher heat and be prone to heat stress. The negative effect of heat stress on poultry birds’ physiology, health, production, welfare, and behaviors are reviewed in detail in this work. The appropriate mitigation strategies for heat stress in poultry are equally explored in this review. Interestingly, each of these strategies finds its applicability at different stages of a poultry’s lifecycle. For instance, gene mapping prior to breeding and genetic selection during breeding are promising tools for developing heat-resistant breeds. Thermal conditioning during embryonic development or early life enhances the ability of birds to tolerate heat during their adult life. Nutritional management such as dietary manipulations, nighttime feeding, and wet feeding often, applied with timely and effective correction of environmental conditions have been proven to ameliorate the effect of heat stress in chicks and adult birds. As long as the climatic crises persist, heat stress may continue to require considerable attention; thus, it is imperative to explore the current happenings and pay attention to the future trajectory of heat stress effects on poultry production.
Article
Full-text available
An experiment was conducted to determine whether ascorbic acid (AA) increases resistance of female Hubbard x Hubbard broiler chicks to multiple concurrent stressors. Stressors imposed from 10 to 17 d posthatch included 2 x 2 x 2 factorial combinations of beak trimming [(B), sham-operated or beak-trimmed and cauterized], coccidiosis [(C), gavage with 0 or 3 x 10(5) sporulated Eimeria tenella oocysts], and heat stress [(H), 28 vs 33 C]. A starter diet was supplemented with AA to provide 0, 150, or 300 ppm (milligrams per kilogram). This resulted in a 2 x 2 x 2 x 3 factorial design with two six-chick replicates of each of the 24 treatment combinations. Data were analyzed using ANOVA and a level of 95% significance. Ascorbic acid increased feed intake and lowered plasma corticosterone and heterophil:lymphocyte ratios. Heat depressed weight gain and feed intake and elevated heterophil:lymphocyte ratios. Heat and AA interacted to improve weight gain and feed intake and lower heterophil:lymphocyte ratios. Coccidiosis depressed weight gain, feed efficiency, and heterophil:lymphocyte ratios. Coccidiosis and AA interacted to increase feed intake and lower plasma corticosterone and heterophil: lymphocyte ratios. Beak trimming increase heterophil:lymphocyte ratios. Beak trimming and AA interacted to increase feed intake and lower heterophil: lymphocyte ratios. Weight gain and feed efficiency decreased whereas heterophil:lymphocyte ratios increased linearly in unsupplemented birds as a function of stressor "order" (the number of stressors imposed simultaneously) indicating an additive effect of systematically increasing the number of stressors. No changes in feed efficiency or heterophil:lymphocyte ratios were detected as a function of stressor order when AA was provided. Ascorbic acid reduced the slope of the regression equation describing the relationship between weight gain and stressor order. It was concluded that AA, particularly at 150 ppm, enhanced performance of broiler chicks exposed to multiple concurrent environmental stressors.
Article
Full-text available
The effects of corticosterone (CORT) administration on the weight of small intestine and the expression of nutrient transporter mRNA in the small intestine of broiler chickens (Gallus gallus domesticus) were investigated. One hundred and eight sevenday-old birds were randomly divided into two equal groups comprising a control group (CTRL) and an experimental group (CORT). CTRL birds were fed a basal diet and the CORT birds were fed a basal diet containing 30 mg corticosterone/kg from d 8 to 21. At 21 d of age, average daily feed intake (ADFI), serum corticosterone level, small intestinal absolute wet weight and relative weight, and relative abundance of SGLT1, CaBP-D28k, PepT1 mRNA in the duodenum and L-FABP mRNA in the jejunum were determined. The results showed that serum corticosterone level, liver weight and small intestinal relative weight (small intestinal wet weight/body weight) of CORT chickens were about 30.15%, 26.72% and 42.20% higher, respectively, than in the CTRL group (p
Article
The intestinal microbiota consists of a vast bacterial community that resides primarily in the lower gut and lives in a symbiotic relationship with the host. A bidirectional neurohumoral communication system, known as the gut-brain axis, integrates the host gut and brain activities. Here, we describe the recent advances in our understanding of how the intestinal microbiota communicates with the brain via this axis to influence brain development and behaviour. We also review how this extended communication system might influence a broad spectrum of diseases, including irritable bowel syndrome, psychiatric disorders and demyelinating conditions such as multiple sclerosis.