By Adu, OA (2022).
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Greener Journal of
Agricultural Sciences Vol. 12(1), pp. 62-68, 2022 ISSN: 2276-7770 Copyright ©2022, the copyright of this article is
retained by the author(s) |
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Performance and haematoserological influence of black and alligator
peppers and their composite mix in broiler chickens
Department of Animal
Production and Health, School of Agriculture and Agricultural Technology,
Federal University of Technology, Akure, P.M.B. 704, Ondo state, Nigeria.
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ARTICLE
INFO |
ABSTRACT |
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Article No.: 012522007 Type: Research |
Background: The experiment was
carried out to assess the influence of varying inclusions of black pepper, alligator
pepper and their composite mix on the performance, haematology
and serum biochemical components of broiler chickens. Methods: Two hundred and ten
(210) day old mixed sex Cobb 500 broiler chicks were allocated to diets
containing 0.25 and 0.50 g/kg each of black pepper, alligator pepper and
their composite mix tagged treatments: B and C, D and E, F and G representing
0.25 and 0.50 g/kg black pepper, alligator pepper and the composite mix
respectively. Treatment A was the control/basal diet. Each treatment was
further divided 3 times with 10 birds per representative group. The birds
received the experimental diets and water ad libitum for 6 weeks (42 days). The initial and final weight
gain as well as the feed intake were captured and recorded to determine the
feed efficiency. At 42nd day, 5 birds per experimental sub-group were
selected randomly and blood collected from the jugular veins for
determination of haematological and serum
biochemical indices. Results: The total weight gain,
feed intake and feed conversion ratio of the broilers fed black and alligator
peppers and their composite were significantly (P < 0.05) better than the
bird on the control diet. However, the phyto-additive
did not have a significant (P > 0.05) influence on the haematological
parameters of the birds when compared with the control. There was a
significant (P < 0.05) reduction in the serum cholesterol and blood
alkaline phosphatase concentrations while the serum total protein was
significantly (P < 0.05) increased. Conclusion: Overall, the phytogens individually improve the performance and haematoserological components of the birds but the
composite mix had better effect on the performance and serological indices of
the broilers. |
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Accepted: 26/01/2022 Published: 22/02/2022 |
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*Corresponding Author Adu Olufemi
Adesanya E-mail: oaadu@futa.edu.ng |
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Keywords: |
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INTRODUCTION
The availability of various medicinal
plants consumed as spices in sub-Saharan African countries is abundant. Among
these plants are black pepper (Piper guineense) and alligator pepper (Aframomum melegueta).
Black and alligator peppers are
reported to be rich in both medicinal and nutritive values (Nosiri
et al., 2013, Uhegbu et al., 2015a). The suitability
of these herbs as medicinal plants is not farfetched from their rich
phytochemical components such as alkaloids, glycosides, tannins, flavonoids,
sterols, triterpenes, and oils which are responsible
for their therapeutic and antimicrobial properties (Okigbo
and Igwe, 2007, Doherty et al., 2010). Previous studies have highlighted the potentials of the seeds of these
spices or
their extracts in alternative medicine. They possess potent antioxidant (Onoja et al., 2014), antibacterial (Ilic
et al., 2010), antidiarrheal (Umukoro and Ashorobi, 2003), anti-inflammatory (Umukoro
and Ashorobi, 2005), antihypercholesterolemic
and blood modulator effects (Adefegha et al., 2017).
Considering the recent
concerns on the extensive use of antibiotics in broiler production (Adu and Olarotimi, 2020), dietary
inclusion of black and alligator peppers could provide a potent alternative in
the management of diseases as well as enhancing the performance of broiler
chickens. Since the blood profiles of an animal forms the basis for determining
its health status and this is directly linked with performance, the effects of
the diets on the haematogical and biochemical
indices, therefore, plays a pivotal role in the overall well
being and the productive performance of the animal. For instance, the
dietary inclusion of alligator pepper meal was discovered to significantly
promote weight gain and recommended for sustainable fish production (Kwankwa et al., 2020). Effiong
and Ochagu (2019) also reported a significant
increase in daily weight gain and feed
conversion ratio of broiler chickens fed diets containing 0.4 % black pepper
seed meal. In another study, Al-Kassie et
al. (2011) included 0.50 to 1.00% of
black pepper in broilers diets and recorded an improved body weight gain, feed
intake and conversion ratio. They also observed a reduced cholesterol, Hb, RBC and H/L ratio concentrations.
On the other hand, black
pepper extracts administered to albino rats at 25 - 75 mg/kg BW was reported to
significantly increase the serum proteins and packed cell volume concentration
while serum cholesterol was significantly reduced (Uhegbu
et al., 2015b). The effects of black pepper on serum enzymes were also recorded
by Uhegbu et al. (2015a). They observed significant
reductions in alanine transaminase, aspartate transaminase and alkaline
phosphatase in female albino rats given aqueous seed extract of black pepper at
5 ml/BW. The red blood cells, white blood cells and hemoglobin concentration of
the rats were significantly increased. Nwozo et al. (2013), in
another their report, also observed a significant decrease in the elevated levels of serum
alanine transaminase and aspartate
transaminase activities of Wistar rats administered
200 to 400 mg/kg BW of alligator pepper. The hypoglycemic effect of alligator
pepper was also documented in previous studies (Akhani
et al., 2004; Al-Amin et al., 2006; Ilic et al.,
2010). The safety of black and alligator peppers was already assured as they
did not have adverse effects on the hematology and blood coagulation, blood
pressure, or heart rate of the animals treated (Weidner and Sigwart,
2000). The aim of the present study is to examine the individualistic and
synergistic effects of these herbal additives on the performance, haematology and serum biochemistry of broiler chickens.
MATERIALS AND
METHODS
Both black and alligator pepper seeds
were sourced and identified at the Universitys herbarium. The seeds were
separated carefully from the twig and all other extraneous materials. The seeds
were air-dried under a shade till a moisture content of 10 -11 % was achieved.
Thereafter, the dried seeds were pulverized into powder to make black pepper
seed powder (BPSP) and alligator pepper seed powder (APSP) using an electric
blender. A total of two hundred and ten
(210) day-old mixed-sexed Cobb 500 broiler chicks were purchased from a
reputable hatchery and used for the experiment at the Poultry Unit of the
Teaching and Research Farm, The Federal University of Technology, Akure. On arrival, they were weighed and randomly assigned
to seven (7) treatments comprising treatments A (control), B (basal + {0.25 g
BPSP/kg}), C (basal + {0.50 g BPSP}/kg), D (basal + {0.25 g APSP}/kg), E (basal
+ {0.50 g APSP}/kg), F (basal + {0.125 g BPSP + 0.125 g APSP}/kg) and G (basal
+ {0.25 g BPSP + 0.25 g APSP}/kg). Each treatment was repeated 3 times with 10
birds per replication in a completely randomized design. Basal broiler starter
and finisher diets (Table 1) were formulated and fed to the birds at 03 weeks
and 4-6 weeks, respectively. The respective total weight gain and feed intake
of the birds were calculated as summations of the weekly weight gains and feed
intake throughout the experimental period.
The feed conversion ratio (FCR) was determined as:
FCR = Total Feed Intake (g)
Total Weight Gain (g)
On the last day of the experiment
(42nd day), five (5) birds per replicate were randomly selected and fasted
overnight. Blood samples were collected through jugular veins puncture and
blood was collected into bottles with EDTA for determination of haematological indices. Another set of blood samples were
collected into dry clean plain centrifuged glass tubes for determination of
serum biochemical parameters. Serum samples were harvested after plain blood
samples were centrifuged for 10 minutes at 3000 rpm. The serum samples were
used for the determination of serum enzymes [alanine transaminase (ALT),
aspartate transaminase (AST) and alkaline phosphatase (ALP)], cholesterol and
proteins [total protein (TP), globulin (GLB) and albumin (ALB)]. The haematological indices determined were packed cell volume
(PCV), haemoglobin concentration (Hb),
red blood cell counts (RBC), Mean corpuscular volume
(MCV), mean corpuscular hemoglobin (MCH) and mean corpuscular hemoglobin
concentration (MCHC) and white blood cell counts (WBC). The WBC differential
counts (granulocytes, lymphocytes and monocytes) were equally determined.
Table 1:
Ingredients Composition of the Experimental Diets
|
Ingredients |
Starter |
Finisher |
|
Maize |
51.00 |
50.00 |
|
Soybean meal |
15.00 |
13.00 |
|
Groundnut cake |
15.00 |
13.00 |
|
Fish Meal (72%CP) |
5.00 |
0.00 |
|
Rice Bran |
0.00 |
13.30 |
|
Corn bran |
10.60 |
6.00 |
|
Bone Meal |
1.50 |
2.50 |
|
Limestone |
1.00 |
1.00 |
|
Salt |
0.35 |
0.35 |
|
Lysine |
0.10 |
0.30 |
|
Methionine |
0.20 |
0.30 |
|
Broiler Premix |
0.25 |
0.25 |
|
Total |
100.00 |
100.00 |
|
Calculated Nutrients |
|
|
|
ME (Kcal/Kg) |
2985.82 |
2964.16 |
|
Crude Protein (%) |
22.60 |
18.56 |
|
Calcium (%) |
1.28 |
1.24 |
|
Phosphorus (%) |
0.52 |
0.56 |
|
Lysine (%) |
1.15 |
1.08 |
|
Methionine (%) |
0.56 |
0.57 |
|
Crude Fibre (%) |
3.68 |
4.85 |
Statistical Analyses
All data collected were subjected to
One-Way analysis of variance (ANOVA) using SAS (2008) version 9.2. Duncan
Multiple Range Test of the same software was used for means comparison where
significant differences existed.
RESULTS AND
DISCUSSION
The results of the performance of the
birds fed different experimental diets are in Table 2. There was an increase in
the total weight gain (TWG) among the birds fed diet containing 0.25 g/kg BPSP
(Diet B) though not significantly (P > 0.05) different from the weights of
the birds on the control diet (Diet A). However, doubling the inclusion rate of
BPSP to 0.50 g/kg diet (Diet C) significantly (P < 0.05) increased the TWG
of the birds when compared with the birds on the control diet. Furthermore, the
inclusions of 0.25 and 0.50 g/kg APSP significantly (P < 0.05) increased the
TWG among the birds on diets D and E when compared with the birds on the
control diet. The composite mix of BPSP and APSP at 0.25 and 0.50 g/kg equally
significantly (P < 0.05) increased the TWG of the birds when compared with
the broilers on the control diet. The TWG recorded among the birds fed the
composite mix was far better than the weights by the birds on all other diets
with birds fed 0.50 g/kg BPSP-APSP mix recording the higher significant (P <
0.05) means when compared with birds on either of the phyto-additives.
The total feed intake (TFI) of the birds on the two phyto-additives
were significantly (P < 0.05) higher than that of the birds on the control
diet. However, the varying inclusions of the composite mix in the diet further enhanced
the TFI of the birds on diets F and G with the broilers on diet G recording the
higher significant (P < 0.05) TFI when compared with birds on other diets.
For the feed conversion ratio (FCR), the phyto-additives
positively influenced the FCR. The inclusion of 0.25 g/kg BPSP did not
significantly (P > 0.05) enhance the FCR unlike the inclusion of 0.50 g/kg
where a significant (P < 0.05) reduction in FCR was recorded. Both the
inclusions of 0.25 and 0.50 g/kg APSP in the diet significantly (P < 0.05)
improved the FCR of the birds when compared with the control. However, broilers
on diets F and G (0.25 and 0.50 g/kg composite mix) presented the best (P <
0.05) FCR.
The improved TWG, FI and
FCR recorded among the birds fed the varying inclusions of the phytogens could be as a result of the antioxidant
properties of black and alligator peppers. Antioxidants have been credited with
having the potentials to positively enhance the performance of poultry birds (Biswas et al 2011). The improved TWG, FI and FCR among the
birds fed diets containing varying inclusions of the phytogens
and their composite indicated that broilers were able to covert feed to muscles
when fed diets supplemented with phytogenic additives. Weight gain, feed intake
and feed conversion ratio are usually the most reliable yardsticks considered
in the measurement of the productivity of diets fed to broiler chickens. The
enhanced performance recorded in all treatments was indicative that broilers
would perform well on diets containing black and alligator peppers at the
inclusion rates of 0.25 to 0.50 g/kg diet. It also indicated that the best
performance could be obtained by feeding the composite mix of the two phytogens as they conferred synergistic effects on the
birds. The excellent performance
recorded by the individual phytogen and their
composite could be due to their rich bioactive components such as tannin,
alkaloid, phytate and saponins.
These phytochemicals were previously explained to increase the growth
performance of animals (Enemor et al., 2014). The finding in the
present study justified the claims of previous studies which documented
improved performances in different classes of livestocks
fed black and alligator peppers (Al-Kassie et al.,
2011, Effiong and Ochagu,
2019, Kwankwa et al., 2020).
The results of the haematological indices of the broilers fed different levels
of the two phytogenic compounds and their composite are in Table 3. From this
study, the haemogram, white blood cell counts and the
differentials were not significantly (P > 0.05) influenced by the inclusions
of the phytogens and their composite. The serum
biochemical indices results of the broilers are equally displayed in Table 4.
It was observed that the serum cholesterol concentration of the birds on the
control diet was significantly (P < 0.05) higher than the cholesterol
concentrations recorded by the birds on all other diets except diet B where a
non-significant (P < 0.05) reduction in cholesterol concentration was
recorded. For the serum enzymes, the inclusions of varying amounts of the phytogens significantly (P < 0.05) lowered serum
concentration of ALP except among the birds fed diet containing 0.25 g/kg BPSP
where there was no statistical (P > 0.05) difference between their ALP
concentration and that of the birds on the control diet. The serum total
protein concentrations of the birds fed varying inclusions of the phytogenic
compounds were significantly (P < 0.05) enhanced when compared with the
birds on the control diet. However, the globulin and albumin concentrations of
the birds were not significantly (P > 0.05) different from what were
recorded by the control birds.
The non-significant
influence recorded in the haematological indices
among birds fed the varying inclusions of the phytogens
and their composite indicated that the health status of the birds was not
compromised. The various haematological indices
studied were within their standard haemtological
reference values range. For instance the haematological
values recorded in this study were within the reference values of RBC (2.0
4.0 x 106mm3), Hb (7.0 13.0
g/dl), PCV (25 45%), MCV (90 140 fl), MCH (33
47 pg) and MCHC (26 35 g/dl) (Harrison and
Lightfoot, 2005). Furthermore, the consistence in white blood cells (WBC)
differential counts recorded across all the treatment diets in this study
showed that the dietary inclusions of the phytogens
and their composite had no significant effect on lymphocyte, monocytes, heterophil, eosinophil, and basophil when compared with
birds on the control diet. This indicated that the birds immunity was not
compromised but rather enhanced. The present study gave credence to the fact
that black and alligator peppers and their composite were safe as phyto-additives in broiler nutrition as previously stated
that they did not have adverse effects on the hematology of farm animals
(Weidner and Sigwart, 2000).
The increased transaminase
in the bloodstream is always linked with hepatocellular damage. Hence, the
insignificant differences recorded in ALT and AST in this study pointed to the
fact that the phytogens and their composite at the
inclusion rates used were not inimical to the livers of the birds. However, the
significant reduction in the serum ALP observed indicated that these phytogens and their composite could be useful in lowering
increased blood concentration of the enzyme which pointed to the therapeutic
effect of these phytogens. This study confirmed the
findings of Nwozo et al. (2013) and Uhegbu et al. (2015a) who documented a significant
reduction in the elevated levels of serum transaminase activities of animals
administered alligator pepper and black pepper respectively. The hypoglycemic
effect of these phytogens and their composites were
clearly illustrated in this study as the birds on the control diet had the
highest serum cholesterol. This agreed with previous reports on the
hypoglycemic potentials of both black and alligator peppers (Uhegbu et al., 2015b, Ilic et
al., 2010). The non-significant difference observed in
the GLB and ALB in this study indicated that the inclusion of the phytogens and their composite did not interfere with
protein metabolism in the liver of the birds. However, the increased total
protein was suggestive that inclusion of these phytogens
enhances protein synthesis in the liver of the animals which agreed with the
report of Uhegbu et al. (2015b).
Table 2: Performance of Broilers fed
Diets Containing BPSP, APSP and their Composite
|
Parameters |
A |
B |
C |
D |
E |
F |
G |
SEM |
P-Values |
|
IBW |
33.00 |
33.12 |
33.08 |
31.99 |
34.20 |
33.09 |
33.14 |
1.00 |
0.19 |
|
TWG |
2600c |
2800bc |
2900b |
2958b |
2890b |
3270ab |
3490a |
110 |
0.03 |
|
TFI |
3500c |
3600b |
3600b |
360ab |
3611b |
3635ab |
3650a |
140 |
0.01 |
|
FCR |
1.35a |
1.29ab |
1.24b |
1.22b |
1.25b |
1.11c |
1.05c |
0.06 |
0.01 |
Means in a
row without a common superscript letter differ (P<0.05) significantly. IBW = Initial Body Weights, TWG =
Total Weight Gain, TFI = Total Feed Intake, FCR = Feed Conversion Ratio. Diets: A (Control/Basal), B (Basal + 0.25 g BPSP/kg diet), C
(Basal + 0.50 g BPSP/kg diet), D (Basal + 0.25 g APSP/kg diet), E (Basal + 0.50
g APSP/kg diet), F (Basal + 0.25 g BPSP-APSP Mix/kg diet), G (Basal + 0.50 g
BPSP-APSP Mix/kg diet).
Table 3: Haematology
of Broilers fed Diets Containing BPSP, APSP and their Composite
|
Parameters |
A |
B |
C |
D |
E |
F |
G |
SEM |
P-Value |
|
PCV (%) |
40.00 |
38.00 |
35.00 |
39.00 |
37.00 |
34.00 |
37.00 |
2.80 |
1.21 |
|
RBC (x106 mm3) |
4.00 |
3.51 |
3.92 |
4.50 |
3.60 |
4.11 |
5.02 |
0.83 |
0.56 |
|
MCHC (g/dl) |
33.00 |
33.00 |
32.00 |
33.00 |
32.00 |
32.00 |
32.00 |
0.62 |
1.18 |
|
MCV (fl) |
100.00 |
110.00 |
95.00 |
89.00 |
100.00 |
87.00 |
80.00 |
17.00 |
0.92 |
|
MCH (pg) |
33.00 |
37.00 |
32.00 |
30.00 |
35.00 |
29.00 |
27.00 |
5.64 |
1.51 |
|
Hb (g/dl) |
13.00 |
13.00 |
12.00 |
13.00 |
12.00 |
11.00 |
12.00 |
0.94 |
0.35 |
|
WBC (x109/l) |
2.91 |
2.90 |
3.11 |
2.52 |
3.90 |
2.33 |
2.11 |
0.91 |
0.26 |
|
GRA (x109/l) |
0.95 |
1.04 |
1.21 |
0.85 |
1.32 |
0.90 |
0.89 |
0.32 |
1.45 |
|
LYM (x109/l) |
1.90 |
1.90 |
1.88 |
1.64 |
2.51 |
1.44 |
1.23 |
0.66 |
1.69 |
|
MON (x109/l) |
0.04 |
0.02 |
0.04 |
0.03 |
0.05 |
0.02 |
0.02 |
0.02 |
1.11 |
Values are means and SEM (Standard
Error of Means). Means in a
row without a common superscript letter differ significantly (P<0.05). PCV = Packed Cell Volume,
RBC = Red Blood Cells, MCHC = Mean Corpuscular Haemaglobin
Concentration, MCV = Mean Corpuscular Volume, MCH = Mean Corpuscular Haemoglobin, Hb = Haemoglobin, WBC = White Blood Counts, GRA = Granulocytes,
LYM = Lymphocytes, MON = Monocytes. Diets: A (Control/Basal), B (Basal +
0.25 g BPSP/kg diet), C (Basal + 0.50 g BPSP/kg diet), D (Basal + 0.25 g
APSP/kg diet), E (Basal + 0.50 g APSP/kg diet), F (Basal + 0.25 g BPSP-APSP
Mix/kg diet), G (Basal + 0.50 g BPSP-APSP Mix/kg diet).
Table 4: Serum Biochemical Components
of Broilers fed Diets Containing BPSP, APSP and their Composite
|
Parameters |
A |
B |
C |
D |
E |
F |
G |
SEM |
P-Values |
|
Chol |
6.84a |
5.40ab |
3.55c |
4.18b |
3.52c |
3.16c |
3.05c |
0.72 |
0.01 |
|
ALP |
2200a |
2200a |
2100b |
1700c |
1200d |
1600c |
1300d |
620 |
0.01 |
|
ALT |
32 |
32 |
31 |
33 |
32 |
31 |
33 |
1.8 |
0.95 |
|
AST |
120 |
110 |
120 |
120 |
120 |
110 |
120 |
12 |
1.23 |
|
TP |
33b |
36a |
36a |
36a |
37a |
36a |
37a |
4.5 |
0.03 |
|
ALB |
12 |
12 |
10 |
8.7 |
10 |
12 |
12 |
3.4 |
0.43 |
|
GLB |
22 |
24 |
26 |
28 |
26 |
24 |
25 |
4.7 |
0.11 |
Values are means and SEM (Standard
Error of Means). Means in a
row without a common superscript letter differ significantly (P<0.05). Chol. (Cholesterol),
Alkaline phosphatase (ALP), Alanine transaminase (ALT), Aspertate
transaminase (AST), TP (Total Protein), ALB (Albumin), GLB (Globulin). Diets: A (Control/Basal), B (Basal + 0.25 g BPSP/kg diet), C
(Basal + 0.50 g BPSP/kg diet), D (Basal + 0.25 g APSP/kg diet), E (Basal + 0.50
g APSP/kg diet), F (Basal + 0.25 g BPSP-APSP Mix/kg diet), G (Basal + 0.50 g
BPSP-APSP Mix/kg diet).
CONCLUSIONS
This study concluded that
the varying inclusions of black pepper, alligator pepper and their composite
had significant enhancement potentials on the performance of broiler chickens
without any adverse effect on the blood profiles of the animals indicating
healthy performance. The phyto-additives also had the
potential of reducing the cholesterol level of the birds thereby providing lean
meat which is healthy to the consumers. The composite mix of these phytogens are therefore recommended at the 0.25 to 0.50
g/kg inclusion rate as the synergistic effect of the composited proved to be of
better performance than the individualist effect of each phytogen.
Competing interests
The
author declares no competing interest.
REFERENCES
1.
Adefegha SA, Olasehinde
TA and Oboh G (2017). Essential oil composition,
antioxidant, antidiabetic and antihypertensive
properties of two Afromomum species. J. Oleo Sci. 66: 5163.
2.
Adu
OA and Olarotimi OJ (2020). Quality
characteristics of eggs from chickens fed diets containing cerium chloride as
rare earth element. Liv. Res. Rural Develop. 32 (4):
1 7.
3.
Akhani SP, Vishwakarma
SL and Goyal RK (2004). Anti-diabetic activity of Zingiber officinale in streptozotocin-induced type I diabetic rats. J. Pharm. Pharmacol. 56:101105.
4.
Al-Amin
ZM, Thomson M, Al-Qattan KK, Peltonen-Shalaby
R and Ali M (2006). Anti-diabetic and hypolipidaemic
properties of ginger (Zingiber officinale)
in streptozotocin-induced diabetic rats. Brit. J. Nutri. 96:660666.
5.
Al-Kassie GAM, Al-Nasrawi MAM and Ajeena SJ (2011). Use of black pepper (Piper nigrum) as feed additive in
broilers diet. Res. Opinions Anim. Vet. Sci. 1
(3): 169-173.
6.
Biswas
A, Ahmed M, Bharti BK and Singh SB (2011). Effect of antioxidants on physio-biochemical and hematological parameters in broiler
chickens at high altitude. Asian-Austral. J. Anim. Sci. 24 (2): 246 - 249.
7.
Doherty
VF, Olaniran OO and Kanife
UC (2010). Antimicrobial activities of Aframomum
melegueta (Alligator pepper). Intl J. Biol. 2(2): 126-131.
8.
Effiong OO and Ochagu
SI (2019). Chemical composition and growth promoting effect of piper guineense leaf and seed meals on broiler chicks at starter
phase. Anim. Res. Intl. 16 (2): 3285 3294
9.
Enemor A, Modie JA
and Ennison B (2014). Biological compounds and their functions. J. Pharm. 78-90.
10.
Harrison
GJ and Lightfoot TL (2005). Clinical avian medicine. Spix
Publ. Inc. Palm Beach, Forida, USA.
11.
Ilic N, Schmidt BM, Poulev and Raskin I
(2010). Toxicological evaluation of grains of paradise (Aframomum melegueta) [Roscoe] K. Schum. J. Ethnopharmacol. 127: 1017.
12.
Kwankwa
T, Ityumbe MS, Ndumari NP, Garba TH, Habib M, Usman A and Sogbesan OA (2020). Effects
of alligator pepper (Aframomum melegueta)
meal additive diets on growth ANS Feed Utilization Clarias
Gariepinus (Burchell,
1822). Intl J Innovative
Studies in Aquatic Biol. & Fisheries
6 (3): 1-6
13.
Nosiri C, Anyanwu
C, Agim C and Nwaogwugwu C.
(2013). Evaluation of Aframomum melegueta
aqueous seed extract on food and water consumption in albino rats. IOSR J.
Pharm. 7 (4): 23-26.
14.
Okigbo RN and Igwe
DI (2007). Antimicrobial effects of Piper guineense
Uziza, and Phyllantus
amarus Ebe-Benizo on Candida
albicans and Streptococcus faecalis.
Acta Microbiol. et Immunolo Hungarica.
54(4): 353-366
15.
Onoja SO, Omeh
YN, Ezeja MI and Chukwu MN
(2014). Evaluation of the in vitro and in vivo antioxidant potentials of Aframomum melegueta methanolic seed extract. J. Trop. Med. 15: 93104.
16.
Uhegbu FO, Imo C and Ugbogu
AE (2015a). Effect
of aqueous extract of Piper guineense seeds on some liver enzymes, antioxidant
enzymes and some hematological parameters in albino rats. Intl J Plant Sci Ecol. 1 (4): 167-171.
17.
Uhegbu FO, Imo C and Ugbogu
AE (2015b). Some biochemical changes in serum of female albino rats administered
aqueous extract of Piper guineense Schumach Seeds. Intl J Biochem.
Res. Rev. 8 (1): 1-7.
18.
Umukoro S and Ashorobi
RB (2003). Pharmacological evaluation of the antidiarrheal activity of Aframomum melegueta
seed. W. Afri.
J. Pharmacol.
Drug Res. 19: 5154.
19.
Umukoro S and Ashorobi
RB (2005). Further evaluation of the anti-inflammatory activity of Aframomum melegueta seed
extract and its possible mechanism of action, Nig. J. Health Biomed. Sci. 4: 3539.
20.
Weidner
MS and Sigwart K (2000). The safety of a ginger
extract in the rat. J. Ethnopharmacol. 73:513520.
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Cite this Article: Adu, OA (2022).
Performance and haematoserological influence of
black and alligator peppers and their composite mix in broiler chickens. Greener Journal of Agricultural Sciences,
12(1): 62-68. |