Research Article Open Access
Effect of Moringa Oleifera Leaf Meal (Molm) on the Growth, Carcass, Heamatology and Biochemical Parameters of Rabbits
Ghomsi MOS1, Enow JT1, Etchu KA1*, Tientcheu BL1, Enamou G1, Chouengouong TM1, Mongo BG1, and Bayemi PH1
1Institute of Agricultural Research for Development (IRAD), BP 2067 Yaoundé, Cameroun
*Corresponding author: Etchu A K, Institute of Agricultural Research for Development (IRAD), Yaoundé, Cameroon, Tel no: (+237) 6777 08 069/ 6991 57 384; E-mail: @
Received: 02 March, 2017; Accepted: 26 April, 2017; Published: 08 May, 2017
Citation: Etchu AK, Ghomsi MOS, Enow JT, (2017) Effect of Moringa Oleifera Leaf Meal (Molm) on the Growth, Carcass,Heamatology and Biochemical Parameters of Rabbits. SOJ Vet Sci 3(3):1-5. DOI: 10.15226/2381-2907/3/3/00133
An experiment was conducted with 30 mixed bred rabbits (6 to 8 weeks old) averaging 592g to assess the performance, haematology, serum biochemistry, carcass and organ weights of growing rabbits fed graded levels of dried Moringa Oleifera Leaf Meal (MOLM) of 0%, 25%, and 50%, as a replacement of Soya Bean Meal (SBM) and groundnut cake in 8-week feeding trial. Feed consumption and weight gain were monitored. Blood samples were collected from the animals through the ear vein for haematology and serum biochemistry, while weight of cut parts and visceral organs were collected from the animals after they were stunned and sacrificed after the 8-week feeding trials and weighed. Results showed that there were significant differences (p < 0.05) in the value obtained for weight gain, feed conversion ratio, total protein and White Blood Cell (WBC). While the results of carcass and organ weight showed significant (P < 0.05) difference in values obtained for live weight, dress weight spleen, head and kidney. While there was no significant difference among the blood constants (VGM and MCHC). Among the leukocyte differential counts examined, lymphocytes, monocytes and eosinophils were not significantly different among the dietary treatments. The results suggest that MOLM possess good dietary protein quality for optimal growth of rabbits and be incorporated in the rabbit’s diets up to 25% inclusion levels without any detrimental effects on the performance, haematology, serum biochemistry and carcass and organ weights of growing rabbits.

Keywords: Moringa leaf; Rabbits; Growth; Carcass; Heamatology
The rabbit (Oryctolagus cuniculus) is the most productive meat producing among all domesticated animals. The feeding habits offer no appreciable competition with man. This is because it can subsist on green as basal diets. In addition to this, rabbits have a number of other characteristics that might be advantageous to subsistence farming system, such as their small body size, short generation interval with a relatively short gestation period of 30-31days. The use of forage and other agro industrial by-products have become an area of interest for many researchers because of the challenges posed by the high cost of conventional feedstuff [1]. In Cameroon, rabbit production is mainly practiced under traditional management systems in rural areas and so has not yet attained its full production potential [2].

Recently, there has been interest in the utilization of Moringa (Moringa Oleifera) commonly called horse radish tree or drum stick tree, as potential inexpensive protein source for livestock feeding. The nutritional qualities of Moringa Oleifera are excellent, which constitutes a source of high quality forage for animals. Also, these leaves are browsed by ruminants and poultry because of its high protein and minerals, by guinea pigs, by rabbits and by cricetoms [3-5].

Serum biochemical analysis is an established means of assessing Toxicological, health and carcass quality status of animal on feeding trials since ingestion of dietary components has measurable effect on carcass quality and may be considered as an appropriate measure of long term nutritional status. This study was therefore, carried out to investigate the effect of feeding graded levels of Moringa Oleifera leaf meal on the growth, carcass, haematology and serum biochemical parameters of rabbits
Materials and Methods
Study Site
The study was conducted at the experimental farm of the Institute of Agricultural Research for Development (IRAD) Nkolbisson, situated in the western suburbs of Yaoundé, Cameroon. This centre is located at 3° 86 longitude North and 11° 5 latitude East. This agro-ecological zone is characterized by minimum temperatures of 19 ° C and maximum of 29° C, a bimodal rainfall of 1500 to 2500 mm/year and a relative humidity that varies between 70% and 90%. The climate is sub-equatorial marked by four seasons [6].
Test Ingredient
Moringa leaves have been Harvested from agro-forestry plot of Irad ekona, by proaning and hand picking, solar dried for 2 days. Then oven dried at a temperature of 50° Centigrade for one hour and air dried under shade to prevent the leaves from being denatured until they will be crispy to touch. The leaves were thereafter crushed with hammer mill before incorporation in the test diets. Three (3) experimental diets were formulated. Diet 1 designated as T0 served as the control diet and contains no (0%) Moringa Oleifera leaf meal. Diet 2 designated as T1, Diet 3 as T2, containing Moringa Oleifera leaf meal at the levels of 25% and 50% as a replacement of protein contain by soya bean meal (SBM) and groundnut cake respectively (Table 1).
Animal material, Experimental diets and Experimental design
Table 1: Composition of Experimental Rations


Ingredients (kg)




Vitamin premix




Bone Meal




Palm Kernel Cake (PKC)




Fish meal




Groundnut cake




Soybean Meal (SBM)












Wheat Bran












Calculated chemical composition

Crudeprotein (%)




Metabolisable energy (Kcal/kg)




T0=0% Moringa oleifera leaf meal T1= 25% Moringa oleifera leaf meal
T2=50% Moringa oleifera leaf meal
Experimental Design and Management of Animals
Thirty weaners rabbits of mixed breeds and sex were use in this study. The animals were between 6 and 8; weeks old and with initial average live weight of 571- 614g. The rabbits were randomly allocated to three (3) treatment diets (T0, T1, T2) with each treatment having five replicates of two rabbits. The animals were house in cages and given an adaptation period of one week to the experimental diets. During this period, they were de-wormed (IVERMET o-1, USO VETERINARIO VMD, Belgium) and given antibiotics (Oxykel 80, KELA N.V, Belgium) against bacterial infections. They were also given an anti-stress (Amin’Total LAPROVET, BP, Cedex 2, France) each time they were manipulated. Routine management practices were carried out during the work. Feed and fresh water was provided ad libitum. Small quantities of 24-h wilted forage were also providing each day.
Data Collection
The rabbits were weighed weekly using weighing balance, before feed was given. Feed intake was obtained by deducting left-over feed from the quantity offered. The data were used to calculate daily weight gain, daily feed intake and feed conversion ratio (FCR). The FCR was calculated by dividing the daily feed intake by the metabolic weight depend on the amount of metabolically active tissue in the body, rather than total body weight; body weight0.75 is generally used to calculate the weight of active tissue.

At the end of the feeding period, the animals (three per treatment) were starved of feed for 24 hour and thereafter slaughter.
Calculated parameters
The calculation of certain parameters was done as follows:
•Simple consumption index = (feed consumption) / (weight gain)
•Feed efficiency relative to metabolic weight = (Feed consumption) / Weight Gain 0.7
Characteristics evaluation
After termination of the feeding experiment, three representative rabbits randomly chosen from each group were fasted for 24 hrs, weighed and handly slaughtered. After complete bleeding. Slaughtered animals were de-skinned, dressed out and the hot carcass including head was weighed and recorded. Edible offals; liver, heart, spleen and kidneys, were weighed.
Blood sample collection, haematology and biochemical analysis
At the end of the feeding period, the animals were starved of feed for 24 hours before blood samples were collected from one rabbit per replicate for haematological and biochemical analysis. Blood samples were collected into labeled Ethylene-Deamine Tetra-Acetic Acid (EDTA) treated tubes for haematological analysis and into tubes without anticoagulant for serum biochemical evaluation. Biochemical analysis in the serum: evaluation of transaminases activities; Total protein; total cholesterol and triglyceride. Biuret method of serum total protein determination was employed in this assay as described by Gornal, et al. [7]. Total cholesterol and triglyceride was determined using colorimetric enzymatic method as described by Trinder, et al. [8]. Alanine amino transferase, Aspartate amino transferase activity was determined using spectrophotometric method [9].
Statistical Analysis
All data were assembled using Excel 2007. The weights, growth rate, feed conversion ratio feed intake and carcass yield and proportions of the internal organs of the animals were subjected to analysis of variance per a completely randomized design and means were separated by the Duncan’s test [10,11].

γi = μ + αi + ei

Where: γi = is the dependent variable (average food consumption, initial average live weight, final average live weight, average weight gain, feed conversion)
μ = general mean
αi = effect of treatments
ei = Residual error
Effects of Moringa Oleifera leaf meal (MOLM) on some growth and carcass parameters
Result of the effect of MOLM on some growth and carcass parameters is shown by (Table 2, 3). The mean feed intake, weight gain and feed conversion ratio are summarized in Table 3 above. Feed intake decreased from 82g/day for the control T0 through 74g/day in diet T1, to 69g/day in diet T2. The feed intake recorded in diet 2 was significantly smaller (P < 0.05) from those of diets 0 and 1. Mean growth rates were similar (P > 0.05) between diet T0 and T1 though the tendency was in the decrease (25, 20 and 20 g/day). There is no difference (P ˃ 0.05) between the control and the other treatment for initial weigh and feed intake. The highest weigh gain is observed for control which is statistically similar (P ˃ 0.05) to diet T1, but different (P ˂ 0.05) to diet T2.

Table 4 shows the effect of MOLM on carcass. There is no difference (P ˃0.05) between the control diet T0 and the other diet T1 and T2 for heart, liver, lungs weight and carcass length.
Effects of Moringa Oleifera leaf meal (MOLM) on hematological and biochemical parameters
The blood hematological and biochemical components of the rabbits are shown in (Table 4,5). The MOLM did not vary the blood characteristics and some biochemical parameter studied. However, the MOLM tended to increase the protein level in the blood and white blood cell in T1 with significant difference (p < 0.05).
Table 2: Chemical Composition of Moringa Oleifera Leaf


DM (%)


ME (Kcal/DM kg)











DM: Dry Matter; CP: Crude Protein; ME: Metabolizable Energy; CF: Crude Fiber; EE: Ether Extract
Table 3: Effects of Moringa Oleifera Leaf Meal (MOLM) on Weights, Growth Rate and Feed Intake





Average initial weight (g) ± SEM

592 ± 76a

614.5 ± 39a

571.9 ± 39a

Mean final weight (g) ± SEM

2012.5 ± 119a

1961.5 ±214a

1630 ± 100b

Total weight gain (g) ± SEM

1420.5 ± 127a

1347 ± 206a

1058 ± 96b

Mean feed intake (g/) ± SEM

4633 ± 627a

4214 ± 457a

4149 ± 182a

Feed conversion ratio

3.25 ± 0.30b

3.16 ± 0.41b

3.93 ± 0.23a


Consumption index relative to metabolic weight

20 ± 1.92ab

19.1 ± 2.14b

22.41 ± 0.92a

mean daily feed intake (g/day) ± SEM

82.74 ± 11a

74.1 ± 5.8ab

69.58 ± 3.2b

Mean daily growth rate
(g/day) ± SEM

25.37 ± 2.28a

20 ± 1.92ab

20 ± 1.92ab

a,b = means on the same row not followed by the same letter are significantly different (p < 0.05)
Table 4: Effects of Moringa Oleifera leaf meal(MOLM) on carcass





Live weight (g)±SEM

1885.7 ± 88a

1740 ± 136a

1448 ± 172b

dress weight (g)±SEM

191.2 ± 21a

178.80 ± 27.8ab

140 ± 25.5b

carcass weight (g)±SEM

1010 ± 61.8a

923 ± 71a

698 ± 72b

Carcass lenght(g)±SEM

34 ± 0.81a

34.5 ± 0.58a

33 ± 2.1a

head weight (g)±SEM

130 ± 7.07a

110 ± 9.12b

108.8 ± 9.78b

liver weight (g)±SEM

40 ± 7.07a

40 ± 7.07a

33.75 ± 4.78a

heart weight (g)±SEM

5 ± 0a

5 ± 0a

5 ± 0a

kidney weight (g)±SEM

16.25 ± 4.78a

12.50 ± 2.88ab

8.75 ± 2.5b

lungs weight (g)±SEM

10 ± 4.08a

12.5 ± 8.66a

10.0 ± 0.00a

a,b = means on the same row not followed by the same letter are significantly different (p < 0.05)
Table 5: Effects of Moringa Oleifera leaf meal (MOLM) on biochemical parameters






45.8 ± 5.7a

48.27 ± 13.67a

43.76 ± 0.115a


137.67 ± 19.09a

124.37 ± 8.38a

136.67 ± 8.96a

Total cholesterol (g/dl)±SEM

0.82 ± 0.35a

1.04 ± 0.19a

1.12 ± 0.34a

Total protein (g/l)±SEM

59.23 ± 2.40b

63.76 ± 1.85ab

64.7 ± 2.86a

Urea (g/l)±SEM

0.48 ± 0.025a

0.45 ± 0.07a

0.48 ± 0.005a

creatinine (g/l)±SEM

13.4 ± 0.85a

12.7 ± 1.30a

13.5 ± 1.05a

a,b = means on the same row not followed by the same letter are significantly different (p < 0.05)
Aspartate Transaminase =AST, Alanine Transaminase=ALT
Table 6: Effects of Moringa Oleifera leaf meal(MOLM) on hematologic parameters





RBC 106/mm3±SEM

6.7 ± 0.5a

6.85 ± 0.24a

7.07 ± 0.5a

WBC (103/mm3) ±SEM

5.5 ± 0.92b

7.34 ± 6.67a

6.26 ± 0.46ab

Hb (g/dl) ±SEM

14.1 ± 0.60a

14.03 ± 0.47a

14.23 ± 0.9a

Platelets (103/mm3) ±SEM

369.67 ± 92.11a

328.3 ± 90.27a

329.33 ± 82.27a

hematocrit (%)±SEM

45.93 ± 2.18a

46.4 ± 1.49a

46.9 ± 2.2a

VGM (fl)±SEM

68.5 ± 2.41a

67.67 ± 0.68a

66.5 ± 1.76a


30.7 ± 0.65a

30.23 ± 0.057a

30.33 ± 0.55a

neutrophils (%)±SEM

32.1 ± 1.57a

28.27 ± 2.59a

32 ± 10.56a

eosinophils (%)±SEM

0 ± 0.00a

 0.03± 0.057a

0 ± 0.00a

basophils (%)±SEM

0.93 ± 00.152a

0.83 ± 0.208a

0.90 ± 0.96a

lymphocytes (%)±SEM

64.53 ± 1.87a

67.06 ± 4.62a

60.43 ± 10.07a

monocytes (%)±SEM

2.43 ± 1.93a

3.8 ± 1.91a

5.66 ± 0.32a

ab = means on the same row not followed by the same letter are significantly different (p < 0.05)
RBC=Red blood cell, Hb=Haemoglobin, WBC=White Blood Cell, MCV=Mean cell volume, MCHC=Mean cell haemoglobin concentration, Mean Corpuscular Volume (MCV), Mean Corpuscular Hemoglobin Concentration (MCHC)
The rabbits weight gains for T1 and T2 diets are different to those obtained (20, 1 and 20,1g / day) by Dougnon, et al. and Esong, et al. [2,5]. On the other hand, the average daily weight gain for control feed (25.37 g/d) is much higher than those reported by these authors. However, the final body weight showed significant difference (P < 0.05) between the treatment T0, T1 and T3 as high weight gain in animals is normally because of increased feed intake. In this study, there was increase in final body weight and body weight gain and confirm the results of Adeniji and Lawal [12]. The result of the present study suggests that, MOLM when fed as source of protein graded level up to 25% could promate the growth of rabbit. In the same time, certain adverse effect could be happened with dosage of moringa 50% due to the high content of some phytochemical compounds (phenols, cumares, alkaloids and tanins) which are naturally occurring at high levels of MOLM [13]. Ufele, et al. show also that Moringa Oleifera leaf meal is non-toxic to rabbits at the 20% level of inclusion [14].

Blood is an important index of physiological and nutritional status in the organism [15]. The effect of MOLM on selected enzymes showed any effect in the activities of aspartate transaminase and alanine transaminase. Transaminase are enzyme markers of hepatic toxicity. There were no significant differences between the tests and control groups for Cholesterol, urea and creatinine. This finding suggests that the MOLM may not have negative effect on the proper functioning of the liver, kidney and muscle. The biochemical values of total protein (59, 2 – 64, 7 g/l), reported in this study Table 3 were generally higher in other tropical areas. The generally higher biochemical values in this study could be due to the high nutritional value of the moringa.

There were no differences between control and test diet for haematological parameters except WBC which suggest that the MOLM could enhance hematopoietic activity and may not precipitate anaemia in a biologic system [16]. The (Mean Corpuscular Volume) MCV, MCH, MCHC, Neutrophils, Lymphocyte, Monocytes and Eosinophils were not significantly affected (P > 0.05) with the inclusion of Moringa leaf meal. This report agrees with the findings of Olatunji and Alagbe, when rabbits were fed vary level MOLM of and the normal range established by Mitruka and Rawnsley [17,18].

The nonsignificant difference (P > 0.05) observed for this parameter is an indication of better utilization of MOLM by the rabbits. The higher value of WBC observed in rabbits fed MOLM based diets compared with the control is an indication that the immunity levels of the rabbits were challenged, which is different from those obtain by Odetola, et al. [19]. According to Soetan, et al. high counts of WBC enhance adaptability to local environment and disease prevalent conditions [20].

The Red blood cell values were not significantly (P > 0.05) influenced with the inclusion of Moringa leaf meal, this means that shows that oxygen and carbon dioxide are well distributed in the body to enhance respiration and good health status. The values recorded fall within the normal recorded by Mitruka and Rawnsley and it agrees with findings of Odetola, et al. [18,19].
This study has demonstrated that Moringa Oleifera leaf meal possess good dietary protein quality for optimal growth of rabbits. It could be used to improve daily weight gain and feed intake of rabbits. And also MOLM can be used to replace such sources protein like soya bean meal and groundnut cake in the rabbit’s diet up to 25% inclusion level without any detrimental effect on the performance, haematology and serum biochemistry of rabbits.
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