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Leverage of Moringa oleifera Supplementation on Performances, Biochemical, and Milk Profiles in Mammals

AAVS_10_9_2043-2050

Review Article

Leverage of Moringa oleifera Supplementation on Performances, Biochemical, and Milk Profiles in Mammals

Haitham Al Masruri1, Rashid Al Zeidi2, Aiman Al Mufarji3, Abd El-Nasser Ahmed Mohammed3, Ahmed Al-Madani4, Al-Hassan Mohammed5*

1Department of Public Health and Animal Care, College of  Veterinary Medicine, King Faisal University, P.O. Box 400, Al-Hassa, Kingdom of Saudi Arabia; 2Department of Clinical Studies, College of Veterinary Medicine, King Faisal University, P.O. Box 400, Al-Hassa, Kingdom of Saudi Arabia; 3Department of Animal and Fish Production, College of Agriculture and Food Sciences, King Faisal University, P.O. Box 400, Al-Hassa, Kingdom of Saudi Arabia; 4Branch of the Ministry of Environment, Water and Agriculture in Jazan Region, KSA; 5Faculty of Human Medicine, Assiut University, Egypt, 71526.

Abstract | Nutritional supplements of Moringa oleifera to animals are considered one of the aids for improving health and production. M. oleifera leaves, seeds, and extracts are administered to animals for therapeutic and nutritional purposes. The effects of using M. oleifera and its extracts on animals’ production and health have shown beneficial effects in several studies. The roles of M. oleifera and its extracts on nutrient digestibility, rumen fermentation and enzyme activities, growth and reproductive performances, antioxidants, and milk production and composition have been well documented. M. oleifera contains valuable chemical constituents such as proteins, essential fatty acids, vitamins, and beta-carotene. The M. oleifera composition varies depending on nutrient availability for production, species, and lifespan of trees. Extracts of leaves and seeds were used for the production of invaluable compounds. Knowledge of M. oleifera impacts on productive, reproductive, and therapeutic performances is more fragmentary and the present review is compiled and discussed owing to the importance of M. oleifera and its purified compounds.

 

Keywords | Moringa oleifera, Growth, Reproduction, Milk, Blood


Received | June 13, 2022; Accepted | July 17, 2022; Published | September 01, 2022

*Correspondence | Al-Hassan Mohammed, Faculty of Human Medicine, Assiut University, Egypt, 71526; Email: aamohammed@kfu.edu.sa

Citation | Al Masruri Haitham, Al Zeidi R, Al Mufarji A, Mohammed AA, Al Madani A, Mohammed H (2022). Leverage of Moringa oleifera supplementation on performances, biochemical, and milk profiles in mammals. Adv. Anim. Vet. Sci. 10(9): 2043-2050.

DOI | http://dx.doi.org/10.17582/journal.aavs/2022/10.9.2043.2050

ISSN (Online) | 2307-8316

 

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Copyright: 2022 by the authors. Licensee ResearchersLinks Ltd, England, UK.

This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).



INTRODUCTION

Moringa oleifera (M. oleifera) is a tree plant generally referred to as a miracle plant. M. oleifera is a nutritious and medicinal tree species-rich in protein, minerals, and vitamins. M. oleifera is a native plant in Pakistan, India, Bangladesh, and Afghanistan (Fahey, 2005). Supplementation of M. oleifera to animals and humans has received increased attention for its high contents of certain micro and macro-nutrients, which are important in medicine and nutrition for both humans and animals (Oyeyinka and Oyeyinka, 2018; Gupta et al., 2018). Leaves of M. oleifera are reported to contain substantial amounts of vitamins such as A, C, and E (Saini et al., 2014a,b; Hekmat et al., 2015), minerals such as potassium, calcium, magnesium, iron, copper, and manganese (Hekmat et al., 2015), nutrients such as protein, fiber, carotenoids, and tocopherols (Jongrungruangchok et al., 2010; Moyo et al., 2011; Saini et al., 2014a,b). Some of the Moringa components are known to scavenge free radicals (DanMalam et al., 2001). Substantial variations in the contents of M. oleifera have been shown such as protein (19-29%), fiber (16-24%), minerals, vitamins, and others according to cultivar and sources (Jongrungruangchok et al., 2010; Moyo et al., 2012; Teixeira et al., 2014; Afzal et al., 2021; Al Mufarji and Mohammed 2022). M. oleifera leaves are known to contain calcium (4X) and protein (2X) compared to milk, vitamin C (7X) compared to oranges, potassium and iron (3X) compared to banana and spinach respectively, and vitamin A (4X) compared to carrots (Thurber and Fahey, 2009; Razis et al., 2014). The leaves of M. oleifera contain beta-carotene and other phytochemicals known for their antioxidant ability (rutin, quercetin, kaempferol, and caffeoylquinic acids); antioxidant vitamins (A, C, and E) and antioxidant micronutrients (zinc and selenium), which play important roles in fertility performance (Jaiswal et al., 2009; Vongsak et al., 2014; Afzal et al., 2020) as well as contributing to an improvement in growth performance (Warastomo et al., 2021; Pandey et al., 2022), blood metabolites (Akanmu et al., 2020; EL-Hedainy et al., 2020), and milk production and composition (Kholif et al., 2016, 2019; Mendoza-Taco et al., 2022). Due to the several aforementioned nutritional benefits of M. oleifera, this review is compiled and discussed such effects on mammals (Figure 1).

 

Nutrient Digestibility, Rumen Fermentation, And Growth Performance

Ruminant animals were supplemented with M. oleifera in different doses for enhancement of feed efficiency, rumen fermentation, and growth performances (Paul et al., 2013; Warastomo et al., 2021; Fadiyimu et al., 2010, 2016, 2017; Abdel-Raheem and Hassan 2021; Pandey et al., 2022). Fadiyimu et al., (2010, 2016; 2017) conducted studies in Nigeria for investigating the effects of the inclusion of 25, 50, 75, and 100% M. oleifera on nutrient digestibility and nitrogen balance of African ewes with an average body weight of 16.1 kg. The inclusion of Moringa in the diet improved the nutrient digestibility and growth characteristics, while the feed intake decreased by increasing the proportion of Moringa in the diet. Supplementing Rhodes hay in Ethiopia with graded levels of dried Moringa leaves improved dry matter intake, increased body weight, and nitrogen retention (Gebregiorgis et al., 2012) and reported that Moringa leaves can serve as a protein supplement for low-quality feeds. EL-Hedainy et al. (2020) conducted a study in Egypt for investigating the effects of 4 g M. oleifera seeds /head for 45 days on the productive performance and body measurements of male Barki five months old. They recorded the ability of M. oleifera seeds to improve the final body weights and daily gains of lambs, while body measurements did not differ significantly between groups. Bhokre et al. (2020) investigated the effects of Moringa leaf meal based diets for 90 days on the biometry and body condition score of Deccani lambs. Their results based on biweekly body measurements indicated that the mean body length, face length, and hip width of the developing Deccani lambs increased linearly throughout the experiment, and body length had a significant difference (P < 0.01) between the treatment groups. They also recorded significantly higher body conditions (BCS) (P < 0.05) in the 25% treated group from the third to sixth week. Warastomo et al. (2021) investigated the effects of moringa leaf flour on the physical properties of lambs with a body weight of 20 kg and aged 7-8 months for 75 days. They recorded that Moringa was not able to improve the physical properties of meat (pH, tenderness, and water holding capacity). Warastomo et al. (2021) investigated the effects of feeding M. oleifera meal (0, 25, and 50) on growth performance of Surti kids aged 6-8 months under intensive system of management for 14 weeks. The lambs showed best results at the supplement level of 25% concerning body weights and biometrics (body length and chest circumference).

The negative effects of replacing soybean meal with M. oleifera leaf meal on ruminal fermentation characteristics were investigated in goats and steers (Elghandour et al., 2017). They observed significant decreases in CH4, ruminal ammonia-N, total protozoal number, and organic matter degradability, as well as increases in CO2 production, fermentation pH, and total bacterial count. Conversely, Abdel-Raheem and Hassan (2021) carried out a study on growing buffalo calves about the effects of M. oleifera dietary inclusion on nutrient digestibility, rumen fermentation, and growth performance. They recorded an improvement in rumen fermentation, growth performance, blood metabolites, and mitigated ammonia and methane values. They attributed the differences between the results to the difference in the environmental conditions, the species, and the age of the animals, as well as the composition and levels of supplementing M. oleifera.

Reproductive Activity

Gonadal dysfunctions and reproductive hormonal imbalances were widely modulated through nutritional ingredients (Nagasawa et al., 1989; Downing et al., 1995; Mohammed and Attaai 2011; Gifre et al., 2017; Senosy et al., 2017, 2018; Mohammed and Farghaly 2018; Mohammed 2018; Mohammed 2019; Mohammed et al., 2012, 2020; 2021, Mohammed and Al-Hozab 2020; Ali et al., 2021), hormonal supplementation (Zarazaga et al., 1996; Mohammed et al., 2011), and both hormonal and nutritional supplementation (Mohammed and Attaai, 2011). Based on the negative influences of increased energy and protein in the diets of humans and animals on health and fertility (McEvoy et al., 1997; Dawuda et al., 2002; Mohammed et al., 2012), and because of the high cost of diet; M. oleifera and their purified extracts were given in small quantity as replacers instead of hormonal stimulation (Odeyinka et al., 2008). In addition, M. oleifera and its purified extracts might be used for treating reproductive dysfunctions.

Barakat et al. (2015) investigated the effect of M. oleifera leaf extract at the level of 20, 50, and 100 μg/ml on the expression of genes related to fertility and the increase of calcium ions in ovine oocytes. They indicated that genes related to oocyte maturation and meiotic progression were affected by M. oleifera extract. Furthermore, M. oleifera along with hormones improved the rate of ovine oocyte maturation and could act to induce mRNA expression and synthesis of the basic maturation-stimulating protein essential for maturation processes. Ajuogu et al. (2019) investigated the effect of M. oleifera leaf powder in levels of 5, 10, and 15 g/kg feed on the concentration of reproductive hormones and semen quality of New Zealand white rabbits. They revealed a significant dose-dependent reduction in the concentration of serum follicle-stimulating (FSH), luteinizing (LH), and estrogen hormones in females.

Sonbarse et al. (2020); Giuberti et al. (2021) recorded that the highest level of M. oleifera significantly increased the progesterone levels whereas the prolactin concentrations were not affected. In males, the concentrations of FSH and LH increased significantly in the M. oleifera treated groups. Semen volume, sperm count, and motility rate were significantly improved in dose-dependent M. oleifera. They added that M. oleifera might be used as an alternative to hormonal treatment to enhance reproductive performance for its high level of beta-carotene, protein, and other fine chemicals. Further studies are still required on the effects of M. oleifera on ovarian follicle development, oocyte quality, oocyte maturation and fertilization, and the viability of the embryos.

Blood Biochemistry

Blood indices and plasma metabolites are indicative of the body’s health in both animals and humans. M. oleifera is widely cultivated as an important vegetable for human consumption (Lin et al., 2018). Therefore, blood indices and plasma metabolites were recorded in different studies on M. oleifera supplementation in both animals and humans (Al Mufarji and Mohammed 2022; Al Mufarji et al., 2022; Al Masruri et al., 2022). Fadiyimu et al. (2010, 2016; 2017) carried out an investigation in Nigeria on the effects of 25, 50, 75, and 100% M. oleifera on blood indices and plasma metabolites of African ewes with an average body weight of 16.1 kg. They showed that the packed cell volume (PCV), hemoglobin (Hb), red blood cells (RBCs), and white blood cells (WBCs) of the animals treated with M. oleifera were within the normal physiological range in contrast to the ewes of the control group, whose values were less than normal. Moyo et al. (2012) examined the antioxidant activity of M. oleifera leaf extract on the enzymatic activity of the liver in goats of South Africa. They showed that M. oleifera extract could be a potential source of compounds with powerful antioxidant potential. Meel et al. (2018) investigated the effect of M. oleifera leaves at levels of 25, 50, 75, and 100% on blood and plasma components of Sirohi goat kids in India. They showed that the red blood cells, hemoglobin, total protein, and albumin increased significantly while the white blood cells and glucose decreased in the 100% treatment. EL-Hedainy et al. (2020) investigated the effect of M. oleifera seeds (4 g/head) for 45 days on growth performance and body parameters of males aged five months in Egypt. They showed the ability of M. oleifera seeds to improve the concentrations of total protein , as well as maintained all blood serum components within the normal range.

The effect of M. oleifera extract (50 mg/kg DM) on blood and plasma measurements of lambs has been investigated by Akanmu et al. (2020). The results revealed that most of the blood treatments were not affected by M. extract treatment as an anti-methanogenetic additive and all the biochemical parameters except for the decreased alkaline phosphatase; did not differ between treatments, as well as reduce intestinal methane emission. They revealed that the extract was not toxic to sheep as an anti-methane additive at a rate of 50 mg/kg DM.

Yasoob et al. (2022) reported that M. oleifera leaf powder when was supplemented to rabbits during heat stress resulted in reduced glucose, total cholesterol, low-density lipoprotein cholesterol, and triglycerides contributing to reduced intestinal methane emissions, alleviate heat stress, and increased meat yield. M. oleifera leaves may improve physiological parameters, and blood and plasma components. M. oleifera contains high lipid contents, thus might be considered as key constituents of the plasma membrane and they are essential for the functionality of all cellular membranes, as well as lipids form membrane vesicles or lipid droplets (LDs) that are involved in the transport of proteins, hormones, or fat-soluble vitamins (A, D, E, and K) in cells and extracellularly, for example in the bloodstream (Vachier et al., 2002). 

Immunity Functions And Antioxidant Activity

Immunity functions and antioxidant activity of animals and humans could be improved through the use of feed additives (Kassab and Mohammed 2013, 2014 a,b; Mohammed 2019; Ali et al., 2021; Ademosun et al., 2019, 2022; Al Mufarji and Mohammed 2022). Bioactive compounds in M. oleifera have been shown to enhance immunity functions, antioxidant activities, and tissue protection in mammals (Kekana et al., 2020; Wen et al., 2022). Wen et al. (2022) examined M. oleifera polysaccharide effects on immune indices of serum and organs in addition to colonic microflora of mice. They indicated that M. oleifera polysaccharide gave a positive effect on immune performance and intestinal health. Kekana et al. (2020) investigated the effect of M. oleifera meal to transition Holstein cows on antioxidant enzymes. The effects of Moringa and its extract on immunity functions and antioxidant activities are attributed to Moringa polyphenols extract, which might have immunomodulatory properties (Adjei-Fremah et al., 2019). M. oleifera leaves contain beta-carotene and other phytochemicals such as rutin, quercetin, kaempferol, and caffeoylquinic acids; antioxidant vitamins such as A, C, and E, and essential micronutrients such as zinc and selenium and all known for their antioxidant abilities. Hassan et al. (2021) reported the great protective effects of M. oleifera leaves extract against diseases and the widely persistent environmental toxins which disrupted cellular metabolic function. Up-regulation of genes for thermo-tolerance, antioxidation, and immunity over supplementing rabbits with oral M. oleifera leaf powder under heat stress was recorded indicating beneficial influences on liver functions in heat-stressed rabbits (Yasoob et al., 2022).

Up-regulation of the antiapoptotic BCL2A1 gene by M. oleifera leaves extract may suggest a protective effect against apoptosis induced due to heat stress. Therefore, further studies are still required to investigate phenolic compounds of M. oleifera for the treatment of various immune diseases.

Milk Production And Composition

Sustainable livestock development of milk and meat production requires appropriate strategies to be applied worldwide for covering the shortage of milk and meat requirements for humans. Because of the increasing demands for meat and milk in the world, specialists continue to explore new approaches to improve meat and milk yield through different nutritional strategies (Stamey et al., 2012; Alshaheen 2016; Hifzulrahman et al., 2019; Wang et al., 2019; Brady et al., 2021). M. oleifera inclusion for ruminants has changed milk yield and improved milk fatty acid profile (Kholif et al., 2016; 2019; Choudhary et al., 2018). Kholif et al. (2016) found that M. oleifera supplementation in lactating Anglo-Nubian goats increased milk production by 24.0%. The contents of saturated fatty acids decrease by 9.0% whereas conjugated linoleic acids (CLAs) increased by 57.0%. Choudhary et al. (2018) found that replacing mixed concentrate ration with 50.0% M. oleifera leaves in lactating Bengal goats contributed to a positive effect on milk yield and composition and increased milk production by 6.0%, milk fatty acid profiles of Nubian goats were enhanced with M. oleifera leaves treatments (10, 20, 40 ml/day) (Kholif et al., 2019). The percentage of saturated fatty acids decreased whereas the of unsaturated fatty acids, conjugated linoleic acid, and the arteriosclerosis index increased. They recommended the use of 20 ml for a practical approach. Olvera-Aguirre et al. (2020) studied the influence of feeding lactating ewes with M. oleifera leaf extracts on milk yield and milk composition. They showed that milk yield and composition were not significantly changed. Effects of M. oleifera essential oils (0.3 and 0.6 ml/day) supplementation on milk quality and fatty acid profile in dairy sheep were investigated by Selmi et al. (2020) and revealed increased milk fat, unchanged protein, decease urea nitrogen, decreased saturated, and decreased unsaturated fatty acid profiles.

Mendoza-Taco et al. (2022) investigated the impacts of M. oleifera leaf extracts (20 ml) on the physicochemical characteristics of yogurt prepared from sheep milk. M. oleifera leaf extracts positively affected the physical and chemical composition of milk and yogurt during storage. Milk production and composition were improved in the previous studies over M. oleifera supplementation due to the nutritional benefits of M. oleifera on nutrient digestibility, rumen fermentation, and growth

CONCLUSIONS AND RECOMMENDATION

The potential properties of M. oleifera as a source of protein and bioactive compounds for animals and humans have been reported in several studies. M. oleifera biomass-derived macromolecules and micromolecules differed according to culture conditions. The biomass-derived macromolecules of M. oleifera have been shown in ruminant species to enhance nutrient digestibility, rumen fermentation, growth performance, antioxidant, and tissue protection. Studies are still required on M. oleifera effects on female and male fertility concerning oocyte, semen quality, and embryo development. Bioactive compounds; carotenoids, could be efficiently transferred to the body and improve body growth and health. The bioactive compounds of M. oleifera as promising protectors of inflammation and oxidative stress processes have been reported in several studies. Moreover, in-vivo and in-vitro studies should be carried out on M. oleifera bioactive compounds to authenticate their possible applications over a wide range of growth, productivity, and reproductive performances, as well as therapeutic approaches in biopharmaceutical industries as potent drugs.

ACKNOWLEDGEMENTS

This work was supported through the Annual Funding track by the Deanship of Scientific Research, Vice Presidency for Graduate Studies and Scientific Research, King Faisal University, Saudi Arabia [GRANT1019].

NOVELTY STATEMENT

The present review article expressed a continuation of a novel dietary supplement of Moringa oleifera based on the previous studies on performances, biochemical, and milk profiles in mammals

CONFLICT OF INTEREST

No conflict of interest for the authors to declare.

AUTHORS contribution

Mohammed participated in experimental design, wrote and submit the review article, and prepared figures. Rashid Al Zeidi, Haitham Al Masruri, Aiman Al Mufarji, Ahmed Al-Madani, and Al-Hassan Mohammed collected references and prepared figures.

REFERENCES

Abdel-Raheem S.M., Hassan E.H. (2021). Effects of dietary inclusion of Moringa oleifera leaf meal on nutrient digestibility, rumen fermentation, ruminal enzyme activities and growth performance of buffalo calves. Saudi J. Biol. Sci. 28: 4430-436. https://doi.org/10.1016/j.sjbs.2021.04.037

Ademosun A.O., Oboh G., Olufunke Florence Ajeigbe O.F. (2022). Influence of Moringa (Moringa oleifera) enriched ice creams on rats’ brain: Exploring the redox and cholinergic systems. Curr. Res. Food Sci. 5: 366-373. https://doi.org/10.1016/j.crfs.2022.01.021

Ademosun S., Ekwemalor K., Asiamah E., Worku M. (2019). Moringa oleifera polyphenols modulate galectin expression in LPS-induced bovine peripheral blood mononuclear cells. J. Dairy Sci. 102: 1.

Adjei-Fremah S., Ekwemalor K., Asiamah E., Worku M. (2019). Moringa oleifera polyphenols modulate galectin expression in LPS-induced bovine peripheral blood mononuclear cells. J. Dairy Sci. 102: 3-4.

Afzal S., Nawaz M.F., Qadir I., Gul S., Yasin G., Ahmad I. (2020). Variability in leaf mineral composition of Moringa oleifera in irrigated plains of Pakistan. South Afr. J. Botany. 129: 442-447. https://doi.org/10.1016/j.sajb.2019.11.025

Afzal A., Hussain T., Hameed A. (2021). Moringa oleifera Supplementation Improves Antioxidant Status and Biochemical Indices by Attenuating Early Pregnancy Stress in Beetal Goats. Front. Nutri., 8. https://doi.org/10.3389/fnut.2021.700957

Ajuogu P. K., Mgbere O. O., Bila D. S., McFarlane J. R. (2019). Hormonal changes, semen quality and variance in reproductive activity outcomes of post pubertal rabbits fed Moringa oleifera Lam. leaf powder. J. Ethnopharmacol. 233: 80–86. https://doi.org/10.1016/j.jep.2018.12.036

Akanmu A.M., Hassen A., Adejoro F.A. (2020). Haematology and serum biochemical indices of lambs supplemented with Moringa oleifera, Jatropha curcas and Aloe vera leaf extract as anti-methanogenic additives. Antibiotics. 9(9): 1–7. https://doi.org/10.3390/antibiotics9090601

Al Masruri H., Al Zeidi, R., Al Mufarji, A., Mohammed A.A. (2022). Moringa oleifera leaves supplementation to anaesthetized mice associated with changes of thermo-tolerance parameters, blood and plasma indices. Fresen. Environ. Bull. 31: 8.

Al Mufarji A., Mohammed A.A. (2022). Organic Moringa oleifera Leaves Chemical Composition and Fatty Acid Profiles and its Effect on Modulation of Blood and Plasma Parameters of Ewes in Subtropics. Adv. Anim. Vet. Sci. 10(6): 1227-1232. https://doi.org/10.17582/journal.aavs/2022/10.6.1227.1232

Al Mufarji A., Mohammed A.A., Al Masruri H., Al Zeidi R. (2022). Modulation Impacts of Moringa oleifera on Thermo-Tolerance Parameters and Blood indices in Subtropical Ewes under Heat Stress (Accepted). https://doi.org/10.17582/journal.aavs/2022/10.7.1641.1648

Ali M.A., Alshaheen T., Senosy W., Kassab A., Mohammed A.A. (2021). Effects of feeding green microalgae and Nigella sativa on productive performance and metabolic profile of Boer goats during peripartum period in subtropics. Fresen. Environ. Bull. 30(07): 8203-8212.

Alshaheen T.A. (2016). Effect of dietary source of omega-3 fatty acid on milk production, some reproductive and blood biochemical parameters of dairy cows during hot summer conditions. Ph.D. College of Food and Agricultural Sciences. King Saud University, KSA.

Barakat I. A. H., Khalil W. K. B., Al-Himaidi A.R. (2015). Moringa oleifera extract modulates the expression of fertility related genes and elevation of calcium ions in sheep oocytes. Small Rumin. Res. 130: 67–75. https://doi.org/10.1016/j.smallrumres.2015.06.011

Bhokre S.M., Rajanna N., Ramana D. B. v, Nagalakshmi D., Kumar M. K., Kumar M.S. (2020). Effect of feeding of Moringa (Moringa oleifera) leaf meal based diets on the biometry and body condition score of Deccani lambs. Int. J. Curr. Microbiol. Appl. Sci. 9(4): 1089–1096. https://doi.org/10.20546/ijcmas.2020.904.129

Brady E.L., Pierce K.M., Lynch M.B., Fahey A.G., Mulligan F.J. (2021). The effect of nutritional management in early lactation and dairy cow genotype on milk production, metabolic status, and uterine recovery in a pasture-based system. J. Dairy Sci. 104(5): 5522-5538. https://doi.org/10.3168/jds.2020-19329

Choudhary R. K., Roy A., Roy P. S., Singh K. M., Kumar P. (2018). Effect of Replacing Concentrate Mixture with Moringa Leaves (Moringa oleifera) on Performance of Lactating Bengal Goats in Kishanganj District of Bihar, India. Int. J. Curr. Microbiol. Appl. Sci. 7: 2895–2900.

Danmalam H.U., Abubakar Z., Katsayal U.A. (2001). Pharmacognostic studies on the leaves of Moringa oleifera, Niger. J. Nat. Prod. Med. 5(1). https://doi.org/10.4314/njnpm.v5i1.11723

Dawuda P.M., Scaramuzzi R.J.,  Leese H.J.,  Hall C.J.,  Peters A.R.,  Drew S.B.,  Wathes D.C. (2002). Effect of timing of urea on the yield and quality of embryos in lactating dairy cows. Theriogenol. 58: 1443–1455. https://doi.org/10.1016/S0093-691X(02)00973-1

Downing J.A., Joss J., Scaramuzzi R.J. (1995). Ovulation rate and the concentrations of gonadotrophins and metabolic hormones in ewes infused with glucose during the late luteal phase of the oestrous cycle. J. Endocrinol. 146: 403–410. https://doi.org/10.1677/joe.0.1460403

Elghandour M.M.Y., L.H. Vallejo, A.Z.M. Salem, M. Mellado, L.M. Camacho M. Cipriano, O.A. Olafadehan, J. Olivares, S. Rojas (2017). Moringa oleifera leaf meal as an environmental friendly protein source for ruminants: Biomethane and carbon dioxide production, and fermentation characteristics. J. Cleaner Prod. 165: 1229-1238. https://doi.org/10.1016/j.jclepro.2017.07.151

EL-Hedainy D. K. A., El-Wakeel E., Rashad A.M.A. (2020). Effect of Moringa seed meal as a feed additive on performance of fattening male Barki sheep. Int. J. Vet. Sci. Res. 6(2): 184–187. https://doi.org/10.17352/ijvsr.000072

Fadiyimu A. A., Alokan J. A., Fajemisin A.N. (2010). Digestibility, nitrogen balance and haematological profile of West African dwarf sheep fed dietary levels of Moringa oleifera as supplement to Panicum maximum. J. Am. Sci. 6(10): 634–643.

Fadiyimu A. A., Alokan J. A., Fajemisin A. N., Onibi G.E. (2016). Feed intake, growth performance and carcass characteristics of West African dwarf sheep fed Moringa oleifera, Gliricidia sepium or cassava fodder as supplements to Panicum maximum. J. Exp. Agric. Int. 1–10. https://doi.org/10.9734/JEAI/2016/25167

Fadiyimu A., Alokan J., Fajemisin A., Onibi G. (2017). Feed Intake, Growth Performance and Carcass Characteristics of West African Dwarf Sheep Fed Moringa oleifera, Gliricidia sepium or Cassava Fodder as Supplements to Panicum maximum. J. Exp. Agric. Int. 14(4): 1–10. https://doi.org/10.9734/JEAI/2016/25167

Fahey J.W. (2005). Moringa oleifera: a review of the medical evidence for its nutritional, therapeutic, and prophylactic properties. Part 1. Trees Life J. 1: 1–15.

Gebregiorgis F., Negesse T., Nurfeta A. (2012). Feed intake and utilization in sheep fed graded levels of dried moringa (Moringa stenopetala) leaf as a supplement to Rhodes grass hay. Trop. Anim. Health Prod. 44(3): 511–517. https://doi.org/10.1007/s11250-011-9927-9

Gifre L., Arís A, Bach À., Garcia-Fruitós E. (2017). Trends in recombinant protein use in animal production. Microb. Cell Fact. 16: 40. https://doi.org/10.1186/s12934-017-0654-4

Giuberti G., Rocchetti G., Montesano D., Lucini L. (2021). The potential of Moringa oleifera in food formulation: a promising source of functional compounds with health-promoting properties, Curr. Opin. Food Sci. 42: 257-269. https://doi.org/10.1016/j.cofs.2021.09.001

Gupta S., Jain R., Kachhwaha S., Kothari S.L. (2018). Nutritional and medicinal applications of Moringa oleifera Lam.—Review of current status and future possibilities. J. Herbal Med. 11: 1–11. https://doi.org/10.1016/j.hermed.2017.07.003

Hassan M.A., Xu T., Tian Y., Zhong Y., Ali F., Yang X., Lu B. (2021). Health benefits and phenolic compounds of Moringa oleifera leaves: A comprehensive review, Phytomed. 93: 2021 https://doi.org/10.1016/j.phymed.2021.153771.

Hekmat S., Morgan K., Soltani M., Gough R. (2015). Sensory evaluation of locally-grown fruit purees and inulin fibre on probiotic yogurt in mwanza, Tanzania and the microbial analysis of probiotic yogurt fortified with Moringa oleifera. J. Health Popul. Nutr. 33, 60–67.

Hifzulrahman M., Abdullah M.U., Akhtar T.N., Pasha J.A., Bhatti Z., Ali M., Saadullah M., Haque M.N. (2019). Comparison of oil and fat supplementation on lactation performance of Nili Ravi buffaloes. J. Dairy Sci. 102(4): 3000-3009. https://doi.org/10.3168/jds.2018-15452

Jaiswal D., Kumar Rai P., Kumar A., Mehta S., Watal G. (2009). Effect of Moringa oleifera lam. leaves aqueous extract therapy on hyperglycemic rats. J. Ethnopharmacol. 123 (3): 392–396. https://doi.org/10.1016/j.jep.2009.03.036

Jongrungruangchok S., Bunrathep S., Songsak T. (2010). Nutrients and minerals content of eleven different samples of Moringa oleifera cultivated in Thailand. J. Health Res. 24: 123–127.

Kassab A.Y., Mohammed A.A. (2013). Effects of dietary live dried yeast on some physiological responses and productive performances in sohagi ewes. Egypt. J. Nutr. Feeds, 16 (2): 215-225

Kassab A.Y., Mohammed A.A. (2014a). Ascorbic acid administration as anti-stress before transportation of sheep. Egypt. J. Anim. Prod. 51 (1): 13-19. https://doi.org/10.21608/ejap.2014.93664

Kassab A.Y., Mohammed A.A. (2014b). Effect of vitamin E and selenium on some physiological and reproductive characteristics of sohagi ewes. Egypt. J. Nutr. Feeds. 17 (1): 9-18.

Kekana T.W., U. Marume M.C. Muya, Nherera-Chokuda F.V. (2020). Periparturient antioxidant enzymes, haematological profile and milk production of dairy cows supplemented with Moringa oleifera leaf meal. Anim. Feed Sci. Tech. 268: 114606. https://doi.org/10.1016/j.anifeedsci.2020.114606

Kholif A.E., Morsy T.A., Goudaa G.A., Anele U.Y., Galyean M.L. (2016). Effect of feeding diets with processed Moringa oleifera meal as protein source in lactating Anglo-Nubian goats. Anim. Feed Sci. Tech. 217: 45-55. https://doi.org/10.1016/j.anifeedsci.2016.04.012

Kholif A. E., Gouda G. A., Galyean M. L., Anele U. Y., Morsy T.A. (2019). Extract of Moringa oleifera leaves increases milk production and enhances milk fatty acid profile of Nubian goats. Agrofor. Syst. 93(5): 1877–1886. https://doi.org/10.1007/s10457-018-0292-9

Li M., Yan J., Zhi X., Wang Y., Hang J., Qiao J. (2019). Chapter 13: Gene Expression during oogenesis and oocyte development. The Ovary (Third Edition), Pages 205-216. https://doi.org/10.1016/B978-0-12-813209-8.00013-3

Lin M., Zhang J., Chen X. (2018). Bioactive flavonoids in Moringa oleifera and their health-promoting properties, J. Functional Foods. 47: 469-479. https://doi.org/10.1016/j.jff.2018.06.011

McEvoy T.G., Robinson J.J., Aitken R.P., Findlay P.A., Robertson I.S. (1997). Dietary excesses of urea influence the viability and metabolism of preimplantation sheep embryos and may affect fetal growth among survivors. Anim. Reprod. Sci. 47(1-2): 71-90. https://doi.org/10.1016/S0378-4320(96)01627-2

Meel P., Gurjar M. L., Nagda R. K., Sharma M. C., Gautam L., (2018). Effect of Moringa oleifera leaves feeding on hemato-biochemical profile of Sirohi goat kids. J. Entomol. Zool. Studies. J. Entomol. Zool. Stud. 6: 41–48.

Mendoza-Taco M. M., Cruz-Hernández A., Ochoa-Flores A.A., Hernández-Becerra J.A., Gómez-Vázquez A., Moo-Huchin V. M., Piñeiro-Vázquez Á., Chay-Canul A. J., Vargas-Bello-Pérez E. (2022). Physicochemical Characteristics of Yogurt from Sheep Fed with Moringa oleifera Leaf Extracts. Animals. 12(1): 110. https://doi.org/10.3390/ani12010110

Mohammed A.A. (2018). Development of oocytes and preimplantation embryos of mice fed diet supplemented with dunaliella salina. Adv. Anim. Vet. Sci. 6: 33-39. https://doi.org/10.17582/journal.aavs/2018/6.1.33.39

Mohammed A.A. (2019). Nigella Sativa oil improves physiological parameters, oocyte quality after ovarian transplantation, and reproductive performance of female mice. Pak. J. Zool. 51 (6): 2225-2231. https://doi.org/10.17582/journal.pjz/2019.51.6.2225.2231

Mohammed A.A., Abd El-Hafiz G.A., Ziyadah H.M.S. (2012). Effect of dietary urea on ovarian structures in Saidi ewes during follicular and luteal phases. Egypt. J. Anim. Prod. 49: 29-35. https://doi.org/10.21608/ejap.2012.94345

Mohammed A.A., Al-Hozab A.A. (2020). +(-)catechin raises body temperature, changes blood parameters, improves oocyte quality and reproductive performance of female mice. Indian J. Anim. Res. 54(5): 543-548. https://doi.org/10.18805/ijar.B-981

Mohammed A.A., Attaai A.H. (2011). Effects of Dietary Urea on timing of embryo cleavages and blood components in Mice. Vet. World. 4(8): 360-363. https://doi.org/10.5455/vetworld.2011.360-363

Mohammed A.A., Farghaly M.M. (2018). Effect of Nigella sativa seeds dietary supplementation on oocyte maturation and embryo development in mice. Egypt. J. Anim. Prod. 55 (3): 195-201. https://doi.org/10.21608/ejap.2018.93241

Mohammed A.A., Al-Hizab F., Al-Suwaiegh S., Alshaheen T., Kassab A., Hamdon H., Senosy W. (2021). Effects of propylene glycol on ovarian Restoration, reproductive performance, Metabolic status and milk production of Farafra ewes in subtropics. Fresen. Environ. Bull. 30(7): 8192-8202.

Mohammed A.A., Ziyad H.M., Abd El-Hafiz G.A. (2011). Changes of follicular fluid composition in relation to dietary urea level and follicle size during follicular and luteal phases in Saidi Ewes. Theriogenol. Insight. 1(1): 31-42.

Moyo B., Masika P., Hugo A., Muchenje V. (2011). Nutritional characterization of Moringa (Moringa oleifera Lam.) leaves. Afr. J. Biotechnol. 10: 12925–12933. https://doi.org/10.5897/AJB10.1599

Moyo B., Oyedemi S., Masika P., Muchenje V. (2012). Polyphenolic content and antioxidant properties of Moringa oleifera leaf extracts and enzymatic activity of liver from goats supplemented with Moringa oleifera leaves/sunflower seed cake. Meat Sci. 91:, 441–447. https://doi.org/10.1016/j.meatsci.2012.02.029

Nagasawa H.,  Konishi R., Yamamoto K., Ben-Amotz A. (1989). Effects of beta-carotene-rich algae Dunaliella on reproduction and body growth in mice. In Vivo. 3(2):79-81.

Odeyinka S.M., Oyedele O.J., Adeleke T.O., Odedire J.A. (2008). Reproductive performance of rabbits fed Moringa Oleifera as a replacement for centrosema pubescens. In: 9th World Rabbit Congress, Verona, Italy, June 10–13, pp. 411–415.

Olvera-Aguirre G., Mendoza-Taco M.M., Arcos-Álvarez D. N., Piñeiro-Vázquez A.T., Moo-Huchin V. M., Canul-Solís J. R., Castillo-Sánchez L., Ramírez-Bautista M. A., Vargas-Bello-Pérez E., Chay-Canul A.J. (2020). Effect of feeding lactating ewes with Moringa oleifera leaf extract on milk yield, milk composition and preweaning performance of ewe/lamb pair. Anim. 10(7): 1–14. https://doi.org/10.3390/ani10071117

Oyeyinka A.T., Oyeyinka S.A., (2018). Moringa oleifera as a food fortificant: Recent trends and prospects. J. Saudi Soc. Agric. Sci. 17: 127–136. https://doi.org/10.1016/j.jssas.2016.02.002

Pandey A., Modi R. J., Lunagariya P. M., Islam M. (2022). Effect of Feeding Moringa oleifera Meal on Growth Performance of Growing Surti Kids under Intensive System of Management. Ind. J. Vet. Sci. Biotech. https://doi.org/10.21887/ijvsbt.18.1.14

Paul L.T.Fowler L.A., Barry R.J.Watts S.A., (2013). Evaluation of Moringa oleifera as a dietary supplement on growth and reproductive performance in zebrafish. J. Nutr. Ecol. Food. Res. 1(4):322-328. https://doi.org/10.1166/jnef.2013.1050

Razis A.F.A., Ibrahim M.D., Kntayya S.B. (2014). Health benefits of Moringa oleifera. Asian Pac. J. Can. Prev. 15: 8571–8576 https://doi.org/10.7314/APJCP.2014.15.20.8571.

Saini R., Prashanth K.H., Shetty N., Giridhar P. (2014a). Elicitors, SA and MJ enhance carotenoids and tocopherol biosynthesis and expression of antioxidant related genes in Moringa oleifera Lam. leaves. Acta Physiol. Plant. 36: 2695–2704. https://doi.org/10.1007/s11738-014-1640-7

Saini R., Shetty N., Prakash M., Giridhar P. (2014b). Effect of dehydration methods on retention of carotenoids, tocopherols, ascorbic acid and antioxidant activity in Moringa oleifera leaves and preparation of a RTE product. J. Food Sci. Technol. 51: 2176 – 2182. https://doi.org/10.1007/s13197-014-1264-3

Selmi H., Bahri A., Ferchichi A., Rouissi H. (2020). Effect of supplementing Moringa oleifera essential oils on milk quality and fatty acid profile in dairy sheep. Ind. J. Anim. Res. 54(7): 879–882. https://doi.org/10.18805/ijar.B-1085

Senosy W., Kassab A.Y., Mohammed A.A. (2017). Effects of feeding green microalgae on ovarian activity, reproductive hormones and metabolic parameters of Boer goats in arid subtropics. Theriogenol. 96: 16-22. https://doi.org/10.1016/j.theriogenology.2017.03.019

Senosy W., Kassab A.Y., Hamdon H.A., Mohammed A.A. (2018). Influence of organic phosphorus on reproductive performance and metabolic profiles of anoestrous Farafra ewes in subtropics at the end of breeding season. Reprod. Domest. Anim. 53(4): 904-913. https://doi.org/10.1111/rda.13183

Singh S., Kate B.N., Banerjee U.C. (2005). Bioactive compounds from cyanobacteria and microalgae: an overview. Crit. Rev. Biotechnol. 25(3): 73-95. https://doi.org/10.1080/07388550500248498

Sonbarse P.P., Kiran K., Sharma P., Parvatam G. (2020). Biochemical and molecular insights of PGPR application for the augmentation of carotenoids, tocopherols, and folate in the foliage of Moringa oleifera, Phytochem. Volume 179: 112506. https://doi.org/10.1016/j.phytochem.2020.112506

Stamey J.A., Shepherd D.M., de Veth M.J., Corl B.A. (2012). Use of algae or algal oil rich in n-3 fatty acids as a feed supplement for dairy cattle. J. Dairy Sci. 95: 5269–5275. https://doi.org/10.3168/jds.2012-5412

Teixeira E., Carvalho M., Neves V., Silva M., Arantes-Pereira L. (2014). Chemical characteristics and fractionation of proteins from Moringa oleifera Lam. leaves. Food Chem. 147: 51–54. https://doi.org/10.1016/j.foodchem.2013.09.135

Thurber M.D., Fahey J.W. (2009). Adoption of Moringa oleifera to combat under-nutrition viewed through the lens of the Diffusion of Innovations theory. Ecol. Food Nutr. 48, 212–225. https://doi.org/10.1080/03670240902794598

Vachier I., Chanez P., Bonnans C., Godard P., Bousquet J., Chavis C. (2002). Endogenous Anti-inflammatory Mediators from Arachidonate in Human Neutrophils. Biochem. Biophys. Res. Commun. 290 (1): 219-224. https://doi.org/10.1006/bbrc.2001.6155

Vongsak B., Sithisarn P., Gritsanapan W. (2014). Simultaneous HPLC quantitative analysis of active compounds in leaves of Moringa oleifera Lam. J. Chromatogr. Sci. 52 (7): 641–645 https://doi.org/10.1093/chromsci/bmt093.

Wang C., Liu Q., Guo G., Huo W.J., Zhang Y.L., Pei C.X., Zhang S.L. (2019). Effects of rumen-protected folic acid and branched-chain volatile fatty acids supplementation on lactation performance, ruminal fermentation, nutrient digestion and blood metabolites in dairy cows. Anim. Feed Sci. Technol. 247: 157-165. https://doi.org/10.1016/j.anifeedsci.2018.11.015

Warastomo M. T., Suryapratama W., Rahardjo A.H.D. (2021). The effect of additional moringa leaf flour (Moringa oleifera) and palm oil in feed on the physical properties of sheep. angon: J. Anim. Sci. Tech. 3(2): 156–165.

Wen Z., Tian H., Liang Y., Guo Y., Deng M., Liu G., Li Y., Liu D., Sun B. (2022). Moringa oleifera polysaccharide regulates colonic microbiota and immune repertoire in C57BL/6 mice, Int. J. Biol. Macromol. 198: 135-146. https://doi.org/10.1016/j.ijbiomac.2021.12.085

Yasoob T.B., Khalid A.R., Zhang Z., Zhu X., Hang S. (2022). Liver transcriptome of rabbits supplemented with oral Moringa oleifera leaf powder under heat stress is associated with modulation of lipid metabolism and up-regulation of genes for thermo-tolerance, antioxidation, and immunity, Nut. Res. 99: 25-39. https://doi.org/10.1016/j.nutres.2021.09.006

Zarazaga L.A., Malpaux B., Chemineau P. (1996). Characteristics of the plasma melatonin rhythm are not modified by steroids during the estrous cycle in lle-de-France ewes. J. Pineal Res. 21: 114-120. https://doi.org/10.1111/j.1600-079X.1996.tb00278.x

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