PHYTOCHEMISTRY AND PHARMACOLOGICAL ACTIVITIES OF MORINGA OLEIFERAHTML Full Text
PHYTOCHEMISTRY AND PHARMACOLOGICAL ACTIVITIES OF MORINGA OLEIFERA
Alemayehu Toma * and Serawit Deyno
Pharmacology Unit, School of medicine, Hawassa University, Hawassa, Ethiopia.
ABSTRACT: Moringa oleifera can grow well in the humid tropics or hot, dry lands, can survive destitute soils, and is little affected by drought. It tolerates a wide range of rainfall with minimum annual rainfall requirements estimated at 250 mm and maximum at over 3000 mm and a pH of 5.0-9.0. Moringa leaves have been reported to be a rich source of β-carotene, protein, vitamin C, calcium and potassium and act as a good source of natural antioxidants; and thus enhance the shelf-life of fat-containing foods due to the presence of various types of antioxidant compounds such as ascorbic acid, flavonoids, phenolics and carotenoids. In the Philippines, it is known as ‘mother’s best friend’ because of its utilization to increase woman’s milk production and is sometimes prescribed for anemia. Moringa oleifera has both nutritional and multi medicinal activity. Some of the medicinal effects include antimicrobial, antifungal, antihypertensive, anti-hyperlipidemic, anti-hyperglycemic, antipyretic, wound healing, antitumor, anticancer, anti-inflammatory and for purification of water. Since, Moringa oleifera can survive drought condition and its diet content is superior to vitamins and even than milk in protein content, its nutritional benefit is indivisible. However, the more rigorous study is required to achieve a level of proof required for full biomedical endorsement of Moringa oleifera.
Moringa Oleifera, Phytochemistry, Pharmacological actions
INTRODUCTION: Moringa oleifera Lam (syn. M. ptreygosperma Gaertn.) is one of the best known and most widely distributed and naturalized species of a monogeneric family Moringaceae 1. The tree ranges in height from 5 to 10 m. It is found wild and cultivated throughout the plains, especially in hedges and in house yards, thrives best under the insular tropical climate, and is plentiful near the sandy beds of rivers and streams 2. It can grow well in the humid tropics or hot, dry lands, can survive destitute soils, and is little affected by drought.
It tolerates a wide range of rainfall with minimum annual rainfall requirements estimated at 250 mm and maximum at over 3000 mm and a pH of 5.0-9.0 3. Moringa leaves have been reported to be a rich source of β-carotene, protein, vitamin C, calcium and potassium and act as a good source of natural antioxidants; and thus enhance the shelf-life of fat-containing foods due to the presence of various types of antioxidant compounds such as ascorbic acid, flavonoids, phenolics and carotenoids 4. In the Philippines, it is known as ‘mother’s best friend’ because of its utilization to increase woman’s milk production and is sometimes prescribed for anemia 5.
Some medicinal properties have been ascribed to various parts of this highly esteemed tree Table 1. Almost all the parts of this plant: root, bark, gum, leaf, fruit (pods), flowers, seed, and seed oil, have been used for various ailments in the indigenous medicine of South Asia, including the treatment of inflammation and infectious diseases along with cardiovascular, gastrointestinal, hematological and hepatorenal disorders 2, 6. The seeds of Moringa are considered to be antipyretic, acrid, bitter and reported to show antimicrobial activity 2. The seed can be consumed fresh as peas; or pounded, roasted, or pressed into sweet, non-desiccating oil, commercially known as ‘Ben oil’ of high quality.
The unique property is the ability of its dry, crushed seed and seed press cake, which contain polypeptides, to serve as natural coagulants for water treatment 7.
Antilithic, rubefacient, vesicant, carminative, antifertility,
anti-inﬂammatory, stimulant in paralytic afﬂictions; act as a
cardiac/circulatory tonic, used as a laxative, abortifacient,
treating rheumatism, inﬂammations, articular pains, lower
back or kidney pain and constipation
TABLE 1: SOME COMMON MEDICINAL USES OF DIFFERENT PARTS OF MORINGA OILEIFERA
|Plant part||Medicinal Uses|
|Root||Antilithic, rubefacient, vesicant, carminative, antifertility, anti-inflammatory, stimulant in paralytic afflictions; act as a cardiac/circulatory tonic, used as a laxative, abortifacient, treating rheumatism, inflammations, articular pains, lower back or kidney pain and constipation|
|Leaves||Purgative, applied as poultice to sores, rubbed on the temples for headaches, used for piles, fevers, sore throat, bronchitis, eye and ear infections, scurvy and catarrh; leaf juice is believed to control glucose levels, applied to reduce glandular swelling|
|Stem bark||Rubefacient, vesicant and used to cure eye diseases and for the treatment of delirious patients, prevent enlargement of the spleen and formation of tuberculous glands of the neck, to destroy tumors and to heal ulcers. The juice from the root bark is put into ears to relieve earaches and also placed in a tooth cavity as a pain killer, and has anti-tubercular activity|
|Gum||Used for dental caries, and is astringent and rubefacient; Gum, mixed with sesame oil, is used to relieve headaches, fevers, intestinal complaints, dysentery, asthma and sometimes used as an abortifacient, and to treat syphilis and rheumatism|
|Flower||High medicinal value as a stimulant, aphrodisiac, abortifacient, cholagogue; used to cure inflammations, muscle diseases, hysteria, tumors, and enlargement of the spleen; lower the serum cholesterol, phospholipid, triglyceride, VLDL, LDL cholesterol to phospholipid ratio and atherogenic index; decrease lipid profile of liver, heart and aorta in hypercholesterolaemic rabbits and increased the excretion of faecal cholesterol|
|Seed||Seed extract exerts its protective effect by decreasing liver lipid peroxides, antihypertensive compounds thiocarbamate and isothiocyanate glycosids have been isolated from the acetate phase of the ethanolic extract of Moringa pods|
Phytochemistry: Moringa oleifera is rich in compounds containing the simple sugar, rhamnose and a fairly unique group of compounds called glucosinolates and isothiocyanates 8. The stem bark has been reported to contain two alkaloids, namely moringine and moringinine 9. Vanillin, β-sitosterol 14, β-sitostenone, 4-hydroxymellin, & octacosanoic acid have been isolated from the stem of M. oleifera 10. Purified, whole-gum exudate from M. oleifera has been found to contain L-arabinose, -galactose, -glucuronic acid, and L-rhamnose, -mannose and -xylose, while a homogeneous, degraded-gum polysaccharide consisting of L-galactose, -glucuronic acid and L-mannose has been obtained on mild hydrolysis of the whole gum with acid. Flowers contain nine amino acids, sucrose, D-glucose, traces of alkaloids, wax, quercetin, and kaempferol; the ash is rich in potassium and calcium. They have also been reported to contain some flavonoid pigments such as alkaloids, kaempferol, rhamnetin, isoquercitrin and kaempferitrin 6, 10.
Antihypertensive compounds thiocarbamate and isothiocyanate glycosides have been isolated from the acetate phase of the ethanol extract of Moringa pods 11. The cytokinins have been shown to be present in the fruit. A new O-ethyl-4-(ά-L-rhamnosyloxy)benzyl carbamate 11 together with seven known bioactive compounds, 4(ά- L-rhamnosyloxy)-benzyl isothiocyanate3, niazimicin 4, 3-O-(6′-O-oleoyl-β-D-glucopyranosyl) -β-sitosterol 15, β-sitosterol-3-O -β -D-glucopyranoside 16, niazirin 12, β-sitosterol 14 and glycerol-1-(9-octadecanoate) 13 have been isolated from the ethanol extract of the Moringa seed 12. Fig. 1 shows the structures of selected phytochemicals from Moringa.
FIG. 1: STRUCTURES OF SELECTED PHYTOCHEMICALS FROM MORINGA: Niazinin A (1), 4-(4’-O-acetyl-α-L-rhamnopyranosyloxy) benzyl isothiocyanate (2), 4-(-L- L-rhamnopyranosyloxy)benzyl isothiocyanate (3), niazimicin (4), 4-(α-L- rhamnopyranosyloxy)benzyl glucosinolate (5), benzyl isothiocyanate (6), aglycon of deoxy-niazimicine (N-benzyl, S-ethylthioformate (7), pterygospermin (8), niaziminin (9+10), O-ethyl-4-( α-L- rhamnopyranosyloxy)benzyl carbamate (11), niazirin (12), glycerol-1-(9-octadecanoate) (13), β-sitosterol (14), 3-O-(6’-Ooleoly-β-o-glucopyranosyl)-β-sitosterol (15), β-sitosterol-3-β-o-glucopyranoside (16).
Lately, interest has been generated in isolating hormones/growth promoters from the leaves of M. oleifera. Modulation of black-gram (Vigna munga L.) has been shown to increase vigorously with the application of an aqueous ethanol extract of M. oleifera leaves, although the nature of the active ingredient is still unknown. Moringa leaves act as a good source of natural antioxidant due to the presence of various types of antioxidant compounds such as ascorbic acid, flavonoids, phenolics, and carotenoids. The high concentrations of ascorbic acid, oestrogenic substances and β-sitosterol 16, iron, calcium, phosphorus, copper, vitamins A, B and C, α-tocopherol, riboflavin, nicotinic acid, folic acid, pyridoxine, β-carotene, protein, and in particular essential amino acids such as methionine, cysteine, tryptophan, and lysine present in Moringa leaves and pods make it a virtually ideal dietary supplement 13.
The composition of the sterols of Moringa seed oil mainly consists of campesterol, stigmasterol, β- sitosterol, D5-avenasterol and clerosterol accompanied by minute amounts of 24 methylene-cholesterol, D7-campestanol, stigmastanol, and 28-isoavenasterol. The sterol composition of the major fractions of Moringa seed oil differs greatly from those of most of the conventional edible oils. The fatty acid composition of M. oleifera seed oil reveals that it falls in the category of high-oleic oils (C18:1, 67.90%–76.00%). Among the other component fatty acids C16:0 (6.04%–7.80%), C18:0 (4.14%–7.60%), C20:0 (2.76%–4.00%), and C22:0 (5.00%–6.73%) are important. Moringa oleifera is also a good source of different tocopherols (α-, γ- and d-); the concentration of those is reported to be 98.82–134.42, 27.90–93.70, and 48.00–71.16 mg/kg, respectively 14.
Medicinal Uses and Pharmacological Properties: Moringa oleifera also has numerous medicinal uses, which have long been recognized in the Ayurvedic and Unani systems of medicine. The medicinal attributes Table 1 and pharmacological activities ascribed to various parts of Moringa are detailed below.
Anti-hypertensive, Diuretic and Cholesterol-Lowering Activities: The widespread combination of diuretic along with lipid and blood pressure lowering constituents make this plant highly useful in cardiovascular disorders. Moringa leaf juice is known to have a stabilizing effect on blood pressure 2. Nitrile, mustard oil glycosides, and thiocarbamate glycosides have been isolated from Moringa leaves, which were found to be responsible for the blood pressure lowering effect. Most of these compounds, bearing thiocarbamate, carbamate or nitrile groups, are fully acetylated glycosides, which are very rare in nature. Bioassay-guided fractionation of the active ethanol extract of Moringa leaves led to the isolation of four pure compounds, niazinin A 1, niazinin 1 B, niazimicin 4 and niazinin A-B which showed a blood pressure lowering effect in rats mediated possibly through a calcium antagonist effect 10, 11, 15.
Another study on the ethanol and aqueous extracts of whole pods and its parts, i.e., coat, pulp, and seed revealed that the blood pressure lowering effect of seed was more pronounced with comparable results in both ethanol and water extracts indicating that the activity is widely distributed. Activity-directed fractionation of the ethanol extract of pods of M. oleifera has led to the isolation of thiocarbamate and isothiocyanate glycosides which are known to be the hypotensive principles. Methyl p-hydroxybenzoate and β-sitosterol 14, investigated in the pods of M. oleifera have also shown promising hypotensive activity. Moringa roots, leaves, flowers, gum and the aqueous infusion of seeds have been found to possess diuretic activity, and such diuretic components are likely to play a complementary role in the overall blood pressure lowering effect of this plant 11, 16.
The crude extract of Moringa leaves significant cholesterol-lowering action in the serum of high-fat diet fed rats which might be attributed to the presence of a bioactive phytoconstituent, i.e. β- sitosterol. Moringa fruit has been found to lower the serum cholesterol, phospholipids, triglycerides, low-density lipoprotein (LDL), very low-density lipoprotein (VLDL) cholesterol to phospholipid ratio, atherogenic index lipid and reduced the lipid profile of liver, heart, and aorta in hyper-cholesteremic rabbits and increased the excretion of fecal cholesterol 17.
Antispasmodic, Antiulcer and Hepatoprotective Activities: M. oleifera roots have been reported to possess antispasmodic activity. Moringa leaves have been extensively studied pharmacologically, and it has been found that the ethanol extract and its constituents exhibit antispasmodic effects possibly through calcium channel blockade. The antispasmodic activity of the ethanol extract of M. oleifera leaves has been attributed to the presence of 4-[α-(L-rhamnosyloxy) benzyl]- o-methyl thiocarbamate 3 (trans), which forms the basis for its traditional use in diarrhea. Moreover, spasmolytic activity exhibited by different constituents provides a pharmacological basis for the traditional uses of this plant in gastrointestinal motility disorder 18.
The methanol fraction of M. oleifera leaf extract showed antiulcerogenic and hepatoprotective effects in rats. Aqueous leaf extracts also showed antiulcer effect indicating that the antiulcer component is widely distributed in this plant 19. Moringa roots have also been reported to possess hepatoprotective activity. The aqueous and alcohol extracts from Moringa flowers were also found to have a significant hepatoprotective effect 21, which may be due to the presence of quercetin, a well-known flavonoid with hepatoprotective activity 20.
Antibacterial and Antifungal Activities: Moringa roots have antibacterial activity and are reported to be rich in antimicrobial agents. These are reported to contain an active antibiotic principle, pterygospermin 8, which has powerful antibacterial and fungicidal effects. A similar compound is found to be responsible for the antibacterial and fungicidal effects of its flowers 22. The root extract also possesses antimicrobial activity attributed to the presence of 4-α-L-rhamnosyloxy benzyl isothiocyanate 3, 23.
The aglycone of deoxy-niazimicine (N-benzyl, S-ethyl thioformate) 7 isolated from the chloroform fraction of an ethanol extract of the root bark was found to be responsible for the antibacterial and antifungal activities. The bark extract has been shown to possess antifungal activity 24, while the juice from the stem bark showed an antibacterial effect against Staphylococcus aureus 17. The fresh leaf juice was found to inhibit the growth of microorganisms (Pseudomonas aeruginosa and Staphylococcus aureus), pathogenic to man 25.
Antitumor, Anticancer and Anti-Inflammatory Activities: Moringa leaves to be a potential source for anti-tumor activity. O-Ethyl- 4-(α-L-rhamnosyloxy) benzyl carbamate 11 together with 4(α-L-rhamnosyloxy)-benzyl isothiocyanate 3, niazimicin 4 and 3-O-(6′-O-oleoyl-β-D gluco-pyranosyl)- β-sitosterol 15 have been tested for their potential antitumor promoting activity using an in vitro assay which showed significant inhibitory effects on Epstein-Barr virus-early antigen. Niazimicin has been proposed to be a potent chemopreventive agent in chemical carcinogenesis 12. The seed extracts have also been found to be effective on hepatic carcinogen-metabolizing enzymes, anti-oxidant parameters and skin papillomagenesis in mice. A seed ointment had a similar effect to neomycin against Staphylococcus aureus pyodermia in mice. It has been found that niaziminin 9 10, a thiocarbamate from the leaves of M. oleifera, exhibits inhibition of tumor-promoter-induced Epstein–Barr virus activation. On the other hand, among the isothiocyanates, naturally occurring 4-[(4′-O -acetyl-α-i -rhamnosyloxy) benzyl] 2, significantly inhibited tumor-promoter induced Epstein–Barr virus activation, suggesting that the isothiocyanate group is a critical structural factor for activity 26.
The crude ethanol extract of dried seeds inhibited the carrageenan-induced inflammation in the hind paw of mice. The hexane fractions of the crude ethanol extract of the dried seeds also inhibited inflammation, and both butanol and water fractions inhibited inflammation. On the other hand, the ethyl acetate fraction caused an increase in inflammation and exhibited toxicity. The mice died after oral administration of the fraction. The crude ethanol extract also inhibited the formation of Epstein-Barr virus early antigen (EBV-EA) induced by 12-0-tetradecanoyl phorbol-13-acetate (TPA) suggesting its antitumor-promoting activity 31.
Other Diverse Activities: Moringa oleifera has also been reported to exhibit other diverse activities. Aqueous leaf extracts regulate thyroid hormone and can be used to treat hyperthyroidism and exhibit an antioxidant effect. A methanol extract of M. oleifera leaves conferred significant radiation protection to the bone marrow chromosomes in mice. Moringa leaves are effective for the regulation of thyroid hormone status 27. A recent report showed that M. oleifera leaf may be applied as a prophylactic or therapeutic anti-HSV (Herpes simplex virus type 1) medicine and may be effective against the acyclovir-resistant variant. Table 1 depicts some common medicinal uses of different parts of this plant. The flowers and leaves also are considered to be of high medicinal value with an antihelmintic activity which is comparable with that of piperazine citrate 28, 35.
Moringa oleifera is coming to the forefront as a result of scientific evidence that Moringa is an important source of naturally occurring phyto-chemicals and this provides a basis for viable future developments. Different parts of M. oleifera are also incorporated in various marketed health formulations, such as Rumalaya and Septilin (the Himalaya Drug Company, Bangalore, India), Orthoherb (Walter Bushnell Ltd, Mumbai, India), Kupid Fort (Pharma Products Pvt. Ltd, Thayavur, India) and Livospin (Herbals APS Pvt. Ltd., Patna, India), which are reputed as remedies available for a variety of human health disorders 17.
Moringa seeds have specific protein fractions for skin and hair care. Two new active components for the cosmetic industry have been extracted from oil cake. Purisoft consists of peptides of the Moringa seed. It protects the human skin from environmental influences and combats premature skin aging. With dual activity, antipollution and conditioning/strengthening of hair, the M. oleifera seed extract is a globally acceptable innovative solution for hair care 36.
The study conducted in India reported that ethanolic and ethyl acetate seed extracts of Moringa oleifera exhibited significant antipyretic activity. Ethyl acetate extract also showed significant percent closure of excision wound. The healing of wounds in case of rats treated with ethyl acetate extract was found to be quicker than the control, which is also comparable with standard (vicco turmeric) 32.
Comparative Effects of Moringa oleifera Lam. tea on normal and hyperglycemic patients conducted in the Philippines showed that blood sugar levels of people in the normal group were not significantly changed 2 h after taking the tea. However, for hyperglycemic individuals, the blood sugar levels significantly dropped after 2 h. A mean drop of 28.15 mg/dl in the blood sugar levels was observed among the hyperglycemic patients. The results point to the benefit of using Moringa oleifera Lam. tea in the management of hyperglycemia 33.
The methanol and water extracts of M. oleifera leaf and root inhibited the 6-hydroxylation of testosterone by CYP3A4 present in human liver microsomes. Activity decreased with increasing inhibitor concentration. The estimated IC50 values are 0.5 and 2.5 mg/ml for methanol and waterleaf extracts, respectively. The human CYP3A4 inhibitory activity exhibited in-vitro makes Moringa a potential risk for herb/ARV interactions for individuals in HAART 34.
Water Purifying Attributes of M. oleifera Seed:
Moringa Seeds as a Coagulant: Moringa seeds are one of the best natural coagulants discovered so far. Crushed seeds are a viable replacement of synthetic coagulants. In Sudan, seed crude extract is used instead of alum by rural women to treat the highly turbid Nile water because of a traditional fear of alum causing gastrointestinal disturbances and Alzheimer’s disease. Moringa seeds are very effective for high turbidity water and show similar coagulation effects to alum 29, 30.
The coagulation effectiveness of M. oleifera varies depending on the initial turbidity, and it has been reported that M. oleifera could reduce turbidity by between 92% and 99% 29. Moringa seeds also have to soften properties in addition to being a pH corrected (alkalinity reduction), as well as exhibiting a natural buffering capacity, which could handle moderately high to high alkaline surface and ground waters. The Moringa seeds can also be used as an antiseptic in the treatment of drinking water. Ongoing research is attempting to characterize and purify the coagulant components of Moringa seeds 7, 29. It is believed that the seed is a natural organic polymer. The active ingredients are dimeric proteins with a molecular weight of about 1300 Da and an isoelectric point between 10 and 11. 29
The protein powder is stable and totally soluble in water. Moringa coagulant protein can be extracted by water or salt solution (commonly NaCl). The amount and effectiveness of the coagulant protein from salt and water extraction methods vary significantly. In crude form, the salt extract shows a better coagulation performance than the corresponding water extract 30. This may be explained by the presence of a higher amount of soluble protein due to the salting-in phenomenon. However, purification of the M. oleifera coagulant protein from the crude salt extract may not be technically and economically feasible.
The coagulation mechanism of the M. oleifera coagulant protein has been explained in different ways. It has been described as adsorption and charge neutralization and inter-particle bridging 30. Flocculation by inter-particle bridging is mainly characteristic of high molecular weight polyelectrolytes. Due to the small size of the M. oleifera coagulant protein (6.5-13 kDa), a bridging effect may not be considered as the likely coagulation mechanism. The high positive charge (pI above 10) and small size may suggest that the main destabilization mechanism could be adsorption and charge neutralization.
Microbial Elimination with Moringa Seeds: Moringa seeds also possess antimicrobial properties. It was reported that a recombinant protein in the seed can flocculate gram-positive and gram-negative bacteria cells. In this case, microorganisms can be removed by settling in the same manner as the removal of colloids in properly coagulated and flocculated water. On the other hand, the seeds may also act directly upon microorganisms and result in growth inhibition. Antimicrobial peptides are thought to act by disrupting the cell membrane or by inhibiting essential enzymes. Moringa seeds could inhibit the replication of bacteriophages. The antimicrobial effects of the seeds are attributed to the compound 4(α-L-rhamnosyloxy) benzyl isothiocyanate 23, 30.
Moringa Seeds as Biosorbent: Moringa seeds could be used as a less expensive biosorbent for the removal of cadmium (Cd) from aqueous media. The aqueous solution of Moringa seed is a heterogeneous complex mixture having various functional groups, mainly low molecular weight organic acids (amino acids). These amino acids have been found to constitute a physiologically active group of binding agents, working even at a low concentration, which because of the ability to interact with metal ions is likely to increase the sorption of metal ions. The proteineous amino acids have a variety of structurally related pH-dependent properties, generating a negatively charged atmosphere and play an important role in the binding of metals 37.
Future Prospects: So far numerous studies have been conducted on different parts of M. oleifera, but there is a dire need to isolate and identify new compounds from different parts of the tree, which have possible antitumor promoters as well as inhibitory properties. Although, preliminary studies are underway in different laboratories to use the antispasmodic, anti-inflammatory, antihypertensive and diuretic activities of M. oleifera seed, these studies should be extended to humans because of the edible nature of the plant. Moringa roots and leaves have been used traditionally to treat constipation.
Studies to verify these claims need to be carried out in the light of the reported antispasmodic activities, which are contrary to its medicinal use as a gut motility stimulant. Earlier studies on the presence of a combination of spasmogenic and spasmolytic constituents in different plants used for constipation might be of some guidance in designing experiments in which the presence of anti-spasmodic constituents at higher doses are explained as a possible mode to offset the side-effects usually associated with the high dose of laxative therapy. Similarly, the known species differences in the pharmacological actions of medicinal plants may also be taken into account when planning studies involving contradictory results. Food plants are considered relatively safe as they are likely to contain synergistic and side effect neutralizing combinations of activities 38.
Moringa oleifera, known to be rich in multiple medicinally active chemicals, may be a good candidate to see if it contains effect enhancing and side-effects neutralizing combinations. Medicinal plants are relatively rich in their contents of calcium channel blockers (CCBs) which are known to possess a wide variety of pharmacological activities such as anti-hypertensive, hepato-protective, antiulcer, antiasthmatic, antispasmodic and antidiarrhoeal 39 and it remains to be seen whether such activities reported being present in Moringa oleifera have a direct link with the presence of CCBs. Niazimicin, a potent antitumor promoter in chemical carcinogenesis is present in the seed; its inhibitory mechanism on tumor proliferation can be investigated by isolating more pure samples. The mechanism of action of M. oleifera as prophylactic or therapeutic anti- HSV medicines for the treatment of HSV-1 infection also needs to be examined.
The available information on the a-, d- and g- tocopherol content in samples of various parts of this edible plant is very limited. β-carotene and vitamins A and C present in M. oleifera, serve as an explanation for their mode of action in the induction of antioxidant profiles, however, the exact mechanism is yet to be elucidated. β-Carotene of M. oleifera leaves exerts a more significant protective activity than silymarin against antitubercular induced toxicity. It would be interesting to see if it also possesses hepatoprotective effect against other commonly used hepatotoxic agents such as CCl4 and galactosamine, which are considered more suitable models and close to human viral hepatitis 40.
Although, Moringa leaves are considered the best protein source, it still has to be shown whether or not this protein source could compete with the more common Protein sources in highly productive growing or milk-producing ruminants. Many studies have also been conducted on the performance of Moringa seeds as an alternative coagulant, coagulant aid and in conjunction with alum for treating wastewater. Therefore, it is important to identify the active constituents of Moringa seed for a better understanding of the coagulation mechanism.
Reports on the antimicrobial effects of the protein purified from M. oleifera are very rare. Since, this plant naturally occurs in varying habitats, it is naïve to expect a great magnitude of variation in the concentration and composition of chemical ingredients in different parts of the tree. However, the extent to which the chemical composition varies in populations adapted to varying habitats is not known. Thus, detailed studies are required to examine this aspect. Because of its multiple uses, the M. oleifera plant needs to be widely cultivated in most of the areas where climatic conditions favor its optimum growth. In this way, a maximum yield of its different useable parts could be achieved to derive the maximal amount of commodities of a multifarious nature for the welfare of mankind 41.
CONCLUSION AND RECOMMENDATION: Moringa oleifera is dicotyledonous which can grow in the tropical and subtropical area. Phyto-chemically Moringa oleifera contains proteins, carbohydrates, tannins, glycosides, fatty acids, flavonoids, and carotenoids. Moringa oleifera has both nutritional and multi medicinal activity. Some of the medicinal effects include anti-microbial, antifungal, antihypertensive, anti-hyperlipidemic, anti-hyperglycemic, antipyretic, wound healing, antitumor, anticancer, anti-inflammatory and for purification of water. Since, Moringa oleifera can survive drought condition and its diet content is superior to vitamins and even than milk in protein content, its nutritional benefit is indivisible.
However, the more rigorous study is required to achieve a level of proof required for full biomedical endorsement of Moringa oleifera. Finally, I strongly recommend a lot to do with Moringa species indigenous to Ethiopia which is called Moringa stenopetala for activities mentioned for Moringa oleifera.
CONFLICT OF INTEREST: Nil
- Nadkarni AK: Indian Materia Medica. Popular Prakashan: Bombay, 1976: 810-816.
- The Wealth of India (A Dictionary of Indian Raw Materials and Industrial Products). Raw Materials, Vol. VI: L-M; Council of Scientific and Industrial Research: New Delhi, 1962: 425-429.
- Palada MC and Changl LC: Suggested cultural practices for Moringa. International Co-operators’ Guide AVRDC. AVRD pub # 2003: 03-545. www.avrdc.org.
- Dillard CJ and German JB: Phytochemicals: nutraceuticals and human health: A review. J Sci Food Agric 2000; 80: 1744-1756.
- Estrella MCP, Mantaring JBV and David GZ: A double-blind, randomized controlled trial on the use of malunggay (Moringa oleifera) for augmentation of the volume of breast milk among non-nursing mothers of preterm infants. Philipp J Pediatr 2000. 49: 3-6.
- Siddhuraju P and Becker K: Antioxidant properties of various solvent extracts of total phenolic constituents from three different Agro-climatic origins of drumstick tree (Moringa oleifera). J Agric Food Chem 2003; 15: 2144-2155.
- Ndabigengesere A and Narasiah KS: Quality of water treated by coagulation using Moringa oleifera Water Res 1998; 32: 781-791.
- Fahey JW, Zalcmann AT and Talalay P: The chemical diversity and distribution of glucosinolates and isothiocyanates among plants. Phytochemistry 2001; 56: 5-51.
- Kerharo PJ: Un remede populaire Sengalais: Le ‘Nebreday’ (Moringa oleifera) employs therapeutics en milieu Africain chimie et pharmacology. Plantes Med Phytother 1969; 3: 14-219.
- Faizi S, Siddiqui B, Saleem R, Saddiqui S and Aftab K: Isolation and structure elucidation of new nitrile and mustard oil glycosides from oleifera and their effect on blood pressure. J Nat Prod 1994; 57: 1256-1261.
- Faizi S, Siddiqui BS, Saleem R, Aftab K, Shaheen F and Gilani AH: Hypotensive constituents from the pods of Moringa oleifera. Planta Med 1998; 64: 225-228.
- Guevara AP, Vargas C and Sakurai H: An antitumor promoter from Moringa oleifera Mutat Res 1999; 440: 181-188.
- Makkar HPS and Becker K: Nutritional value and anti-nutritional components of whole and ethanol extracted Moringa oleifera Anim Feed Sci Technol 1996; 63: 211-228.
- Anwar F and Bhanger MI: Analytical characterization of Moringa oleifera seed oil grown in temperate regions of Pakistan. Journal Agric Food Chem 2003; 51: 6558-6563.
- Faizi S, Siddiqui B, Saleem R, Siddiqui S, Aftab K and Gilani A: Novel hypotensive agents, niazimin A, niazimin B, niazicin A and niazicin B from Moringa oleifera; Isolation of first naturally occurring carbamates. J Chem Soc Perkin Trans 1994b; I: 3035-3640.
- Faizi S, Siddiqui BS, Saleem R, Siddiqui S, Aftab K, and Gilani AH: Fully acetylated carbamate and hypotensive thiocarbamate glycosides from Moringa oleifera. Phytochemistry 1995; 38: 957-963.
- Mehta LK, Balaraman R, Amin AH, Bafna PA and Gulati OD: Effect of fruits of Moringa oleifera on the lipid profile of normal and hypercholesterolemic rabbits. J Ethnopharmacol 2003; l86: 191-195.
- Gilani AH, Aftab K and Suria A: Pharmacological studies on hypotensive and spasmodic activities of pure compounds from Moringa oleifera. Phytother Res 1994a; 8: 87-91.
- Pal SK, Mukherjee PK and Saha BP: Studies on the antiulcer activity of Moringa oleifera leaf extract on gastric ulcer models in rats. Phytother Res 1995a; 9: 463-465.
- Gilani AH, Janbaz KH and Shah BH: Quercetin exhibits hepatoprotective activity in rats. Biochem Soc Trans 1997; 25: 85.
- Ruckmani K, Kavimani S, Anandan R and Jaykar B: Effect of Moringa oleifera Lam on paracetamol-induced hepatotoxicity Indian J Pharm Sci 1998; 60: 30-35.
- Das BR, Kurup PA, Rao PL and Narasimha Rao PL: The antibiotic principle from Moringa pterygosperma. VII. Antibacterial activity and chemical structure of compounds related to pterygospermin. Indian J Med Res 1957; 45: 191-196.
- Eilert U, Wolters B and Nadrtedt A: The antibiotic principle of seeds of Moringa oleifera and Moringa stenopetala. Planta Med 1981; 42: 55-61.
- Bhatnagar SS, Santapau H, Desai JDH, Yellore S and Rao TNS: The biological activity of Indian medicinal plants. Part 1. Anti-bacterial, anti-tubercular and antifungal action. Indian J Med Res 1961; 49: 799-805.
- Caceres A, Cabrera O, Morales O, Mollinedo P and Mendia P: Pharmacological properties of Moringa oleifera. 1: Preliminary screening for antimicrobial activity. J Ethnopharmacol 1991; 33: 213-216.
- Caceres A and Lopez S: Pharmacologic properties of Moringa oleifera: 3: Effect of seed extracts in the treatment of experimental Pyoderma. Fitoterapia 1991; 62: 449-450.
- Tahiliani P and Kar A: Role of Moringa oleifera leaf extract in the regulation of thyroid hormone status in adult male and female rats. Pharmacol Res 2000; 41: 319-323.
- Trapti R, Vijay B, Komal, Aswar P and Khadabadi S: Comparative studies on anthelmintic activity of Moringa oleifera and Vitex negundo. Asian J Research Chem 2009; 2(2).
- Muyibi SA and Evison LM: Optimizing physical parameters affecting coagulation of turbid water with Moringa oleifera Water Res 1995b; 29: 2689-2695.
- Francis K and Amos B: Effectiveness of Moringa oleifera seed as a coagulant for water purification. African Journal of Agricultural Research 2009; 4(1): 119-123.
- Guevara AP, Carolyn V and Milagros U: Anti-inflammatory and antitumor activities of seeds extracts of Malunggay, oleifera. http://www.stii.dost. gov
- Hukkeri V, Nagathan C, Karadi R and Patil B. Antipyretic and wound healing activities of Moringa oleifera in rats. http:// www.ijpsonline.com
- Michael P and Howell H: Comparative effects of Moringa oleifera tea on normal and hyperglycemic patients. http://www.ehealthinternational.org/
- Monera1 G: Moringa oleifera leaf extracts inhibit 6β-hydroxylation of testosterone by CYP3A4. J Infect Developing Countries 2008; 2(5): 379-383.
- Bhattacharya SB, Das AK and Banerji N: Chemical investigations on the gum exudates from Sonja (Moringa oleifera). Carbohydr Res 1982; 102: 253-262.
- Stussi IA, Freis O, Moser P and Pauly G: Laboratories Sérobiologiques Pulnoy, France 2002. http://www. laboratoiresserobiologiques.com
- Sharma P, Kumari P, Srivastava MM and Srivastava S: Removal of cadmium from aqueous system by shelled Moringa oleifera seed powder. Bioresour Technol 2006; 97: 299-305.
- Gilani AH, Bashir S, Janbaz KH and Shah AJ: Presence of cholinergic and calcium channel blocking activities explains the traditional use of Hibiscus rosasinensis in constipation and diarrhea. J Ethnopharmacol 2005a; 102: 289-294.
- Stephens RL Jr and Rahwan RG: Antiulcer activity of the calcium antagonist propyl-methyleneiodioxyindene-V, localization of the site of action. Gen Pharmacol 1992; 23: 193-196.
- Gilani AH and Janbaz KH: Preventive and curative effects of Berberis aristata fruit extract on paracetamol and CCl4-induced hepatotoxicity. Phytother Res 1995; 9: 489-494.
- Farooq A, Sajid L, Muhammad A and Anwarul H: Moringa oleifera: A food plant with multiple medicinal uses. Phytother Res 2007; 21: 17-25.
How to cite this article:
Toma A and Deyno S: Phytochemistry and pharmacological activities of Moringa oleifera. Int J Pharmacognosy 2014; 1(4): 222-31. doi link: http://dx.doi.org/10.13040/IJPSR.0975-8232.IJP.1(4).222-31.
This Journal licensed under a Creative Commons Attribution-Non-commercial-Share Alike 3.0 Unported License.
A. Toma* and S. Deyno
Pharmacology Unit, School of medicine, Hawassa University, Hawassa, Ethiopia.
05 January 2014
27 February 2014
30 March 2014
01 April 2014