Sesbenia grandiflora: An all-round tree
Avinash B. Thalkari1*,
Pawan N. Karwa2, Priyanka S. Chopane1,
Krushna. K. Zhambare1,
Pallavi S. Shinde2, Thalkari A.B.1
1SBSPM’S B- Pharmacy
College, Ambajogai-431517, Maharashtra.
2Gurukrupa Institute
of Pharmacy (Degree), Near Chatrapatthi Sugar
Factory,
NH- 222 Gadi
Road, Majalgaon-431131, Maharashtra.
*Corresponding Author E-mail: avinashthalkari@rediffmail.com
ABSTRACT:
The history of herbal
medicines is as old as human civilization. Sesbania
sesban Linn. (fabaceae)
is to be found in all geographical plains of India and are commonly are known
to be Jayanti. The leaves of Sesbania Sesbanhastra are been designed as a purgative,
demulcent, maturant, Anthelmintic and for also for
all inflammation and related pains . It a herb which is used in
traditional system of medicine to carry all the the
leaves of Sesbania grandiflora have
been used in local traditional medicine since ancient times. The various
traditional medicinal plants are casted in the treatment of diabetes
mellitus and many other diseases since past decade. The antioxidant property of
Agati is due to the presence of phytochemical
constituents making it a potent anticancer and hepatoprotective agent. The
below paper is a study that is intended with various properties, chemicaltests, different types of screening and also their
uses which were carried out on the flowers of Sesbania
grandiflora. According to the survey of the WHO almost 80% of people living
in developing countries depend on the traditional medicines to maintain their
health care.
KEYWORDS: Traditional,
Medicinal, Microscopy, Inflammation, Analysis.
INTRODUCTION:
In India, we are
using plants and herbs as the basic source of medicine as they are very rich in
medical content. Sesbani sesban Linn., commonly known as ‘Egyptian Susan’ is one
of the six species of genus Sesbania that is
commonly found in tropical region of India. The plant is grown due to its
property of nitrogen fixing ability and as wind shades.(1)Small tree
are mostly seen in the India or Southeast Asia and needs hot and humid
tropical climate areas in the in the world. In Australia and in India, plantations
have attained heights of about 8m in under 3 years.
Sesbania is grown as a cover crop and green manure in the
summer months. When the process of growing cover of the crop or the plant the
soil incorporation is a important factor in case of
the sesbania it does well incorporation while
becomes green or soon after flowering for the purpose of soil improvement. The
major plus point obtained from growing Sesbania
is the addition of organic matter that is needed to be added in the desert
soils. During the breakdown of organic matters by microorganisms, compounds are
formed which are resistant to decomposition – such as gums, waxes and Resins.
The tree are useful in the forage, firewood, pulp and paper, food, green manure
and landscape decoration.(2) The phytochemicals are mostly important
resources for medicinal uses. The plant products are becoming more popular than
the synthetic drugs due to the property of low toxicity and long standing
experience of exposure of these drugs in ethnic medicine system like Ayurveda.
It is cultivated as an ornamental plant, grows wild in hedges and shady
forests.(3) The leaf is widely used in detoxification process of manacle.
S. grandflora leaves are highly nutritious and
have been shown to contain significant amounts of proteins, fat, carbohydrates,
fiber, and minerals such as iron, calcium, and phosphorus. The new grown leaves
are edible and are quite often used as a part of the meals. In the rural areas
of the Tangail district of Bangladesh, the villagers use it as a remedy for
diarrhea. Oral administration of crude ethanolic extracts of Sesbania grandiflora reduces the number and
duration of defecation episodes.(4) Nutraceuticals are the emerging
era in the treatment and prevention of cancer, neurodegenerative diseases,
cardiovascular diseases, and diabetes mellitus. In 2014, WHO reported the
global prevalence of diabetes mellitus was estimated 9% among adult and 1.5
million deaths.(5) The whole plant parts from the top to the
bottom of Sesbani grandiflora posses different therapeutic values. They also play a role
in the preparations of different dosage forms such as paste, cream, powder,
tablets, capsules, tincture, extracts, and tonic. Steamed flowers are used as a
traditional Indonesian dish.(6) It was certainly introduced into the
Philippines. This tree occurs also in India to the Mascarene Islands, through
Malaya to tropical Australia, and is planted in other tropical countries(7)
It is well adapted to hot, humid environments and does not grow well in
the subtropics particularly in areas with temperatures below about 100C.(8)
Wound healing involves various steps like coagulation, formation of granulation
tissue, coagulation and acquisition of wound strength.(9)
Synonyms:
Robinia grandiflora (L),
Aeschynomene grandiflora (L),
Agati grandiflora(L.) (6)
Sesban grandiflora Poir.(7)
Common names:
Australian Corkwood
tree, Tiger Tongue, West Indian Pea, White Dragon Tree.(6)
Arabic: Sesaban
Bengali: Jainti, Jayant
Burmese:Yay-tha-kyee, Yethugyi(10)
Chamorro: caturay,
katurai.(7)
English: Common sesban, Egyptian rattle pod, Frother,
River bean, Sesban, Sesbania,
Corkwood tree, Scarlet wisteria, Sesban, Vegetable
hummingbird
French: Agati
a grandesfleurs. (10)
Hawaiian:Ohaike‘oke‘o.(7)
Hindi: Jainti,
Jait, Rawasan
Indonesian: Janti, Jayanti, Puri
Javanese: Janti
Luganda: Mubimba, Muzimbandeya(10)
Marathi: Hadga
Palauan: Katurai.
Samoan: Sepania.(7)
Sanskrit: Jayanti, Jayantika
Spanish: Ańilfrancés,
Tamarindillo(10)
Tahitian: Afai,
Ofai, Ouai, Oufai.
Tamil: Agathi,
Agati(7),Champai,
Chithagathi, Karunchembai
Thai: Sami, Saphaolom
Vietnamese: Dien-dien(10)
Morphological characters:-
S.grandiflora is a small, erect,
fast-growing perennial (4-5 m in just 6 months), and sparsely branched tree
that reaches an average height of about 10-15 m and a diameter up to 12 cm
(fig. 1A). The leaves are pari-pinnately compound up
to 15-25 cm long with 20-50 leaflets in pairs, dimensions 12-44x5-15 mm, oblong
to elliptical in shape and opposite arrangement. Single leaflet is 2-4 cm long
and 10-15 mm in breadth, linear, oblong, mucronate, deciduous, stipulus lanceolate orsetaceous
deciduous (fig. 1B-C) .The bark is light gray, corky and deeply furrowed and
the wood is soft and white (fig. 1D). The flower clusters hanging at the leaf
base. They are fleshy with 2-5 large or giant showy white petals. They are
7.5-10.0 cm long with short axillary racemes, curved about 3 cm wide before
opening. Flowers are arrangement to pea flowers with five petals that are
differentiated into a standard, wing, and keel petals. The standard petal of
the flowers is seen usually upright, the wing of the petals spread out on
opposite if the flower and the keel is when observed was found to be
boat-shaped and in this species is curved down and away from the flower (fig.
1E). The Fruit, The fruit looks like flat, long and thin green beans. Pod looks
like sub-cylindrical, straight or slightly curved up to 30-45 cm long and 5-8
mm wide, straw-colored or reddish-brown, containing from 15-50 pale-colored
seeds. Seed: The seed is 3-4.5 mm x 2 mm x 2 mm, sub-cylindrical or bean like,
elliptical, olive-green or red brown, 6-8 in a pod. There are 55-80 seeds per
gram.
Fig. 1: S.
Grandiflora small branched tree (A), leaves (B-C), stems (D), and
flowers (E)Powder Microscopy.(5)
Phytochemicals,
Phytochemical screening and study Phytochemical Substances:-
1]Phytochemicals,
Phytochemical screening :
A] Phytochemicals:
The freshly prepared
organic extracts are qualitatively tested to detect the presence of various
categories of phytochemicals. These are then identified by characteristic color
changes as are previously described. The total flavonoid content is then
estimated using quercetin as a reference compound. The total tannin content of S.grandiflora was determined by Folin-Coicalteu method as previously described.(4) The
phytochemical constituents of Sesbania grandiflora
are alkaloids, flavonoids, glycosides, tannins, steroids, proteins,
carbohydrates, terpenoids, anthraquinone and saponin.(6).Preliminary
Phytochemical screening revealed the presence of triterpenoids, carbohydrates,
vitamins, amino acids, proteins, tannins, Saponins glycosides and steroids.
Flowers contain cyanidin and delphinidin glucosides. The Pollen play an
important role and pollen tubes contain alpha-ketoglutaric, oxaloacetic and
pyruvic acids as a main content. The observations suggests that, previous
phytochemical study of the plant led to the isolation of oleanolic acid,
stigmasta-5, 24(28)-diene-3-ol-3-0-β-D-galactopyranoside,
fatty acids and also the amino acids. Various types of lignins
composed of guaiacyl, syringyl
and P-hydroxyphenylpropane building units and also
antitumor principal kaempferol disaccharide.(10)
B]phytochemical
screening:
The plant Sesbania grandiflora (Linn) contains Grandifloral, arginine, cystine, histidine, isolucine, phenylalanine, tryptophan, valine, threonine,
alanine, aspargine, aspartic acid and a saponin
yielding oleanolic acid, galactose, rhamnose and glucuronic acidand
it also contains flavonol glycoside, kaempfrol. The various extracts of Sesbania
grandiflora i.e. Petroleum ether, Chloroform, Ethylacetate,
Methanol, and Hydroalcoholicmedium were subjected to
qualitative chemical analyses to detect the presence of various
phytoconstituents.(2)
Phytochemical
study:
A] On Bioactive
compounds:-
The leaves of plant
samples are firstly air-dried and then ground into uniform powder. The aqueous
extract of each sample is then prepared by soaking 100g of dried, powdered
sample in 200ml of distilled water for 12 hour. The extracts were filtered
using whattman Filter paper No.42 (125mm).
Phytochemical tests were carried out on the aqueous extract and on the powdered
specimens.(8)
B] Phytochemical
substances:-
The nutritive value
of S. grandiflora leaves contains moisture about 73.1 g, protein 8.4g,
fat 1.4g, minerals 3.1g, crude fibers 2.2g, carbohydrates 11.8 mg, energy 93
mg, calcium 1,130 mg, phosphorus 80 mg, and iron 3.9 mg. The literature survey
of this plant revealed that this plant possesses protein and amino acids:
arginine, cysteine, histidine, isoleucine, phenylalanine, tryptophan, valine,
threonine, alanine, asparagine, aspartic acid, leucocyanidin and cyaniding. Sugar
derivatives are galactose and rhamnose. The phytochemical substances of S.
grandiflora various parts contain several kinds of alkaloids,
triterpenoids, carbohydrates, saponin, tannin, chlorogenic acid, flavonoid,
anthocyanin, steroidal glycosides and phenolic compounds. Three is flavonoids, isovestitol, medicarpin, and sativan,
along with other known compound, betulinic acid, were
isolated from the root. The active ingredients in the seeds are leucocyanidin
and cyaniding. The active ingredients in flowers are cyaniding, delphinidin
glucosides, tannins, keampferol, grandiflora,
proteins, oleanolic acid, cysteine, isoleucine, asparagine, phenylalanine,
valine, nicotinic acid and vitamin C.(5)
Powder Microscopy:
Studies on the leaves helped
to be very useful in identification of unique diagnostic characters like
presence of 1to 4 layered angular collenchymatous
tissue near the vascular bundle towards the lower region, Hence the powder
microscopic studies of the leaf leads to the diagnostic characters of the plant
that can go a long way in pharmacognosy and authentic identification
1] Powder Microscopic Studies:
Leaflets of S. grandiflora
are dorsiventral, upper and lower epidermis are single layered covered by thin
cuticle. Upper epidermis is followed by 2-3 layers of narrowly arranged angular
collenchymatous cells and 1-4 layers of closely
arranged parenchymatous cells in the form of neck of the round bottom flask
(Figure 2, 5). Centre portion of the midrib region is occupied by well developed vascular bundle which is conjoint,
collateral, closed with metaxylem facing towards the lower region and
protoxylem facing towards the upper region (Figure 2, 4). Lower region of the
leaf let is planoconvexin structure consisting of 2-3
layers of angular collenchymas followed by 1-3 layers
of parenchyma. About 1-4 layers of cells are arranged near the vascular bundle
region (Figure 3). Microscopically laminar region shows single layered upper and
lower epidermis, 2 layered palisade parenchyma and loosely arranged spongy
parenchyma cells (Figure 6). Stomata are of anisocytic,
present on both surfaces but more towards the lower surface (Figure 7).The
quantitative values of the upper and lower surface of stomatal index is
15-20-26 per sq mm, and 16-22-28 per sq mm respectively. The palisade ratio is 4.20-5.50 per sq mm. The vein islet number is 20-30 per sq mm and the upper and lower surface Stomatal number is
4-6-8 per sq mm,5-7-9 per sq
mm respectively. Diagnostic characters of Agathi·
Presence of 1to 4 layered angular collenchymatous
tissue near the vascular bundle towards the lower region. There was the
presence of the prominent 2-3 layered narrowly arranged angular collenchymatous cells and 1-4 layers of closely arranged
parenchymatous cells in the form of neck of the round bottom flask towards the
upper epidermal layer. Presence of anisocytic type of
stomata on both surfaces of the leaf let, more towards the lower surface·
Presence of conjoint, collateral, closed Vascular bundle in the midrib region
of the leaf let. Physicochemical Studies The results of physicochemical studies
are presented in table 1. Further, the sample tested positive for saponins
which is evident by the percentage of chloroform and petroleum ether extracts.
The sample also contained traces of tannins. The swelling index was found to be
9ml and the foaming index is <100. The sample contains inorganic
constituents like bicarbonates (HCo3), sulphates (SO4), chlorides (Cl3), calcium
(Ca), Sodium (Na), calcium phosphate (CaPO4), iron (Fe) and magnesium
(Mg).Fluorescence Studies The fluorescence behavior of the powder with
different reagents under day light and short ultra violet light showed distinct
characteristic features. The details are depicted in table 2.Thin layer
chromatography studies (Table3)Thin layer Chromatography study has been carried
out with petroleum ether, Chloroform and ethanol extracts by using solvents
such as benzene: ethanol (19:1), Chloroform: methanol (19:1) and Toluene: ethyl
acetate (90:10) respectively. Plates viewed under ordinary light, UV long wave
365nm and UV short wave 254nm. Rf values of the various spots were calculated.
The Rf value of the petroleum ether extract has shown nine spots 0.08,0.13, 0.2,
0.5, 0.58, 0.71, 0.8, 0.86, 0.94; similarly Chloroform extract 0.05,
0.19, 0.28, 0.77
Table 1: Table 1:
Physicochemical Analysis
Sr.No. |
Extractives |
Solvent system |
Spraying reagent |
Rf. Values |
1 |
Petroleum-either 60-80°C |
Benzene: Ethanol (19:1) |
10%H2SO4 in Methanol |
0.08, 0.13, 0.2, 0.5, 0.58, 0.71, 0.8, 0.86, 0.94. |
2 |
Silica gel 60 F 254 pre coated sheets |
Chloroform: Methanol (19:1) |
10%H2SO4 in Methanol |
0.05, 0.19, 0.28, 0.35. |
3 |
Silica gel 60 F 254 pre coated sheets |
Toluene: Ethyl acetate (90:10), |
10%H2SO4 in Methanol |
0.05, 0.14, 0.29, 0.54, 0.77. |
Table 2: Fluorescence Studies
[Powder (P) + reagent] |
Ordinary light |
U.V. Long wave 365 nm |
U.V. Short wave 254 nm |
Powder |
G |
FL.W |
G |
P + Water |
G |
Dark Y |
G |
P + 1N. HCl |
Br |
Br |
Dark G |
P + 1N. NaOH |
G |
Mustard |
Dark G |
P+1N. NaOH In MeOH |
Dark G |
Light lemon Y |
Dark G |
P + 50% KOH |
Dark G |
Pinkish O |
Deep G |
P + 50% H2SO4 |
Deep G |
Br |
G |
P + Con. H2SO4 |
Bl |
FL G |
G Bl |
P + 50% HNO3 |
Br |
Br |
G |
P + Con.HNO3 |
Br |
Light Br |
Br G |
P + Acetic acid |
Bl Br |
O |
Dark G |
P + Iodine water |
G |
Dark Br |
G |
(G: Green; Bl: Black; Br:
Brown; Y: Yellow Fl: Fluorescent; O: Orange; B:Blue;Cr: Cream; W:
White)
Table 3: Thin Layer
Chromatographic (TLC) Studies
SR. No. |
Parameters |
Results |
1 |
% Foreign matter (w/w) |
< 2 |
2 |
% Lossondryingat1100C.(w/w) |
9.51 |
3 |
% Ash content (w/w) |
8.65 |
4 |
% Water soluble ash (w/w) |
1.74 |
5 |
% Acid insoluble ash (w/w) |
0.26 |
6 |
% Extractive values: (w/w) |
|
a. Petroleum ether |
6.92 |
|
b. Chloroform |
2.46 |
|
c. Ethanol |
2.46 |
|
7 |
% Solubility at room temp.(w/w) |
|
a. Ethanol |
24.86 |
|
b. Water |
41.71 |
|
8 |
% Extractable matter (Hot) (w/w) |
51.10 |
9 |
% Tannins (w/w) |
Traces |
10 |
Swelling index (w/w) |
9ml |
11 |
Foaming index (w/w) |
< 100 |
12 |
Organic constituents (Qualitative) |
Steroid, saponin |
13 |
Inorganic constituents (Qualitative) |
HCO3, SO4, Cl3, Ca, Mg, Na, CaPO4, Fe |
Fig. 2 T.S. of the leaf (Leaf let) 10x X 4x Ground plan
Fig. 3 Lower region enlarged 10x X 40x Ground plan
Fig. 2 Vascular bundle enlarged 10x X 40x
Fig. 5. Upper region enlarged 10x X 40x
Fig. 6. Laminar region enlarged 10x X 40x
Fig. 7. Epidermal peeling showing stomata 10x X 40x (Anisocytic
type of stomata) Lower Region
Figure 2 - 7: Microscopical
characteristics of Sesbania grandiflora (L.)
PERS COL: Collenchyma, PAR: Parenchyma, PAL: Palisade tissue, SPG: Spongy
Parenchyma, UEP: Upper Epidermis, VB: Vascular Bundle. (11)
2] Chromatography
analysis:
A number of
preliminary analytical works are to conducted based
on TLC and HPLC methods. TLC mobile system chosen was chloroform–methanol
(8.5:1.5); while other solvent systems could not separate the sample very well.
Likewise, a reversed phase system did not show a good separation in terms of
spot number and shape. Regarding TLC analyses, the majority of chemical
constituents were apparently consisted ofpolyphenol
and terpenoid groups as the plate showed some spots with fluorescence under UV
light 366 nm and more spots after being sprayed with vanillin reagent, on the
other hand, had a very few numbers on 254 nm
Figure 8. TLC
profile of S. grandiflora extract on silica plate, mobile phase was
chloroform–methanol (8.5:1.5). The profile on UV light 254 nm (A), on 366 nm
(B), and after sprayed with vanilin-H2SO4 (C).
HPLC is a
reproducible, rapid, and efficient method now becoming a reference in an
analytical procedure in modern industry. The best system for S. grandiflora
was achieved with acetonitrile-water (2:8) and flow rate at 0.5 mL/min (Figure
3). The peaks were increased in number compared to the mixture of 1:9;
moreover, their shapes were symmetric. In total there were nine peaks appeared
by the system, while the latter only produced four peaks. Interestingly, this
feature was exhibited less than 10 min. Considering efficiency as a major issue
in manufacturing, this HPLC system can be employed. The lambda used was 340 nm.
Figure 9.
Chromatogram profile of S. grandiflora with mobile phase
acetonitrile-water (2:8) and flow rate of 0.5 mL/min (A), chromatogram on the
ratio of 9:1 (B).
3] Antibacterial
test:
Out of 20 samples
examined, the most potent samples were exhibited by the S. grandiflora
flower and C. specious rhizome extracts. Their inhibition diameter was found to
be of 18.0 mm and 13.6 mm, respectively (positive control erythromycin =
18.0mm) (Figure 10).
Figure 10.
Inhibition zones of C. odorata, I. verum, S. grandiflora, P. alba, and P. rubra against
S. mutans.
A: The middle is the
positive control (erythromycin) while the others showed mild activities;
B: The
activity of S. grandiflora extractat
concentrations of 2.5%, 5.0% and 10.0%, respectively. 1: C. odorata; 2:I. verum;
3: S. grandiflora; 4: P. alba; 5: P. rubra. (12)
Meanwhile, the
flowers of C. roseus, T. eracta, P. alba, and
the rhizomes of A. calamus, C. heyneana, Z.
amaricans, I. cylindrica,
Z. cassumunar exhibited moderate activities with
a diameter inhibition ranging from 5.0 mm to 12.3 mm. The remaining samples C.
odorata flower, A. purpurata,
C. rotundus, C. soloensis,
and C. zedoaria rhizomes, in contrast, showed
a weak inhibition with an inhibition diameter less than 5 mm or being inactive
(0 mm) (Table 1), while DMSO did not show any inhibition effects.
Uses:
1] Medicinal Uses:
The following are
the few medicinal uses of the plant Sesbaniagrandiflora
used in the various field of medicine
·
In
Ayurveda, it can act as a remedy for various infections and diseases.
·
Fresh
leaves are used as an ailment for migraine, sinusitis, rheumatism, arthiris, gout and wound healing.
·
Leaves
are also used as tonic or paste to treat oral and throat infections.
·
The
juice extracted from the flowers of Sesbania
grandiflora are used for treating nightbliness,
headache and constipation.
·
Bark
is used to treat diarrhea, small pox, malaria, eruptive fever and gonorrhea.
·
The
roots of red flowered variety Sesbania
grandiflora can act as remedy to cure the rheumatism.
·
The oil of Sesbania grandiflora seed
has anthelmintic activity. (6)
·
Pods pale yellow, linear, usually 10-20 cm long, cylindrical or
compressed, rarely oblong; up to 40 seeds are found in a pod; seeds oblong or
sub quadrate, brown or dark green mottled with black.
·
The leaves and tender branches of sesban
are are high in protein content (20-25% crude
protein) and have high digestibility when consumed by ruminants, such as cattle
and goats. Particular Anti-nutritional factors are found to be present in sesban fodder. Feeding sesban
fodders to monogastric animals (such as chickens, rabbits, and pigs) is not
recommended.
·
Reports of feeding sesban to ruminant’s
conflict:-Trials in Australia feeding sesban
to heifers showed live weight gains, but trials with young goats in Samoa found
a lack of weight gain. Till the further research gives an clear guideline
caution should be followed in feeding ruminants with sesban
fodder at more than 10-20 percent of diet.
Soil
improvement:
Sesban
establishes quickly and grows rapidly. In Africa it is often allowed to grow
scattered throughout annual crop fields for the nitrogen it provides. It has
been used as experimental alley cropping method to provide much and green
leaf manure to intercrops. Sesban has
shallow roots.
Wood:
Sesban's wood is light in
weight compared to the woods of Calliandra and
Leucaena, but it is often harvested for firewood in Africa and India. It
has been used in India to make charcoal. The wood is not durable and should not
be considered for timber use. The branches have been used as a source of the
poles in temporary structures for the sheds and mud daub huts. As the sesban grows so rapidly, it has potential for
pulpwood production. Plantings at about 10,000 trees have produced 15-20 tons
of woody biomass (dry weight) in one year.
Food:
Flowers of sesban
are known to be added to stews and omelets in some regions, but it is
mainly as a decorative agent (10)
2] Traditional Uses:
In the Folk
Medicine it is resorted to be aperient, diuretic, emetic, emmenagogue,
febrifuge, laxative, and tonic. Agati is a commercially
used remedy for bruises, catarrh, dysentery, eyes, fevers, headaches, smallpox,
sores, sore throat, and stomatitis many more diseases. Different parts of this
plant are used in Siddha system of Indian traditional medicine for the
treatment of the various ailments including anemia, bronchitis, fever,
headache, ophthalmia, nasal catarrh, inflammation, leprosy, gout and rheumatism
In addition, S. grandiflora is mentioned as a potent antidote for
tobacco and smoking-related diseases. (7)
The root-bark
obtained from the bark of the red-flowered is useful in vitiated condition of vata and arthralgia. The bark has the astringent, cooling,
bitter, tonic, anthelmintic and febrifuge properties. The scabies can be
treated by the pounded bark. The juice of the bark is good for dyspepsia,
diarrhea and gastralgia. The leaves are acrid, bitter, sweet, cooling,
aperient, tonic and diuretic and contain a non-poisonous saponine
like substance. The leaf juice is used is nasal catarrh, nyctalopia and cephalagia. Disinfestation of the mouth and throat and also
in the stomatalgia can be cured btmy
cheating the leaves.(5). The flowers possess an cooling, bitter,
astringent, acrid and antipyretic. The juice of the flowers is applied to the
eyes to cure the nyctalopia and is immensely used in the treatment of the
intermittent fevers. The fruits are sweet, bitter, laxative and alexiteric and
are useful in flatulent-colic, astringent, cooling, bitter, tonic,
anthelmintic, febrifuge, cure scabies, dyspepsia, diarrhea and gastralgia,
astringent, antipyretic, for nyctalopianaemia,
emaciation and vitated conditions of tridosa.(2)
3] Therapeutic Uses
a) Antibacterial
and antifungal activity:
Polyphenolic
extracts (PE) of Sesbania grandiflora flower
was evaluated using both in vitro and in situ methods. In
vitro studies of PE of Sesbania
grandiflora has showed inhibitory effect against Staphylococcus aureus, Shigellaflexnesi, Salmonella typhi, E.coli and Vibriocholera. Among all this microbes, S.aureus
was more sensitive and showed minimuminhibition at a
concentration 0.013mg/ml. The ethanolic and aqueous extracts of Sesbania grandiflora leaves was screened for
their antibacterial activity against Staphylococcus aureus, E.coli, Klebiella pneumonia, Pseudomonous
aeruginosa and Bacillus subtilus using
agar diffusion technique. The study showed a significant antibacterial activity
of ethanolic extract on Staphylococcus and E.coli. A comparative study
on antibacterial activity of ethanolic leaves extracts of Sesbaniagrandiflora
using agar diffusion technique against E.coli and Pseudomonas
aeruginosa exhibited a significant inhibitory effect on Pseudonomas
aeroginosa producing a zone of inhibition of 12mm
at a concentration of 100μl. Even the two fungal pathogens Candia
albicans and Aspergillus niger were
inhibited by Sesbania grandiflora leave
extract. The minimum inhibitory concentration (MIC) and zone of inhibition was
determined in Sesbania grandiflora ethanolic
root extract by disc diffusion technique against Staphylococcus aureus,
Staphylococcus epidermis, E.coli and Bacillus subtilis at different
concentration. The highest zone of inhibition (25.7mm) was obtained for
Staphylococcus epidermis at a dosage of 250mg/disc, where as
E.coli showed lowest inhibition zone of1.5mm at a concentration of
50mg/disc.
b) Antituberculosis activity:
The chemical
components namely isolflavonoids, isolated from Sesbania grandiflora root extract has exhibited
maximum antituberculosis activity against
Mycobacterium tuberculosis H37Rv.
c) Anthelmintic
activity:
Anthelminitic activity was
studied in acetone, ethanol and aqueous extracts of Sesbania
grandiflora flowers at a concentration of 100,150,200mg/ml. The ethanolic
extract of flower showed a significant anthelmintic activity (Pheretimaposthuma) at a concentration of200mg/ml.
The presence of various phytochemical contributes anthelmintic property. A
effect of the anthelmintic activity of aqueous extract obtained from the Sesbania grandiflora leaves was carried out against Acaridiagalli revealed a definite anthelmintic
efficiency, which was mainly because of the presence of phytochemicals like
flavonoid, phenol, tannin, alkaloid, saponin, steroids and terpenoids. A comparative
study on antihelmintic property of Sesbania grandiflora alcoholic extract showed a
significant effect against Indian earthworm. A dosage of 50mg/ml, not only
showed paralysis, but also caused death of worm in a shorter period of time
when compared to standard drug Piperazine Citrate. Sesbania
grandiflora seed oil exhibited highly significant anthelmintic activity at a
concentration of 100mg/ml against Pheritimapasthumain
both parameters (paralysis and death) when compared to standard drug Piperazine
citrate(10mg/ml).
d)Antidiabetic
property:
Significant
anthelmintic activity at a concentration of 100mg/ml against Pheritimapasthumain both parameters (paralysis and death) when
compared to standard drug Piperazine citrate(10mg/ml).
e) Antidiabetic
property:
The 70% alcoholic
extract of Sesbania grandiflora flower has
shown a significant antidiabetic activity in alloxan induced diabetic rats at a
dose of 250mg/kg and 500mg/kg administrated for 28days. Even a marked reduction
in serum total cholesterol, TG, SGOT, SGPT and BUN was observed. The
histopathological studies showed the repair and regeneration of the damage
islet of pancreatic cell.
f) Hepatoprotective
activity:
Hepatoprotective
activity of aqueous extract of Sesbania
grandiflora leaves was studied in albino rats. The rats orally fed with carbon
tetrachloride to induce liver damage at a dosage of 500mg/kg b.wt. Treatment of rats using aqueous extract has shown a
decline in serum level of glutamic pyruvate transaminase(SGPT), alkaline
phosphatase(ALP) and total bilirubin, cholesterol. A study done on the
hepatoprotective activity of petroleum ether extract of Sesbania
grandiflora fruit has shown a significant reduction in ALT, AST, ALP and total
bilirubin level at a dosage of400mg/kg of b.wt in
ethanol induced heptotoxic rats. Histopathological
studies has also revealed the presence of normal liver cells.
g) Antioxidant
activity and Cardio protective activity:
The Cardio
protective activity of Sesbania grandiflora
was evaluated against cigarette smoke exposed rats. The adult male Wister-
Kyoto rats were exposed to cigratte smoke for
90daysand orally treated with Sesbania
grandiflora aqueous leave extract for 3 weeks at a dose of1000mg/kg of body
weight. After treatment there was a significant decrease in the activity of
serum lactate dehydrogenase, cardiac superoxide dismutase, glutathione
reductase, glutathione–S-transferase and glucose 6 phosphate dehydrogenase.
h) Wound healing
activity:
Wound healing
activity was evaluated in wistar rats using excision
and incision wound Model. The methanolic extract of Sesbania
grandiflora bark showed positive wound healing activity when the concentration
of 10% w/w in Wistar albino rats using excision wound model when compared to
standard 1% Framycetin sulphate.
i) Antiulcer activity:
The ethanolic
extracts of Sesbania grandiflora leave at a
dosage of 250mg and 500mg/Kg of body weight had showed reduction (50% and
74.22%) in ulcer of ethanol induced adultalbino rats
when compared to the control group. Omeprazole was used as standard drug.
j) Anticancer
activity:
Sesbania grandiflora methanolic leave extracts had repored potent antiproliferative activity in human lung
cancer cell line, A549 by activating caspase 3 leading to cell dealth byapoptosis. Hematological
profile such as RBC, Hb and lymphocyte were also reported to be normal.
k)
Anti-inflammatory activity:
Methanolic extract
of leaves of Sesbania grandiflora has
revealed anti-inflammatory activityin formaldehyde
induced rat paw oedema model at dosage of 400mg/kg of
body weight. Inthis study 0.5mg/kg of Dexamethanone was used as standard drug.
l) Antiurolithiatic activity:
The leaves of Sesbania grandiflora exhibited good antiurolithiatic activity in rats induced with calcium
oxalate type stones.
m) Immunomodulatory
activity:
The oral
administration methanolic extract of Sesbania grandiflora
at a dose of 200and400mg/kg has reported a significant immunomodulatory
activity in rats induced by sheep red blood cells to create hypersensitivity.
n) Antiviral
activity:
Methanolic flower
extracts of Sesbania grandiflora showed
significant antiviral activity against herpex
simplex-1, herpex simplex-2, vaccinia, vesicular
stomatitis anad cox sickie. The antiviral activity is
mainly due to flavonoid content.(6)
4] Other uses:
Various medicinal
uses for Sesbania Sesban
have been mostly recorded in Africa and Asia. The leaves and flowers are used
in the medicinal poultices and teas, which are said to possess an effect of
astringency, or contraction of body tissues. Gum production from the bark is
use of the tree. leaf of Sesbani Sesban has traditionally been used as purgative,
demulcent, maturant, anthelmintic and for all pains
and inflammation (1).
CONCLUSION:
Medicinal plants or
ethno medicine are in practice from Ancient times in
many cultures and Sesbaniagrandiflora is
one among them. As the pharmacologists are looking forward to develop new drugs
from natural sources, development of modern drugs from Sesbaniagrandiflora
can be emphasized for the control of various diseases. In recent
years, ethno medicinal studies received much response
as thus leads to the numerous little known and unknown medicinal qualities seen
in the plant parts. The new trend of the antimicrobial drug preparation
will help to be an alternative medicine for the novel synthetic drugs.
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(www.elsevier.com/locate/apjtb)
Received on 28.06.2019
Modified on 18.07.2019
Accepted on 10.08.2019 ©A&V
Publications All right reserved
Res. J. Pharmacognosy
and Phytochem. 2019; 11(3):114-122.
DOI: 10.5958/0975-4385.2019.00020.7