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CHAPTER-II
8
2. REVIEW OF LITERATURE
2.1 Past work on the plant Dalbergia paniculata, Cyathea gigantea,
Colebrookea oppositifolia and Entada pursaetha
An extensive literature survey has been carried out on selected
plants Dalbergia paniculata, Cyathea gigantea, Colebrookea oppositifolia
and Entada pursaetha along with their chemical constituents and biological
properties as described below.
List of Dalbergia paniculata,. (www.IPNI.org)
TABLE No. 2.1
PLANT NAME PLANT NAME PLANT NAME
Dalbergia acuta Dalbergia cucullata Dalbergia glabra
Dalbergia altissima Dalbergia cujabensis Dalbergia glandulosa
Dalbergia amerimnum Dalbergia cuscatlanica Dalbergia glaziovii
Dalbergia aturensis Dalbergia debilis Dalbergia glomerata
Dalbergia barretoana Dalbergia decipularis Dalbergia gracilis
Dalbergia berteroi Dalbergia delavayi Dalbergia granadillo
Dalbergia brasiliensis Dalbergia densa Dalbergia grandistipula
Dalbergia brownei Dalbergia densiflora Dalbergia guttembergii
Dalbergia calderonii Dalbergia ecastaphyllum Dalbergia hepperi
Dalbergia calycina Dalbergia elegans Dalbergia hiemalis
Dalbergia campechiana Dalbergia enneandra Dalbergia hortensis
Dalbergia candenatensis Dalbergia enneaphylla Dalbergia hygrophila
9
Dalbergia cearensis Dalbergia ernest Dalbergia hypargyrea
Dalbergia chontalensis Dalbergia ferrugineo-
tomentosa Dalbergia hypoleuca
Dalbergia chontalensis Dalbergia foliolosa Dalbergia intermedia
Dalbergia cibix Dalbergia frutescens Dalbergia intibucana
Dalbergia congestiflora Dalbergia funera Dalbergia inundata
Dalbergia cubilquitzensis Dalbergia gautieri Dalbergia iquitosensis
2.2 Botanical Description of Dalbergia paniculata:
An attempt was made to bring out the details of each plant like its
origin and life history. The genus Dalbergia belongs to the family Fabaceae.
The Dalbergia genus is considered to be of medicinal importance
because of the presence of isoflavonoid glycosides and steroids in
various parts of the plant. The genus consists of 300 species and about
25 species occur in India. Many species of Dalbergia are important timber
trees, valued for their decorative and often fragrant wood, rich in aromatic
oils.
2.3 Geographical distribution of D. paniculata
The Plant is found in many parts of India. In Indian Subcontinent:
India - Goa, Gujarat, Haryana, Karnataka, Kerala, MadhyaPradesh,
Maharashtra, Meghalaya, Orissa, Rajasthan, Tamil Nadu, Uttar Pradesh.
Nepal, Andaman and Nicobar, Cambodia, Laos, Myanmar, Vietnam.
10
2.4 Taxonomical Classification of 1 D. paniculata
Kingdom : Plantae
Division : Magnoliophyta
Class : Magnoliopsida
Order : Fabales
Family : Fabaceae
Genus : Dalbergia
Species : paniculata
2.5 Vernacular names of D. paniculata:
Dalbergia paniculata is commonly called as Padru pachhali, Patri.
Hindi : Dhobein
Kannada : Biluga-Damara
Marathi : Sondhara
Tamil : Paingannni
Telugu : Sopera
2.6 Phytochemistry:
Several efforts made by eminent researchers on the isolation and
identification of compounds from various parts of D.paniculata, contibuted
enormous literature on the phytochemical work of the selected plants.
11
Caviunin Dalpalatin
Dalpaniculin Dalpanol
Dalpatein Dehydrodalpan ol-O-glucoside
Sitosterol
The presence of Caviunin and sitosterol from their Phytochemical
study on leaves of Dalbergia paniculata was reported by J.R. Rao, M.A.
Ahamed., 1992. In 1972 D. Adinaraya, J. R. Rao. isolated two
Isoflavanoid glycosides dalpanitin & dalpatin and they isolated dalpanol in
12
1975 from Dalbergia paniculata. J.R. Rao, S.R. Rao., Dalpaniculin, a
C- glycosylisoflavone from Dalbergia paniculata seeds in 1991.
2.7 Biological Activities:
A Careful review on different biological activities done was carried
out for the selected four plants and concluded below.
There are no published pharmacological reports till now on this
plant. Dalbergia genus possesses immense traditional application. So far,
a few species have been screened for their biological activity and
experimental results have shown a wide spectrum of such effects, the
important ones are as follows:
Alcoholic extract of D. sisso leaves have shown peripheral
analgesic activity and central analgesic activity in various models viz;
acetic acid induced writhings, hot plate method, tail-clip test in mice and
Randoll-selitto assay. Similar activity has also been reported in ethanolic
extract of D. lanceolata bark. The alcoholic extract of D. sisso leaves
extract also showed antipyretic activity in Brewers yeast induced pyrexia in
rats reported by A. V. Misar, M. Kale, M. Joshi and A.M. Mujbumder., 2005
The ethanolic extract of D. sisso leaves significantly inhibited
carragenin, kaolin, and nystatin induced paw edema as well as the weight
of granuloma induced by the cotton pellet. It also inhibited dye leakage in
acetic acid –induced vascular permeability test in mice (49). Biochanin- A
(5,7-dihyddroxy –4-methoxy isoflavone) isolated from flowers of D.
sissoids have shown to possess anti –inflammatory activity against PGE,
13
bradykinin, 5-HT and histamine induced rat hind paw odema in dose
dependent manner.
The petroleum ether, alcohol and aqueous extracts of D.lanceolaria
had been found effective against arthritis when tested against
formaldehyde-induced arthritis in young growing albino rats by R.H. Singh
and G.N. Chaturvedi., 1966.
Citric acid extract of bark of D. melanoxylon have shown significant
antibacterial activity against gram-negative bacteria (Escherichia coli,
Pseudomonas aeruginosa, Salmonella typhimurium and Yersinia pestis)
and gram-positive bacteria (Bacillus subtilis, Klebsiella pneumoniae, and
Staphylococcus aureus). The plant has potential antifungal activity against
Candida albicans and Aspergillus niger reported by M. Gundidga and N.
Gaza., 1993.
The decoction of dried leaves of D. sisso possesses antidiarrhoeal
activity. The ethanolic extract of the bark of D.lanceolaria have shown
activity against castor oil and magnesium sulphate induced diarrhoea in
albino mice.
The lyophilized aqueous extract (LAE) of D. monetaria have shown
a dose dependant inhibition of gastric lesions induced by indomethacin,
ethanol, pylorus ligature and hypothermic–restraint stress on oral
administration.
The oil extracted from wood scrapings of D. sisso has shown dose
dependent larvicidal activity, growth inhibiter and repellant action against
Anopheles stephensi, Ades aegypti and culex quinquefasciatus.
14
The extracts and formononetin an isoflavone from the bark of D.
frutescans have shown significant activity against Giardia intestinalis with
an IC 50 value of 30ng/ml (approx. 0.1 µm) as compared to the value for
metronidazole, the current drug of choice of 100 ng/ml (approx. 0.6 µm)
Khan et al., 2000.
The flavanoids isolated from air dried powdered heartwood of D.
louvelli showed antiplasmodial activity with IC 50 values ranging from 5.8
to 8.7 um. Triterpenoid glycosides, DSS, isolated from the root of
D.saxatilis have shown antifertility activity in female wistar rats at the dose
rate of 200mg/kg body weigtt at the premating period, inhibiting the
conception in 71.4% of the treated animals. Fertility index was 107.82
compared to 373.5 for control rats.
Butein isolated from D. odorifera have shown to inhibit the iron-
induced lipid peroxidation in rat brain homogenate in concentration
dependant manner with an IC 50 value 3.3±0.4µm. It was as potent as α-
tocopherol in reducing the stable free radical diphenyl-2-picarylhydryl
(DPPH) with an IC0.200 value 9.2±1.8 µm. It also inhibited the activity of
xanthine oxidase with IC 50 value 5.9±0.3µm. Butein scavenged the
peroxyl radical derived from 2,2-azobis (2-amidinopropane)
dihydrochloride (AAPH) in aqueous phase. Butein have also shown to
inhibited copper-catalyzed oxidation of human lowdensity lipoprotein (LDL)
in a concentration dependent manner. Butein caused endothelium
dependant relaxation of rat aorta, precontracted with phenylephrine.
Ethanolic extracts of the stem bark of the D. cultrate Grati and D.
nigrescens Kurz were found to exhibit a significant antitumor promoting
15
activity on TPA (12-o-tetradecanoylphorbol-13-acetase, EBV-EA (Epstein
Barr virus early antigen) and TPAinduced EBV-EA activation.
The genus Dalbergia though known for its timber value also
possesses significant medicinal properties. Most of the work carried out on
the various species is on the extracts of the different parts. The biological
screening of D.paniculata will help to further explore the medicinal
potential.
2.8 List of Cyathea gigantean (ww.IPNI.org)
TABLE No. 2.2
PLANT NAME PLANT NAME PLANT NAME
Cyathea abbottii
Cyathea abbottii
Cyathea acanthophora
Cyathea acrostichoides
Cyathea acuminata
Cyathea affinis
Cyathea
Cyathea chinensis
Cyathea christii
Cyathea cincinnata
Cyathea cinerea
Cyathea coactilis
Cyathea colensoi
Cyathea confirmis
Cyathea corcovadensis
Cyathea costalisora
Cyathea costulisora
Cyathea crassa
Cyathea croftii
Cyathea cucullifera
Cyathea gleichenioides
Cyathea gregaria
Cyathea grevilleana
Cyathea halconensis
Cyathea hancockii
Cyathea havilandii
Cyathea henryi
Cyathea
heterochlamydea
Cyathea hooglandii
Cyathea hookeri
Cyathea hornei
Cyathea horridula
16
Cyathea hotteana
Cyathea humilis
Cyathea Hunsteiniana
Cyathea hymenodes
Cyathea imbricata
Cyathea imrayana
Cyathea incana
Cyathea incisoserrata
Cyathea inquinans
Cyathea insulana
Cyathea javanica
Cyathea nigrolineata
Cyathea nigropaleata
Cyathea nilgirensis
Cyathea nockii
Cyathea obtusiloba
albidosquamata
Cyathea alderwereltii
Cyathea alleniae
Cyathea alpicola
Cyathea amboinensis
Cyathea amintae
Cyathea andersonii
Cyathea aneitensis
Cyathea annae
Cyathea apiculata
Cyathea apoensis
Cyathea approximata
Cyathea archboldii
Cyathea ascendens
Cyathea atropurpurea
Cyathea australis
Cyathea baileyana
Cyathea deckenii
Cyathea decrescens
Cyathea dicksonioides
Cyathea dimorpha
Cyathea doctersii
Cyathea dregei
Cyathea dryopteroides
Cyathea edanoi
Cyathea elongata
Cyathea erinacea
Cyathea eriophora
Cyathea
esmeraldensis
Cyathea everta
Cyathea exilis
Cyathea excavata
17
Cyathea balanocarpa
Cyathea batjanensis
Cyathea biformis
Cyathea borneensis
Cyathea boytelii
2.8.1 Botanical Description of Cyathea gigantea :
An attempt was made to bring out the details of each plant like its
origin and life history. The genus Cyathea belongs to the family
Cyatheaceae. The Cyatheaceae is the scaly tree fern family and includes
the world's tallest tree ferns, which reach heights up to 20 m. They are
also very ancient plants, appearing in the fossil record in the late Jurassic,
though the modern genera likely appeared in the Tertiary. Cyatheaceae is
the largest family of tree ferns, including about 500 species.
Cyatheaceae are leptosporangiate ferns, the most familiar group
of monilophytes (korall, et al., 2006). The Cyatheaceae usually have a
single, erect trunk-like rhizome (stem). Their fronds (leaves) are also very
large, some of the largest in the plant kingdom. Some species have fronds
reaching 3-4 m in length, and have a final crown width of some 6 m. The
fronds are circinate before unfolding and usually pinnately or bipinnately
compound, with leaflets that are deeply pinnately lobed. The large leaves
are covered in scales and hairs and bear sori (spore clusters) on the
underside (Judd et al., 2008). The sori are often covered by a flap of tissue
called an indusium, a useful characteristic for classifying the Cyatheaceae.
Some indusia are cup-shaped (cyatheoid), while others are hood-shaped
18
(hemitelioid), enclose the sorus (sphaeropteroid) or scaly. Like most ferns,
members of the Cyatheaceae are homosporous. Cyatheaceae are found
in both New and Old World tropical wet montane forests and cloud forests,
with some species extending into south-temperate regions (Korall et al.,
2007). Most Cyatheaceae are terrestrial, with one sometimes
being epiphytic and others having a creeping habit, but these are
exceptions to the family norm.
2.8.2 Geographical distribution of C.gigantea:
Cyathea gigantea is a species of tree fern native to northeastern to
southern India, SriLanka, Nepal to Myanmar, Thailand, Laos, Vietnam,
the Malay Peninsula, as well as central Sumatra and western Java. In
India it is spread all over the country and grows in moist areas up to
1000m.
2.8.3 Taxonomical Classification of C. gigantea:
Kingdom : Plantae
Division : Pteridophyta
Class : Pteridopsida
Order : Cyatheales
Family : Cyatheaceae
Genus : Cyathea
Species : gigantea
19
2.8.4 Vernacular namesofC.gigantea:
Cyathea gigantea is also called as Alsophilla gigantea
Wallich exW. J. Hooker, 1844.
2.8.5 Phytochemistry:
Several efforts made by eminent researchers on the isolation and
identification of compounds from various parts of C.gigantea, contibuted
enormous literature on the phytochemical work of the selected plants.
Sitosterol Hentriacontane
Oleanolic acid Diploterol
R. K. Juneja, S. C. Sharma and J. S. Tandon., in 1990 did their
Phytochemical work on tree fern Cyathea gigantea and identified
20
hentriacontane, β-sitostenone, β-sitostanone, diploterol, sitosterol, hopan-
29-ol, and oleanolic acid from the hexane soluble fraction of the plant.
Das Talukdar, M. Dutta Choudhury, M.Chakraborty, B.K. Dutta in
2010 done Phytochemical work and confirmed the presence of alkaloids,
steroids, flavonoids, reducing sugar and tannins.
2.8.6 Biological Activities:
A Careful review on different biological activities done was carried
out for the selected four plants and concluded below.
The reported pharmacological work related to Cyathea species was
as follows:
The in vitro antioxidant potential of the crude extract (CE),
precipitate (PPT), aqueous fraction (AQF), n-butanolic fraction (BUF) and
ethyl acetate fraction (EAF) from C. phalerata was evaluated through the
scavenging of diphenyl-1-picryl-hydrazyl-hydrate (DPPH), superoxide
anion (O2•−) (nitroblue tetrazolium assay) and hydroxyl radicals (OH•)
(deoxyribose assay), and lipid peroxidation in rat liver homogenate. In
these assays, it was observed that EAF had marked antioxidant potential,
especially as a scavenger of the OH• radical and in inhibiting lipid
peroxidation. The in vivo evaluation of oxidative stress (DNA
fragmentation, membrane lipoperoxidation and carbonyl protein formation)
and the antioxidant defenses (concentration of reduced glutathione, as
well as catalase and glutathione S-transferase activities) were measured
in mice pre-treated with EAF (10, 30 or 100 mg/kg, orally) and later
exposed to carbon tetrachloride (CCl4). The EAF decreased thiobarbituric
21
acid reactive substances levels, DNA damage and carbonyl protein
contents, and increased catalase and glutathione S-transferase activities.
Based on these results, it is concluded that the EAF from C.
phalerata protects liver from oxidative stress induced by CCl4 in mice and
these effects are probably related to the antioxidant activity associated
with the free radical scavenging property of this fraction reported by
Mariana Appel Hort et al., 2007.
2.9 List of Colebrookea oppositifolia (ww.IPNI.org)
TABLE No. 2.3
Colebrookea oppositifolia.Sm.
Colebrookea oppositifolia.Lodd
Colebrookea ternifolia.Roxb
2.9.1 Botanical Description of Colebrookea oppositifolia:
The genus Colebrookea belongs to the family Lamiaceae with
Shrubs which are erect, densely lanate-tomentose. Stems are yellow-
brown. Leaves sometimes in whorls of 3, oblong-elliptic, dentate. They
are distributed worldwide and they belong to seed-forming, dicotyledonous
plants, comprises over 240 genera and 6500 species, following the family
circumscription of (Cantino et al. 1992). The main centre of diversity is the
Mediterranean region to central Asia. Members are found in tropical and
temperate regions. About 60 genera with ± 980 species occur in the Sub-
Saharan African region (Klopper et al. 2006).
22
2.9.2 Geographical distribution of C.oppositifolia :
The plant is distributed throughout India, Pakistan, South-west
China (Yunnan), Nepal, Myanmar, Thailand, Indo- China. It grows in
Savanna forests, thickets in hot, dry regions up to 200-200 meters.
2.9.3 Taxonomical Classification of C.oppositifolia:
Kingdom : Plantae
Phylum : Eudicots
Class : Asterids
Order : Lamiales
Family : Lamiaceae
Genus : Colebrookea
Species : oppositifolia
2.9.4 Vernacular names of C.oppositifolia :
Telugu : jolidi, tolisi
Kannada : thuggi gida
Marathi : bhaman, bhamini, bhamni
Tamil : vitupucittalai
Oriya : tulia
Lepcha : umhyemkung
Hindi : binda, kala-bansa, pansra, bhirmoli,
23
2.9.5 Phytochemistry:
Several efforts made by eminent researchers on the isolation and
identification of compounds from various parts of C.oppositifolia and
E.pursaetha contibuted enormous literature on the phytochemical work of
the selected plants.
Chrysin Negletein
Ladanein Verbascoside
Fan Yang, Xing- Cong Li and Han-Qing Wang..1996., Isolated
flavonoid aglycones – chrysin, negletein, ladanein. Flavonoid glycosides –
negletein 6-glucoside;5,7,2’ –trihydroxyflavone 2’- glucoside from
Colebrookea oppositifolia.
24
A acylated flavone glycoside i.e., Phenylethanoid – verbascoside
(also called acetoside or kusaginin) was isolated from Colebrookea
oppositifolia by Reddy RV, Reddy BA and Gunasekar.D., in 2009.
2.9.6 Biological Activities:
A Careful review on different biological activities done was carried
out for the selected four plants and concluded below.
The methanolic and aqueous extracts of different parts
of Colebrookia oppositifolia were examined for antibacterial activities in
vitro by an agar diffusion method. Antibacterial activity of leaves, shoots,
and roots ofColebrookia oppositifolia was assessed against Gram positive
and Gram negative bacteria that were isolated and identified from water
samples by the API 20E method. Extract of roots showed more
antibacterial activities against Staph. aureus and B. cereus var. mycoides,
Pseudomonas aeruginosa, Klebsiella pneumonia, andShigella flexneri at
37°C, than extracts from leaves and shoots. The low est MIC (minimum
inhibitory concentration) and MBC (minimum bactericidal concentration)
were observed in roots as compared to shoots and leaves reported by
Ahmed et al., 2009.
The effect of aqueous extract of colebrookea oppositifolia on
bioavailability of amoxycilline in rabbits vide by Das et al., 2004.
Oral feeding of male rats with the ethanolic leaf extract of
Colebrookia oppositifolia at dose levels of 100 and 200 mg/kg for 8-10
weeks did not cause body weight loss, while the weights of testes and
epididymides were significantly decreased. Seminal vesicles and ventral
25
prostate showed a significant reduction at the higher dose only. Treated
animals showed a notable depression of spermatogenesis and this
antifertility studies of Colebrookea oppositifolia leaf extract in male rats
with special reference to testicular cell population dynamics was reported
by Gupta et al., 2001.
Synergistic interaction between amphotericin B (AmB) and
acteoside, isolated from the aerial parts of Colebrookea oppositifolia.
Acteoside alone exhibited no intrinsic antifungal activity but it showed a
potent synergism in combination with AmB against selected pathogenic
species, with fractional inhibitory concentration indices in the range of
0.0312 to 0.1562. The combination of 3.12 micrograms ml-1 and 12.5
micrograms ml-1 concentration of acteoside with sub-MICs of AmB
resulted in a potent fungicidal effect and also significantly exhibited an
extended post-antifungal effect. The data presented here supports
synergism between acteoside and AmB and therefore it is proposed that a
prospective new management strategy for therapeutic application of this
combination should be explored and was reported.
26
2.10 List of Entada pursaetha (ww.IPNI.org)
TABLE No. 2.4
PLANT NAME PLANT NAME PLANT NAME
Entada adans Entada abyssinica Entada acaciifolia
Entada adenanthera Entada africana Entada arborea
Entada arenaria Entada bacillaris Entada bequaerti
Entada boiviniana Entada borneensis Entada camerunensis
Entada chiliantha Entada cirrhosa Entada claessensii
Entada coulteria Entada dolichorrhachis Entada duparquetiana
Entada durissima Entada entada Entada flexuosa
Entada formosana Entada gandu Entada gigalobium
Entada gigas Entada glandulosa Entada gogo
Entada grandidieri Entada gandu Entada gigalobium
Entada adans Entada abyssinica Entada acaciifolia
Entada adenanthera Entada africana Entada arborea
Entada arenaria Entada bacillaris Entada bequaerti
Entada boiviniana Entada borneensis Entada camerunensis
Entada chiliantha Entada cirrhosa Entada claessensii
Entada coulteria Entada dolichorrhachis Entada duparquetiana
Entada durissima Entada entada Entada flexuosa
27
2.10.1 Botanical Description:
An attempt was made to bring out the details of each plant like its
origin and life history. An attempt was made to bring out the details of each
plant like its origin and life history. Entada pursaeta DC (Elelphant creeper)
belonging to the family Mimosae. Mimoseae is a tribe of leguminous plants
in the subfamily Mimosoideae. Where this is treated as a family of its own
(e.g. in the Cronquist system), the Mimoseae become the
subfamily Leguminosae-Mimosoideae belonging to order fabales.
(http://hortiplex.gardenweb.com/plants/p1/gw3000319.html). This is the
third largest family of flowering plants is the legume family, with more than
18, 000 species.
2.10.2 Geographical distribution of E.pursaetha:
It is distributed in India, it is endemic woody liana rarely distributed
in the subtropical Evergreen forests of Western Ghats of Karnataka,
Tamilnadu Kerala and Eastern Ghats of Andhra Pradesh.
2.10.3 Taxonomical Classification of E. pursaetha:
Kingdom : Plantae
Division : Pteridophyta
Class : Rosidae
Order : Fabales
Family : Mimosoideae
Genus : Entada
Species : pursaetha
28
2.10.4 Vernacular names of E. pursaetha:
Telugu : Tikka tivva Tilokayalo, Gila teega,
Peddamudupu.
Hindi : Barabi
Tamil : Irikki
Sanskrit : Bidhanta
Kannada : Ganape kayi
Popular name : Nicker bean.
2.10.5 Phytochemistry:
Several efforts made by eminent researchers on the isolation and
identification of compounds from various parts of E.pursaetha contibuted
enormous literature on the phytochemical work of the selected plants.
Amyrin Quercetin
Cyanidin Gallic Acid
29
Dopamine
Bark and seeds contain significant amounts of saponins including
an anti-tumour saponin, entanin, which on hydrolysis yields entagenic
acid. Seeds also contain a fixed oil, proteins, albumins and globulins,
essential amino acids, fatty acids such as oleic and linoleic acids;
phaseoloidin, tyrosine glucoside and dopamine glucoside and many
minerals. A new triterpenoid, entagenic acid and a crystalline sapogenin
have also been isolated from the seeds. Myristic, palmitic, stearic,
arachidic, behenic, and linolenic acids have been obtained from seed oil
hydrolysate. Seed oil also contains triglycerides comprised of
monounsaturated diolein and dilinolein, saturated oleolinolein,
dioleolinolein, trioleein, oleodilinolein and trilinolein. Pericarp contains β-
sitosterol, α-amyrin, quercetin, cyanidin chloride and gallic acid. Kernel
contains oleanolic and echinocytic acids and methyl mercaptan (the text
book of Indian Medicinal Plants by P.C. Khare, The Medicinal plants of
Bangladesh)
2.10.6 Biological Activities:
A Careful review on different biological activities done was carried
out for the selected four plants and concluded below.
30
The antioxidant activity of the crude methanolic extract of the seeds
of Entada pursaetha was reported.
Five new triterpenoid saponins, pursaethosides A-E (1-5), were
isolated from the n-BuOH extract of the seed kernels of Entada pursaetha
along with the known phaseoloidin. The structures of 1-5 were elucidated
mainly by spectroscopic data interpretation and chemical degradation.
Pursaethosides C-E (3-5) possess as a common structural feature
entagenic acid as aglycon, which is rare among triterpene saponins.
Compounds 2-4 and phaesolidin were found to be not cytotoxic when
tested against HCT 116 and HT-29 human colon cancer cells.
Antibacterial and molecular docking studies of entagenic
acid, a bioactive principle from seed kernel of Entada pursaetha reported.
2.11. Objective and scope of work
The practice of herbal medicine dates back to the very earliest
periods of known human history. There is evidence that herbs have been
used in the treatment of diseases and for revitalizing the body system in
almost all ancient civilizations. There is a rapid progress in various fields of
human activity, the field of medicine and its allied sciences. All these have
made rapid strides.
Majority of the present day diseases are due to the shift in the
balance of the pro-oxidant and the antioxidant homeostatic phenomenon
in the body. The antioxidant defense systems, can only protect the body
when the amount of free radicals are within the normal physiological level;
but when this balance is shifted towards more of free radicals, it leads to
31
oxidative stress which may result in tissue injury and subsequent
diseases. (Rakesh and Rajesh, 2006)
The present study on these four Traditional Indian medicinal plants has
been aimed to focuss for their anti-inflammatory, anti-oxidant and
hepatoprotective potentials. The idea stemmed from the following fact:
� According to folkloric use, the plants were not screened for the
treatment of anti-inflammatory and hepatoprotective conditions.
� The plant C.gigantea is becoming an endangered species now a
days and this enabled the author to perform individual studies and
also to identify the novel bioactivities from this amazing plant.
� The species Dalbergia, Cyathea, Colebrookea and Entada were
used traditionally in several formulations and this prompted the
author to develop formulations for producing significant activity in
anti-inflammatory and hepatoprotective studies.
� Colebrookea and Entada have not been screened for antidiabetic
activity.
On the basis of the survey of ethnomedical, folkloric information and
literature, the following plants were selected:
Dalbergia paniciulata, Cyathea gigantea, Colebrookea oppositifolia
and Entada pursaetha.
32
2.12 The objective of the proposed work:
The purpose of this research work is to investigate the
pharmacological activities and phytochemistry of these plants in a
scientific manner. The different steps adopted are given here under.
2.13 Collection of plant materials and extraction:
Exhaustive and upto date review of literature for antioxidant, anti-
inflammatory, hepatoprotective activities and their methods of screening ,
phytochemical and pharmacological review of the selected plants were
conducted.
The freshly collected leaves of the plants were shade dried and
powdered. The powdered materials were then subjected to maceration.
Dried powdered leaves of Dalbergia paniculata, Cyathea gigantea,
Colebrookea oppositifolia and Entada pursaetha were separately
macerated successively three times with methanol: water (70:30) for 10
days. The extracts thus obtained were concentrated under vacuum at
temperature of 430 c by using rotary evaporator.
2.14 Phytochemical Studies:
The extracts were tested for phyto-constituents by different
chemical tests and the prepared extracts have been subjected to column
chromatography over silica gel column with solvents of increasing order of
polarity. The separated constituents were characterized with the help of
spectroscopy, melting point, Co-TLC, etc.
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2.15 Antioxidant studies:
Sometimes endogenous antioxidants and the protective
mechanisms are found to be insufficient. Hence, the search for exogenous
antioxidants is continued. Recently, intensive research has been carried
out to characterize the antioxidant properties of extracts from several plant
materials. Hence the plant extracts were studied for in vitro antioxidant
free radical scavenging activity against superoxide, hydroxyl and DPPH
radicals.
2.16 Acute toxicity studies:
Toxicity studies conducted as per accepted protocol drawn under
OECD-425 guidelines for rats. The acute toxicity study was aimed at
establishing the therapeutic index i.e. the ratio between the
pharmacologically effective dose and the lethal dose, and also to perform
the primary screening.
2.17 Anti-inflammatory studies:
All the extracts were screened for anti-inflammatory activity using
carrageenan-induced rat paw oedema method. To assess the folk claims
and to find out the active constituents responsible for anti-inflammatory
activity.
2.18 Hepatoprotective studies:
All the extracts were screened for the hepatoprotective nature
against paracetamol-induced hepato-toxicity in rats, to know the
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hepatoprotective potential of the crude extract and inorder to know the
fraction / phytoconstituent responsible for the hepatoprotective activity.
2.19 Documentation of results:
The results were tabulated and statistical significance (significance:
*P<0.05, **P<0.01, *P<0.001) of results was carried out by using unpaired
student’s t-test.