A Review on Pharmacological Profile for Phytomedicine Known as Gloriosa superba Linn.
Hemant Badwaik*, Tapan Kumar Giri , D.K. Tripathi , Mukesh Singh and Abdul
Hanif Khan
Rungta College of Pharmaceutical
Sciences and Research, Bhilai (C.G)
ABSTRACT:
Application indigenous natural products has been
alternative way to replace synthetic medicine Gloriosa superba is a well known ethnomedicinal plant which is used in Ayurveda.
Photochemical studies of G. superba shows
presence of colchicin, b-siltosterol, long chain fatty acids, b and g-lumiccolchicines, 2-hydroxy-6-methoxy benzoic, luterlin, N-formyl-deacetyl colchicines and new colchicine
glycoside, 3-O-demethylcolchicine-3-O-alpha-D- glucopyranoside.
FDA-approved use of Colchicine is to treat gout (it
is one of the active ingredients of anti-gout tablets marketed by Merck &
Co.). It is also used as an anticancer, antimicrobial, antifungal,
anticoagulant, antilipoxygenase agent and antidote in
snake bite. However, ingestion of all parts of the
plant is extremely poisonous and can be fatal. The commonest clinical
presentation of poisoning is severe gastroenteritis with nausea, vomiting, diarrhoea with b leading to dehydration, hypovolaemic shock and acute renal failure. Gloriosa superba usually
multiply by corm and seeds but due to low germination capability it restricts
for the regeneration. Therefore, in order to safeguard and preserve this
important plant biotechnological approachs would be
very useful. Micropropagation of Gloriosa superba meets ever increasing demands
for colchicine. The availability from both wild and
cultivated sources make the plant of Gloriosa superba a potential source of Colchicine
in India.
KEYWORDS: Gloriosa superba Linn., 3-O-demethylcolchicine-3-O-alpha-D- glucopyranoside, antitumor, gout, gastroenteritis.
INTRODUCTION:
According to one of the ancient proverbs in
India,” there is no plant on earth which
has no medicinal property.” A large number of plants have been used by man from ancient times as medicine for curing
various ailments. In recent times there
is an upsurge of interest and focus on the
importance of medicinal plants and traditional health systems in solving the health care problems of the world1.
Although the modern medicine has developed so much improves to useful in
treating many horrible human diseases, but not in reasonable cost. Herbal
renaissance is happing all over the globe as herbal products are symbol of safty as compare to synthetic medicine. Tradinal
system of medicine is found to have utilities as many accounts. Due to
population rise adequate supply of drug and high cost of treatment, side
effects along with drug resistance has been encountered in synthetic drugs,
which has leads to elevated emphasis for use of plants to treat human diseases2.
The World Health Organization (WHO) has
previously recognized to re-establish the tradinal
knowledge of medicine among our conventional theaters. Tradinal
knowledge since 200 B.C. in Ayurveda is very well
recognized especially in India among tribal people. In India, the population of
tribal people is around 53 million along with 555 tribal groups or communities,
which are reside in forest and surroundings. These people have enormous
indigenous knowledge which is possible
tool to explore for novel cost-effective plants for medicine. Several medicinal
plants were originally identified developed through the indigenous knowledge
thus ethinomedicines have played key role in
development of drugs in modern system of medicine.
Gloriosa superba is
one of the oldest ingredient of species from ancient time. Being native
form India specially Southern India. It
is known as
glory lily and climbing lily- in English; Karihari-
in Hindi; Langli- in Sanskrit, Agnishike
in Kannada, Nabhikkodi in Tamil, Karianag
in Marathi 3,4,5 .The genus Gloriosa is
comprised of about 10 to 15 known species such as Gloriosa superba Linn, G luteo,
G plantii, G.latifolia, G magnifica, G rothschildiana, G abysstinica, G longifolia, G
simplex. The important species found in India are G superba
and G.rothschildiana6..
Fig. (1). Image of Gloriosa
superb linn.
Description:
Climbing, sometimes erect herb up to 4 m long; stem
annual, glabrous and sparsely branched; tuber perennial, horizontal, abruptly
bent in a V or L shape, roots fibrous. Leaves in whorls of 3–4, opposite or
alternate, simple, sessile; blade ovate to lanceolate,
6–15(–20) cm × 1.5–4 cm, base obtuse, apex of upper leaves with or without 1–2
cm long tendril, parallel-veined. Flowers axillary,
solitary, bisexual, regular, 6-merous, 4.5–7 cm in diameter, showy, pendulous;
pedicel 4–20 cm long; perianth segments free, lanceolate or oblanceolate,
5–7(–9) cm × 1(–2) cm, often with undulate margins, strongly reflexed when mature, persistent, usually yellow and red,
less often yellow, red or white; stamens with filaments 2–5 cm long, spreading,
anthers 7–10 mm long, opening by longitudinal slits; ovary superior, 3-celled, carpels coherent only by their inner margins, style filiform, 2–4(–5.5) cm long, bent at a right angle basally.
Fruit a loculicidal, oblong capsule 4–6 cm × 1–2 cm,
containing up to 20(–40) seeds. Seeds ovoid, 4–5 mm in diameter, surrounded by
a fleshy, red sarcotesta7.
Ethnomedicinal /
Traditional Uses:
Gloriosa superba is
a well known ethnomedicinal plant which is used in Ayurveda. Its use in the Indian traditional folk medicine
is also well documented. Plant pacifies vitiated kapha,
indigestion, fever, arthritis, obstructed labor, cardio-myopathy,
skin diseases, in higher dose or without purification, it is highly poisonous. In Ayurveda and yunani systems of medicine, the tuber of plant is well
known due to its pungent, bitter, acrid, heating, anthelmintic,
laxative, alexiteric and abortifacient
nature. It is widely used in the treatment of ulcers, leprosy, piles,
inflammations, abdominal pains, intestinal worms, thirst, bruises, infertility
and skin problem8. However, ingestion of all parts of the plant is
extremely poisonous and can be fatal 9. The tuber also claims
antidotal properties to snake-bite and in India it is commonly placed on window
sills to deter snakes. Many cultures
believe the species to have various magical properties10. Tribals
crush roots of the plant in water and apply on head for curing baldness. To
avoid painful delivery, Gonds and Bharias
of Patalkot, apply rhizome extract over the navel and
vagina. It induces labour pain and performs normal
delivery. According to Bhumkas of Patalkot,
this dose may lead to abortion if given to a lady with pregnancy of 1 or 2
months11. Since the rhizome is having abortive action, this is
prescribed for normal delivery12.
Phytochemistry:
Photochemical studies show that all
parts of the plant, especially the tubers are extremely toxic due to the
presence of a highly active alkaloid, Colchicine. The
species also contains another toxic alkaloid, Gloriosine13. Alkaloids are structurally heterogeneous
class of secondary biomolecules
derived from basically five amino acids ornithine, lysine, phenylalanine, tyrosine and tryptophan14. Along with these
two important alkaloids the other compounds such as lumicolchicine,
3-demethyl-N-deformyl-N-deacetylcolchicine, 3-demethylcolchicine, N-formyl deacetylcolchcine have been isolated from the plant15,16.
G. superba
seeds contain new colchicine glycoside, 3-O-demethylcolchicine-3-O-alpha-D-
glucopyranoside17. Colchicin, b-siltosterol, long chain fatty acids, b and g-lumiccolchicines, 2-hydroxy-6-methoxy benzoic acid from
tubers and root while luterlin, N-formyl-deacetyl colchicines from flower have been isolated18,
19, 20. Isolated, purified 3-monomeric monocot mannose-binding lectins
from G. superba
evaluated for antipoxviral
activity 21.
Colchicine:
Fig. (2). Structure of colchicine
(N-[(7S)-1,2,3,10- tetramethoxy-9-oxo-5,6,7,9-tetrahydrobenzo[a]heptalen- 7-yl]acetamide)22,23.
G. superba
is also known for its
colchicines content which finds use to treat arthritis24. Biosynthetic
enhancement of colchicines production on the root culture of G. superba by aluminium chloride as an elictor
was successfully observed25. Colchicine is
synthesized using mainly aromatic amino acids such as tryptophan, phenylalanine
and tyrosine. Biosynthesis of colchicine studied
using in vitro supply of exogenous precursor from G. superba and B5 medium.
Pharmacological Activities:
G. superba
is used in treatment of
gout and rheumatism. In small doses it act as tonic, stomatic
and anthelmentic26.
Antifungal activity:
Excellent antifungal activity has been reported o of
tuber extract against Candida albicans, Microsporum canis and
Staphylococcus aures27. Aqueous and alcoholic extracts of leaves
also showed significant
antimicrobial and antifungal activity28.
Enzyme inhibitory activity:
Rhizome extract of Gloriosa superba have been screened against lipoxygenase, acetylcholinesterase,
buterylcholinesterase and urease
in which wonderful inhibition was observed on lipoxygenase26, 29.
Treatment of snake bite:
Plant extract showed potent neutralising
effect against venom 26, 30.
Antitumor/cytogenic
activity:
G.superba screened for metaphase chromosome
preparation in adult mosquitoes using an inoculation technique for colchicine like substances using mosquito cytogenic assay have shown increased metaphasic
chromosome31. Colchicine affect cell
membrane structure indirectly by inhibiting the synthesis of membrane
constituent. It binds to tubeline preventing its polymerisation into microtubules. This anti-mitotic
property disrupts the spindle apparatus that separates chromosome through
metaphase, cells with high metabolic rates are most implicated by the arrest of
mitosis32.
Antipoxviral
activity:
The presense of mannose
derivative and oligomanose carbohydrates has shown
inhibition against Man lectin. It has been found cytotoxic to BSC-I cell line33.
Anticoagulant activity:
Ethanolic and aqueous extract of Gloriosa superba has displayed anticoagulant
property34.
Toxicity/Poisoning:
The colchicine which is major
component of G. superba
is mainly responsible for toxic effect35. The commonest clinical
presentation of poisoning is severe gastroenteritis with nausea, vomiting, diarrhoea with blood leading to dehydration, hypovolaemic shock and acute renal failure. Muscle weakness, hypoventilation, ascending polyneuropathy, bone marrow depression and coagulation
disorders are the other features of poisoning. Death in severe poisoning occurs
due to shock or respiratory failure although haemorrhagic
or infective complications may cause death after the first day36, 37.
Description of clinical
effects in poisoning:
1. Cardiovascular: There is no direct effect on
the heart, but fluid and electrolyte loss, often causes hypovolaemic
shock manifested by hypotension and tachycardia.
2. Respiratory: Respiratory failure is thought
to be due to the paralysis of intercostal muscles
rather than the direct depression of the respiratory centre by colchicine38.
3. Central nervous system (CNS): There is progressive paralysis of the central
nervous system and peripheral nervous system38.
4. Peripheral nervous system: Ascending polyneuropathy, weakness, loss of deep tendon reflexes may
be described.
5. Skeletal and smooth muscle: Colchicine could have a direct toxic effect on skeletal
muscles causing muscular weakness. Rhabdomyolysis may
occur with significant increase in muscle enzymes and myoglobinuria
as a result of direct muscular damage. Muscle weakness that may persist for
many weeks may contribute to respiratory deficiency39.
6. Gastrointestinal: Gastroenteritis including nausea, vomiting, diarrhoea with blood accompanied by colic and tenesmus. Loss of fluids and electrolytes leads to hypovolaemia. Intestinal ileus
may develop within the first few days and may persist up to a week40.
7. Hepatic: Colchicine
may exert direct hepatic toxicity with moderate cytolysis.
8. Renal: Any direct toxic effect of the toxin
on kidney is not clear. Renal failure is
probably secondary to excess fluid loss or hypovolaemia
and is preceded by oliguria and haematuria. Proteinuria could
also occur41.
9. Endocrine and reproductive systems: Vaginal
bleeding has been reported as a feature of intoxication. Tubers are used as an abortifacient
in some countries.
10. Dermatological: Alopecia usually occurs one
or two weeks after the ingestion of G. superba. A case
of generalized depilation has also been reported13.
11. Eye, ear, nose, and throat: Subconjunctival haemorrhages have
been observed. Burning and rawness of the throat may be early symptoms of
toxicity13.
12. Fluid and electrolyte disturbances: There is
an extensive fluid and electrolyte loss due to intense vomiting and diarrhoea or sometimes due to haemorrhages.
Hypokalaemia, hypocalcaemia, hypophosphataemia
and hyponatraemia may occur41.
13. Haematological: Colchicine has a
depressant action on the bone marrow which is characterized by a transient leucocytosis followed by leucopenia. It could also cause
thrombocytopenia that may give rise to various coagulation disorders resulting
in vaginal bleeding, conjunctival and gastrointestinal
haemorrhages .Severe thrombocytopenia occurring
within 6 hours of poisoning has been documented. Anaemia
may occur, mostly secondary to haemorrhages42.
Conservation:
Gloriosa superba usually
multiply by corm and seeds but due to low germination capability it restricts
for the regeneration. Therefore, in order to safeguard and preserve this
important plant biotechnological approachs would be
very useful.
Clonal propagation of G.
superba from apical bud and node segment of shoot
tip, cultured on solidified agar (0.8% w/v) Gamborg’s
B5 medium containing BA, IAA, Kinetin, NAA, IBA or 2,4-D. The cultures were
maintained under fluorescent light at 25-27ºC. Primary cultures were initiated
in solid B5 containing 0.5 to 1 mg/L BA and 0.01-0.5 mg/L IAA, transferred to
shoot multiplication media, shoot proliferation occurred via adventitious bud
formation within 4-8 weeks43. In vitro propagation and corm
formation in G. superba
is also reported44. Micropropagation of Gloriosa superba L. Through High Frequency Shoot Proliferation has
been studeeded. The survival rate of regenerants was found to be 85 - 90%45.
CONCLUSION:
Application indigenous natural products has been
alternative way to replace synthetic medicine. Gloriosa superba is a well known ethnomedicinal plant which is used in Ayurveda.
Photochemical studies of G. superba shows
presence of a highly active alkaloid, Colchicine. FDA-approved use of colchicine
is to treat gout (it is one of the active ingredients of anti-gout tablets
marketed by Merck & Co.), though it is also occasionally used in veterinary
medicine to treat cancers in some animals. It is also used as an antimicrobial,
antifungal, anticoagulant, antilipoxygenase agent and
antidote in snake bite. However, ingestion of all
parts of the plant is extremely poisonous and can be fatal. The
commonest clinical presentation of poisoning is severe gastroenteritis with
nausea, vomiting, diarrhoea with bleading
to dehydration, hypovolaemic shock and acute renal
failure. Gloriosa superba usually
multiply by corm and seeds but due to low germination capability it restricts
for the regeneration. Therefore, in order to safeguard and preserve this
important plant biotechnological approachs would be
very useful. Micropropagation of Gloriosa superba meets ever increasing demands
for colchicine. The availability from both wild and
cultivated sources make the plant of Gloriosa superba a potential source of Colchicine
in India.
REFERENCES:
1.
Nair C.K. ‘Ethino medicinal
plants to fight Neoplastic diseses’,
Ethinomedicine:a source of commentary therapeutics.
2010; 203-226.
2.
Shrivastava A. et.al. ‘Indigenous herbal medicines: tribal
formulations and tradinal herbal practices, aavishkar publishers and distributors .2008; 440.
3.
Nankarni K.M, ‘Indian materia medica’, 3rd
edition, mumbai popular prakashan
. 1996; 579.
4.
Kirthikar K.R., Basu B.D., ‘Indian medicinal plant’, 2nd edition
, allahbad popular publication.1935;2525-2526.
5.
Khare C.P., ‘Indian
medicinal plants: an illustrated dictionary’, Springer VerlagBerlin
/Heidelberg. 2007; 293-294.
6.
http://WWW.hort.purdue.edu/newcrop/crop facts heets/gloriosa.html.
7.
The Ayurvedic Pharmacopoieia
of India,part I, volume III, 106.
8.
Kirtikar,
KR and Basu, BD. Indian Medicinal Plants, Vol.
I-IV. International Book Distributor, Dehradun,
India. 1935.
9.
Senanayake,
N and Karalliedde, L., Acute poisoning in Sri Lanka;
an overview. Ceylon Medical Journal. 31(2); 1986: 61-71.
10.
Watt, JM and Breyer-Brandwijk,
MG., The medicinal and poisonous plants of southern and eastern Africa.
E. & S. Livingstone, Edinburgh. 1962.
11.
http://WWW.disabled-world.com/artman/publish/glori.html/Rare
Herb of Patalkot: Gloriosa superba.
12.
Duke, JA., Handbook of medicinal
herbs. CRC Press, USA .1985.
13. Gooneratne BWM., Massive
generalized alopecia after poisoning by
G. superba. Br
Med J. 1; 1983:1023-1024.
14. Thakur
RS, Potesilova H, Santavy
F., Substances from plants of the subfamily Wurmbaeoideae
and their derivatives. Part LXXIX.
Alkaloids of the plant Gloriosa superba L. Planta Medica. 3; 1975: 201-209.
15.
Sugandhi, R., Biodiversity
conservation and patenting and property
right of tribal medicine of medicinal plants of India. 10th Asian Symposium on
Medicinal Plants, Spices and other Natural products (ASOMPS X). Dhaka,
Bangladesh, 18-23 November, 2000.
16. Chulabhorn,
M, Somsak, R. et. al., Biodiversity and natural
product drug discovery, Pure and Appl. Chem. 70 (11); 1998: 2065-2072.
17.
Suri, O.P., B.D. Gupta,
and K.A. Suri; A new glycoside,
3-O-demethylcolchicine-3-O-alpha-d-glucopyranoside from Gloriosa
seeds. Natural Product Letters. 15; 2001: 217-219.
18.
Srivastava UC,
Chandra V, Gloriosa superba Linn. (kalihari) - An
important colchicines. 1977.
19.
Clewer HWV,
Green SS, Tutin F,
The constituents of Gloriosa superba. J. Chem.
107; 1915: 835–846.
20.
Capraro HG, Brossi A, In the alkaloids. A. Brossi. Academic
Press. 23; 1984:1- 7.
21.
Kaur, A., S.S. Kamboj, and J. Singh; Purification of 3 monomeric
monocot mannose-binding lectins and their evaluation
for antipoxviral activity: potential application
in multiple viral diseases caused by
enveloped viruses. Biochemistry and Cell Biology. 85; 2007: 88-95.
22.
Dictonary of Alkalods, second edition,CRC
press.443.
23.
Cerquaglia C, Diaco M, Nucera G, Regina
ML, Montalto M,
Manna R, Pharmacological and
Clinical Basis of Treatment
of Familial Mediterranean
Fever (FMF) with Colchicine or
Analogues: An Update. Current
Drug Targets - Inflammation & Allergy. 4; 2005: 117-124.
24.
Bellet, P., and J.C. Gaignanlt; Gloriosa superba Linn and
the production of colchicinic substances. Annales Pharmaceutiques Francaises . 43; 1985:345-347.
25.
Ghose, B.et.al.,Enhanced colchicin
production in root cultures of Glorisa superba by direct and indirect precursors of the
biosynthetic pathways. Biotechnology Letters. 24; 2002 :231-234.
26.
Samy, R.P., Thiwan,M.M. et. Al.,Ethinobotonical
survey of folk plants for the treatment of snake bites in northen
part of Tamilnadu. India. Journal of Ethinopharmacolgy. 115; 2008:302-312.
27.
Khan, H. et.al., Enzyme inhibition activity of
extract from rhizomes of Glorisa superba
Linn. Journal of Enzyme inhibition and medicinal chemistry. 6; 2007:722-725.
28.
Subhasni R. et. al.,Antimicrobial activity of aqueous and alcoholic extract
of Gloriosa superba Linn.,
Proc Int. Congress on “Ayurveda-2000”:216.
29.
Haroon, K. et. al., Enzyme
inhibition activities of the extract from rhizomes of Gloriosa superba Linn. Journal of enzyme
inhibition and medicinal chemistry. 22(6); 2008:722-725.
30.
Ramar, P.S. et. al., Ethinobotanical survey of folk plants for treatment of
snakebites in southern part of Tamilnadu, India.
Journal ethinopharmacology. 115(2); 2008:302-312.
31.
Jitpakdi, A.W. et.al.,
Screening of ten plant species for metaphase chromosome preparation in adult
mosquitoes using an inoculation technique. Journal of Medical Entomology . 36; 1999:892-895.
32.
Kumar, L.S., Doubling of chromosomes induced by gloriosine isolated from G. superba Linn., Nature . 171;
1953:791-792.
33.
Amandeep K. et. al.,Purification
of 3 monomeric monocot mannose-binding lectins and
their evaluation for antipoxviral activity:
potential applications in multiple
viral diseases caused
by enveloped viruses. Biochemistry
and cell biology
= Biochimie et biologie
cellulaire . 85(1); 2007: 88-95.
34.
Stitaya S, Porntipa P, Biodiversity and
natural product drug
discovery. Pure Appl. Chem.
70(11); 1988: 2065-2072.
35.
Vishwanathan, N. And B.S. Joshi.,Toxic constituent of some Indian plants. Current
Science. 52; 1983: 1-8.
36.
Mendis, S,. Colchicine cardiotoxicity
following ingestion of Gloriosa superba tubers.
Postgraduate Medical Journal. 768; 1989:752-755.
37.
Jayaweera, D.M.A.,Medicinal Plants Used in Ceylon. 1982; Vol.
3.Colombo: National Science Council of Sri Lanka.
38.
Angunawela RM and Fernando HA
,Acute ascending polyneuropathy
& dermatitis following poisoning by tubers of G. Superba. Ceylon Medical Journal . 16; 1971: 233-235.
39.
Wijesundere A ,Plant
poisons. Ceylon Medical Journal . 31(2);
1986:89-91.
40.
Ellenhorn MJ, Schonwald S, et.al., Ellenhorn's
Medical toxicology: diagnosis & treatment of human poisoning, 2nd ed. 1996.
41.
Murray SS, Kramlinger KG, McMichan JC and Mohr DN, Acute toxicity after excessive
ingestion of colchicine. Mayo Clin Proc .
58; 1983: 528-532.
42.
Saravanapavananthan T .,Plant
poisoning in Sri Lanka. Jaffna Medical
Journal. 20(1) ;1985: 17-21.
43.
Samarajeewa, P.K., M.D. Dassanayake, and S.D.G. Jayawardena,
Clonal propagation of Gloriosa
superba. Indian Journal of Experimental Biology . 31;
1993:719-720.
44.
Somani, V.J., C.K. John,
and R.J. Thengane, In vitro propagation and corm
formation in Gloriosa superba. Indial of Journal
of Experimental Biology. 27; 1989: 578-579.
45.
Roy. K., Sayeed Hassan A.K.M.and Shyamal, Micropropagation of Gloriosa superba L. Through High Frequency Shoot Proliferation.
Plant Tissue Cult. 15(1); 2005: 67-74.
Received on 30.01.2011
Accepted on 28.02.2011
© A&V Publication all right reserved
Research Journal of Pharmacognosy and
Phytochemistry. 3(3): May- June 2011, 103-107