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