Journal of Atoms and Molecules

  

J. Atoms and Molecules/ 4(1); 2014 / 635–644 Nidavani R B et al

Review article

PHARMACOLOGY OF CELOSIA ARGENTEA L.

Ramesh B. Nidavani * , Mahalakshmi AM, Seema M, Krishna KL

  Department of Pharmacology, JSS College of Pharmacy, JSS University, Sri Shivarathreeshwara Nagar, Mysore-570 015, India.

  

Received on: 22-01-2014 Revised on: 06-02-2014 Accepted on: 23–02–2014

ABSTRACT:

Celosia argentea L. (family-amaranthaceae) is widely used in traditional medicine to cure several

disorders such as fever, diarrhea, mouth sores, itching, wounds, jaundice, gonorrhea, and

inflammation. A variety of phytoconstituents are isolated from the C. argentea L. which includes

triterpenoid saponins, celosin E, celosin F and celosin G together with a known compound

cristatain, betalains, nicotinic acid, celogenamide-A, celogentin A–D, H, J and K. The plant having

potential pharmacological values screened for its various pharmacological activities, namely, anti-

inflammatory, immunostimulating, anticancer, hepatoprotective, antioxidant, wound healing,

antidiabetic and antibacterial activities which are reported in the extracts of different parts and its

phytoconstituents of this plant. An overview and details of the pharmacological investigations on

the C.argentea L. is presented in this review.

  KEY WORDS: Celosia argentea. L, Celosin, ethnomedicinal plant, ethnopharmacology

  INTRODUCTION:

  Human beings have been aware of medicinal plants as long ago as 3,000 BC

  [1]

  . Virtually every indigenous culture in the world uses medicinal plants in some form or other for treatment of ailments. The actual knowledge of medicinal plants is possessed by a select group of practitioners, who determine the nature of the ailments and then prescribe remedies. Although indigenous cultures possess a holistic view of ailments and their cure, medicinal plants do form a major part of indigenous medicinal or traditional medicinal practices. Since the advent of modern or allopathic medicine, traditional medicine lost quite a bit of ground, being determined to be somewhat similar to superstitious beliefs or even quackery by allopathic doctors.

  • Corresponding author Ramesh B. Nidavani, Email: rameshnidavani@jssuni.edu.in Tel: +91 – 9980335197
However, in recent periods, traditional medicine has made a major come-back. It has been realized that a number of important modern pharmaceuticals have been derived from, or are plants used by indigenous people

  [2]

  argentea L. and 6 varieties of Celosia cristata

  It is having an erect, coarse, simple, branched, smooth annual herb, normally about 0.5 to 1.5 m in height but sometimes much taller. It has

  C. argentea L. plant is an annual dicotyledon.

  [13] .

  area of tropical Africa. C. argentea L. grows as a weed during rainy season throughout India, and other tropical regions of the world mainly Sri Lanka, Yeman, Indonesia, America and West indies. In India plants are chopped and used as feed for chickens and as forage for cattle

  trigyna ) is a potherb throughout the savanna

  It is common in West Africa, from Sierra Leone to Nigeria. It is also available in Ethiopia, Somalia, Kenya, other parts of East Africa, Mexico and Central Africa. In the rainforest zone of Nigeria, Benin, Cameroon, Gabon, and Togo it is cultivated as vegetable. The wild form (sometimes referred to as C.

  C. argentea L. is known worldwide, its use for food is geographically much more limited.

  [12] .

  vegetable

  argentea L. are routinely used as leafy

  . There are more than seventy different species are identified and among all including C.

  [11]

  L. was investigated in China using sequence- related amplified polymorphism

  Genetic diversity of 16 varieties of C.

  . A number of modern drugs like aspirin, atropine, ephedrine, digoxin, morphine, quinine, reserpine, tubocurarine and artimisinin, are examples, which were originally discovered through observations of traditional cure methods of indigenous peoples

  [10] .

  . It is commonly named as semen celosiae, celosia, silver cock’s comb, cock’s comb, quail grass, woolflower in English. In India locally it is named as sitivara, vitunnaka, sunishannaka (Sanskrit), indivara, survali, safed murga (Hindi), annesoppu, and kanne hoo (Kannada)

  [9]

  . An Indian origin, C. argentea L., is a plant of tropical origin and known for its very brilliant colors and traditional uses

  [8]

  Amongst the different plants of the Celosia species, C. argentea L. is an important tropical leafy vegetable crop of high nutritional and medicinal value

  [7] .

  The Celosia species is a small genus of edible and ornamental plants belonging to Amaranthacea. The generic name is derived from the Greek word kelos, meaning "burned," and refers to the flame-like flower heads. The flowers of the species are commonly known as wool-flowers, brain celosia or cockscombs, if the flower heads are crested by fasciation, it is called as Velvet flower (in Mexico). The plants are well known in East Africa’s highlands and are used under their Swahili name, mfungu

  [5,6] .

  . In the developed countries, 25% of the medicinal drugs are based on plants and their derivatives. Medicinal plants are the major components of all indigenous or alternative systems of medicine. Medicinal plants are sources and can be a good start for the discovery of new chemical compound

  [4]

  The Indian sub-continent comprising of the countries India, Pakistan, and Bangladesh form one of the richest sources of traditional medicinal practices in the whole world. Overall, the alternative medicinal systems of India uses more than 7500 plant species. The various traditional medicinal systems practiced in the above countries are the well known homeopathic, Ayurvedic, Unani, and the Siddha systems of medicine with their well-defined formulations and selection of medicinal plants. Phytochemicals are used as templates for lead optimization programs, which are intended to make safe and effective drugs

  [3] .

DISTRIBUTION AND DESCRIPTION:

  few branches, at least until it approaches the time for flowering. The leaves are alternate entire or rarely lobed, light green. They are typically 2x6 cm, although those on flowering shoots are slightly longer. Even the green foliage may contain large amounts of betalain pigments. The often brilliantly colored flowers are borne in dense heads. Most occur in spikes, and stand like spears in the garden bed. But certain cultivated forms have compact or feathery clusters due to fasciation. The flowers yield large numbers of seeds in black colour and are about 1 mm in diameter. The flowers blooms from late summer through late fall

  [29]

  [30] .

  . The leaves and flowers are used as edible and are grown for such use in Africa and Southeast Asia

PHARMACOLOGICAL ACTIVITY:

TRADITIONAL USES:

  [16,17,18]

  [26]

  The following manifestations can be made on the basis of this comprehensive perusal of literature, that the plant C. argentea L. is being used traditionally, due to their immense therapeutic potential to treat/cure various diseases. It is a rich source of bioactive compounds like, phenolics and triterpenes are present in plant and exhibit with wide range of health benefits. Many studies demonstrated significant anti-inflammatory, immune- stimulating, antidiarrheal, anticancer, hepatoprotective, antimetastatic, antioxidant, wound healing, antidiabetic, antimitotic, antibacterial, antifungal activities and others. These pharmacological activities and identified compounds provide solid scientific evidence for some of the traditional therapeutically claims of C. argentea L.. A variety of phytoconstituents has been isolated from the different parts of C. argentea L. Thus, there remains a tremendous scope for further scientific exploration of C. argentea L. to establish their therapeutic efficacy and commercial exploitation.

  CONCLUSION:

  . The C. argentea L. displays a wide range of pharmacological activities with correlate to mechanistic possibilities over respective disorders and ephemeral overview of its pharmacological activities, has been presented in Table 3.

  [31]

  In the recent years, the use of herbal products has been increasing in developing countries. Plants have always been an attractive source of drugs. On the other hand, intricate ways of molecular interactions and bioactivity mechanisms of the extracts or their bioactive constituents provide a challenge to the scientists

  The whole plant is known for its usage in the treatment of diarrhea, piles, bleeding nose, inflammation, haematological, gynaecologic disorders and also as disinfectant

  [15]

  . In India, the plant is well known for treatment of mouth sores, blood diseases and used as an aphrodisiac

  , and also flowers of the plant are used against snakebite

  [28]

  . In screening of Taiwanese crude flower extract of C. argentea L. was found antibacterial effect against Streptococcus mutants

  [27]

  . In Vietnam, this plant is used as hemostatic herb

  . In Riau province, Sumatra (Indonesia) antibacterial assay of extracts of 114 species were tested and C. argentea L. was found to have activity against cough and jaundice

  . The seed paste is used to cure ovarian and uterine diseases

  [23]

  [19,20]

  . In Indian folk medicine, it is widely used for the treatment of diabetes mellitus

  [21]

  . In China, plant is well known for cold, gastrointestinal diseases, rheumatoid arthritis

  [22]

  and as fertility regulating agent

  . The traditional

  [25]

  Yao communities of China use the stem, leaf,

  flower and seed of C. argentea L. for the treatment of hemorrhoids, leucorrhea, and profuse uterine bleeding

  [24]

  . In USA, midwifery, rural Honduras practice C.

  [6,13,14,] .

  decoction for hemorrhage

  argentea L. for encouraging lactation and its

  REFERENCES:

  13. Lost Crops of Africa: Volume II: Vegetables, 2006.

  21. Vetrichelvan T, Jegadeesan M, Devi B.

  20. Katewa SS, Chaudhary BL, Jain A. Folk herbal medicines from tribal area of Rajasthan, India. J Ethnopharmacol 2004;94:41-6.

  Medicinal plant diversity of Sitamata wildlife sanctuary, Rajasthan, India. J Ethnopharmacol, 2005;102:143-57.

  19. Jain A, Katewa SS, Galav PK, Sharma P.

  18. Anonymous. The wealth of India. New Delhi, India: Council scientific and Industrial research, 414-5,1992.

  ed., Allahabad; 2053- 2054, 1935.

  nd

  17. Kirtikar K, Basu L. Indian Medicinal Plants, Vol. III 2

  16. Jain SK, DeFilipps RA. Medicinal plants of India, United State of America Reference Publication Inc., US, 1991.

  15. Wiart C. Medicinal plants of Southeast Asia, Pelanduk Publications, 2000.

  14. Jain GC. Hepatoprotective activity of ethanolic extract of Celosia argentea Linn. seeds in rats. J Phytological Res 2005;18(1):87-90.

  12. Uusiku NP, Oelofse A, Duodu KG, Bester MJ, Faber M. Nutritional value of leafy vegetables of sub-Saharan Africa and their potential contribution to human health: A review, J Food Compos Anal 2010;23:499-509.

  1. Sofowora A. Medicinal Plants and Traditional Medicinal in Africa. John Wiley and Sons, New York, 256, 1982.

  11. Feng N, Xue Q, Guo QH, Zhao R, Guo ML. Genetic Diversity and Population Structure of Celosia argentea and Related Species Revealed by SRAP. Biochem Genet 2009;47:521-32.

  10. Wee YC. A Guide to Medicinal Plants, Singapore Science Centre Publication, Singapore, 1992.

  9. Koh HL, Chua TK, Tan CH A Guide to Medicinal Plant, an Illustrated, Scientific and Medicinal Approach, World Scientific, Singapore, 292, 2009.

  8. Aladesanwa RD, Adenawoola AR, Olowolafe OG. Effects of atrazine residue on the growth and development of celosia (Celosia argentea) under screen house conditions in Nigeria. Crop Protection 2001;20:321-4.

  7. Germplasm Resources Information Network. United States Department of Agriculture. 2001; accessed on December 2, 2013.

  Argentea L. Int J Pharm Pharm Sci 2013;5(3):54-9.

  6. Ramesh BN, Mahalakshmi AM, Mallappa SH. Towards a better understanding of an updated Ethnopharmacology of Celosia

  5. Busia K. Medical provision in Africa – Past and present. Phytotherap Res 2005;19:919-23.

  4. Balunas MJ, Kinghorn AD. Drug discovery from medicinal plants. Life Sci 2005;78:431-41.

  3. Gilani AH, Rahman AU. Trends in ethnopharmacology. J Ethnopharmacol 2005;100:43-9.

  2. Balick JM, Cox PA. Plants, People and Culture: the Science of Ethnobotany, Scientific American Library, New York, 228, 1996.

  Anti-diabetic activity of alcoholic extract of Celosia argentea LINN. seeds in rats. Biol Pharm Bull 2002;25:526-8.

  22. Zheng XL, Xing FW. Ethnobotanical study on medicinal plants around Mt.Yinggeling, Hainan Island, China. J Ethnopharmacol 2009;124:197-210.

  Celosia argentea and Cucurbita moschata

  39. Rukhsana AR, Manohar JP, Priyanka G, Areej S. Evaluation of antioxidant potential of Celosia argentea extracts.

  38. Iwalewa EO, Adewunmi CO, Omisore NO, Adebanji OA, Azike CK, Adigun AO, et al. Pro- and antioxidant effects and cytoprotective potentials of nine edible vegetables in southwest Nigeria. J Med Food 2005;8(4):539-44.

  37. Jain GC. Hepatoprotective activity of ethanolic extract of Celosia argentea Linn. seeds in rats. J Phytological Res 2005;18(1):87-90.

  36. Santosh SB, Sohan SC, Anupama AS, Devanand BS, Manohar JP. Anti- inflammatory activity of an isolated flavonoid fraction from Celosia argentea Linn. J Medicinal Plants Res 2008;2(3):52-4.

  Celosia argentea seeds. Biol Pharm Bull 1998;21(11):1154-9.

  35. Hayakawa Y, Fujii H, Hase K, Ohnishi Y, Sakukawa R, Kadota S, et al. Anti- metastatic and immunomodulating properties of the water extract from

  antitumor activities. Chem Pharm Bull 2011;59(5):666-71.

  argentea and their anti-inflammatory and

  34. Wu Q, Wang Y, Guo M. Triterpenoid saponins from the seeds of Celosia

  extracts on anti-DNP IgE antibody production in mice. Arerugi 1994;43(5):652-9. [Article in Japanese]

  33. Imaoka K, Ushijima H, Inouye S, Takahashi T, Kojima Y. Effects of

  23. Kong YC, Jing-Xi X, But PPH. Fertility regulating agents from traditional Chinese medicines. J Ethnopharmacol 1986;15:1- 44.

  Immunostimulating activity of Celosian, an antihepatotoxic polysaccharide isolated from Celosia argentea. Planta Med 1997;63(3):216-9.

  32. Hase K, Basnet P, Kadota S, Namba T.

  31. Ramesh BN, Mahalakshmi AM. Teak (tectona grandis linn.): A renowned timber plant with potential medicinal values. Int J Pharm Pharm Sci 2014;6(1):48-54.

  30. Grubben GJH, Denton OA. Plant Resources of Tropical Africa 2. Vegetables. PROTA Foundation, Wageningen; Backhuys, Leiden; CTA, Wageningen, 2004.

  29. Houghton PJ, Osibogun IM. Flowering plants used against snakebite. J Ethnopharmacol 1993;39:1-29.

  28. Chen CP, Lin CC, Tsuneo N. Screening of Taiwanese crude drugs for antibacterial activity against Streptococcus mutans. J Ethnopharmacol 1989;27:285-95.

  27. Dung N, Loi DT. Selection of traditional medicines for study. J Ethnopharmacol 1991;32:57-70.

  Medicinal plants from Riau Province, Sumatra, Indonesia. Part 2: antibacterial and antifungal activity. J Ethnopharmacol 1995;45:97-111.

  26. Grosvenor PW, Supriono A, Gray DO.

  25. Ticktin T, Dalle SP. Medicinal plant use in the practice of midwifery in rural Honduras. J Ethnopharmacol 2005;96:233-48.

  24. Li S, Long C, Liu F, Lee S, Guo Q, Li R, et al. Herbs for medicinal baths among the traditional Yao communities of China. J Ethnopharmacol 2006;108:59-67.

  Pharmacog J 2013: 5(3):140-141.

  40. Malomo SO, Ore A, Yakubu MT. In vitro and in vivo antioxidant activities of the aqueous extract of Celosia argentea leaves. Ind J Pharmacol 2011;43(3):278-

  46. Priya KS, Arumgam G, Rethinam B, Wells A, Babu M. Celosia argentea Linn. leaf extract improves wound healing in a rat burn wound model. Wound Repair Regen 2004;12(6):618-25.

  argentea L. for Skin Depigmentation. J Oleo Sci 2002;51:203-6.

  53. Sawabe A, Nomura M, Fujiharay Y, Tada T, Hattori F, Shiohara S, et al. Isolation and Synthesis of Cosmetic Substances from African Dietary Leaves, Celosia

  52. Praveen S, Gali V, Sunder S, Santhosh G, Bimlesh K. Anti-diarrhoel activity of leaf extract of Celosea argentea in experimentally induced diarrhea rats. J Advanced Pharm Techn Res 2010;1(1):41-8.

  51. Jun’ichi K, Hayato S. Kazutaka S, Koichi T, Hiroshi M. Celogentins A-C, New Antimitotic Bicyclic Peptides from the Seeds of Celosia argentea. J Org Chem 2001;66:6626-33.

  Celosia argentea . Tetrahedron 2003;59:5307-15.

  50. Hayato S, Hiroshi M, Shigeo I, Jun’ichi K. New antimitotic bicyclic peptides, celogentins D–H, and J, from the seeds of

  49. Morita H, Shimbo K, Shigemori H, Kobayashi J. Antimitotic activity of moroidin, a bicyclic peptide from the seeds of Celosia argentea. Bioorg Med Chem Lett 2000;10:469-71.

  Anti-diabetic activity of alcoholic extract of Celosia argentea Linn. seeds in rats. Biol Pharm Bull 2002;25(4):526-8.

  48. Vetrichelvan T, Jegadeesan M, Devi BA.

  47. Santhosh G, Prakash T, Kotresha D, Roopa K, Surendra V, Divakar G. Anti- diabetic activity of Celosia argentea rootin streptozotocin-induced rats. Int J Green Pharm 2010; July-September:206-11.

  Ethnopharmacological approaches to wound healing—Exploring medicinal plants of India. J Ethnopharmacol 2007;114:103-13.

  85.

  45. Kumar B, Vijayakumar M, Govindarajan R, Pushpangadan P.

  Celosia argentea . Int J Pharmacog 1993;31:223-4.

  Contribution to Indigenous Drugs Part-I

  44. Shah MB, Patel KN, Chauhan MG.

  Antimicrobial activity of six selected plants against some strains of pathogenic organisms. J Microbio Antimicrobials 2012;4(3):54-9.

  43. Kasim LS, Ayodele O, Effedua HI, Adejumo OE, Ekor M, Fajemirokun TO.

  A, Shanmuga PK, Radhakrishnan N, Babu M. Antibacterial activity of two plant extracts on eight burn pathogens. J Ethnopharmacol 2003;86:59- 62.

  42. Gnanamani

  Celosia argentea L. Bull Inst Compr Agr Sci Kinki Univ 1993;7:9-15.

  41. Akiyoshi S, Yoshinobu N, Masayo I, Yoshiharu M, Tadashi O. Investigation of glycosides in the leaves of African

  54. Kachchhi NR, Parmar RK, Tirgar PR, Desai TR, Bhalodia PN. Evaluation of the antiurolithiatic activity of methanolic extract of Celosia Argentea roots in rats. Int J Phytopharmacol 2012;3(3):249-55.

  Tables:

Table 1: Taxonomy of C. argentea L.

  Kingdom Plantae Super division Spermatophyte Division Magnoliophyta Class Magnoliopsida Order Carypphyllales Family Amaranthaceae Genus Celosia Species Argentia Table 2: The morphological features of C. argentea L.

  [6,13] Part Macroscopic features

  Leaves Alternate, linear to lanceolate, entire and to 5cm long Flowers Small, in dense erect spikes up to 8 cm long, white to purple, without petals Fruits Membranaceous, utricles, seeds shining black and about 1.5 mm in diameter Seeds Small (between 1-5 millimeters) and round, with a black or reddish-black exterior and a thin, brittle outer skin

  

Table 3: Summary of Pharmacological activities of C. argentea L.

  Seeds Ethanolic extract Carbon tetrachloride (CCl 4 ) induced hepatic damage in rats Significant reduction in lipid peroxidation (TBARS) and an elevation in antioxidant defense parameters [37] .

  C, indicant, (3Z)- hexenyl-1-O-(6-O- α-rhamnopyranosyl- β-glucupyranoside,

  The antioxidant activity of extract may be due to phenolic and flavonoid components of the extract [40] . Leaves Aqueous extract In-vivo by cadmium (Cd)- induced oxidative stress in Wistar rats The antioxidant activity of extract may be due to phenolic and flavonoid components of the extract [40] . Leaves Glycosides: citrusin

  Leaves Aqueous extract In-vitro ammonium thiocyanate, reducing power, and membrane stabilizing models

  In-vitro DPPH free radical assay All extracts showed antioxidant property [38] .

  Whole plant Boiled, cold, and methanolic extracts

  Antioxidant activity Aerial parts, Seeds, Root

Total phenols In-vitro antioxidant

methods Suppressing free radicles possibly due to abundant polyphenols [39] .

  Boiled, cold, and methanolic extracts Hemagglutination assay in bovine erythrocytes method All extracts showed membrane stabilizing capacity in supports by plants antioxidant property [38].

  Cytoprotective activity Whole plant

  Suggested for further study [34] Hepatoprotective activity

  Pharmacological activity Parts Extract / Possible chemical constituents Screening method employed Possible mechanistic action Immunological activity Seeds Celosian Chemical and immunological liver injury model (in-vivo and in-vitro)

  [36] for anti-inflammatory activity Seeds Triterpenoid saponins: celosin E, celosin F, celosin G, and cristatain in-vitro anti- inflammatory screening models

  Carrageenan induced rat paw edema acute inflammatory & cotton pellet induced chronic inflammatory methods Flavonoids are responsible

  Anti-inflammatory activity Leaves Ethanolic extract: flavonoid fraction

  Antimetastatic activity Seeds intraportal injection of colon 26-L5 carcinoma cells model Anti-metastatic effect is based on its immunomodulating effect due to induction of cytokines such as IL-12, IL-2 and IFN- gamma leading to a Th1 dominant immune state and activating macrophages to the tumoricidal state [35] .

  In-vitro methods Suggested for further study [34] .

  Anti-cancer activity Seeds Triterpenoid saponins: celosin E, celosin F, celosin G, and cristatain

  Study suggests that suppression of IgE antibody in certain allergic disorders [33] .

  (DNP) antibody responses in mice model

  Acts as immunostimulating; Celosian is induced production of TNF-alpha, IL-1 beta, NO and IFN-gamma [32] . Seeds anti-Dinitrophenyl

  In-vitro DPPH method Not showed antioxidant property by glycosides of C. argentea L. [41] .

  Antimitotic activity Seeds Moroidin- a bicyclic peptide Microtubule assembly assay Inhibits the polymerization of tubulin [49] . Seeds Celogentins D,E,F,G, H and J- bicyclic peptides Microtubule assembly assay Inhibits the polymerization of tubulin [50] .

  Showed MIC to about 50mg/ml against Salmonella typhi, 50mg/ml against Escherichia coli and 100mg/ml against Staphylococcus aureus [43]

  Suggests that, extract may possess as insulin-like effect on peripheral tissuesby either promotingglucose uptake or metabolism [47] . Seeds Ethanolic extract Hypoglycaeimic action in alloxan-induced diabetic rats Suggested for further study [48] .

  Leaves Ethanolic extract Rat burn wound model Mitogenic and motogenic promotion of dermal fibroblasts [45,46] Anti-diabetic activity Root Ethanolic extract Hypoglycaeimic action in streptozotocin induced diabetic rats

  Not showed any MIC [43] Wound healing activity

  Antifungal activity Leaves Ethanolic extract; tannin & alkaloids (fairly present) screened against pathogenic fungi namely, strains of C. albicans , T. metagophyte, M. furfur by agar-well diffusion assays

  Diuretic activity Seeds Ethanolic extract On albino rats and human volunteers Suggested for further study [44]

  Leaves Ethanolic extract

  Leaves Ethanolic extract; tannin & alkaloids (fairly present) Screened against pathogenic bacteria namely, strains of A. flavus, E. coli, P. aeruginosa, S. typhi and S. aureus by agar- well diffusion assays

  (3Z)-hexenyl-1-O- β-glucupyranoside, (7E)-6,9- dihydromegastigma- 7-ene-3-one-9-O- β- glucupyranoside,

  , and Vibrio Suggested further study for elucidating antibacterial molecule from C. argentea L. [42] .

  Antibacterial activity Leaves Ethanolic extract Disc-diffusion and MIC method by using pathogenic bacteria namely strains of E. coli , Staphylococcus , Klebsiella , Pseudomonas , Streptococcus , Shigella, Salmonella

  (glucose) tend to have growth promoting activity whereas those without sugar moiety may have growth inhibitory activity [41] .

  Bioassay of germinating lettuce seeds Compounds with sugar moiety

  C, indicant, (3Z)- hexenyl-1-O-(6-O- α-rhamnopyranosyl- β-glucupyranoside, (3Z)-hexenyl-1-O- β- glucupyranoside, (7E)-6,9- dihydromegastigma- 7-ene-3-one-9-O- β- glucupyranoside,

  Growth activity Leaves Glycosides: citrusin

  • Suggested for further study [44]
Seeds Celogentins A, B and C- bicyclic peptides Microtubule assembly assay Inhibits the polymerization of tubulin [51] .

  Anti-diarrheal activity Leaves Ethanolic extract Castor oil induced, Charcoal meal test and

  PGE2 induced diarrhea methods Study suggests that, the antidiarrheal effect may be by reduction of gastrointestinal motility by tannins and flavonoids [52] .

  Skin Depigmentation Leaves Eugenyl O-β-D- glucopyranoside (citrusin C)

  External application method Citrusin C showed strong tyrosinase inhibitory activity [53] .

  Anti-urolithiatic activity Roots Methonolic extract Ethylene glycol induced urolithiasis Wister rat model The extract having anti- urolithiatic effect [54] .

  

C.argentea L., Celosia argentea L.; TNF-alpha, tumor necrosis factor-alpha; IL-1 beta, interleukin-

  1 beta; NO, nitric oxide; IFN-gamma, gamma interferon; Th1, T-helper cell 1; DPPH, 1,1-diphenyl- 2-picrylhydrazyl; MIC, minimum inhibitory concentration; A. flavus, Aspergillus flavus; E. coli,

  

Escherichia coli; P. aeruginosa, Pseudomonas aeruginosa; S. typhi, Salmonella typhi; S. aureus,

Staphylococcus aureus; C. albicans, Candida albicans , T. metagophyte, Trichophyton metagophyte;

M. furfur, Malassezia furfur ; and PGE2, Prostaglandin E2.

  How to cite this article:

  Nidavani R B, Mahalakshmi AM, Seema M, Krishna KL “Pharmacology of Celosia argentea L.” J. Atoms and Molecules, 4(1), 2014: 635 – 644.