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Ali Esmail Al-Snafi. et al. / Journal of Pharmaceutical Biology, 5(4), 2015, 254-261.

Journal of Pharmaceutical Biology


www.jpbjournal.com e-ISSN - 2249-7560
Print ISSN - 2249-7579

THE CHEMICAL CONSTITUENTS AND PHARMACOLOGICAL


IMPORTANCE OF CELOSIA CRISTATA – A REVIEW
Ali Esmail Al-Snafi*
Department of Pharmacology, College of Medicine, Thi qar University, Nasiriyah, Iraq.

ABSTRACT
Celosia cristata (Family: amaranthaceae) is widely used in traditional medicine to cure several disorders. Many
sensitive ingredients were isolated from different parts of the plant. The recent studies showed that the plant exerted a wide
range of pharmacological activities. The chemical constituents and pharmacological activities of Celosia cristata were
presented in this review.

Keywords: Celosia cristata, Pharmacological Importance, Chemical constituent.

INTRODUCTION
Medicinal plants are the Nature’s gift to human Foxtail amaranth, Fire-flame bush, Shinaji tea and
beings to help them pursue a disease-free healthy life. Woodfordia [58,60].
Plants are a valuable source of a lot of secondary
DESCRIPTION
metabolites. Two thirds of the new chemicals identified
This species is an annual herb, hairless entirely.
yearly were extracted from higher plants. 75% of the
The stem is erect, thick, little branched, green or tinged
world’s population used plants for therapy and
with red, ridged, and flat near the upper part. The simple
prevention. In the US, where chemical synthesis
leaves are alternate, petiolate; the blade is long-elliptical
dominates the pharmaceutical industry, 25% of the
to ovally lanceolate, 5-13cm long, 2-6cm wide, acuminate
pharmaceuticals are based on plant-derived chemicals.
or attenuate at the apex, gradually narrow and decurrent at
Recent studies showed that medicinal plants exerted a
the base, and entire marginally. Occurring on top of the
wide range of pharmacological effects. The major
stem, the spikes are flat, succulent, crest-like or
pharmaceutical companies are currently conducting
featherlike; down their middle are numerous flowers;
extensive research on plant materials to introduced new
the perianthial segments are light red to purplish red,
drugs in the medical practice [1-57]. This review will
yellowish white or yellow, elliptically ovate, pointed at
highlight the chemical constituents and pharmacological
the tip, 5 in number; the bract, bractlet and perianthial
activities of Celosia cristata.
segment are scarious; each flower has 5 stamens whose
filaments are joined together to form a cup at the base.
Nomenclature and classification
The fruit is an egg-shaped utricle, which is wrapped in the
The Celosia species is a small genus of edible
persistent perianth and becomes circumscissile when ripe.
and ornamental plants belonging to Amaranthacea. The
The seed is kidney-shaped, black, and lustrous [58,61-62].
generic name is derived from the Greek word kelos,
meaning "burned," and refers to the flame-like flower Distribution
heads. Celosia cristata is a member of the genus Celosia, It is common in Africa, South America, India
and is commonly known as cockscomb, since the flower and some parts of Asia [63].
looks like the head on a rooster (cock). It belongs to the
class Magnoliopsida, order Caryophyllales and family Traditional uses
Amaranthaceae [58-59].Common name: Cockscomb, Seeds were used as demulcent; for painful
Crested celosia, Yellow toreador, Red cockscomb, micturition and for dysentery. Flowers were edible in

Corresponding Author:- Ali Esmail Al-Snafi Email:- aboahmad61@yahoo.com

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India, they were also used medicinally in menorrhagia and inorganic elements are abundant, the amount of fat in
and as an astringent which are used to treat bloody stool, seed is about 10.1% [70].
hemorrhoid bleeding and diarrhea; the seed decoction is The total polyphenols, flavonoids and tannin
used to treat dysentery [63-66]. contents of methanolic extracts on the cockscome flowers
The flowers were also used as astringent, styptic, were 6.80, 2.34 and 6.23mg/g extract residue, respectively
depurative, uterine sedative, constipating, antibacterial, [71]. Cochliophilin A (5-hydroxy-6, 7-methylenedioxyfla-
and corrective of urinary pigments, febrifuge and vone), known as a host-specific attractant towards the
alexeteric. They were useful in the conditions of kapha zoospores of Aphanomyces cochlioides was isolated
and pitta, leprosy, burning sensation, skin diseases, from Celosia cristata, that is susceptible to the pathogen.
diarrhoea, dysentery, fever, headache, hemorrhoids, Its content in Celosia seedlings was quantified as 1.4 µg/g
herpes, internal hemorrhage, leukorrhea, liver disorders, fresh weight. A new isoflavone, cristatein (5-hydroxy-6-
menorrhagia, ulcers, and wounds. Juice of leaves was hy-droxymethyl -7,2 0 -dimethoxyisoflavone, 2), and five
used in bilious sickness. They were also valued as a known flavonoids were also identified [72-73].
stimulant in pregnancy. The seed was hypotensive and The changes of flavonoid compounds in Flos
ophthalmic. It was used in the treatment of bloodshot Celosiae cristatae were determined after carbonizing
eyes, blurring of vision, cataracts and hypertension. The processed. Among the ten batches of processing samples,
flower and seed were astringent, haemostatic, parasiticide these components were not determined in two batches,
and poultice. They were used in the treatment of bloody but were found in the other eight bathes, with the content
stool, haemorrhoid bleeding, uterine bleeding, of kaempferol as 0.002 -.025 % and isorhamnetin as 0.001
leucorrhoea and diarrhea [60]. -0.011 % [74].
The plant was also used for the treatment of Five saponin, cristatain , celosin A , celosin B ,
fatigue, atherosclerosis, leucorrhoea and osteoporosis. Its celosin C and celosin D were isolated from the seeds
seeds have been used for removing “liver-heat” of Celosia cristata [75]. A new triterpenoid saponin,
improving eyesight, clearing wind- and as an anti- semenoside A, was isolated from Semen Celosia cristatae
inflammatory agent [59]. [76]. Two glycoproteins, CCP-25 and CCP-27 were
purified from the leaves of Celosia cristata [77].
Pats used: Fruit and seeds were used medicinally [67]. However, eighteen compounds were isolated and
fifteen compounds were identified, they were p-
Physicochemical characteristics [68] (w/w%) hydroxyphenylethanol, kaempferol, quercetin, cristatain,
Total ash value 5.54, acid insoluble ash 1.14, celosin A, celosin B, celosinⅠ, celosinⅡ, sphingosine,
water soluble ash 2.78, sulphated ash 0.8, moisture β-sitosterol, stearic acid, stigmasterol, daucosterol,
content 5.4, loss on drying 5.8, stomatal number 172 and palmitinic acid and n-hexacosoic acid [78].
stomatal index 25.
Pharmacological effects
Chemical constituents Hemostatic effect
The preliminary phytochemical analysis on the Five days after mice were given decoction of
extracts of Celosia cristata showed the presence Flos Celosiae cristatae with the dosage of 17g/kg,they
flavonoids, mucilages, phenolic compounds & tannins, were compared with a control group. It emerged that the
saponins, triterpenoids, alkaloids, carbohydrates, bleeding time (BT) was shortened greatly (P0.01). Seven
proteins, amino acids, gums and steroids [63,68]. days after rabbits were given the same decoction with the
The plant contained betanin, and several sterols. dosage of 1.7g/kg, it was found that the coagulation time
The inflorescence contained amarantin, isoamarantin, (CT), prothrombin time (PT) and plasma recovery (PRT)
celosianin and isocelosianin. The seeds contain 10.1- were shortened (P0.05), and the euglobulin lysis time
12.8% of protein and yield 7.2-7.9% fatty oil. The plant (ELT) was markedly shortened(P0.01)in comparison with
also contained choline esters of hyaluronic acid [64,67]. control [79].
Six compounds were isolated from the ethanolic
extract of Celosia cristata, and identified as 4- Hepatoprotective effects
hydroxyphenethyl alcohol, kaempferol, quercetin, β- A new triterpenoid saponin, semenoside A, was
sitosterol, 2-hydrox octadecanoic acid and stigmasterol isolated from Semen Celosia cristatae. The
[69]. hepatoprotective activity of semenoside A with an oral
The analysis of Celosia cristata L. Showed that dose of 1.0, 2.0 and 4.0mg/kg, respectively, were
the protein content in dried samples is about 19.40%, investigated by carbon tetrachloride (CCl4)-induced
24.60% and 27.04% in the inflorescence, leaf and stalk hepatotoxicity in mice. The results indicated that it had
and seed respectively. These proteins are rich in all kinds significant hepatoprotective effects (p < 0.01) [76].
of amino acid; many kinds of vitamins such as B1, B2, C, Cristatain saponin exhibited significant
E and beta-carotene are in high content and dietary fiber hepatoprotective effect on carbon tetrachloride (CCl4) -

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and N, N-dimethylformamide (DMF)-induced which suggesting the Celosia cristata L. ethanol extract
hepatotoxicity in mice, which were evidenced by might be used as hydration and anti-wrinkle agents [82].
significant decreases in the values of asparate The antioxidant compounds and antioxidant
aminotransferase (AST), alanine aminotransferase (ALT) activities of the methanolic extracts and solvent fractions
and alkaline phosphatase (ALP) of serum and from cockscome flowers were studied. To determine the
histopathological examinations compared to controls [75]. antioxidant compounds in the methanolic extract and
The antioxidant potential and protective effects solvent fractions, the total polyphenol, flavonoid and
of Celosia cristata L. (Family: Amaranthaceae) flower tannin were measured by spectrophotometric methods.
(CCF) extracts on tert-butyl-hydroperoxide (t-BHP)- These were evaluated for antioxidative activities by
induced oxidative damage in the hepatocytes of Chang DPPH and ABTS radical scavenging activities. The total
cells and rat livers was studied . In vitro, CCF extracts polyphenol, flavonoids and tannin contents of methanolic
exhibited protective effect through their radical extracts on the cockscome flowers were 6.80, 2.34 and
scavenging ability to enhance cell viability, prevent 6.23mg/g extract residue, respectively. The DPPH and
reactive oxygen species (ROS) generation, and inhibit ABTS radical scavenging activities of the methanolic
mitochondrial membrane depolarisation in t-BHP-induced extracts on the cockscome flowers were 52.43 and
hepatotoxicity in Chang cells. In vivo, oral feeding of 107.01mg Trolox equivalent antioxidant capacity per g
CCF (100mg and 500mg/kg of body weight) to rats for extract residue, respectively [71].
five consecutive days before a single dose of t-BHP The antioxidant activity test of Celosia cristata
(2mmol/kg, i.p.) showed a significant (p<0.05) protective antiviral proteins (CCP-25 and CCP-27) using ferric
effect by lowering serum levels of glutamate oxaloacetate reducing antioxidant power (FRAP) assay in vitro
transaminase (GOT) and glutamate pyruvate transaminase indicated that these proteins are strong antioxidants. The
(GPT). The extract decreased the hepatic levels of lipid increase in activities of redox-enzymes such as
peroxidation (MDA) and serum level of triglyceride (TG) peroxidase, catalase and polyphenol oxidase on tobacco
against t-BHP-induced oxidative stress [80]. The mosaic virus (TMV) inoculation of test plants was
histopathological hepatic lesions induced by inhibited when plants were treated with CCP-25 before
administration of CCl4 were remarkably ameliorated by TMV inoculation. The activity of phenylalanine ammonia
cristatain. Furthermore, it appeared that luteolin display lyase, involved in biosynthesis of antioxidative
hepatoprotective property in CCl4 induced liver injury in compounds was also inhibited [77].
mice [78].
Adipogenic effect
Cytotoxic effects The in vitro the capacity of a Celosia
The cytotoxicity of water and organic solvent cristata extract to impact the adipogenic potential of
extracts was determined in the fibroblast cells Cos7 and in native human adipose tissue progenitor
four cancer cell lines: HeLa, HepG2, SK-Hep1 and LS cells, i.e. commitment and differentiation towards
174T. The aqueous extracts were also screened against adipogenic lineage, was evaluated. Native adipose tissue
BVDV and HBV, whereas organic solvent extracts were progenitor cells were isolated by
assayed on T. brucei. IC50 of the water extracts against immunoselection/depletion approaches from human
Cos7, HeLa, HepG2, SK-Hep1 and LS 174T were 263.9, subcutaneous adipose tissues. Two distinct cell culture
2773.5, 200, 180 and >200 μg/ml respectively. IC50 of conditions were used to assess the effect of Celosia
CH2Cl2 extracts against HeLa and Cos 7 were 472.0 cristata extract on commitment and differentiation of
and 136.0 μg/ml, while IC50 of MeOH extracts progenitor cells. Cells were cultured either in
against the same cell lines, were 499.8 and 77.2 differentiation medium for 10 days in the
respectively [81]. presence/absence of Celosia cristata extracts to study the
impact on differentiation or first cultured in a
Antioxidant effects commitment-inducing medium, with or without Celosia
The anti-oxidant and anti-aging activity of cristata extract, for 48 h and then cultured 10 days in
Celosia cristata were studied. Celosia cristata L. ethanol differentiation medium to assess the impact on
extract had anti-oxidant activity in a dose-dependent commitment. In both experimental series, the fate of
manner in 1-diphenyl-2-picryl-hydrazyl (DPPH) radical progenitor cells was studied by quantification of lipids
scavenging. Ethanol extract had anti-oxidant activity in a and by determining the expression of key genes involved
dose-dependent manner. Silica dose-dependently in adipogenesis. The Results showed that Celosia
increased the intracellular ROS generation in RAW 264.7 cristata extract reduces lipid content of progenitor cells
cells. Celosia cristata L. ethanol extract showed anti- undergoing differentiation. This reduction correlates with
aging effects, the hyaluronidase inhibitory effects and a reduced expression of C/EBPα. When progenitor cells
elastase activity inhibitory effects were relatively strong, are placed in commitment-inducing conditions, Celosia
cristata extract induces a more potent reduction of lipid

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content. This reduction correlates with a decrease in the two tobamo viruses, tobacco mosaic virus and sunnhemp
expression levels of master genes involved in rosette virus, and citrus ring spot virus (ungrouped), were
adipogenesis: the genes of transcription factors PPARγ2 purified from the dried leaves of Celosia cristata. These
and C/EBPα as well as marker genes coding for LPL and proteins, called CCP-25 and CCP-27, have M(r) 25 and
GPDH [83]. 27 kDa. Their concentration was found to vary between
the pre-flowering and post-flowering stages of C. cristata
Antimicrobial and anthelmintic effects 90% lesion formation at a concentration of 20-30 µg ml(-
Celosia cristata flowers showed antioxidant 1). They were resistant to proteases in the native state, but
properties and antimicrobial effect. It also had sun were readily digested when denatured. Both of them
protection effects [84]. The antimicrobial properties of imparted actinomycin D sensitive resistance by inhibiting
ethanolic, methanolic and other solvent extracts local lesions on Nicotiana tabacum cv. Samsun NN by
of Celosia cristata L. was evaluated against tobacco mosaic virus. Their application, individually, also
microorganisms, Staphylococcus aureus, Bacillus resulted in high resistance in systemic hosts to sunnhemp
subtillus, Salmonella typhimurium, Escherichia coli, rosette virus, and citrus ring spot virus [88].
Pseudomonas aeruginosa and Candida albicans. The Antiviral protein and antioxidant activity:
minimal inhibitory concentration (MIC) values of the Proteins CCP-25 and CCp-27 isolated from Celosia
extracts against animal pathogenic bacteria and yeast cristata leaves studied for correlation between its antiviral
were assessed using the broth microdilution methods. and antioxidant activity. Antiviral proteins showed strong
Results showed that the different extracts differed clearly antioxidant activity through increase in activities of redox
in their antimicrobial activities. MIC values in the range enzymes such as peroxidase, catalase and polyphenyl
of 0.125 to 1mg/ml hexane fraction of methanolic and oxidase. It was evaluated using ferric reducing antioxidant
ethanolic extracts exhibited good activity power assay [89].
against Staphylococcus aureus (0.125mg/ml), Bacillus The chloroform, methanol and aqueous extract
subtillus (0.5mg/ml) and Candida albicans (1mg/ml) and of Celosia cristata leaves (100 mg/ml and 200 mg/ml)
dichloromethane fraction showed similar results [85]. were used to determine the paralysis and mortality of
Preinoculation treatment with Celosia cristata earthworms (used as it shows resemblance with intestinal
leaf extract prevented lesion production by sunnhemp roundworm parasites anatomically and physiologically) in
rosette virus, tobacco mosaic virus and potato virus X in comparison with albendazole (100 mg/ml and 200
several local lesion hosts. The extract inhibited lesion mg/ml). Worms placed in both aqueous and methanol
formation only in treated areas, and did not act on the extracts of C. cristata showed significant paralysis and
virus directly, but only via the host. The persistence of leads mortality in dose dependent manner. Chloroform
inhibitory activity in test hosts for up to 6 days indicates extract showed no significant activity against the worms.
that the site of virus attachment is blocked The results revealed that the aqueous extract had higher
semipermanently [86]. significant anthelmintic activity than methanol extract
Two N-terminally blocked antiviral [63].
glycoproteins, CCP-25 and CCP-27 were purified from
the leaves of Celosia cristata [77]. Other pharmacological effects
Study the anti-BVDV toxicity on EBTr cells, Celosia cristata was considered as one of the
anti-BVDV protection in EBTr cells and anti-HBV effect herbal therapy acting as antitussive [67]. Choline esters of
in Hep G2, showed that the plant had no anti-BVDV hyaluronic acid from the plant, when fed to rats, showed
toxicity on EBTr cells, anti-BVDV protection in EBTr antiulcer and gastro-protective effect [64].
cells, but it had anti-HBV effect in Hep G2 in high The plant prevented fluoride toxicity, the food
concentration [81]. supplemented with calcium can reduce the effect of high
An antiviral protein named CCP-27 was purified fluorine, and the food supplemented with both calcium
from the leaves of Celosia cristata at the post-flowering and Celosia cristata extracts is better. The water extract
stage by anion-exchange, cation-exchange, and gel- of Celosia cristata could enhance immune function of
filtration chromatography. It exhibited resistance against mice.
sunnhemp rosette virus in its test host Cyamopsis Celosia cristata could strengthen the mouse
tetragonoloba. It also exhibited deoxyribonuclease endurance and increase the deposit of muscle glycogen
activity against supercoiled pBlueScript SK+ plasmid and hepatic glycogen. The ethanol extract of Celosia
DNA. It was found to nick supercoiled DNA into nicked cristata possesses the actions of lowing lipids and MDA
circular form at lower protein concentration followed by and may prevent fatty liver. The water extract of Celosia
nicked to linear form conversion at higher protein cristata exhibits a killing effect on Trichomonas
concentration. CCP-27 also possesses strong ribonuclease vaginalis. Celosia cristata injection exhibits obvious
activity against Torula yeast rRNA [87].Two antiviral effect of inducing abortion in second trimester on
glycoproteins, active against mechanical transmission of pregnant mice, guinea pig and rabbit [62].

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CONCLUSION effects. This review was designed to highlight the


The recent pharmacological studies showed that chemical constituents and pharmacological activities of
Celosia cristata exerted wide range of pharmacological Celosia cristata.

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