Evaluation of Anthelmintic Activity of Different Extracts of Careya arborea
Manbir Kaur*, Ravika Nanda, Rupinder Kaur, Pooja Kohar
Department of Pharmacy,
Global Group of Institutes, Amritsar
*Correspondence: manbirmanu@yahoo.com
DOI: https://doi.org/10.71431/IJRPAS.2025.4112
Article Information
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Abstract
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Research Article
Received: 24/02/2025
Accepted: 26/02/2025
Published: 01/03/2025
Keywords
Anthelmintic;
Acetone extract; Careya arborea; earthworms; tubers.
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This
study evaluates the anthelmintic activity of various extracts of Careya
arborea, a medicinal plant traditionally used in ethnomedicine. Soxhlet
extraction method, was employed
to isolate bioactive compounds. The anthelmintic efficacy was assessed
against earthworms using standard assays that measured
paralysis and mortality rates at various concentrations (25 and 50 mg/mL). The results indicated a significant dose-dependent effect,
with acetone extracts demonstrating the highest activity,
effectively inducing paralysis and mortality in the test organisms. These
findings support the traditional use of Careya arborea and suggest
its potential as a natural anthelmintic agent, warranting further
investigation into its active constituents and mechanisms of action.
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INTRODUCTION
Throughout
history, people have sought remedies for their ailments by exploring the
natural world. The use of medicinal plants dates back to ancient times,
initially driven by instinctual observations akin to those made by animals.
During this era, knowledge about the causes of illnesses and the therapeutic
properties of plants was limited, relying primarily on experiential evidence
[1]. Over time, however, the rationale behind the use of specific medicinal
plants for treating particular diseases began to emerge. This gradual shift led
to a departure from empirical approaches towards a more evidence-based
framework. Prior to the emergence of iatrochemistry in the 16th century, plants
served as the primary source of treatment and prevention. Despite the
advancement of synthetic drugs, the declining efficacy and increasing
contraindications associated with their use have revived interest in natural
remedies. As a result, the utilization of natural drugs has once again become a
relevant and topical area of exploration [2].
Helminths
multicellular worms, encompass various types including nematodes (roundworms),
cestodes (tapeworms), and trematodes (flatworms), which commonly inhabitthe
human gut. Among the most prevalent intestinal helminths are Ascaris lumbricoides (roundworm),
Trichiuristrichiuria (whipworm), Ancylostoma
duodenale, and Necatoramericanicus
(hookworms), collectively known as geohelminths or soil-transmitted helminths.
These infections are endemic in tropical and subtropical regions of the
developing world, particularly in areas lacking adequate water and sanitation
facilities [3, 4]. Recent estimates indicate staggering numbers of infections,
with A. lumbricoides affecting over a
billion people, T. trichiura795
million, and hookworms 740 million individuals [5].
Although
intestinal helminths rarely result in mortality, they exert a profound impact
on the health and nutritional status of affected individuals, particularly
children [6,7]. Beyond health implications, helminth infections hamper physical
and cognitive development in children, hamper educational attainment, and
impede overall economic progress [8,9].
Helminth
infections affect approximately one-third of the global population, making them
one of the most prevalent infectious disease agents worldwide. These infections
pose persistent challenges to public health, particularly in developing regions
[10]. Approximately 2 billion people, more than a quarter of the world's
population, are affected by helminthic parasites, representing a significant
burden in developing countries, particularly among children. If left untreated,
most helminth infections can evolve into chronic inflammatory disorders,
leading to both immediate and delayed-onset pathology [11,12]. In developing
regions such as Sub-Saharan Africa, Asia, and the Americas, an estimated one
billion individuals are infected with one or more helminth species
[13].Helminths are classified into two major phyla; nematodes and
platyhelminths [14]. Nematodes, also known as roundworms, encompass
soil-transmitted helminths and filarial worms responsible for lymphatic
filariasis (LF) and onchocerciasis.[16][17]
Plant profile
Careya arborea Roxb,
commonly known as wild guava and belonging to the family Lecythidaceae, Careya arborea, belonging to the
Lecythidaceae family, is a tree species native to the Indian Subcontinent,
Afghanistan, and Indochina. In Hindi, it is known as Kumbhi, while in English,
it is referred to as the Slow Match Tree and is popularly referred to as
Padmaka or Kumbhi in Ayurveda. This tree can be distinguished by its thick,
dark grey bark, large showy flowers, and leaves that turn red in winter. It
possesses significant medicinal value, with most of its plant parts utilized in
traditional systems of medicine. The plant has been recognized for its
antimicrobial, astringent, demulcent, antitumor, antipyretic, antipruritic,
hepatoprotective, antioxidant, CNS activity, antileishmanial, antidiarrheal,
anticoagulant, analgesic, antitumour, and cytotoxic properties [23-26, 31-38].
Phytoconstituents
of Careya arborea
The
plant has been extensively investigated and chemical constituents from the
barks, leaves and seeds of the plant have been reported to include
triterpenoids, flavonoid, coumarin saponins and tannins. Careya arborea also contains five Saponins (sapogenols- careyagenol
A, B, C, D and E); sterols, α-spinosterol and α-spinosterone.
Table 1:
Phytoconstituents present in different parts of Careya arborea [27-30]
Plant Part
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Phytoconstituents
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Roots
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Phyto-estrogens, Sito-sterol
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Stem bark
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lupeol, β-sitosterol, betulin, betulinic acid,
1-[5-(1,3-benzodioxol-5-yl)-1-oxo-2,4 pentadienyl] piperidine
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Seeds
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α–spinasterol, Δ22-stigmastenol
Triterpenoids: Barringtogenol C
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Leaves
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Careyagenolide, maslinic acid, 2α hydroxyursolic
acid n-hexacosanol, α–spinasterol, taraxerol, taraxeryl acetate,
β-sitosterol, ellagicacid and quercitin, Triterpene ester-careaborin, Tannins
valoneicacid dilactone
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Flowers
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Steroids and triterpenoids,
Phenols, Tannins
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MATERIALSAND METHODS:
Plant
Material
The stem bark of plant is procured from Triputi region
of Andhra Pradesh and was verified by Dr. K. Madhava Chetty, faculty of botany
at Sri Venkateswara University, Tripura,
Andhra
Pradesh. The specimen is assigned an accession no. 6310 and was deposited at
the herbarium section of departmental museum for reference.
Preparation of the
Extracts:
The
collected plant materials (tubers) were initially washed under running tap
water and then dried. Subsequently, they were finely ground to a powder. The
powder was carefully sieved using a commercial sieve with a mesh size of
approximately 60mm to ensure uniform particle size. The sieved powder was then
labeled and stored in airtight bottles for future use.
To
prepare the extracts, precise amounts of the powdered sample (35g) were weighed
and placed in a Soxhlet extraction apparatus. Acetone and hydroalcoholic
extracts were prepared by using 250ml of solvent separately. The extraction
process was conducted for 24 hours with each solvent to obtain the plant
extracts.
Collection of
Animal and Experiment:
The
assay was conducted using adult earthworms due to their structural and
physiological similarities to the intestinal roundworm parasites found in
humans. Earthworms are readily available and are commonly utilized for initial in-vitro
evaluations of anthelmintic compounds.
Figure 1:
Earthworms
Prepared
extracts of Careya arborea were
assessed for their anthelmintic activity against earthworms. Before commencing
the experiment, all test solutions and standard drug solutions were freshly
prepared as follows:
·
For 25mg/ml: 625mg of respective extract
was dissolved in 25ml of dimethyl sulfoxide.
·
For 50mg/ml: 1.2gm of acetone extract was
dissolved in 25ml of dimethyl sulfoxide.
·
For Albendazole Standard Drug (20mg/ml):
400mg of albendazole standard drug was dissolved in 20ml of dimethyl sulfoxide.
Two
groups of earthworms, each of approximately equal size, were placed in 25ml
solutions with two different concentrations (25,50mg/ml) of the extracts in
petri dishes. Albendazole (20mg/ml) served as the reference standard, while
acetone was used as the control. The time taken for paralysis and the time of
death of the worms were determined. Paralysis was recorded when no movement
could be observed in the worms except when vigorously shaken. The time of death
was noted when the worms showed no movement even when shaken vigorously.
Figure 2 a. Albendazole
(20mg/ml) b. Acetone Extract (50mg/ml) c. Acetone
Extract (25mg/ml)
RESULTS AND DISCUSSION
Anthelmintic
activity of different extracts and standard drug
The
result in the Table II depicts the time taken for paralysis and death of worms
when treated with different concentrations. The standard drug, albendazole
showed paralysis at 18 to 21secs and death after 35 to 37secs at 20mg/ml
concentration. Acetone extract of C.
arborea plant in concentrations 25 and 50 mg/ml showed paralysis of worms
within 28 to 33secs and death within 45 to 52 secs depending on the
concentration (Table 2).
Table
2: Anthelmintic activity with different
extracts of C. arborea tuber and
standard drug
Concentration
(mg/ml)
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Acetone
Extract
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Hydroalcoholic
Extract
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Standard
Drug Albendazole
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Paralysis (secs)
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Death (secs)
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Paralysis (secs)
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Death (secs)
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Paralysis (secs)
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Death (secs)
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25 mg
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34 ± 1.41
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52.5± 0.707
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-
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-
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20
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37
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50 mg
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28.5 ± 0.707
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44.5 ± 0.7
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420
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-
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Std (Albendazole)
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20
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37
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-
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-
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Control
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51
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152
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-
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-
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Figure 3: Anthelmintic activity with different extracts of C. arborea tuber and standard drug
It
was observed that the acetone extract (50mg/ml) of Careya arborea tuber is more potent than the acetone extract
(25mg/ml) and their activities were comparable with the standard drug
albendazole (20 mg/ml). Hydroalcoholic Extract at both concentrations did not
show significant results.
CONCLUSION
In the evaluation of the anthelmintic activity of the Careya arborea, extraction was done
using organic solvent acetone and aqueous solvent. The result depicted that the
acetone extract (50mg/ml) showed the
promising activity. From the above work it can be concluded that Careya arborea can prove to be a good
source of herbal drug aiding to explore anthelmintic lead that is helpful in
combating the diseases caused by helminths. Intensive investigations related to
bioactive constituents for specific pharmacological action, their mechanism of
action, safety, and efficacy could be the future research interests, to explore
the plant exhaustively. There is a great promise for the development of novel
drugs from C. arborea to treat many
human syndromes as a result of its effectiveness and safety
ACKNOWLEDGEMENT:
We are thankful to the management of Global Group of
Institutes for providing all necessary facilities during this study.
REFERENCES:
1. Stojanoski, N. Development of health culture in
Veles and its region from the past to the end of the 20th century. Veles:
Society of science and art, 1999; 13:34-34.
2. Kelly, K. The history of medicine. New York:
Facts On File, 2009.
3. Savioli, L. and Albonico, M. Focus:
Soil-transmitted helminthiasis. Nature Reviews Microbiology, 2004;
2(8): 618-619.
4. Cappello, M. Global health impact of
soil-transmitted nematodes. The Pediatric infectious disease journal, 2004;
23(7): 663-664.
5. De Silva, N.R., Brooker, S., Hotez, P.J.,
Montresor, A., Engels, D. and Savioli, L. Soil-transmitted helminth infections:
updating the global picture. Trends in parasitology, 2003; 19(12):
547-551.
6. Stephenson, L.S., Latham, M.C. and Ottesen,
E.A. Malnutrition and parasitic helminth infections. Parasitology, 2000;
121(S1): 23-38.
7. Chway, H.M., Montresor, A., Tielsch, J.M.,
Jape, J.K., Albonico, M., Savioli, L. and Stoltzfus, R.J. Low dose daily iron
supplementation improves iron status and appetite but not anemia, whereas
quarterly anthelminthic treatment improves growth, appetite and anemia in
Zanzibari preschool children. The Journal of nutrition, 2004; 134(2):
348-356.
8. Drake, L.J., Jukes, M.C.H., Sternberg, R.J. and
Bundy, D.A.P., October. Geohelminth infections (ascariasis, trichuriasis, and
hookworm): cognitive and developmental impacts. In Seminars in
Pediatric Infectious Diseases, 2000; 11(4): 245-251.
9. Guyatt, H. Do intestinal nematodes affect
productivity in adulthood?. Parasitology Today, 2000; 16(4):
153-158.
10. Hotez, P.J., Brindley, P.J., Bethony, J.M.,
King, C.H., Pearce, E.J. and Jacobson, J., 2008. Helminth infections: the great
neglected tropical diseases. The Journal of clinical investigation, 118(4):
1311-1321.
11. King, C.H. Lifting the burden of
schistosomiasis—defining elements of infection-associated disease and the
benefits of antiparasite treatment. The Journal of infectious diseases, 2007;
196(5): 653-655.
12. Budke, C.M., Jiamin, Q.I.U., Qian, W. and
Torgerson, P.R. Economic effects of echinococcosis in a disease-endemic region
of the Tibetan Plateau. American Journal of Tropical Medicine and
Hygiene, 2005; 73(1): 2-10.
13. Hotez, P.J., Molyneux, D.H., Fenwick, A.,
Kumaresan, J., Sachs, S.E., Sachs, J.D. and Savioli, L. Control of neglected
tropical diseases. New England journal of medicine, 2007; 357(10):
1018-1027.
14. Hotez, P.J., Brindley, P.J., Bethony, J.M.,
King, C.H., Pearce, E.J. and Jacobson, J. Helminth infections: the great
neglected tropical diseases. The Journal of clinical investigation, 2008;
118(4): 1311-1321.
15. Breedlove, B. and Bradbury, R. Tapeworm
Enigma. Emerging Infectious Diseases, 2022; 28(6):
1306.
16. Jourdan, P.M., Lamberton, P.H., Fenwick, A. and
Addiss, D.G. Soil-transmitted helminth infections. The lancet, 2018;
391(10117): 252-265.
17. Novianty, S., Dimyati, Y., Pasaribu, S. and
Pasaribu, A.P. Risk factors for soil-transmitted helminthiasis in preschool
children living in farmland, North Sumatera, Indonesia. Journal of
tropical medicine, 2018.
18. Mascarini-Serra, L. Prevention of
soil-transmitted helminth infection. Journal of global infectious
diseases, 2011; 3(2): 175-182.
19. Sharma, S., Hashmi, M.F. and Alhajjaj, M.S.
Stat Pearls Publishing. Treasure Island (FL): 2021 Aug, 4.
20. Jourdan, P.M., Lamberton, P.H., Fenwick, A. and
Addiss, D.G. Soil-transmitted helminth infections. The lancet,
2018; 391(10117): 252-265.
21. Das, A.K. Hepatic and biliary ascariasis. Journal
of Global Infectious Diseases, 2014; 6(2), pp.65-72.
22. Ambardar, N. and Aeri, V. A better
understanding of traditional uses of Careya
arborea Roxb.: Phytochemical and pharmacological review. CELLMED, 2013;
3(4): 281.
23. Das, M.C. Triterpenoid sapogenols from the leaves
of Careya arborea: structure of
careyagenolide. Phytochemistry, 1982; 21(8): 2069-2073.
24. Basak, A., Banerjee, S.K., Bose, L. and Basu,
K. CHEMICAL EXAMINATION OF LEAVES OF CAREYA-ARBOREA. JOURNAL OF THE
INDIAN CHEMICAL SOCIETY, 1976; 53(6): 639-640.
25. Mahato, S.B. and Dutta, N.L. Sterols from Careya arborea. Phytochemistry, 1972;
11(6),: 2116-2117.
26. Talapatra, B., Basak, A. and Talapatra, S.K.
TERPENOIDS AND RELATED-COMPOUNDS. 20. CAREABORIN, A NEW TRITERPENE ESTER FROM
THE LEAVES OF CAREYA-ARBOREA. Journal
of the Indian Chemical Society, 1981; 58(8),: 814-815.
27. Gupta, R.K. Tannin bearing plants of India from
denuded wastelands. J Econ Tax Bot, 1981; 2: 139-155.
28. Haloi, K., Kalita, E. and Kalit, J.C. Effects
of methanolic root extract of Careya
arborea Roxbon ovarian histology of albino mice. Nebio, 2010;
1(1).
29. Manbir Kaur, Rakesh Yadav. Pharmacognostic,
ethno-pharmacological, phytochemical and pharmacological profile of wild guava
I.E. Careyaarborearoxb. Int J Curr Pharm Res 2017;9 (3):1-7.
30. Kumar, R.S., Sundram, R.S., Sivakumar, P.,
Nethaji, R., Senthil, V., Murthy, N.V. and Kanagasabi, R. CNS activity of the
methanol extracts of Careya arborea
in experimental animal model. Bangladesh Journal of Pharmacology, 2008;
3(1): 36-43.
31. Senthilkumar, N., Badami, S., Cherian, M.M. and
Hariharapura, R.C. Potent in vitro cytotoxic and antioxidant activity of Careya
arborea bark extracts. Phytotherapy Research: An International Journal
Devoted to Pharmacological and Toxicological Evaluation of Natural Product
Derivatives, 2007; 21(5): 492-495.
32. Ramesh, H.A. and Shenoy, D.B. Effect of Careya
arborea extracts on wound healing activity in rats. International
Journal of Analytical, Pharmaceutical and Biomedical Sciences, 2013; 2
(1): 36-42.
33. Rayhana, B., Sheliya, M.A., Pillai, K.K., Aeri,
V. and Sharma, M. Evaluation of anti-inflammatory effect of Careya arborea in CFA induced chronic
inflammation. Int. J. Pharm. Sci. Rev. Res, 2014; 26(2):
292-298.
34. Chothani, D.L. and Patel, N.M. Anti-allergic
potential of methanolic extract of leaves and fruits of Careya arborea. Journal of Pharma Sci Tech, 2014; 4(1):
29-31.
35. Shinde, G.S., Karadi, R.V., Khedkar, A.S.,
Dere, P.J., Mandavkar, Y.D. and Khalure, P.R. Screening of Careya arborea Roxb
for their anticonvulsant properties in experimental animals. International
Journal of Green Pharmacy (IJGP), 2013; 7(1).
36. Kumar, K., Mruthunjaya, K., Kumar, S. and
Mythreyi, R. Anti-ulcer activity of ethanol extract of the stem bark of Careya
arborea Roxb. International Current Pharmaceutical Journal, 2013;
2(3): 78-82.
37. Karunakar, N., Pillai, K.K., Husain, S.Z. and
Rao, M. Investigations of anti-inflammatory activity of Jigrine. Indian
journal of physiology and pharmacology, 1997; 41: 134-138.
38. Sambath Kumar, R. Hepatoprotective and in vivo
antioxidant effects of Careya arborea
against carbon tetrachloride induced liver damage in rats. Int J Mol
Med Adv Sci., 2005; 1: 418-424.