In vitro anthelmintic efficacy of aqueous extracts from Coriandrum sativum seeds and Swertia chirata plant against Haemonchus contortus in Barbari goats


163 / 41

Authors

  • RAMAKANT Department of Veterinary Medicine, College of Veterinary Science and Animal Husbandry, Acharya Narendra Deva University of Agriculture and Technology Kumarganj-224 229 Ayodhya, Uttar Pradesh, India image/svg+xml
  • Arbind Singh Department of Livestock Farm Complex, College of Veterinary and Animal Sciences, Sardar Vallabhbhai Patel University of Agriculture and Technology Meerut-250 110, India image/svg+xml
  • Prem Sagar Maurya Department of Veterinary Parasitology, College of Veterinary and Animal Sciences, Sardar Vallabhbhai Patel University of Agriculture and Technology Meerut-250 110, India image/svg+xml
  • TARUN KUMAR SARKAR Department of Veterinary Medicine, College of Veterinary and Animal Sciences, Sardar Vallabhbhai Patel University of Agriculture and Technology Meerut-250 110, India image/svg+xml
  • VIKAS JAISWAL Department of Veterinary Pathology, College of Veterinary and Animal Sciences, Sardar Vallabhbhai Patel University of Agriculture and Technology Meerut-250 110, India image/svg+xml
  • DEVESH KUMAR YADAV Department of Animal Genetics and Breeding, College of Veterinary and Animal Sciences, Sardar Vallabhbhai Patel University of Agriculture and Technology Meerut-250 110, India image/svg+xml
  • AMIT KUMAR VERMA Department of Veterinary Medicine, College of Veterinary and Animal Sciences, Sardar Vallabhbhai Patel University of Agriculture and Technology Meerut-250 110, India image/svg+xml

https://doi.org/10.56093/ijans.v96i7.175813

Keywords:

Anthelmintic activity, Barbari goat, Coriandrum sativum, Haemonchus contortus, In vitro assay, Swertia chirata

Abstract

The present study explored the laboratory-based anti-parasitic potential of water extracts of coriander (Coriandrum sativum) seeds and entire Swertia chirata plant against Haemonchus contortus parasite, collected directly from Barbari goats. The faecal samples were cultured to harvest infectious third-stage (L3) larvae. Subsequently, PCR testing on the ITS-2 ribosomal DNA region was utilized to verify the parasite as H. contortus. To evaluate the deworming potential of the plant extracts, both egg hatch assays (EHA) and larval paralysis assays (LPA) were performed at four different dosage levels: 12.5, 25, 50, and 100 mg/ml. Phosphate-buffered saline (PBS) was used as a negative baseline, while Closantel (0.5 mg/ml) served as the positive control. Findings revealed that the coriander seed extract showed dose dependent effectiveness, successfully preventing 27.49% to 86.94% of the eggs from hatching and paralyzing 35.07% to 89.93% of the larvae. However, aqueous extract of S. chirata proved to be considerably more effective. It restricted 43.64 and 93.12%, egg hatching and stopped larval movement by 47.40% to 94.10%. As expected, the closantel control achieved total elimination in both tests. Ultimately, these experiments demonstrated that both botanical extracts successfully cleared H. contortus in a lab setting, with S. chirata standing out as the highly superior candidate.

Downloads

Download data is not yet available.

References

1. Ahmed A H, Ejo M, Feyera T, Regassa D, Mummed B and Huluka S A. 2020. In vitro anthelmintic activity of crude extracts of Artemisia herba-alba and Punica granatum against Haemonchuscontortus. Journal of Parasitology Research 2020: 4950196. https://doi.org/10.1155/2020/4950196. DOI: https://doi.org/10.1155/2020/4950196

2. Aleem A and Kabir H. 2018. Review of Swertia chirata as traditional uses to its phytochemistry and pharmacological activity. Journal of Drug Delivery and Therapeutics 8(5-s): 73–78. DOI: https://doi.org/10.22270/jddt.v8i5-s.1957

3. Bott N J, Campbell E B, Beveridge I, Chilton N B, Ress D, Hunt PW and Gasser R B. 2009. A combined microscopic-molecular method for the diagnosis of Strongylide infections in sheep. International Journal for Parasitology 39: 1277–1287. DOI: https://doi.org/10.1016/j.ijpara.2009.03.002

4. BrahmaA, Das S, Kumar D, Bordoloi G, Pandit S, Bera S, Ghosh J D and Jas R. 2015. Prevalence of gastrointestinal parasites in black Bengal goats of Sunderban Delta in West Bengal. International Journal of Parasitology Research 7(1): 56–159.

5. Coles G C, Jackson F, Pomroy W E, Prichard R K, Von Samson-Himmelstjerna G, Silvestre A, Taylor M A and Vercruysse J. 2006. The detection of anthelmintic resistance in nematodes of veterinary importance. Veterinary Parasitology 136(3-4): 167–185. DOI: https://doi.org/10.1016/j.vetpar.2005.11.019

6. Dehuri M, Palai S, Mohanty B and Malangmei L. 2021. Anti- helminthic activity of plant extracts against gastrointestinal nematodes in small ruminants: A Review. Pharmacognosy Reviews 15(30): 117–127. DOI: https://doi.org/10.5530/phrev.2021.15.14

7. Demeler J, Gill J H, Von Samson-Himmelstjerna G and Sangster N C. 2013. The in vitro assay profile of macrocyclic lactone resistance in three species of sheep trichostrongyloids. International Journal for Parasitology: Drugs and Drug Resistance 3: 109–118. DOI: https://doi.org/10.1016/j.ijpddr.2013.04.002

8. Dhama K, Chakraborty S, Mahima, Wani M Y, Verma A K, Deb R, Tiwari R and Kapoor S. 2013. Novel and emerging therapies safeguarding health of humans and their companion animals: A review. Pakistan Journal of Biological Sciences 16(3): 101–111 DOI: https://doi.org/10.3923/pjbs.2013.101.111

9. Edwards E E, Bridget C G, Williamson L H, Storey B E and Sakamoto K. 2016. Pathology of Haemonchus contortus in New World camelids in the southeastern United States: A Retrospective Review 28: 105–109. DOI: https://doi.org/10.1177/1040638716628587

10. Eguale T, Tilahun G, Debella A, Feleke A and Makonnen E. 2007. In vitro and in vivo anthelmintic activity of crude extracts of Coriandrum sativum against Haemonchus contortus. Journal of Ethnopharmacology 110: 428–433. DOI: https://doi.org/10.1016/j.jep.2006.10.003

11. Hou B, Yong R, Wuen J, Zhang Y, Buyin B, Subu D, Zha H, Li H and Hasi S. 2022. Positivity rate investigation and anthelmintic resistance analysis of gastrointestinal nematodes in sheep and cattle in Ordos. China. Animals 12(7): 891. DOI: https://doi.org/10.3390/ani12070891

12. Jaiswal K, Mishra S and Pandey J. 2020. In Vitro assessment of the anthelmintic activity of the crude extracts of Coriandrum sativum (Linn.): Seeds. International Journal of Pharmacy and Pharmaceutical Research 19(3): 320-329.

13. Kaplan R M, Vidyashankar A N. 2012. An inconvenient truth: Global worming and anthelmintic resistance. Veterinary Parasitology 186: 70–78. DOI: https://doi.org/10.1016/j.vetpar.2011.11.048

14. Kotze A C and Prichard R K. 2016. Anthelmintic Resistance in Haemonchus contortus: History, Mechanisms and Diagnosis. Advances in Parasitology 93: 397–428. DOI: https://doi.org/10.1016/bs.apar.2016.02.012

15. Khanal S, Shakya N, Nepal N and Pant D. 2014. Swertia chirata: The Himalayan Herb. International Journal of Applied Science and Biotechnology 2(4): 389-392. DOI: https://doi.org/10.3126/ijasbt.v2i4.11281

16. Laribi B, Kouki K, M’Hamdi M and Bettaieb T. 2015. Coriander (Coriandrum sativum L.) and its bioactive constituents. Fitoterapia 103: 9–26. DOI: https://doi.org/10.1016/j.fitote.2015.03.012

17. Mahima, Rahal A, Deb R, Latheef S K, Samad H A, Tiwari R, Verma A K, Kumar A and Dhama K. 2012. Immunomodulatory and therauptic potential of herbal, traditional / indigenous and ethano-veterinary medicine. Pakistan Journal of Biological Sciences 15(16): 754–774. DOI: https://doi.org/10.3923/pjbs.2012.754.774

18. Niezen J H, Waghorn T S, Charleston W A G and Waghorn G C. 1995. Growth and gastrointestinal nematode parasitism in lambs grazing either lucerne (Medicago sativa) or sulla (Hedysarum coronarium) which contains condensed tannins. The Journal of Agricultural Science 125: 281–289. DOI: https://doi.org/10.1017/S0021859600084422

19. Ramakant, Sarkar T K, Verma A K, Maurya P S, Thakur V, Singh A, Rawat S, Chandra G, Maurya P K and Gautam S. 2024a. Prevalence of Gastrointestinal Parasitic infections in Goats in Western Uttar Pradesh, India. Acta Scientific Veterinary Sciences 6(6): 17–27. DOI: https://doi.org/10.31080/ASVS.2024.06.0881

20. Ramakant, Sarkar T K, Verma A K, Maurya P S, Thakur V, Singh A, Jaiswal V, Rawat S, Maurya P K and Gautam S. 2024b. In vitro anthelmintic activity of aqueous extracts of seven medicinal plants against Haemonchus contortus in goats. International Journal of Advanced Biochemistry Research SP-8(6): 51–58. DOI: https://doi.org/10.33545/26174693.2024.v8.i6Sa.1254

21. Ramakant, Sarkar T K, Verma K, Maurya P S, Jaiswal V, Singh A, Thakur V and Rawat S. 2025. PCR based identification of different strongyle species in goats of western Uttar Pradesh, India. Indian journal of Animal Science 95(1): 13–17. DOI: https://doi.org/10.56093/ijans.v95i1.157162

22. Ramakant, Sarkar T K, Maurya P S, Singh A, Jaiswal V, Pal A, Yadav D K and Verma A K. 2026. In vivo anthelmintic efficacy, hematobiochemical and antioxidant effects of Swertia chirata in Barbari goats naturally infected with Haemonchus contortus. Tropical Animal Health and Production 58(6): 392. DOI: https://doi.org/10.1007/s11250-026-05204-5

23. Santos F O, Lima H G, Santos N S S, Serra T M, Uzeda R S U, Reis I M A, Botura M B, Branco A and Batatinha M J M. 2017. In vitro anthelmintic and cytotoxicity activities the Digitaria Insularis (Poaceae). Veterinary Parasitology 245: 48–54. DOI: https://doi.org/10.1016/j.vetpar.2017.08.007

24. Shamim A, Sajid, M S, Khan M N, Imran M and Saqib M. 2018. Peptides isolation from crude somatic antigens of Haemonchus contortus through SDS-PAGE. Indian Journal of Animal Research 52: 914–916. DOI: https://doi.org/10.18805/ijar.v0iOF.8473

25. Sinha S K, Pati S and Shahi S. 2023. Medicinal value of Chiraita: A review. European Chemical Bulletin 12(1, S): 158–162.

26. Soulsby E J L. 1982. Helminths, Arthropods and Protozoa of Domesticated Animals. 7th edn., ELBS, Bailliere Tindall, London pp. 763–778.

27. Tan T K, Panchad C, Lee L V, Ngui R, Sharma S K R and Lim A L Y. 2014. Co-infection of Haemonchuscontortus and Trichostrongylus spp. among livestock in Malaysia as reveled by amplification and sequencing of internal transcribed spacer Π DNA region. MBC Veterinary Research 10: 38. DOI: https://doi.org/10.1186/1746-6148-10-38

28. Thienpont D, Rochette F and Vanparijs O F J. 1986. Diagnosing helminthiasis by coprological examination. 2ndedn., Janssen Research Foundation, Beerse, Belgium pp. 205.

29. Varady M and Corba J. 1999. Comparison of six in vitro tests in determining benzimidazole and levamisole resistance in Haemonchus contortus and Ostertagia circumcincta of sheep. Veterinary Parasitology 80: 239–249. DOI: https://doi.org/10.1016/S0304-4017(98)00211-8

30. Veerakumari L and Munuswamy N. 2000. In vitro effect of some anthelmintics on lactate dehydrogenase activity of Cotylophoron cotylophorum (Digenea, Paramphistomidae). Veterinary Parasitology 91(1–2): 129–140. DOI: https://doi.org/10.1016/S0304-4017(00)00258-2

Downloads

Published

2026-07-24

Issue

Section

Articles

How to Cite

RAMAKANT, Singh, A., Maurya, P. S., SARKAR, T. K. ., JAISWAL, V. ., YADAV, D. K. ., & VERMA, A. K. . (2026). In vitro anthelmintic efficacy of aqueous extracts from Coriandrum sativum seeds and Swertia chirata plant against Haemonchus contortus in Barbari goats. The Indian Journal of Animal Sciences, 96(7), 527–531. https://doi.org/10.56093/ijans.v96i7.175813
Citation