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Analgesic activity of aqueous and methanol fruit pulp extracts of Hyphaene thebaica (Arecaceae) (Linn) mart in mice

  • Francis Désiré Bomba Tatsinkou ORCID logo EMAIL logo , Georlin E. Fotabong , Bibiane A. Wandji , Marius Mbiantcha , Erastus N. Nembo , Armel Jackson Seukep , Elisabeth M. Zeuko’o , Telesphore B. Nguelefack and Emmanuel A. Asongalem
Published/Copyright: February 11, 2025

Abstract

Objectives

Pain affects about one in every five persons and is considered a major global health burden. Hyphaene thebaica (Arecaceae), is a medicinal plant used in Cameroon, fruit pulp are macerated and orally administered in traditional medicine to treat various ailments, including hypertension, pain, and inflammation. This study aimed to evaluate the pain-killing effect of fruit pulp extracts of H. thebaica in mice.

Methods

Aqueous (AEHT) and methanol (MEHT) extracts were prepared from fruit pulp of H. thebaica, followed by a qualitative phytochemical analysis. The extracts were given orally at doses of 100, 200, and 400 mg/kg in acute pain models such as acetic acid, formalin, hotplate, and capsaicin. Control groups included distilled water (negative), and diclofenac, morphine, ruthenium red, diazepam (positive). Naloxone pretreatment was used to assess opioid pathway involvement. Locomotor and sedative effects were evaluated using rota-rod and open-field tests. Acute toxicity was assessed at 2,000 mg/kg.

Results

Phytochemical tests revealed saponins, flavonoids, tannins, and phenols. Both extracts greatly decreased the writhing induced by acetic acid. MEHT inhibited both phases of formalin-induced pain (p<0.01). Both extracts significantly inhibited hotplate-induced nociception (p<0.001), partially reversed by naloxone, except for MEHT. In the capsaicin test, extracts produced a remarkable reduction of paw licking time (p<0.01). No motor coordination alteration or acute toxicity effects were observed.

Conclusions

The findings demonstrated the analgesic activity of AEHT and MEHT, mediated by the stimulation of opioids and blockage of vanilloid receptors pathways.


Corresponding author: Francis Désiré Bomba Tatsinkou, Department of Biomedical Sciences, Faculty of Health Sciences, 107749 University of Buea , P.O. Box 63, Buea, Cameroon; and Laboratory of Animal Physiology and Phytopharmacology, Faculty of Science, University of Dschang, P.O. Box 67, Dschang, Cameroon, E-mail:

Acknowledgments

We are grateful to the traditional herbalist Ms. Marie Fidelie Mbezele who provided plant materials and the University of Buea for providing all the facilities.

  1. Research ethics: The protocol for the experiments with animals underwent review and approval by the Institutional Animal Ethics Committee of the University of Buea (UB-IACUC N°18/2023).

  2. Informed consent: Not applicable.

  3. Author contributions: Francis Desire Bomba Tatsinkou, Emeleke Fotabong Georlin, and Emmanuel Acha Asongalem designed, collected data, and wrote the manuscript; Francis Desire Bomba Tatsinkou, and Emmanuel Acha Asongalem supervised the work and analyzed the data; Bibiane Aimee Wandji, Marius Mbiantcha, Erastus Nembu Nembo, Armel Jackson Seukep, Elisabeth Menkem Zeuko’o, and Telesphore Benoit Nguelefack reviewed the paper draft. All authors read and approved the final version of the manuscript.

  4. Use of Large Language Models, AI and Machine Learning Tools: None declared.

  5. Conflict of interest: The authors state no conflict of interest.

  6. Research funding: None declared.

  7. Data availability: All data supporting the findings of this study are available within the paper. Should any raw data files be needed in another format they are available from the corresponding author upon reasonable request.

References

1. Zimmer, Z, Fraser, K, Grol-Prokopczyk, H, Zajacova, A. A global study of pain prevalence across 52 countries: examining the role of country-level contextual factors. Pain 2022;163:1740–50. https://doi.org/10.1097/j.pain.0000000000002557.Search in Google Scholar PubMed PubMed Central

2. Raja, SN, Carr, DB, Cohen, M, Finnerup, NB, Flor, H, Gibson, S, et al.. The revised International Association for the study of pain definition of pain: concepts, challenges, and compromises. Pain 2020;161:1976–82. https://doi.org/10.1097/j.pain.0000000000001939.Search in Google Scholar PubMed PubMed Central

3. Soomro, S. Oxidative stress and inflammation. Open J Immunol 2019;9:1. https://doi.org/10.4236/oji.2019.91001.Search in Google Scholar

4. Henschke, N, Kamper, SJ, Maher, CG. The epidemiology and economic consequences of pain. Mayo Clin Proc 2015;90:139–47. https://doi.org/10.1016/j.mayocp.2014.09.010.Search in Google Scholar PubMed

5. Arendt-Nielsen, L, Belton, J, Cardosa, M. Beyond the study of pain: the evolving role of the International Association for the Study of Pain in global advocacy. Pain 2023;164:S22–s6. https://doi.org/10.1097/j.pain.0000000000003064.Search in Google Scholar PubMed

6. Park, HJ, Moon, DE. Pharmacologic management of chronic pain. Korean J Pain 2010;23:99–108. https://doi.org/10.3344/kjp.2010.23.2.99.Search in Google Scholar PubMed PubMed Central

7. Hewitt, DJ, Hargreaves, RJ, Curtis, SP, Michelson, D. Challenges in analgesic drug development. Clin Pharmacol Terapeutics 2009;86:447–50. https://doi.org/10.1038/clpt.2009.161.Search in Google Scholar PubMed

8. Sook-Ha, F, Noraisah, AA, Dayang, FB. Evaluation of analgesic activity of the methanol extract from the galls of Quercus infectoria (olivier) in rats. Evid base Compl Alternative Med 2014:6. https://doi.org/10.1155/2014/976764.Search in Google Scholar PubMed PubMed Central

9. Kebbou, A, Laaradia, M, Oufquir, S, Aarab, A, Gabbas, Z, Rais, H, et al.. Antioxidant activity, anti-inflammatory and analgesic effects of Caralluma europaea (Eddaghmouss) in mice. Online J Biol Sci 2019;19:272–85. https://doi.org/10.3844/ojbsci.2019.272.285.Search in Google Scholar

10. WHO. WHO traditional medicine strategy: 2014–2023. Geneva, Switzerland: World Health Organization; 2013.Search in Google Scholar

11. Adebayo, SA, Dzoyem, JP, Shai, LJ, Eloff, JN. The anti-inflammatory and antioxidant activity of 25 plant species used traditionally to treat pain in southern African. BMC Compl Alternative Med 2015;15:159. https://doi.org/10.1186/s12906-015-0669-5.Search in Google Scholar PubMed PubMed Central

12. Bomba, FD, Wandji, BA, Piegang, BN, Awouafack, MD, Sriram, D, Yogeeswari, P, et al.. Antinociceptive properties of the aqueous and methanol extracts of the stem bark of Petersianthus macrocarpus (P. Beauv.) Liben (Lecythidaceae) in mice. J Ethnopharmacol 2015;174:66–73. https://doi.org/10.1016/j.jep.2015.08.004.Search in Google Scholar PubMed

13. Mokale Kognou, AL, Kopa Kowa, T, Pateriya, P, Narayan Pal, P, Mouokeu, RS, Tchinda Tiabou, A, et al.. Pharmacological evidence of Vitex thyrsiflora, Entandrophragma cylindricum, and Anonidium mannii used for the management of inflammation in Cameroon. J Basic Clin Physiol Pharmacol 2020;31:20190053. https://doi.org/10.1515/jbcpp-2019-0053.Search in Google Scholar PubMed

14. Jiofack, T, Fokunang, C, Guedje, N, Kemeuze, V, Fongnzossie, E, Nkongmeneck, BA, et al.. Ethnobotanical uses of medicinal plants of two ethnoecological regions of Cameroon. Int J Med Med Sci 2010;2:60–79.Search in Google Scholar

15. Betti, JL, Yemefa’a, MSR, Tarla, NF. Contribution to the knowledge of non wood forest products of the far north region of Cameroon: medicinal plants sold in the Kousséri market. J Ecol Nat Environ 2011;3:241–54.Search in Google Scholar

16. Hassan, M, Ali, S, Abu-Almaaty, A, Abbas, O. Seed on some haematological, biochemical and histological features of albino rats. J Cytol Histol 2018;9:2.10.4172/2157-7099.1000494Search in Google Scholar

17. Mohamed, AA, Khalil, AA, El-Beltagi, HE. Antioxidant and antimicrobial properties of kaff maryam (Anastatica hierochuntica) and doum palm (Hyphaene thebaica). Grasas Aceites 2010;61:67–75. https://doi.org/10.3989/gya.064509.Search in Google Scholar

18. Abd el Halim, NAF. Effect of doum fruit (Hyphaene thebaica) extract on some biochemical parameters, enzyme activities and histopathological changes of pancreas in alloxan induced diabetic rats. Food Nutr Sci 2020;11:207–19. https://doi.org/10.4236/fns.2020.113016.Search in Google Scholar

19. Shehu, B, Gidado, A, Buratai, L. Hypoglycaemic, hypolipidaemic and possible toxicity of the methanolic fruit pulp extract of hyphane thebaica (L) Mart in alloxan–induced diabetic rats. J Med Applied Bioscien 2014;6:1–10.Search in Google Scholar

20. Khallaf, ISA, Wahman, R, Farghaly, HSM, Bayoumi, SAL. The inhibitory effect of doum palm (Hyphaene thebaica l. mart.) leaves extract on α-glucosidase activity. Bull Pharmaceut Sci 2022;45:163–76. https://doi.org/10.21608/bfsa.2022.239375.Search in Google Scholar

21. Ndam, L, Mih, A, Fongod, A, Tening, A, Tonjock, R, Enang, J, et al.. Phytochemical screening of the bioactive compounds in twenty (20) Cameroonian medicinal plants. Int J Curr Microbiol App Sci. 2014;3:768–78.Search in Google Scholar

22. OECD. Guideline for the testing of chemicals. acute oral toxicity e acute toxic 904 class method: test no-423. Paris, France: Organization for Economic Cooperation and Development; 2001, 905:906 p.Search in Google Scholar

23. Asongalem, EA, Foyet, HS, Ekobo, S, Dimo, T, Kamtchouing, P. Antiinflammatory, lack of central analgesia and antipyretic properties of Acanthus montanus (Ness) T. Anderson. J Ethnopharmacol 2004;95:63–8. https://doi.org/10.1016/j.jep.2004.06.014.Search in Google Scholar PubMed

24. Gou, KJ, Zeng, R, Dong, Y, Hu, QQ, Hu, HW, Maffucci, KG, et al.. Anti-inflammatory and analgesic effects of Polygonum orientale L. Extracts. Front Pharmacol 2017;8:562. https://doi.org/10.3389/fphar.2017.00562.Search in Google Scholar PubMed PubMed Central

25. Rezaee-Asl, M, Sabour, M, Nikoui, V, Ostadhadi, S, Bakhtiarian, A. The study of analgesic effects of Leonurus cardiaca L. in Mice by formalin, tail flick and hot plate tests. Int Sch Res notices 2014;2014:687697.10.1155/2014/687697Search in Google Scholar PubMed PubMed Central

26. Sałat, K, Filipek, B. Antinociceptive activity of transient receptor potential channel TRPV1, TRPA1, and TRPM8 antagonists in neurogenic and neuropathic pain models in mice. J Zhejiang Univ – Sci B 2015;16:167–78. https://doi.org/10.1631/jzus.b1400189.Search in Google Scholar

27. Bridi, H, Ccana-Ccapatinta, GV, Stolz, ED, Meirelles, GC, Bordignon, SAL, Rates, SMK, et al.. Dimeric acylphloroglucinols from Hypericum austrobrasiliense exhibiting antinociceptive activity in mice. Phytochemistry 2016;122:178–83. https://doi.org/10.1016/j.phytochem.2015.12.012.Search in Google Scholar PubMed

28. Shajib, MS, Akter, S, Ahmed, T, Imam, MZ. Antinociceptive and neuropharmacological activities of methanol extract of Phoenix sylvestris fruit pulp. Front Pharmacol 2015;6:162449. https://doi.org/10.3389/fphar.2015.00212.Search in Google Scholar PubMed PubMed Central

29. Saxena, M, Saxena, J, Nema, R, Singh, D, Gupta, A. Phytochemistry of medicinal plants. J Pharmacogn Phytochem 2013;1:168–82.Search in Google Scholar

30. Takahashi, RN, de Lima, TC, Morato, GS. Pharmacological actions of tannic acid; II. Evaluation of CNS activity in animals. Planta Med 1986:272–5. https://doi.org/10.1055/s-2007-969150.Search in Google Scholar PubMed

31. Derouich, M, Bouhlali, EDT, Hmidani, A, Bammou, M, Bourkhis, B, Sellam, K, et al.. Assessment of total polyphenols, flavonoids and anti-inflammatory potential of three Apiaceae species grown in the Southeast of Morocco. Sci Afr 2020;9:e00507. https://doi.org/10.1016/j.sciaf.2020.e00507.Search in Google Scholar

32. Nayeem, N, Imran, M, Asdaq, SMB, Rabbani, SI, Alanazi, FA, Alamri, AS, et al.. Total phenolic, flavonoid contents and biological activities of stem extracts of Astragalus spinosus (Forssk.) Muschl. grown in Northern border province, Saudi Arabia. Saudi J Biol Sci 2022;29:1277–82. https://doi.org/10.1016/j.sjbs.2021.12.029.Search in Google Scholar PubMed PubMed Central

33. Ghule, R, Venkatnarayanan, R, Thakare, S, Jain, H, Ghule, P. Analgesic activity of Cuscuta campestris Yuncker a parasitic plant grown on Nerium indicum Mill. J Adv Pharm Educ Res 2011;1:45–51.Search in Google Scholar

34. Davies, P, Bailey, PJ, Goldenberg, MM, Ford-Hutchinson, AW. The role of arachidonic acid oxygenation products in pain and inflammation. Annu Rev Immunol 1984;2:335–57. https://doi.org/10.1146/annurev.iy.02.040184.002003.Search in Google Scholar PubMed

35. Collier, HO, Dinneen, LC, Johnson, CA, Schneider, C. The abdominal constriction response and its suppression by analgesic drugs in the mouse. Br J Pharmacol Chemother 1968;32:295–310. https://doi.org/10.1111/j.1476-5381.1968.tb00973.x.Search in Google Scholar PubMed PubMed Central

36. Katole, NT, Kale, JS, Salankar, HV. Evaluation of the antinociceptive action of simvastatin in mice. Cureus 2022;14:e26910. https://doi.org/10.7759/cureus.26910.Search in Google Scholar PubMed PubMed Central

37. Ayanaw, MA, Yesuf, JS, Birru, EM. Evaluation of analgesic and anti-inflammatory activities of methanolic leaf and root extracts of Gomphocarpus purpurascens A. Rich (asclepiadaceae) in mice. J Exp Pharmacol 2023;15:1–11. https://doi.org/10.2147/jep.s361194.Search in Google Scholar PubMed PubMed Central

38. Sudo, RT, Neto, ML, Monteiro, CE, Amaral, RV, Resende, ÂC, Souza, PJ, et al.. Antinociceptive effects of hydroalcoholic extract from Euterpe oleracea Mart. (Açaí) in a rodent model of acute and neuropathic pain. BMC Compl Alternative Med 2015;15:208. https://doi.org/10.1186/s12906-015-0724-2.Search in Google Scholar PubMed PubMed Central

39. Sengupta, R, Sheorey, SD, Hinge, MA. Analgesic and anti-inflammatory plants: an updated review. Int J Pharmaceut Sci Rev Res 2012;12:114–9.Search in Google Scholar

40. Aburas, K, Misbah, A, Fehelbum, H, Abukhdir, A. Analgesic effect by using hot Plat and tail flick test in rats models for aqueous Moringa oleifer extract. Libyan J Med Res 2023;17:107–19. https://doi.org/10.54361/ljmr.17-21.Search in Google Scholar

41. Caterina, MJ, Schumacher, MA, Tominaga, M, Rosen, TA, Levine, JD, Julius, D. The capsaicin receptor: a heat-activated ion channel in the pain pathway. Nature 1997;389:816–24. https://doi.org/10.1038/39807.Search in Google Scholar PubMed

42. Szolcsányi, J. Capsaicin and sensory neurones: a historical perspective. Prog Drug Res 2014;68:1–37. https://doi.org/10.1007/978-3-0348-0828-6_1.Search in Google Scholar PubMed

43. Meza, RC, Ancatén-González, C, Chiu, CQ, Chávez, AE. Transient receptor potential vanilloid 1 function at central synapses in health and disease. Front Cell Neurosci 2022;16:864828. https://doi.org/10.3389/fncel.2022.864828.Search in Google Scholar PubMed PubMed Central

44. Khalil, M, Alliger, K, Weidinger, C, Yerinde, C, Wirtz, S, Becker, C, et al.. Functional role of transient receptor potential channels in immune cells and epithelia. Front Immunol 2018;9:174. https://doi.org/10.3389/fimmu.2018.00174.Search in Google Scholar PubMed PubMed Central

45. Tripathi, K. Essentials of medical pharmacology, 5th ed. New Delhi, India: Jaypee Brothers Medical Publishers; 2004.Search in Google Scholar

Received: 2024-08-10
Accepted: 2024-12-31
Published Online: 2025-02-11

© 2025 Walter de Gruyter GmbH, Berlin/Boston

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