Home Aqueous extract of dry powder blend of seeds and leaves of Picralima nitida (Stapf) T. & H. Durand reduce pain and inflammation in animal models
Article
Licensed
Unlicensed Requires Authentication

Aqueous extract of dry powder blend of seeds and leaves of Picralima nitida (Stapf) T. & H. Durand reduce pain and inflammation in animal models

  • Abayomi M. Ajayi EMAIL logo , Akinyinka O. Alabi , Adaeze Adebesin , Benneth Ben-Azu and Solomon Umukoro
Published/Copyright: June 29, 2020

Abstract

Objectives

Blend of seeds and leaves of Picralima nitida herein referred to as West African Durand powder (WDP) was investigated for antinociceptive and anti-inflammatory properties.

Methods

Acute toxic effect of the aqueous extract was evaluated in mice of both sexes. Antinociceptive effect of WDP (100–400 mg/kg) was evaluated in models of acetic acid-induced writhing and thermal nociception on hot plate in mice. Carrageenan-induced paw oedema and air pouch rat models were used to evaluate the anti-inflammatory activity of the extract.

Results

WDP (2,000 mg/kg) showed no toxic effect in mice. WDP at 100, 200 and 400 mg/kg inhibited abdominal writhings by 59.9, 66.0 and 79.0%, respectively. There was a significant increase in reaction time on the hot plate tests in mice treated with WDP (400 mg/kg). The paw oedema was reduced by WDP (100, 200 and 400 mg/kg) 5 h post-carrageeenan. Exudate volume was significantly reduced to 39.8 and 44.8% by 200 and 400 mg/kg WDP, respectively. WDP reduced Leucocytes counts (23.3 and 57.1%, respectively) and neutrophil counts (28.1 and 60.0%, as well as reduced nitrites, malondialdehyde levels and increased glutathione concentrations in the air pouch.

Conclusions

These results suggest that aqueous extract of blend of seeds and leaves of P. nitida possesses antinociceptive and anti-inflammatory properties.


Corresponding author: Abayomi M. Ajayi, PhD, Department of Pharmacology & Therapeutics, Faculty of Basic Medical Sciences, College of Medicine, University of Ibadan, Ibadan, Oyo, Nigeria, Mobile: +2348103861380, E-mail:

Acknowledgments

Authors acknowledge technical assistance provided by Mr Olatunde Matthews of the Department of Pharmacology and Therapeutics, University of Ibadan.

  1. Research funding: None declared.

  2. Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission. AMA and AOA designed the experiments, AMA, AOA, AA, BB and SU performed the experiments, analyzed data and read the manuscript.

  3. Competing interests: Authors state no conflict of interest.

  4. Informed consent: Informed consent was obtained from all individuals included in this study.

  5. Ethical approval: All experiments were carried out with strict compliance to The “Principle of Laboratory Animal Care” (NIH Publication No. 85-23) and ethical guidelines for investigation of experimental pain in conscious animals. Having conducted similarly related investigations in rodents, the local institutional review board deemed the study exempt from review.

References

1. Edeoga, HO, Okwu, DE, Mbaebie, BO. Phytochemical constituents of some Nigerian medicinal plants. Afr J Biotech 2005;4:685–8. https://doi.org/10.5897/ajb2005.000-3127.Search in Google Scholar

2. Cowan, MM. Plant products as antimicrobial agents. Clin Microb Rev 1999;12:564–82. https://doi.org/10.1128/cmr.12.4.564.Search in Google Scholar

3. Sofowora, A, Ogunbodede, E, Onayade, A. The role and place of medicinal plants in the strategies for disease prevention. AJTCAM;2013;10:210–29. https://doi.org/10.4314/ajtcam.v10i5.2.Search in Google Scholar

4. Aslam, MS, Ahmad, MS, Mamat, AS, Ahmad, MZ, Salam, F. An update review on polyherbal formulation: a global perspective. Sys Rev Pharm 2016;7:35–41. https://doi.org/10.5530/srp.2016.7.5.Search in Google Scholar

5. Kale, OE, Akinpelu, OB, Bakare, AA, Yusuf, FO, Gomba, R, Araka, DC, et al. Five traditional Nigerian Polyherbal remedies protect against high fructose fed, streptozotocin-induced type 2 diabetes in male Wistar rats. BMC Comp and Alter Med 2018;18:160. https://doi.org/10.1186/s12906-018-2225-6.Search in Google Scholar

6. Nafiu, MO, Hamid, AA, Muritala, HF, Adeyemi, SB. Preparation, standardization, and quality control of medicinal plants in Africa. In: Kuete, V, editor. Medicinal spices and vegetables from Africa. Therapeutic potential against metabolic, inflammatory, infectious and systemic diseases. Cambridge, Massachusetts: Academic Press; 2017;pp. 171–204.10.1016/B978-0-12-809286-6.00007-8Search in Google Scholar

7. Oreagba, IA, Oshikoya, KA, Amachree, M. Herbal medicine use among urban residents in Lagos, Nigeria. BMC Comp and Alter Med 2011;11:117. https://doi.org/10.1186/1472-6882-11-117.Search in Google Scholar

8. Che, CT, Wang, ZJ, Chow, MS, Lam, CW. Herb-herb combination for therapeutic enhancement and advancement: theory, practice and future perspectives. Molecules 2013;18:5125–41. https://doi.org/10.3390/molecules18055125.Search in Google Scholar

9. Ajanohoun, JE, Aboubakar, N, Diamante, K, Ebot, ME, Ekpere, JA, Enow-Orock, EG, et al. Contribution to ethnobotanical and floristic studies in Cameroun. Traditional medicine and Pharmacopoeia. Technical and Research Commission of the Organisation of African Unity. Lagos, Nigeria: OAU/STRC; 1996;pp. 60–1.Search in Google Scholar

10. Irvine, FR. Woody plants of Ghana. London: Oxford University Press; 1961;pp. 629–30.Search in Google Scholar

11. Erharuyi, O, Falodun, A, Langer, P. Medicinal uses, phytochemistry and pharmacology of Picralima nitida (Apocynaceae) in tropical diseases: a review. Asian Pac J Trop Med 2014;7:1–8. https://doi.org/10.1016/s1995-7645(13)60182-0.Search in Google Scholar

12. Iwu, M. Hand book of African medicinal plants. U.S.A.: CRC Press Inc.; 1993; pp. 219–21.Search in Google Scholar

13. Dapaah, G, Koffuor, GA, Mante, PK, Ben, IO. The possible mode of antitussive and expectorant activity of the ethanol seed extracts of Picralima nitida ((Stapf) Th. & H. Durand). J Trad Comple Med 2017;7:133–40. https://doi.org/10.1016/j.jtcme.2016.05.003.Search in Google Scholar

14. Ezeamuzie, IC, Ojinnaka, MC, Uzogara, EO, Oji, SE. Anti-inflammatory, antipyretic and anti- malarial activities of a West African medicinal plant- Picralima nitida. Afr J Med Med Sci 1994;23:85–90.Search in Google Scholar

15. Duwiejua, M, Woode, E, Obiri, DD. Pseudo-akuammigine, an alkaloid from Picralima nitida seeds, has anti-inflammatory and analgesic actions in rats. J Ethnopharmacol 2002;81:73–9. https://doi.org/10.1016/s0378-8741(02)00058-2.Search in Google Scholar

16. Saxton, JE. Alkaloids of Picralima nitida. In: Manske, RHF, editor. The alkaloids: Chemistry and physiology. New York: Academic Press; 1960, vol 8, pp. 122–9.Search in Google Scholar

17. Corbett, AD, Menzies, JRW, Macdonald, A, Paterson, SJ, Duwiejua, M. The opioid activity of akuammine, akuammicine and akuammidine: alkaloids from Picralima nitida (family Apocynaceae). Br J Pharmacol 1996;119:334.Search in Google Scholar

18. Duwiejua, M, Obiri, DD, Zeitlin, IJ, Waterman, PG. Antiinflammatory activity in extracts from Picralima nitida (Fam. Apocynaceae). Br. J. Pharmacol 1995;116:360.Search in Google Scholar

19. Ansa-Asamoah, R, Ampofo, AA. Analgesic effect of crude extracts of P. nitida seeds. Afri J Pharmacol 1986;1:35–8.Search in Google Scholar

20. Igboasoiyi, AC, Essien, EE, Eseyin, OA, Ubam, G. Screening of the seed of Picralima nitida for hypoglycaemic activity. Pak J Biol Sci 2007;10:828–30. https://doi.org/10.3923/pjbs.2007.828.830.Search in Google Scholar

21. Olajide, OA, Velagapudi, R, Okorji, UP, Sarker, SD, Fiebich, BL. Picralima nitida seeds suppress PGE2 production by interfering with multiple signalling pathways in IL-1β-stimulated SK-N-SH neuronal cells. J Ethnopharmacol 2014;152:377–83. https://doi.org/10.1016/j.jep.2014.01.027.Search in Google Scholar

22. Fakeye, TO, Itiola, OA, George, AO, Odelola, HA. Antimicrobial property of Picralima nitida stem bark extract in cream formulations. Pharm Biol 2004;42:274–9. https://doi.org/10.1080/13880200490511765.Search in Google Scholar

23. Falodun, AT, Ajayi, CO, Obuotor, EM, Adepiti, AO, Akanmu, MA, Elujoba, AA. Antiplasmodial properties, toxicity and novelty-induced behaviour of a formulation from Picralima nitida and Alstonia boonei. Euro J Med Plants 2015;8:112–20. https://doi.org/10.9734/ejmp/2015/17211.Search in Google Scholar

24. Awodele, O, Oreagba, IA, Odoma, S, Silva, JA, Osunkalu, VO. Toxicological evaluation of the aqueous leaf extract of Moringa oleifera Lam. (Moringaceae). J. Ethnopharmacol 2012;139:330–6. https://doi.org/10.1016/j.jep.2011.10.008.Search in Google Scholar

25. Evans, WC (ed.). Trease and evans pharmacognosy. 15th ed. Edinburgh: Habid, W.B Saunders; 2002.Search in Google Scholar

26. Harborne, JB. Phytochemical methods. A guide to modern techniques of plant analysis; 1998, vol 279. Springer Science & Business Media, Berlin/Heidelberg, Germany.Search in Google Scholar

27. Sofowara, A. Medicine plants and traditional medicine in Africa. Ibadan, Nigeria: Spectrum Books Ltd.; 1993.Search in Google Scholar

28. Thaipong, K, Boonprakob, U, Crosby, K, Zevallos, C, Bryne, DH. Comparison of ABTS, DPPH, FRAP, and ORAC assays for estimating antioxidant activity from guava fruit extracts. J Food Comp Analy 2006;19:669–75. https://doi.org/10.1016/j.jfca.2006.01.003.Search in Google Scholar

29. Sultana, B, Farooq, A, Muhammad, A. Effect of extraction solvent/technique on the antioxidant activity of selected medicinal plant extracts. Molecules 2009;14:2167–80. https://doi.org/10.3390/molecules14062167.Search in Google Scholar

30. National Institute of HealthGuide for the care and use of laboratory animals. National Academic Press, Washington DC; 1996.Search in Google Scholar

31. Zimmermann, M. Ethical guidelines for investigations of experimental pain in animals. Pain 1983;16:109–10. https://doi.org/10.1016/0304-3959(83)90201-4.Search in Google Scholar

32. OECD. OECD/OCDE guidelines for acute toxicity of chemicals. Paris, France: Organization for Economic Co-operation and Development: No 423; 2001.Search in Google Scholar

33. Koster, R, Anderson, M, DeBeer, EJ. Acetic acid for analgesic screening. Fed. Proc. 1959;18:412.Search in Google Scholar

34. Archer, J. Tests for emotionality in rats and mice: a review. Anim Behav. 1973;21:205–35. https://doi.org/10.1016/s0003-3472(73)80065-x.Search in Google Scholar

35. Winter, CA, Risley, EA, Nuss, CW. Carrageenan – induced oedema in the hind paw of the rat as an assay for anti – inflammatory drugs. Proc Soc Exp Biol Med 1962;111:544–7. https://doi.org/10.3181/00379727-111-27849.Search in Google Scholar

36. Martin, SW, Stevens, AJ, Brennan, BS, Davies, D, Rowland, M, Houston, JB. The six-day-old rat air pouch model of inflammation: characterization of the inflammatory response to carrageenan. J Pharmacol Tox Methods 1994;32:139–47. https://doi.org/10.1016/1056-8719(94)90067-1.Search in Google Scholar

37. Gornall, AG, Bradwill, CJ, David, MM. Determination of serum proteins by means of the biuret reaction. J Biol Chem 1949;77:167–82. https://doi.org/10.1159/000219790.Search in Google Scholar

38. Nagababu, E, Rifkind, JM, Sesikeran, B, Lakshmaiah, N. Assessment of antioxidant activities of Eugenol by in vitro and in vivo methods. Methods Mol Biol 2010;610:165–80. https://doi.org/10.1007/978-1-60327-029-8_10.Search in Google Scholar

39. Sin, YM, Pook, SH, Tan, TM, Petterssoon, A, Kara, AU, Teh, WF. Changes in Gluthathione and its associated enzymes during Carrageenan-induced acute inflammation in mice. Comp Biochem Physiol 1997;116C:191–5. https://doi.org/10.1016/s0742-8413(96)00201-0.Search in Google Scholar

40. Asare, GA, Addo, P, Bugyei, K, Gyan, B, Adjei, S, Otu-Nyarko, LS, et al. Acute toxicity studies of aqueous leaf extract of Phyllanthus niruri. Interdisciplinary Toxicol 2011;4:206–10. https://doi.org/10.2478/v10102-011-0031-9.Search in Google Scholar

41. Menzies, JRW, Paterson, SJ, Duwiejua, M, Corbett, AD. Opioid activity of alkaloids extracted from Picralima nitida (family Apocynaceae). Eur J Pharmacol 1998;350:101–8. https://doi.org/10.1016/s0014-2999(98)00232-5.Search in Google Scholar

42. Duarte, IDG, Nakamura, M, Ferreira, SH. Participation of the sympathetic system in acetic acid-induced writhing in mice. Braz J Med Biol Res 1998;21:341–3.Search in Google Scholar

43. Rossato, MF, Oliveira, SM, Trevisan, G, Rotta, M, Ferreeira, J. Structural improvement of compounds with analgesic activity: AC-MPF4, a compound with mixed anti-inflammatory and antinociceptive activity via opioid receptor. Pharmacol Biochem Behav 2015;129:72–8. https://doi.org/10.1016/j.pbb.2014.12.001.Search in Google Scholar

44. De Souza, MM, Pereira, MA, Ardenghi, JV, Mora, TC, Bresciani, LF, Yunes, RA, et al. Filicene obtained from Adiantum cuneatum interacts with the cholinergic, dopaminergic, glutamatergic, GABAergic, and tachykinergic systems to exert antinociceptive effect in mice. Pharmacol Biochem Beh 2009;93:40–6. https://doi.org/10.1016/j.pbb.2009.04.004.Search in Google Scholar

45. Liu, Y, Yin, D, Chen, L, Qu, W, Chen, C, Laudon, M, et al. Piromelatine exerts antinociceptive effect via melatonin, opioid, and 5HT1A receptors and hypnotic effect via melatonin receptors in a mouse model of neuropathic pain. Psychopharmacology 2014;230:3973–85. https://doi.org/10.1007/s00213-014-3530-5.Search in Google Scholar

46. Shubayev, VI, Kato, K, Myers, RR. Cytokines in pain. In: Kruger, L, Light, AR, editors. Translational pain research: from mouse to man. Boca Raton, FL: CRC Press/Taylor & Francis; 2010.10.1201/9781439812105-c8Search in Google Scholar

47. Posadas, I, Bucci, M, Roviezzo, F, Rossi, A, Parente, L, Sautebin, L, et al. Carrageenan-induced mouse paw oedema is biphasic, age-weight dependent and displays differential nitric oxide cyclooxygenase-2 expression. Br J Pharmacol 2004;142:331–8. https://doi.org/10.1038/sj.bjp.0705650.Search in Google Scholar

48. Lo, TN, Almeida, AP, Beavan, MA. Dextran and carrageenan evoke different inflammatory response in rat with respect to composition of infiltrates and effect of indomethacin. J Pharmacol Exp Ther 1982;221:261–7.Search in Google Scholar

49. Salvemini, D, Wang, ZQ, Wyatt, PS, Bourdon, DM, Marino, MH, Manning, PT, et al. Nitric oxide: a key mediator in the early and late phase in carrageenan-induced rat paw inflammation. Br J Pharmacol 1996;118:829–38. https://doi.org/10.1111/j.1476-5381.1996.tb15475.x.Search in Google Scholar

50. Omote, K, Hazama, K, Kawamata, T, Nakayaka, Y, Toriyabe, M, Namiki, A. Peripheral nitric oxide in carrageenan-induce inflammation. Brain Res 2001;912:171–5. https://doi.org/10.1016/s0006-8993(01)02733-0.Search in Google Scholar

51. Abramson, SB. Nitric oxide in inflammation and pain associated with osteoarthritis. Arthritis Res Ther. 2008;10:1–7. https://doi.org/10.1186/ar2463.Search in Google Scholar

52. Demir, E, Kaya, B, Soriano, C, Creus, A, Marcos, R. Genotoxic analysis of four lipid-peroxidation products in the mouse lymphoma assay. Mutat Res 2011;726:98–103. https://doi.org/10.1016/j.mrgentox.2011.07.001.Search in Google Scholar

Received: 2019-09-09
Accepted: 2020-04-09
Published Online: 2020-06-29

© 2020 Walter de Gruyter GmbH, Berlin/Boston

Articles in the same Issue

  1. Frontmatter
  2. Review
  3. Update of hypothyroidism and its management in Unani medicine
  4. Original Articles
  5. 6-OHDA mediated neurotoxicity in SH-SY5Y cellular model of Parkinson disease suppressed by pretreatment with hesperidin through activating L-type calcium channels
  6. Modulation of sleep using electrical vestibular nerve stimulation prior to sleep onset: a pilot study
  7. Nitric oxide mediates the antidepressant-like effect of modafinil in mouse forced swimming and tail suspension tests
  8. Effect of mobile phone usage on cognitive functions, sleep pattern, visuospatial ability in Parkinsons patients; a possible correlation with onset of clinical symptoms
  9. Food-added azodicarbonamide alters haematogical parameters, antioxidant status and biochemical/histomorphological indices of liver and kidney injury in rats
  10. Conditioned medium from the human umbilical cord-mesenchymal stem cells stimulate the proliferation of human keratinocytes
  11. p53 upregulated mediator of apoptosis (Puma) deficiency increases survival of adult neural stem cells generated physiologically in the hippocampus, but does not protect stem cells generated in surplus after an excitotoxic lesion
  12. In vitro antioxidants and hepatoprotective effects of Pleurotus tuber-regium on carbon tetrachloride–treated rats
  13. Mitigative effect of Momordica cymbalaria fruit extract against sodium fluoride induced hepatotoxicity in Wistar male albino rats
  14. Amine-modified kaolinite clay preserved thyroid function and renal oxidative balance after sub-acute exposure in rats
  15. Aqueous extract of dry powder blend of seeds and leaves of Picralima nitida (Stapf) T. & H. Durand reduce pain and inflammation in animal models
  16. Methanol extract of Caesalpinia benthamiana normalizes blood pressure and attenuates oxidative stress in uninephrectomized hypertensive rats
  17. Evaluation of antidiabetic effect of Cistus salviifolius L. (Cistaceae) in streptozotocin-nicotinamide induced diabetic mice
  18. Correlation between biofilm formation and antimicrobial susceptibility pattern toward extended spectrum β-lactamase (ESBL)- and non-ESBL-producing uropathogenic bacteria
Downloaded on 22.9.2025 from https://www.degruyterbrill.com/document/doi/10.1515/jbcpp-2019-0212/html
Scroll to top button