30DEC

Libyan International Conference for Health Sciences

The First Libyan International Conference for Health Sciences (2024): Open University, Tripoli, Libya
Mediterranean Journal of Pharmacy and Pharmaceutical Sciences
https://app.periodikos.com.br/journal/medjpps/article/doi/10.5281/zenodo.7905327

Mediterranean Journal of Pharmacy and Pharmaceutical Sciences

Original article

Characterizations of the active ingredients of methanol extract of weaver ant and its analgesic activity in mice

Deborah O. Momo , Osaro Iyekowa, Omonkhelin J. Owolabi

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Abstract

Pain according to WHO has been one of the greatest issues to plague man, in the bid to handle this issue of pain, man has sought to look for other means to reduce pain to its bare minimum. This study aims to investigate the analgesic activity of the methanolic extract of the African weaver ant using acetic acid-induced writhing, hot plate method, and formalin-induced pain models in Swiss mice. In the acetic acid test, the methanolic extract of Oecophylla longinoda (OL) was administered orally at 200 and 400 mg/kg body weight. In contrast, aspirin was administered at 100 mg/kg and tween 80 served as standards. In the hot plate and formalin models, the extract was administered orally at two doses of 200 and 400 mg/kg while pentazocine at 10 mg/kg and tween 80 at 10 mg/kg served as standards. The methanolic extract of OL exhibited significant analgesic activity in all the models, with none less than the standard significant difference (p<0.05) by increasing the reaction time of the mice after treatment in comparison to the control. The 400 mg/kg extract in the acetic acid-induced writhing response has a percentage inhibition of 52.7%, which shows how well the extract inhibits pain in mice. The methanolic extract significantly reduced pain response in mice, with a p-value of 0.03, 0.02, and 0.001 in all the test models, respectively. OL increased the pain threshold over time and significantly reduced the writhing response that mice experience from acetic acid. Furthermore, pretreatment with OL significantly and dose-dependently decreased the early and late phases of formalin-induced pain in mice. Thus, these findings suggest that the methanolic extract of OL acts on central and peripheral pain pathways.

Keywords

Analgesic, Nigeria, nociceptive, Oecophylla longinoda, pain, weaver ant

References

  1. Merskey H (1979) Pain terms: a list with definitions and notes on usage. Recommended by the lASP Subcommittee on Taxonomy. Pain. 6 (3): 249-252. PMID: 460932.
  2. Xu S, Wei W, Shen Y, Hao J, Ding C (1996) Studies on the anti-inflammatory, immunoregulatory, and analgesic actions of Melatonin. Drug Development Research. 39 (2): 167-173. doi. 10.1002/(SICI)1098-2299 (199610) 39:2167
  3. Baldry PE (2004) Acupuncture, trigger points, and muscular skeletal pain. 3rd ed., London, Churchill Livingston. UK. ISBN: 9780443066443.
  4. Watson J (1981) Pain mechanisms - a review: ii. Afferent pain pathways. Australian Journal of Physiotherapy. 27 (6): 191-198. doi: 10.1016/S0004-9514(14)60759-5
  5. Vardanyan RS, Hruby VJ (2016) in Synthesis of best-seller drugs. Academic press. doi: 10.1016/C2012-0-07004-4
  6. Vardanyan RS, Hruby VJ (2006) in Synthesis of Essential Drugs. Elsevier Science. doi: 10.1016/B978-0-444-52166-8.X5000-6
  7. Kohn DK, Wixson S, White WJ, Benson J (1997) Anesthesia and analgesia in laboratory animals. Academic Press. 6. 83-99. doi: 101016/B978-0-12-417570-9.X5000-4
  8. Langford DJ, Mogil JS (2008) Pain testing in the laboratory mouse. Anesthesia and analgesic in laboratory animals, 2nd Ed. Elsevier Inc. ISBN: 9780080559834.
  9. Khatun A, Rahman M, Rahman Md M, Hossain H, Jahan IA (2016) Antioxidant, antinociceptive and CNS activities of Viscum orientale and highly sensitive quantification of bioactive polyphenols by UPLC. Frontiers in Pharmacology. 7 (285708). doi: 10.3389/fphar.2016000176
  10. Graven-Nielson T, Arendt-Nielsen L (2010) Assessment of mechanisms in localized and widespread musculo-skeletal pain. Nature Reviews Rheumatology. 6 (10): 599-606. doi: 10.1038/nrrheum.2010.107
  11. Smart KM, Blake C, Staines A, Doody C (2010) Clinical indicators of 'nociceptive', 'peripheral neuropathic' and 'central' mechanisms of musculoskeletal pain. A Delphi survey of expert clinicians. Manual Therapy. 15 (1): 80-87. doi: 10.1016/j.math.2009.07.005
  12. Merskey H, Bogduk N (1994) Classification of chronic pain. Second edition (Revised). Seattle: IASP Press; 1974-2024. ISSN: 0301-3959.
  13. Baron R (2000) Peripheral neuropathic pain: from mechanisms to symptoms. The Clinical Journal of Pain. 16 (2S): S12-S20. doi: Nil.
  14. Hanson JR (2003) Natural Products: The secondary metabolite. Cambridge: Royal Society of Chemistry. ISBN: 0-85404-490-6.
  15. Baron R, Binder A, Wasner G (2010) Neuropathic pain: diagnosis, pathophysiological mechanisms, and treatment. The Lancet Neurology. 9 (8): 807-819. doi: Nil.
  16. Hanson JR (2003) Natural Products: The secondary metabolite. Cambridge: Royal Society of Chemistry. ISBN: 0-85404-490-6.
  17. Iyekowa O, Momo DO, Agbonifo E, Ngbodin J, Akinyemi K, Samuel VE, Chioma CG, Obasuyi EI, Adeyeye DO (2022) Bioactive chemical constituents screening and inhibitory activities of methanol extract of Oecophylla Longinoda (Tailor Ant) Against Some pathogens. NIPES Journal of Science and Technology Research. 4 (3): 80-86. doi: 10.37933/nipes/4.3.2022.9
  18. Trease GE, Evans WC (2009) Pharmacognosy. 16th edition. Saunders Ltd, Elsevier. ISBN: 978-0-7020-2933-2.
  19. Koster R, Anderson M, De Berar EJ (1959) Acetic acid for analgesic screening. Federation proceedings. 18: 412-416. Corpus ID: 20863822.
  20. Dias RJ, Patil CR, Bansod KU, Mali KK (2022) Laboratory manual in Pharmacology. Publisher: Trinity Publishing House, Satara. ISBN: 978-81-9552200-0-8.
  21. Franzotti EM, Santos CVF, Rodrigues HMSL, Mourao RHV, Andrade MR, Antoniolli AR (2000) Anti-inflammatory, analgesic activity and acute toxicity of Sida cordifolia L. (Malva-branca). Journal of Ethnopharmacology. 72 (1-2): 273-238. doi: 10.1016/S0378-8741(00)00205-1
  22. Shibata M, Ohkubo T, Takahash H, Inoki R (1989) Modified formalin test, characteristic biphasic pain response. Pain. 38 (3): 755-759. doi: 10.1016/0304-3959(89)90222-4
  23. Lorke D (2083) A new approach to practical acute toxicity testing. Archives of Toxicology. 54 (4): 275-287. doi: 10.1007/BF1234480
  24. Morales-Lázaro S, Llorente I, Sierra-Ramírez F, Simon SA, Islas LD, Rosenbaum T (2016) Inhibition of TRPV1 channels by a naturally occurring omega-9 fatty acid reduces pain and itch. Nature Communications. 7: 13092. doi. 10.1038/ncomms13092
  25. Farag MA, Gad MZ (2022) Omega-9 fatty acids: potential roles in inflammation and cancer management. Genetic Engineering Biotechnology. 20: 48. 16. doi: 10.1186/s43141-022-00329-0
  26. Harima A, Shimizu H, Takagi H (1991) Analgesic effect of L- arginine in patients with persistent pain. European Neuropsychopharmacology. 1 (4): 529-533. doi: 10.1016/0924-977x(91)90006-g
  27. Egashira K, Hirooka Y, Kuga T, Mohri M, Takeshita A (1996) Effects of l-arginine supplementation on endothelium-dependent coronary vasodilation in patients with angina pectoris and normal coronary arteriograms. Circulation. 94: 130-134. doi: 10.1161/01.CIR.94.2.130
  28. Guido F, Regina S, Manfred M, Rene O, Wolfgang D (1999) Species-specific production of microbial volatile organic compounds (MVOC) by airborne fungi from a compost facility. Chemosphere. 395: 795-810. doi: 10.1016/s0045-6535(99)00015-6
  29. Fialho MFP, Brusco I, Brum ES, Piana M, Boligon AA, Trevisan G, Oliveira SM (2017) Buddleja thyrsoides Lam. crude extract presents antinociceptive effect on an arthritic pain model in mice. Biochemical Journal. 474 (17): 2993-3010. doi: 10.1042/BCJ20170008
  30. Xin Q, Bai B, Liu W (2017) The analgesic effects of oxytocin in the peripheral and central nervous system. Neurochemistry International. 103: 57-64. doi: 10.1016/j.neuint.2016.12.021
  31. Janssen P, Niemegeers CJ, Dony JG (1963) The inhibitory effects of Fentanyl and other morphine like analgesics on the warm water induced tail withdrawal reflex in rats. Arzneimittelforschung. 13: 502-507. PMID: 13957426.
  32. S. Hunskaar O, Fasmer B, Hole K (1985) Formalin test in mice, a useful technique for evaluating mild analgesics. Journal of Neuroscience Methods. 14 (1): 69-76. doi: 10.1016/0165-0270(85)90116-5
  33. Clavelou P, Dallel R, Orliaguet T, Woda A, Raboisson P (1995) The orofacial formalin test in rats: effects of different formalin concentrations. Pain. 62 (3): 295-301. doi: 10.1016/0304-3959(94)00273-H
  34. Ricciotti E, FitzGerald GA (2011) Prostaglandins and inflammation. Arteriosclerosis, Thrombosis, and Vascular Biology. 31 (5): 986-1000. doi: 10.1161/ATVBAHA.110.207449
  35. Shreedhara CS, Vaidya VP, Vagdevi HM, Latha KP, Muralikrishna KS, Krupanidhi AM (2009) Screening of Bauhinia purpurea Linn. for analgesic and anti-inflammatory activities. Indian Journal of Pharmacology. 41 (2): 75-79. doi: 10.4103/0253-7613.51345
  36. McDonald J, Lambert DG (2005) Opioid receptors. Continuing Education in Anesthesia Critical Care and Pain. 5 (1): 22-25. doi. 10.1093/bjaceaccp/mki004
  37. Okokon JF, Davis K, Nwidu LL (2016) Anti-inflammatory and antinociceptive activities of Solenostemon monostachyus aerial part extract in mice. Avicenna Journal of Phytomedicine. 6 (3): 284-294. PMID: 27462551.

Submitted date:
04/05/2023

Reviewed date:
05/02/2023

Accepted date:
05/07/2023

Publication date:
07/21/2023

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