DOI QR코드

DOI QR Code

Antioxidant Effects of Berchemia berchemiaefolia in Nerve Pain Models

  • Lee, Gil-Hyun (Department of Clinical Laboratory Science, Kyungwoon University) ;
  • Hyun, Kyung-Yae (Department of Clinical Laboratory Science, DongEui University) ;
  • Choi, Seok-Cheol (Department of Clinical Laboratory Science, Catholic University of Pusan)
  • Received : 2017.11.14
  • Accepted : 2017.12.06
  • Published : 2017.12.31

Abstract

Berchemia berchemiaefolia (BB) are climbing plants or small to medium-sized trees that live in Africa, Asia and America. We performed the present study to investigate whether oral administration of Berchemia berchemiaefolia extract (BBE) protects SD rats from pain. The SD rat experimental groups were divided into four groups. Two of the animal model groups were fed on BBE (200 mg/kg or 100 mg/kg). We performed oral acute toxicity test to determine the optimal oral dose of BBE. To explore if BBE alleviated pain in the SD rat, we undertook the tail flick latency test and formalin test. Additionally, we conducted the anti-oxidative test. The findings of the present study suggest that Berchemia berchemiaefolia extract exhibits strong antioxidant and analgesic activities.

Keywords

References

  1. Beltramo M1, Bernardini N, Bertorelli R, Campanella M, Nicolussi E, Fredduzzi S, Reggiani A. CB2 receptor-mediated antihyperalgesia: possible direct involvement of neural mechanisms. European Journal of Neuroscience. 2006. 23: 1530-1538. https://doi.org/10.1111/j.1460-9568.2006.04684.x
  2. Bojovic O, Bramham CR, Tjolsen A. Chronic morphine treatment enhances sciatic nerve stimulation-induced immediate early gene expression in the rat dorsal horn. Acta Neurobiologiae Experimentalis. 2015. 75: 305-313.
  3. Cimanga K, Ying L, De Bruyne T, Apers S, Cos P, Hermans N, Bakana P, Tona L, Kambu K, Kalenda DT, Pieters L, Vanden Berghe D, Vlietinck AJ. Radical scavenging and xanthine oxidase inhibitory activity of phenolic compounds from Bridelia ferruginea stem bark. Journal of Pharmacy and Pharmacology. 2001. 53: 757-761. https://doi.org/10.1211/0022357011775893
  4. Connor M. Allopurinol for pain relief: more than just crystal clearance? British Journal of Pharmacology. 2009. 156: 4-6. https://doi.org/10.1111/j.1476-5381.2008.00065.x
  5. Evers S. Facial pain: Overlapping syndromes. Cephalalgia. 2017. 37: 705-713. https://doi.org/10.1177/0333102417703761
  6. Hogan D, Baker AL, Moron JA, Carlton SM. Systemic morphine treatment induces changes in firing patterns and responses of nociceptive afferent fibers in mouse glabrous skin. Pain. 2013. 154: 2297-2309. https://doi.org/10.1016/j.pain.2013.05.033
  7. Kaulmann A, Bohn T. Carotenoids, inflammation, and oxidative stress- -implications of cellular signaling pathways and relation to chronic disease prevention. Nutrition Research. 2014. 34:907-929. https://doi.org/10.1016/j.nutres.2014.07.010
  8. Kishore RK, Halim AS, Syazana MS, Sirajudeen KN. Tualang honey has higher phenolic content and greater radical scavenging activity compared with other honey sources. Nutrition Research. 2011. 31: 322-325. https://doi.org/10.1016/j.nutres.2011.03.001
  9. Li C, Yi LT, Geng D, Han YY, Weng LJ. Hepatoprotective effect of ethanol extract from Berchemia lineate against CCl4-induced acute hepatotoxicity in mice. Pharmaceutical Biology. 2014. 53: 767-772.
  10. Mfotie Njoya E, Munvera AM, Mkounga P, Nkengfack AE, McGaw LJ. Phytochemical analysis with free radical scavenging, nitric oxide inhibition and antiproliferative activity of Sarcocephalus pobeguinii extracts. BMC Complementary and Alternative Medicine. 2017. 17: 199-207. https://doi.org/10.1186/s12906-017-1712-5
  11. Mor D, Kendig MD, Kang JW, Gemikonakli G, Austin PJ, Kalman E, Corbit LH. Peripheral nerve injury impairs the ability to maintain behavioral flexibility following acute stress in the rat. Behavioral Brain Research. 2017. 328: 123-129. https://doi.org/10.1016/j.bbr.2017.04.003
  12. Palle P, Ferreira FM, Methner A, Buch T. The more the merrier? scoring, statistics and animal welfare in experimental autoimmune encephalomyelitis. Lab Anim. 2016. 50: 427-432. https://doi.org/10.1177/0023677216675008
  13. Pillarisetti S, Khanna I. A multimodal disease modifying approach to treat neuropathic pain-inhibition of soluble epoxide hydro lase (sEH). Drug Discovery Today. 2015. 20: 1382-1390. https://doi.org/10.1016/j.drudis.2015.07.017
  14. Planjar-Prvan M, Bielen I, Baraba R, Buljan R. Pathophysiologic basis of the treatment of neurogenic pain. Acta Medica Croatica. 2004. 58: 197-205.
  15. Ray K, Fahrmann J, Mitchell B, Paul D, King H, Crain C, Cook C, Golovko M, Brose S, Golovko S, Santanam N. Oxidationsensitive nociception involved in endometriosis-associated pain. Pain. 2015. 156: 528-539. https://doi.org/10.1097/01.j.pain.0000460321.72396.88
  16. Rosa KA, Gadotti VM, Rosa AO, Rodrigues AL, Calixto JB, Santos AR. Evidence for the involvement of glutamatergic system in the antinociceptive effect of ascorbic acid. Neuroscience Letters. 2005. 381: 185-188. https://doi.org/10.1016/j.neulet.2005.02.032
  17. Russo R, Cristiano C, Avagliano C, De Caro C, La Rana G, Raso GM, Canani RB, Meli R, Calignano A. Gut-brain axis: role of lipids in the regulation of inflammation, pain and CNS diseases. Current Medi Chem. Curr Med Chem. 2017. 16. doi: 10.2174/0929867324666170216113756. [Epub ahead of print].
  18. Siahposht-Khachaki A, Pourreza P, Ezzatpanah S, Haghparast A. Nucleus accumbens dopamine receptors mediate hypothalamus -induced antinociception in the rat formalin test. European Journal of Pain. 2017. 21: 1285-1294. https://doi.org/10.1002/ejp.1029
  19. Srinivasan V, Pandi-Perumal SR, Spence DW, Moscovitch A, Trakht I, Brown GM, Cardinali DP. Potential use of melatonergic drugs in analgesia: mechanisms of action. Brain Research Bulletin. 2010. 81: 362-371. https://doi.org/10.1016/j.brainresbull.2009.12.001
  20. Straub JO. Environmental risk assessment for new human pharmaceuticals in the European Union according to the draft guideline/discussion paper. Toxicology Letters. 2001. 131: 137-143.
  21. Taherian A, Sameni H, Sadeghi S, Taherian M. The role of opioid receptors on anti-nociceptive effects of hydroalcoholic extract of securigera securidaca L. seed in albino mice. Journal of Pain. 2016. 17: 55.
  22. Toyama S, Shimoyama N, Shimoyama M. The analgesic effect of orexin-A in a murine model of chemotherapy-induced neuropathic pain. Neuropeptides. 2017. 61: 95-100. https://doi.org/10.1016/j.npep.2016.12.007
  23. Umar AH, Suleiman I, Muhammed H. Effect of low dose lead (Pb) administration on tail immersion test and formalin-induced pain in wistar rats: possible modulatory role of cobalt (II) chloride. Nigerian Journal of Physiological Sciences. 2017. 31: 161-164.
  24. Wang ZY, Liu JG, Li H, Yang HM. Pharmacological effects of active components of chinese herbal medicine in the treatment of Alzheimer's disease: a review. The American Journal of Chinese Medicine. 2016. 44: 1525-1541. https://doi.org/10.1142/S0192415X16500853
  25. Ye L, Xiao L, Bai X, Yang SY, Li Y, Chen Y, Cui Y, Chen Y. Spinal mitochondrial-derived ROS contributes to remifentanil-induced postoperative hyperalgesia via modulating NMDA receptor in rats. Neuroscience Letters. 2016. 634: 79-86. https://doi.org/10.1016/j.neulet.2016.09.016
  26. Zhou F, Zhang W, Zhou J, Li M, Zhong F, Zhang Y, Liu Y, Wang Y. Involvement of endoplasmic reticulum stress in formalininduced pain is attenuated by 4-phenylbutyric acid. Journal of Pain Research. 2017. 10: 653-662. https://doi.org/10.2147/JPR.S125805
  27. Zuntini Viscardi D, Arrigo JD, Correia CA, Kassuya CA, Cardoso CA, Maldonade IR, Argandona EJ. Seed and peel essential oils obtained from Campomanesia adamantium fruit inhibit inflammatory and pain parameters in rodents. PLOS One. 2017. 12: 1-15.