Neoboutonia velutina Prain is a small tree of 6-12 m, found in tropical areas of Africa (Cameroon, Zimbabwe, Malawi, Nigeria, Angola and Southern Sudan). This plant is used in Cameroonian traditional medicine for the treatment of central nervous system diseases like epilepsy and for the treatment of hepatitis. In our knowledge, there are no published studies on biological activity of N. velutina. In the present study, in vivo animal models of epilepsy (strychnine, pentylenetetrazol and Picrotoxin-induced convulsions) and insomnia (diazepam -induced sleep) were used to evaluate the anticonvulsant and sedative properties of N. velutina. The aqueous extract of the leaves of N. velutina protected mice against strychnine (p<0.05), pentylenetetrazol (p<0.01), and picrotoxin (p<0.001)-induced seizures. The extract strongly increased the total sleep time induced by diazepam (50 mg/kg i.p.) but did not significantly precipitate the onset of sleep. The results lead to the conclusion that the extract of N. velutina possesses anticonvulsant and sedative properties in mice and could explain its use in traditional medicine for the treatment of epilepsy and insomnia.
Published in | Journal of Diseases and Medicinal Plants (Volume 1, Issue 2) |
DOI | 10.11648/j.jdmp.20150102.11 |
Page(s) | 24-30 |
Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
Copyright |
Copyright © The Author(s), 2015. Published by Science Publishing Group |
Neoboutonia velutina, Aqueous Extract, Anticonvulsant, Sedative
[1] | Engel J., Timothy J.R.A., Pedley., Aicardi J., Dichler A.M., Heinemann U., Moshé S., Porter J.R., Taylor D.C., 1997. Epilepsy: a comprehensive textbook. Lippicot Roven Publisher. 500 p. |
[2] | WHO., 2013. Aide-mémoire N°165. Epilepsie: étiologie, épidémiologie et pronostic. |
[3] | Njamshi A., Dongmo L., Simi V., Echoufo B., Pepouoni M.N., Kamndem P., Atchou G., 2002. Epilepsy in rural Cameroun: the alarming prevalence rates in the Mbam valley. 169th conference of the swiss society of neurology in Zoug. pp. 23-25. |
[4] | Taylor D. J., Lichstein K.L., Durrence H., Reidel B. W., Bush A. J., 2005. Epidemiology of Insomnia, Depression, and Anxiety. SLEEP, Vol. 28, No. 11. |
[5] | Adjanohoun E. J., 1988. Contribution aux études ethnobotaniques et floristiques en République populaire du Congo. ACCT, Paris, pp : 605. |
[6] | Iwu M. M., 1993. Handbook of African medicinal plants. CRC Press. Boca Raton fl., ISBN-10: 084934266X. |
[7] | Purves, Dale, Augustine, G.J., Fitzpatrick, D., Hall, W.C., LaMantia, A., McNamara, J.O., White, L.E., 2008. Neuroscience, 4th ed. Sinauer Associates, pp. 137–138. |
[8] | Ngo Bum E., Nkantchoua G.N., Njikam N., Taiwe G.S., Ngoupaye G.T., 2010. Anticonvulsant and sedative activity of leaves of senna spectabilis in mice. International j. pharmacol. 6(2): 123-128. |
[9] | Ngo Bum E., Taiwe S.G., Moto O.F., Ngoupaye T.G., Nkontchoua N.C.G., 2009a. Anticonvulsant, anxiolytic and sedative properties of roots of Nauclea latifolia Smith in mice. Epilepsy behav. 15: 434-440. |
[10] | Hema B., Bhupendra S., Mohamed Saleem T.S., Gauthaman K., 2009. Anticonvulsant Effect of Drosera burmannii Vahl. Int. J. Appl. Res.Nat. 2(3): 1-4. |
[11] | Rakotonirina S. V., Ngo Bum E., Rakotonirina A., Bopelet M., 2001. Sedative properties of the extract of the rhizome of Cyperus articulatus. Fitoterapia 72: 22-29. |
[12] | Engelborghs S., D’Hooge R., De Deyn P. P., 2000. Pathophysiology of epilepsy. Review article. Acta neurol.belg. 100: 201-213. |
[13] | Trailovic S. M., and Varagic V. M., 2007. The effect of invermectin on convulsions in rats produced by lidocaine and strychnine. Vet. Res. Commun. 31: 863-872. |
[14] | Park H. G., Yoon S. Y., Choi J. Y., Lee G. S., Choi J. H., et al., 2007. Anticonvulsant effect of Wogonin isolated from Scutellaria baicalensis. Eur. J. Pharmacol. 574: 112-119. |
[15] | Findlay, G.S., Wick M. J., Mascia M. P., Wallace D., Millier G. W., Harris R. A., Blednov Blednov Y. A., 2002; Transgénic expression of a mutant glycine receptor decrease alcohol sensitivity of mice. J. Pharmacol. Exp. Ther. 300: 526-534. |
[16] | Loscher, W., Fassbender C. P., Nolthing B., 1991. The role of technical, biological and pharmacological factors in the laboratory evaluation of anticonvulsant drugs 11. Maximal electroshock seizure models. Epilepsy Res. 8: 79-84. |
[17] | Rizuj S., Muker D., and Mathur., 1980. A new report of possible source of natural herbicide. Indian J. Exp. Biol. 18:777–778. |
[18] | Caceres A., Lopez B.R., Giron M.A., Logemann H., 1991. Plants used in Guatemala for the treatment of dermatophytic infections: Screening for antimycotic activity of 44 plant extracts. J. Ethnopharmacol. 31:263–276. |
[19] | Rogawski M. A., 1992. The NMDA receptor, NMDA antagonists and epilepsy therapy. A status report. Drugs 44: 279-292. |
[20] | De Deyn P. P., D’Hooge R., Marescau B., Pei Y-Q., 1992. Chemical model of epilepsy with some reference to their applicability in the development of anticonvulsant. Epilepsy Res. 12: 87-110. |
[21] | Nicoll, R.A., 2007. Introduction to the pharmacology of CNS drugs. In: Katzung, B.G. (Ed.), Basic and Clinical Pharmacology. McGraw-Hill Medical, San Fransisco, pp. 333–346. |
[22] | Karunakar H., Shalin P T., Arun B J., Shastry C. S., Chandrashekhar K. S., 2009. Anticonvulsant activity of Carissa carandas Linn. root extract in experimental mice. Trop. J. Pharm. Res. 8 (2): 117-125. |
[23] | Ngo Bum E., Dawack D. L., Schmutz M., Rakotonirina S.V., Rakotonirina A., 2004a. Anticonvulsant activity of mimosa pudica decoction. Fitotherapia. 75: 310-315. |
[24] | Ngo Bum E., Ngah E., Ekoundi B. C., Dong C., Ayissi M. R. E., Rakotonirina S.V., Rakotonirina A., 2004b. The decoction of passiflora edulis possesses sedative and anticonvulsant properties in mice. African j. trad. Complem. Altern. Med. 1: 63-71. |
[25] | Rang H. P., Dale M. M., Ritter J. M., 1999. Pharmacology, Churchill Livingstone, London, pp: 531. |
[26] | Bruneton J., 1999. Pharmacognosie, phytochimie des plantes médicinales. Lavoisier, Paris ISBN: 27430003154. |
APA Style
Germain Jean Magloire Ketcha Wanda, Steve Guemnang Ngitedem, Sefirin Djiogue, Franklin Zemo Gamo, Dieudonne Njamen. (2015). Anticonvulsant and Sedative Properties of Leaves of Neoboutonia velutina (Euphorbiaceae) Prain in Mice. Journal of Diseases and Medicinal Plants, 1(2), 24-30. https://doi.org/10.11648/j.jdmp.20150102.11
ACS Style
Germain Jean Magloire Ketcha Wanda; Steve Guemnang Ngitedem; Sefirin Djiogue; Franklin Zemo Gamo; Dieudonne Njamen. Anticonvulsant and Sedative Properties of Leaves of Neoboutonia velutina (Euphorbiaceae) Prain in Mice. J. Dis. Med. Plants 2015, 1(2), 24-30. doi: 10.11648/j.jdmp.20150102.11
AMA Style
Germain Jean Magloire Ketcha Wanda, Steve Guemnang Ngitedem, Sefirin Djiogue, Franklin Zemo Gamo, Dieudonne Njamen. Anticonvulsant and Sedative Properties of Leaves of Neoboutonia velutina (Euphorbiaceae) Prain in Mice. J Dis Med Plants. 2015;1(2):24-30. doi: 10.11648/j.jdmp.20150102.11
@article{10.11648/j.jdmp.20150102.11, author = {Germain Jean Magloire Ketcha Wanda and Steve Guemnang Ngitedem and Sefirin Djiogue and Franklin Zemo Gamo and Dieudonne Njamen}, title = {Anticonvulsant and Sedative Properties of Leaves of Neoboutonia velutina (Euphorbiaceae) Prain in Mice}, journal = {Journal of Diseases and Medicinal Plants}, volume = {1}, number = {2}, pages = {24-30}, doi = {10.11648/j.jdmp.20150102.11}, url = {https://doi.org/10.11648/j.jdmp.20150102.11}, eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.jdmp.20150102.11}, abstract = {Neoboutonia velutina Prain is a small tree of 6-12 m, found in tropical areas of Africa (Cameroon, Zimbabwe, Malawi, Nigeria, Angola and Southern Sudan). This plant is used in Cameroonian traditional medicine for the treatment of central nervous system diseases like epilepsy and for the treatment of hepatitis. In our knowledge, there are no published studies on biological activity of N. velutina. In the present study, in vivo animal models of epilepsy (strychnine, pentylenetetrazol and Picrotoxin-induced convulsions) and insomnia (diazepam -induced sleep) were used to evaluate the anticonvulsant and sedative properties of N. velutina. The aqueous extract of the leaves of N. velutina protected mice against strychnine (p<0.05), pentylenetetrazol (p<0.01), and picrotoxin (p<0.001)-induced seizures. The extract strongly increased the total sleep time induced by diazepam (50 mg/kg i.p.) but did not significantly precipitate the onset of sleep. The results lead to the conclusion that the extract of N. velutina possesses anticonvulsant and sedative properties in mice and could explain its use in traditional medicine for the treatment of epilepsy and insomnia.}, year = {2015} }
TY - JOUR T1 - Anticonvulsant and Sedative Properties of Leaves of Neoboutonia velutina (Euphorbiaceae) Prain in Mice AU - Germain Jean Magloire Ketcha Wanda AU - Steve Guemnang Ngitedem AU - Sefirin Djiogue AU - Franklin Zemo Gamo AU - Dieudonne Njamen Y1 - 2015/05/28 PY - 2015 N1 - https://doi.org/10.11648/j.jdmp.20150102.11 DO - 10.11648/j.jdmp.20150102.11 T2 - Journal of Diseases and Medicinal Plants JF - Journal of Diseases and Medicinal Plants JO - Journal of Diseases and Medicinal Plants SP - 24 EP - 30 PB - Science Publishing Group SN - 2469-8210 UR - https://doi.org/10.11648/j.jdmp.20150102.11 AB - Neoboutonia velutina Prain is a small tree of 6-12 m, found in tropical areas of Africa (Cameroon, Zimbabwe, Malawi, Nigeria, Angola and Southern Sudan). This plant is used in Cameroonian traditional medicine for the treatment of central nervous system diseases like epilepsy and for the treatment of hepatitis. In our knowledge, there are no published studies on biological activity of N. velutina. In the present study, in vivo animal models of epilepsy (strychnine, pentylenetetrazol and Picrotoxin-induced convulsions) and insomnia (diazepam -induced sleep) were used to evaluate the anticonvulsant and sedative properties of N. velutina. The aqueous extract of the leaves of N. velutina protected mice against strychnine (p<0.05), pentylenetetrazol (p<0.01), and picrotoxin (p<0.001)-induced seizures. The extract strongly increased the total sleep time induced by diazepam (50 mg/kg i.p.) but did not significantly precipitate the onset of sleep. The results lead to the conclusion that the extract of N. velutina possesses anticonvulsant and sedative properties in mice and could explain its use in traditional medicine for the treatment of epilepsy and insomnia. VL - 1 IS - 2 ER -