Anticonvulsant Activity of Hippocratea welwitschii Oliv. (Celastraceae) Root Extracts on Chicks and Swiss Mice

http://www.doi.org/10.26538/tjnpr/v8i1.48

Authors

  • Kamal J. Muhammad Chemistry Advanced Research Centre, Sheda Science and Technology Complex, Sheda- Abuja-Nigeria
  • Michael O. Afolayan Chemistry Advanced Research Centre, Sheda Science and Technology Complex, Sheda- Abuja-Nigeria
  • Uzama Danlami Chemistry Advanced Research Centre, Sheda Science and Technology Complex, Sheda- Abuja-Nigeria
  • Paul C. Onyenekwe Biotechnology Advanced Research Centre, Sheda Science and Technology Complex, Sheda- Abuja-Nigeria
  • Mohammed G. Magaji Department of Pharmacology and Therapeutics, Ahmadu Bello University, Zaria-Nigeria

Keywords:

Beam Walking Assay, Pentylenetetrazole, Strychnine, Seizure, Hippocratea welwitschii, Epilepsy

Abstract

Dried roots of Hippocratea welwitschii are a prevalent traditional medication for the management of epilepsy in the traditional ‘Ukanafum’ system of medicine in the Akwa Ibom, South Southern, Nigeria. Various extracts of the root of the plant namely: n-hexane, ethyl acetate, methanolic, aqueous and crude extracts were subjected to anticonvulsant evaluation using the maximal electroshock test (MEST) in chicks, subcutaneous pentylenetetrazole (scPTZ) and strychnine induced seizures test in mice. The neurotoxic potential of the extracts was assessed using beam walking assays in mice. The n-hexane (250 mg/kg), methanol (250 mg/kg) and aqueous (125 and 250 mg/kg) extracts produced 30% protection against seizure induced by MEST. The methanol extract (250 mg/kg) and crude extract (125 mg/kg) showed 80% and 70% protection in the scPTZ test, respectively. Similarly, the aqueous extract at 125 mg/kg protected 60% of the mice against seizure induced by strychnine. In the beam walking assay test, only the methanol extract produced a significant (p < 0.05) increase in the number of foot slips and the time taken to complete the task. In conclusion the various extracts of the root of Hippocratea welwitschii demonstrated anticonvulsant activity and deserve further study on the isolation and elucidation of the anticonvulsant active compounds and possible mechanism of anticonvulsant action.

References

Muhammad KJ, Jamil S, Basar N, Magaji MG.

Anticonvulsant studies on the isolated compounds from the

leaves of Scurrula parasitica L (Loranthaceae). Malaysian J

Fund Appli Sci. 2019; 15(6): 806-810.

Yemitan OK, Adeyemi OO. Antiepileptogenic and

anticonvulsant actions of Dalbergia saxatilis (Hook, F.) in

sub-toxic chemical kindling and toxic convulsant models.

Eur J Med Plants. 2013; 3(2): 288-296.

Thurman DJ, Beghi E, Begley CE, Berg AT, Buchhalter JR,

Ding D, Hesdorffer DC, Hauser WA, Kazis L, Kobau R,

Kroner B, Labiner D, Liow K, Logroscino G, Medina MT,

Newton CR, Parko K, Paschal A, Preux PM, Sander JW,

Selassie A, Theodore W, Tomson T, Wiebe S, ILAE

Commission on Epidemiology. Standards for epidemiologic

studies and surveillance of epilepsy. Epilepsia. 2011; 52(7):

–26.

World Health Organization. Neurological Disorders: Public

Health Challenges, Geneva, Switzerland. 2006.

Hirak KM, Chandi CK, Sanjay KD, Lakshmikanta G, Bijan

KG. Epilepsy and its Management: A Review. Journal of

Pharma Sci Tech. 2012; 1(2): 20-26.

Simonato M, Brooks-Kayal AR, Engel J Jr, Galanopoulou

AS, Jensen FE, Moshe SL, O’Brien TJ, Pitkanen A, Wilcox

KS, French JA. The challenge and promise of antiepileptic

therapy development in animal models. Lancet Neurol. 2014;

(9): 949–960.

Musa MA, Abdullahi IM, Kamal MJ, Magaji GM.

Phytochemical screening and anticonvulsant studies of ethyl

acetate fraction of Globimetula braunii on laboratory

animals. Asian Pac J Trop Biomed. 2014; 4(4): 285–289.

Hela SI, Megahed HS, Salem SM, Youness ER.

Monotherapy versus polytherapy in epileptic adolescents.

Maced J Med Sci. 2013; 6(2):174-177.

Jaafar KM, Shajarahtunnur J, Norazah B. Antioxidant

Activity of Leaf Extracts of Globimetula braunii (Engler)

van Tiegh Parasitizing on Piliostigma thonningii and Parkia

biglobosa. J. Teknol. 2017; 79: 43–47.

Tripathi AS, Chitra V, Sheikh NW, Mohale DS, and Dewani

AP. Immunomodulatory Activity of the Methanol Extract of

Amorphophallus campanulatus (Araceae) Tuber. Trop J

Pharma Res. 2010; 9(5): 451-454.

Gurib-Fakim A. Medicinal plants: traditions of yesterday and

drugs of tomorrow. Mol asp Med. 2006; 27(1): 1-93.

Rates SMK. Plants as source of drugs. Toxicon. 2001; 39(5):

-613.

Burkill HM. The useful plants of West Tropical Africa, 2nd

ed., vol. 2. The White Friars Press limited, Great Britain.

; 352-364.

Onyekere PF, Enebechi CK, Nnamani DO, PeculiarOnyekere CO, Okonta EO. Phytochemical analysis and

antimicrobial activity of methanol extract of the leaves of

Hippocratea Welwitschii OLIV. (CELASTRACEAE).

African J Pharm Res Develop. 2019; 11(2): 106 – 115.

Swinyard EA, Kupferberg HJ. Antiepileptic drugs: detection,

quantification, and evaluation. Fed Proc. 1985; 44(10):

–2633.

Sayyah M, Valizadeh J, Kamalinejad M. Anticonvulsant

activity of the leaf essential oil of Laurus nobilis against

pentylenetetrazole and maximal electroshock-induced

seizures. Phytomed. 2002; 9: 212-216.

Swinyard EA, Woodhead JH, White HS, Franlin MR.

General principles: Experimental selection, quantification

and evaluation of anticonvulsants. In R. H. Levy, R. H.

Mattson, B. Melrum, J. K. Penry, F. E. Dreifuss (Eds.).

Antiepileptic Drugs (3rd Edition). 1989; 85-102). New York:

Raven press.

Porter RJ, Cereghino JJ, Gladding GD, Hessie BJ,

Kupferberg HJ, Scoville B, White BG. Antiepileptic drug

development program. Cleveland Clin Quart. 1984; 51(2):

-305.

Stanley JL, Rachael JL, Brown TA. McDonald ML, Dawson

RG, Reynolds SD. The mouse beam walking assay offers

improved sensitivity over the mouse rotarod in determining

motor coordination deficits induced by benzodiazepines. J

Psychopharm. 2005; 19(3): 221-227.

Obiloma AA, Ogbonna PC, Okere TO, Adumanya OC,

Maduforo AN. Chemical Composition of Hippocratea

welwitchi: a Common Indigenous Spice Consumed in Southeastern Nigeria. J Diet Assoc Nigeria. 2017; 8: 131-135.

Okwute SK, Okoh-Esene RU, Okogun JI. Two Triterpenoids

Isolated from the Root of Hippocratea welwitschii

(celastraceae)-oliv. UW. Trends in Sci Technol J. 2018; 3(2):

–540.

Illodigwe EE, Akah PA, Okoye TC, Omeje EO.

Anticonvulsant effects of a glycoside isolated from the leaf

of Spathodea campanulata P. Beauv. J Med Res. 2010;

(18): 1894-1900.

Swinyard EA, Woodhead JH. General principles of

detection, quantification and evaluation of anticonvulsants in

Antiepileptic drugs woodbury DM. Penry JK and Pippenger

CE, eds, Raven press. 1982; 113.

White HS, Woodhead JH, Franklin MR, Swinyard EA, Wolf

HH. Experimental selection qualification and evaluation of

antiepileptic drugs 4thedn. Levy LH. Mattson RH and

Meldrum BS. Eds. Raven press, New Work. 1995; 99-100.

Sayyah M, Nadjafnia L, Kamalinejad M. Anticonvulsant

activity and chemical composition of Artemisia dracunculus

L. essential oil. J Ethnopharmacol 2004; 94: 283-287.

Subramaniam S, Rho JM, Penix L, Donevan SD, Fielding

RP, Rogawski MA. Felbamate block of the N-methyl-Daspartate receptor. J Pharmacol Exp Ther 1995; 273(2): 878-

Prigol M, Brüning CA, Godoi B, Nogueira CW, Zeni G. mTrifluoromethyl-diphenyl diselenide attenuates

pentylenetetrazole-induced seizures in mice by inhibiting

GABA uptake in cerebral cortex slices. Pharmacol Rep 2009;

: 1127- 1133.

Czapin ́ski P, Blaszczyk B, Czuczwar SJ. Mechanisms of

action of antiepileptic drugs. Curr Top Med Chem 2005; 5:

-14.

Sun XY, Zhang L, Wei CX, Piao HR, Quan ZS.

Characterization of the anticonvulsant activity of doxepin in

various experimental seizure models in mice. Pharmacol Rep

; 61: 245-251.

Yudkoff M, Daikhin Y, Nissim I, Horyn O, Luhovyy B,

Lazarow A. Short-term fasting, seizure control and brain

amino acid metabolism. Neuro chem Int 2006; 48: 650-656.

Yang J, Wetterstrand C, Jones RS. Felbamate but not

phenytoin or gabapentin reduces glutamate release by

blocking presynaptic NMDA receptors in the entorhinal

cortex. Epilepsy Res 2007; 77(23): 157-164.

Mante PK, Adongo DW, Woode E, Kukuia KKE, Elvis

OforiAmeyaw, EO. Anticonvulsant Effect of Antiaris

toxicaria (Pers.) Lesch. (Moraceae) Aqueous Extract in

Rodents. Hindawi Publishing Corporation ISRN

Pharmacology. 2013; 9.

Bigler ED. “Comparison of effects of bicuculline, strychnine,

and picrotoxin with those of pentylenetetrazole on photically

evoked after discharges,” Epilepsia. 1977; 18(4): 465–470.

Trailovic SM, Varagic VM. The Effect of Ivermectin on

Convulsions in Rats Produced by Lidocaine and Strychnine.

Vet Res Comm. 2007; 31: 863–872

Kehne JH, Kane JM, Miller FP, Ketteler HJ, Braun DL,

Senyah Y, Chaney SF, Abdallah A, Dudley MW, Ogden

AM, Palfreyman MG. MDL 27, 531 selectively reverses

strychnine-induced seizures in mice. BJ. Pharmacol. 1992;

: 910-916.

Published

2024-02-01

How to Cite

Muhammad, K. J., Afolayan, M. O., Danlami, U., Onyenekwe, P. C., & Magaji, M. G. (2024). Anticonvulsant Activity of Hippocratea welwitschii Oliv. (Celastraceae) Root Extracts on Chicks and Swiss Mice: http://www.doi.org/10.26538/tjnpr/v8i1.48. Tropical Journal of Natural Product Research (TJNPR), 8(1), 6045–6050. Retrieved from https://tjnpr.org/index.php/home/article/view/3431