Anticonvulsant Studies on Ethanol Leaf Extract of Cadaba farinosa Forssk. in Experimental Models doi.org/10.26538/tjnpr/v6i8.21

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Muhammad A. Tijjani
Hamidu Usman
Aishatu Muhammad
Mohammed G. Magaji
Abdullahi H. Yaro
Halimatu S. Hassan
Umar U. Pateh
Mohammed I. Sule
Lawan B. Inuwa

Abstract

Cadaba farinosa Forssk. is widely distributed in tropical and sub-tropical regions. It is used in the treatment of pains, dysentery, rheumatism, cough, fever, as antidote and neurological disorders. The study evaluated the anticonvulsant activity of the ethanol leaf extract (CEE) of the plant in Swiss mice using maximal electroshock test (MEST), pentylenetetrazole (PTZ), strychnine (STN) and 4-aminopyridine (4-AP) induced seizures tests. The intraperitoneal (i.p.) median lethal dose (LD50) of CEE was found to be 2154.1 mg/kg body weight in mice. There was no significant protection against maximal electroshock induced seizures in all treated groups and no difference in their mean recovery time. Only the standard drug (phenytoin) showed 40% protection. The extract did not protect the mice against pentylenetetrazole induced seizures at all doses. However, there was significant increase in the mean onset of seizures at all doses. There was significant (p ≤ 0.05) 16.7% protection exhibited by the extract at 150 and 300 mg/kg. The extract at 75 mg/kg exhibited the highest protection of 83.3% against STN induced seizures in mice. At 75 mg/kg the extract exhibited highest protection of 83.3% against strychnine induced seizures in mice. Phenobarbitone caused an increase in the mean onset with 50% protection. The extract (300 mg/kg) offered 100% protection against 4-aminopyridine induced seizures in mice higher than that produced by phenobarbitone. However, there was no significant difference in the onset of seizure in the unprotected animals. The results suggest that ethanol leaf extract of Cadaba farinosa possesses anticonvulsant properties.

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How to Cite
A. Tijjani, M., Usman, H., Muhammad, A., G. Magaji, M., H. Yaro, A., S. Hassan, H., U. Pateh, U., I. Sule, M., & B. Inuwa, L. (2022). Anticonvulsant Studies on Ethanol Leaf Extract of Cadaba farinosa Forssk. in Experimental Models: doi.org/10.26538/tjnpr/v6i8.21. Tropical Journal of Natural Product Research (TJNPR), 6(8), 1286-1289. https://tjnpr.org/index.php/home/article/view/1309
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References

Sander JWAS and Shorvon SD. Epidemiology of epilepsies. J Neurol Neurosurg Psych. 1996; 61:433-443.

Verma M, Pandeya SN, Singh KN, Stables JP. Anticonvulsant activity of schiff bases of Isatin derivatives. Acta Pharm. 2004; 54:49–56.

Siddiqui N, Pandeya SN, Khan SA, Stables J, Rana A, Alam M. Synthesis and anticonvulsant activity of sulfonamide derivatives-hydrophobic domain. Bioorg Med Chem Lett., 2007; 17: 255–259.

Yogeeswari P, Sriram D, Veena V, Kavya R, Rakhra K, Ragavendran JV. Synthesis of aryl semicarbazones as potential anticonvulsant agents. Biomed Pharmacother. 2005; 59:51-55.

Agarwal N and Mishra P. Synthesis of 4-aryl substituted semicarbazones of some terpines as novel anticonvulsants. J Pharm Pharm Sci. 2004; 7:260-264.

Smith MC and Bleck TP. Convulsive Disorders: toxicity of anticonvulsants. Clin Neuropharmacol. 1991; 14:97-115.

Mattson RH. Efficacy and adverse effects of established and new antiepileptic drugs. Epilepsia. 1995; 36(2): S13- S26.

SamrJn EB, van Duijn CM, Koch S, Hiidesmaa VK, Klepel H, Bardy AH, Mannagetta GB, Deichl AW, Gaily E, Granstron ML, Meinardi AH, Grobbee DE, Hofman A, Janz D, Lindhout D. Maternal use of antiepileptic drugs and the risk of major congenital malformations: a joint European prospective study of human teratogenesis associated with material epilepsy. Epilepsia. 1997; 38:981.

Akerele O. Medicinal plants and primary health care: an agenda for action. Fitoter. 1988; LIX: 355-363.

Farnsworth NR. Screening plants for new medicines. In E.O. Wilson, (Ed.), Biodiversity, Part II Washington: National Academy Press; 1989. 83-97 p.

Raza M, Choudary MI, Atta-ur-Rahman. Anticonvulsant medicinal plants. In Atta-urRahman (Ed.), Studies in Natural Product Chemistry Netherlands: Elsevier Science Publishers; 1999. Vol 22: 507-553 p.

Brain KR and Turner TD. The Practical Evaluation of Phytopharmaceuticals. Wright Science Technica. Bristol. 1975. 140-154 p.

Silva LG, Lee IS, Kinghorn DA. Special problem with the extraction of plants. In: Cannell RJP, ed. Natural Products

Isolation. New Jersey, USA: Humana Press Inc; 1998. 343- 364 p.

Evans MC. Textbook of Pharmacognosy (12th ed.) London: Balliere Tindall; 1983. 322-383 p.

Evans MC. Textbook of Pharmacognosy (13th ed.) London: Balliere Tindall; 1996. 247-762 p.

Evans MC. Textbook of Pharmacognosy (15th ed.) London: Balliere Tindall, Singapore: Harcourt Brace and Company Asia Pte. Ltd.; 2002. 13-53, 117-139, 227, 293-334, 471- 511p.

Lorke D. A new approach to practical acute toxicity testing, Arch. of Toxicol., 1983; 54(4): 275-287.

Swinyard EA and Kupferberg HJ. Antiepileptic drugs: detection, quantification and evaluation. Fed Proceed. 1985; 44:39-43.

Browning R. The electroshock model, neuronal network and antiepileptic drugs. In C. M. Faingold and G. H. Fromm (Eds.), Drugs for control of Epilepsy: Actions on neural networks in seizure disorders Boca Raton, FL: CRC Press; 1992. 195-211 p.

Swinyard EA, Woodhead JH, White HS, Franklin MR. General Principles: Experimental selection, quantification and evaluation of anticonvulsants. In R. Levy, R. Mattson,B. Meldrum, J. K. Penry, and F. E. Dreifuss (Eds.), Antiepileptic Drugs New York: Raven Press;1989. 85-103 p.

Porter RJ, Cereghino JJ, Gladding GD. Antiepileptic Drug Development Livingstone: Elselvier science limited; 1984. 515, 550-557, 585 p.

Yamaguchi SI and Rogawski MA. Effects of anticonvulsant drugs on 4-aminopyridine-induced seizure in mice. Epilep Res. 1992; 11:9-16.

Raza M, Shasheen F, Chaudhary MI, Suria A, Attaur- Rahman, Sombati S, DeLorenzo RJ. Anticonvulsant activities of the FSI subfraction isolated from roots of Delphinium denudatum. Phytother Res. 2001; 15:426-430.

Rho JM and Sanker R. The Pharmacological basis of antiepileptic drug action. Epilepsia, 1999; 40:1471-1483.

DeSarro A, Cecchetti V, Fravolin Naocari F, Tabarrini O, DeSarro G. Effects of novel 6-defluroquinolones and Classic quinolones on Pentylenetetrazole-induced seizure in mice. Antimicrob Agents Chemother. 1999; 43:1729-1736.

Loscher W, Honack D, Fassbender CP, Nolting B. The role of technical biological and pharmacological factors in the laboratory evaluation of anticonvulsant drugs III Pentylenetetrazole seizure models. Epilep Res. 1991; 8:171- 189.

Meldrum BS. Update of mechanism of Action of Antiepileptic Drugs. Epilepsia. 1996; 37(6): 6-11.

Larson MD. An analysis of the action of strychnine on the recurrent IPSP and amino acid-induced inhibitions in the cat’s spinal cord. Brain Res. 1969; 15:185-200.

Du W, Bautista JF, Yang H, Diezz-Sampedro A, You SA, Wang L. Calcium-sensitive channelopathy in human epilepsy and paroxysmal movement disorder. Nat Genet. 2005; 37: 733-738.

Wickenden AD. Potassium channels as antiepileptic drug targets. Neuropharmacol. 2002; 43: 1055-1060.