scholarly journals Evaluation of Anticonvulsant Activity of 80% Methanolic Root Bark Extract and Solvent Fractions of Pentas schimperiana (A. Rich.) Vatke (Rubiaceae) in Swiss Albino Mice

2021 ◽  
Vol 2021 ◽  
pp. 1-7
Author(s):  
Nebeyi Fisseha ◽  
Workineh Shibeshi ◽  
Daniel Bisrat

Background. Epilepsy is one of the most common serious neurological disorders, responsible for substantial morbidity and mortality due to limited efficacy and negative properties of antiepileptic drugs. Medicinal plants are believed to be an important source of new chemical substances with potential therapeutic effects. Pentas schimperiana (A. Rich.) Vatke is a medicinal plant used in Ethiopian traditional medicine for the treatment of epilepsy. However, it lacks scientific investigation on its anticonvulsant activity. Therefore, this study was conducted to evaluate the anticonvulsant activity of 80% methanol root bark extract and solvent fractions of Pentas schimperiana (A. Rich.) Vatke in mice. Methods. Anticonvulsant activity was evaluated by using the pentylenetetrazole and maximal electroshock-induced seizure test. The 80% methanolic root bark extract was subjected to successive fractionation with solvents differing polarity, i.e., chloroform, butanol, and water. The test groups received 100, 200, and 400 mg/kg bodyweight of extract and its solvent fractions. Result. The ME400 and BF400 at the higher dose exhibited a significant ( p < 0.001 ) anticonvulsant effect in both the pentylenetetrazole and maximal electroshock-induced seizure test compared with control. However, chloroform fraction only showed a significant ( p < 0.001 ) anticonvulsant effect in the PTZ-induced seizure test, while aqueous fraction had least anticonvulsant activity in both seizure-induced tests. Phytochemical screening of Pentas schimperiana (A. Rich.) Vatke root bark extract revealed the presence of alkaloids, saponins, flavonoids, phenols, steroids, terpenoids, and tannins. Conclusion. This study indicated that the plant has anticonvulsant activity and is considered as a potential source to develop a new antiepileptic drug.

2021 ◽  
Vol 36 (2) ◽  
pp. 121-130
Author(s):  
Tewodros Agedew ◽  
Teshome Nedi ◽  
Shemsu Umer ◽  
Workineh Shibeshi

Epilepsy is a chronic non-communicable disease characterized by recurrent seizures. According to 2019 WHO report, it affects about 50  million people globally and nearly 80% of them live in low-and middleincome countries. Current antiepileptic drugs have several limitations including lack of response in significant number of patients and intolerable adverse drug reactions. Buddleja polystachya Fresen. (Buddlejaceae) is a medicinal plant used for the treatment of epilepsy in Ethiopian traditional medicine, where the dried leaves are crushed, mixed with local alcoholic beverage and taken orally. Thus, this study was conducted to evaluate the anticonvulsant activity of the 80% methanol leaf extract and solvent fractions of B. polystachya in mice models of seizure. The dried and powdered leaves of B.  polystachya were extracted using cold maceration with 80% methanol (1:5 w/v), and the resulting crude extract was fractionated using chloroform and n-butanol to get chloroform, n-butanol and aqueous fractions. Anticonvulsant activities of B. polystachya crude extract and solvent fractions at doses of 100, 200 and 400 mg/kg were evaluated using pentylenetetrazol (PTZ) and maximal electroshock (MES)–induced seizures in mice (n = 6). In addition, motor coordination effects were assessed using rotarod test. Sodium valproate (200 mg/kg), phenytoin (25 mg/kg) and diazepam (5 mg/kg) were used as standards for PTZ, MES and rotarod tests, respectively. Distilled water or 2% tween 80 was used as negative control. All doses of the crude extract exhibited a significant (p < 0.001) anticonvulsant property in both PTZ and MES tests compared with negative control. Similarly, the n-butanol fraction exerted significant (p < 0.001) anticonvulsant effects in both seizure models. However, the chloroform fraction (200 and 400 mg/kg) showed a significant (p < 0.001) anticonvulsant effect in only PTZ-induced seizure model. The aqueous fraction was devoid of any anticonvulsant activity in both models. The crude extract and fractions did not exert any significant changes in motor coordination. Preliminary phytochemical screening of the crude extract and solvent  fractions revealed the presence of flavonoids, phenols, tannins, steroids, terpenoids and saponins. In conclusion, the results of this study indicated that the plant has a promising anticonvulsant activity and could be considered as a potential source to develop new  anticonvulsant drug.


2008 ◽  
Vol 120 (2) ◽  
pp. 255-258 ◽  
Author(s):  
J. Ya’u ◽  
A.H. Yaro ◽  
M.S. Abubakar ◽  
J.A. Anuka ◽  
I.M. Hussaini

2020 ◽  
Vol 20 (2) ◽  
pp. 144-154
Author(s):  
Olayemi K. Wakeel ◽  
Oluropo B. Awosan ◽  
Oyetunji T. Kolawole ◽  
Akeem A. Ayankunle ◽  
Olukunle J. Onaolapo ◽  
...  

Objective: To determine the potential effect of Pyrenancantha staudtii extract on experimentally induced seizures in mice and to evaluate the role of benzodiazepines, naloxone, and serotonin within these pathways. Methods: Animal behaviours were evaluated using open field, hexobarbitone-induced sleep model, and anticonvulsant activity using picrotoxin-, or strychnine-, or isoniazid-induced convulsions. Attempt to understand the mode of action of the anticonvulsant activity of the plant, three notable antagonists (flumazenil, 3 mg/kg; naloxone 5 mg/kg, i.p., and cyproheptadine, 4 mg/kg, i.p) were used. Results: The results revealed a significant (p < 0.05) reduction in the frequency of rearing and grooming episodes compared with the control. The extract of P. staudtii potentiates the sleeping time of hexobarbitone-induced hypnosis in a dose-related manner. P. staudtii stem bark extracts significantly (p<0.05) prolonged the onset of a seizure and attenuated the duration of seizure in a dose-dependent manner in picrotoxin- and or isoniazid-induced seizures. While, P. staudtii stem bark extract at all doses (100, 200, and 400 mg kg-1) though significantly prolonged the onset of action, but did not confer any significant changes on the duration, as well as mortality in this strychnine-induced seizure model. However, the anticonvulsant activity of the methanolic extract of P. staudtii was significantly reversed following intraperitoneal pre-treatment with flumazenil (GABA receptor antagonist) and naloxone (opioid receptor antagonist) but not cyproheptadine (5-HT2 receptor antagonist) in picrotoxin-induced convulsion. Conclusion: The data obtained suggest that methanol extract of P. staudtii possessed significant anticonvulsant effect, thereby confirming the traditional uses of P. staudtii in the treatment of epilepsy; mechanisms of which could involve the interaction with GABAergic and or opioidergic system.


2014 ◽  
Vol 29 (1) ◽  
pp. 161-165 ◽  
Author(s):  
M. G. Magaji ◽  
M. Mohammed ◽  
R. A. Magaji ◽  
A. M. Musa ◽  
I. Abdu-Aguye ◽  
...  

2018 ◽  
Vol 14 (2) ◽  
pp. 113
Author(s):  
Jamilu Ya’u ◽  
Sani Malami ◽  
Zachariah Bako ◽  
Maimouna Moustapha ◽  
Abdullahi H. Yaro

Author(s):  
PRIYADARSHINI SHOUGRAKPAM ◽  
ABHISHEK BHATTACHARJEE ◽  
NGANGOM GUNINDRO ◽  
SANJENBAM RITA

Objective: To compare anticonvulsant activity of methanol extracts of Sapindus emarginatus (MESE) and Acorus calamus (MEAC) in experimental seizure models in mice. Methods: Hind limb tonic extension (HLTE) in Maximal electroshock (MES) seizure and clonic seizure in Pentylenetetrazol (PTZ) seizure models were assessed. Group I (control) mice received 1% gum acacia in distilled water (1 ml/100 g). Topiramate (50 mg/kg) was administered in group II (standard) animals. Group III and IV mice were treated with 200 and 400 mg/kg of MESE, respectively. Mice in group V and VI were given MEAC at the dose of 200 and 400 mg/kg, respectively. Drugs were given orally suspended in 1% gum acacia suspension (1 ml/100 g) for 7 d. Next day after 1 h of drug administration, the seizure was induced for evaluation. Results: Anticonvulsant property of both extracts was confirmed by reduction (p<0.001) in HLTE phase in MES model; delayed onset of the clonic seizure (p<0.001) and its shortened phase (p<0.001) in PTZ model when compared with the control. MESE-200 mg/kg produced significantly longer (p<0.001) HLTE phase with lower protection (40.34%) among the different doses of the extracts. Clonic seizure onsets and durations in PTZ model were comparable among the different extract-treated groups; however, mortality was higher (66.6%) with MESE-200 mg/kg. Conclusion: Anticonvulsant activity of MESE and MEAC was evident; however, MESE at the dose of 200 mg/kg was less effective.


Author(s):  
Nishanta Thakuria ◽  
Swarnamoni Das ◽  
Babul Dewan

ABSTRACTObjective: To assess the anticonvulsant activity of ethanolic extract of Citrus maximus (EECM) leaves of maximal electroshock seizure (MES) andpentylenetetrazol (PTZ)-induced seizure models on albino (Wistar strain) rats and mice.Methods: Anticonvulsant activity was carried out by MES model and PTZ-induced clonic convulsions model; in each model, albino rats (Wistar strain)of either sex were taken and divided into five groups, each consisting of 6 rats. One group was used as control (3% w/v gum acacia), one as standard(phenytoin), and three groups for the test drug of EECM leaves (doses of 50, 100, and 200 mg/kg) treatment. The reduction in time or abolition of tonicextensor phase of MES-convulsions was recorded for all the animals. In PTZ model, either delay or complete abolition of convulsions in rats treatedwith diazepam and EECM leaves was noted for all the animals.Result: EECM leaves reduced the extensor phase of convulsion in MES in a dose-dependent manner and decrease in the duration of convulsions in PTZmodel with increasing dose. Anticonvulsant activity was seen maximum at the dose of 200 mg/kg.Conclusions: Thus, from the above two seizure models of MES and PTZ, it can be concluded that EECM leaves have got an anticonvulsant effect in anincreasing dose-dependent manner.Keywords: Anticonvulsant, Citrus maximus, Maximal electroshock seizure, Pentylenetetrazol.


Author(s):  
Kayalvizhi M. K. ◽  
Sathiya Vinotha A. T.

Background: The objective of the study was to evaluate the anticonvulsant activity of nicardipine in wistar albino rats.Methods: Anticonvulsant activity of nicardipine in a dose 10 mg/kg, and its effect with the standard drug lamotrigine (5 mg/kg) was studied in a maximal electroshock seizures (MES) experimental animal model.Results: Nicardipine in dose of 10 mg/kg showed significant anticonvulsant effect (p<0.001) and combination with standard drug lamotrigine (p<0.001) also showed more significant anticonvulsant effect in MES model.Conclusions: Nicardipine is having anticonvulsant activity and it also potentiates the anticonvulsant effect of lamotrigine in MES model.


2015 ◽  
Vol 4 (4) ◽  
pp. 231-234
Author(s):  
Kamaluddeen Garba ◽  
◽  
Abdullahi Yaro Hamza ◽  

The current antiseizure drugs present with side effects, some of which can lead to discontinuation of epilepsy pharmacotherapy, and a sizeable number of other drugs being less efficacious. Medicinal plants are used for the treatment of epilepsy in Nigeria. The aim of this study is to evaluate the anticonvulsant activity of the stem bark extract of Trichilia roka in mice and chicks. Anticonvulsant screening was carried using pentylenetetrazole (PTZ), strychnine (STN) and picrotoxin (PCT) induced seizures while Maximal electroshock (MEST) test in day old chicks. Preliminary phytochemical screening of the extracts was carried out on the extract using conventional protocols. The LD50 was determined in mice. The intraperitoneal LD50 was calculated to be 118.32 mg/kg in mice. Flavonoids, tannins, alkaloids, saponins, glycosides, anthraquinones and steroids were found to be present. Significant (p≤0.05) prolongation of the mean onset of seizures was recorded with Trichilia roka (15 and 30 mg/kg) compared with normal saline treated groups in PTZ induced seizures. Trichilia roka at all the doses tested did not significantly reduce the mean recovery time of seizures induced by MEST. The extract at 7.5 and 15 mg/kg prolonged the latency of convulsion induced by STN. The extract failed to show significant prolongation of the latency of seizures induced by picrotoxin. It can then be inferred, that Trichilia roka contained bioactive constituents that are beneficial in petit mal epilepsy and justify their use in Traditional Medicine.


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