Anticonvulsant Activity of 80% Methanol Leaf Extract and Solvent Fractions of Buddleja polystachya Fresen. (Buddlejaceae) in Mice

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.

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Antioxidant and Anti-Melanogenic Activities of Pakoba Leaves (Syzygium sp) from North Celebes

ICONIET PROCEEDING ◽

10.33555/iconiet.v2i2.15 ◽

2019 ◽

Vol 2 (2) ◽

pp. 79-83

Author(s):

Dela Rosa ◽

Catherine Roeroe ◽

Agustina Susanti

Keyword(s):

Antioxidant Activity ◽

Crude Extract ◽

Leaf Extract ◽

Methanol Extract ◽

Chloroform Fraction ◽

Aqueous Fraction ◽

Ic50 Value ◽

Dpph Method ◽

Good Potential ◽

Crude Methanol Extract

In this research the potential of Pakoba leaf extract to be used as antioxidant and skin whitening (anti-melanogenic agent) is investigated. The antioxidant activity of Pakoba leaves were studied using DPPH method and the result showed that the 80 percent methanol crude extract has strong antioxidant activity with an IC50 value of 22.66 ± 1.02 μg/ml. The aqueous fraction of the sample has an IC50 value of 53.30 ± 1.42 μg/ml, followed by n-butanol fraction (53.63 ± 1.45 μg/ml) and chloroform fraction (511.54 ± 1.59 μg/ml). The anti-melanogenic activity of the crude methanol extract showed IC50 value of 316.56 ± 11.04 μg/ml. Thus, it isconcluded that crude extract of Pakoba leaves shows good potential as the antioxidant source although it does not show good anti- melanogenic activity.

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

Advances in Pharmacological and Pharmaceutical Sciences ◽

10.1155/2021/6689879 ◽

2021 ◽

Vol 2021 ◽

pp. 1-7

Author(s):

Nebeyi Fisseha ◽

Workineh Shibeshi ◽

Daniel Bisrat

Keyword(s):

Anticonvulsant Activity ◽

Bark Extract ◽

Anticonvulsant Effect ◽

Chloroform Fraction ◽

Therapeutic Effects ◽

Maximal Electroshock ◽

Root Bark ◽

Aqueous Fraction ◽

Potential Source ◽

Substantial Morbidity

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.

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Evaluation of the antidiarrheal activity of 80% methanol extract and solvent fractions of the leaf of Bersama abyssinica fresen (Melianthaceae) in mice

BMC Complementary Medicine and Therapies ◽

10.1186/s12906-021-03498-6 ◽

2022 ◽

Vol 22 (1) ◽

Author(s):

Mihret Ayalew ◽

Azmeraw Bekele ◽

Mestayet Geta Mengistie ◽

Seyfe Asrade Atnafie

Keyword(s):

Crude Extract ◽

Intestinal Motility ◽

Castor Oil ◽

Negative Control ◽

Experimental Models ◽

Chloroform Fraction ◽

Traditional Use ◽

Aqueous Fraction ◽

Antidiarrheal Activity

Abstract Introduction The use of traditional medicinal plants in the management of diarrhea has long been practiced in Ethiopia. B. abyssinica fresen is one of the plants traditionally used to treat diarrhea whereas an in vivo study had not yet been conducted. Thus, this study aimed to evaluate the antidiarrheal activity of crude extract and solvent fractions of the leaf of B. abyssinica in mice. Methods Cold maceration within 80% methanol was used to extract the leaf powder and extract of the leaf was fractionated using n-hexane, chloroform, and distilled water. The in vivo antidiarrheal activity of crude extracts and solvent fractions were tested in experimental models of castor oil-induced diarrhea, enteropooling, and antimotility test. Five groups each with 6 mice were used under the three antidiarrheal models. Positive controls were treated with loperamide 3 mg/kg and atropine 5 mg/kg and 2% tween 80 was used in the treatment of negative controls. The extract and solvent fractions were administered at doses of 100, 200, and 400 mg/kg. Time of onset of diarrhea, number and weight of total and wet feces, the percent reduction in the number of wet feces, weight and volume of intestinal contents, and percent inhibition of intestinal motility were recorded. Data were analyzed using SPSS version 20. Result Defecation of castor oil-induced diarrheal or loose stools was inhibited (p < 0.01 to p < 0.001) at 200 mg/kg and 400 mg/kg of crude extract and aqueous fraction. The crude extract and the aqueous fraction at three doses (p < 0.01 to p < 0.001), the chloroform fraction at 200 mg/kg and 400 mg/kg (p < 0.01 to p < 0.001), and the n-hexane fraction at 400 mg/kg (p < 0.05) reduced intraluminal fluid accumulation compared with the negative control. Castor oil-induced intestinal motility was significantly suppressed with the three-doses of aqueous fraction (p < 0.05 to p < 0.001), 200 mg/kg and 400 mg/kg of crude extract (p < 0.05 to p < 0.01), 400 mg/kg of chloroform and n-hexane (p < 0.01 to p < 0.001) compared with negative control. Conclusion The crude extract, aqueous, and chloroform fractions of B. abyyssinica leaves have promising anti-diarrheal effects, supporting the plant's traditional use to treat diarrhea.

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In vitro and In vivo Anticonvulsant Effect of Hydroalcoholic Extract of Moringa stenopetala in Mice Models

Journal of Complementary and Alternative Medical Research ◽

10.9734/jocamr/2020/v12i330208 ◽

2021 ◽

pp. 16-23

Author(s):

Samson Sahile Salile ◽

Teferra Abula

Keyword(s):

Crude Extract ◽

Anticonvulsant Activity ◽

Statistical Significance ◽

Southern Ethiopia ◽

P Value ◽

Anticonvulsant Effect ◽

Significant Activity ◽

Moringa Stenopetala

Background: Epilepsy is a debilitating neurological disorder that directly affects approximately 65 million people worldwide. In the search of safe and effective antiepileptics traditional treatment practices are one area of research to obtain novel molecules. Moringa stenopetala root is claimed to be used for epilepsy treatment in Konso area, Southern Ethiopia. But there was no scientific research evidence for the claimed use of the plant. Objective: This study was conducted to explore the anticonvulsant activity of hydro-alcoholic (80% methanol) extract of root of Moringa stenopetala. Methods: The dry residues of the plant extract was used for the test. In vitro 0Mg2+ mice model at dose 0.7 mg/kg of extract, diazepam(3μM) and untreated brain slice groups were used to compare the presence of seizure like event (SLE). In vivo pentylenetetrazol (PTZ) model with 85 mg/kg subcutaneously was used to compare the seizure on set time with two extract doses and diazepam 5 mg/kg. The data was presented with mean± standard error. In maximum electric shock (MES) model 54 mA was passed for 0.2 second transauricularly in mice. The mean time of hind limb extension was recorded for doses 400 mg/kg and 800mg/kg of the extract and 10 mg/kg phenytoin. The means were compared for statistical significance using one way ANOVA post hoc LSD whereas proportions were compared using Fishers exact test with P-value < .05. Results: M. stenopetala extract has shown statistically significant anticonvulsant activity in vitro compared to control (P<.05). A positive control, the known anticonvulsant diazepam (3μM), showed significant anticonvulsant activity (P<.05). In vivo MES model showed statistically significant anti-seizure activity at both doses (P<.05). But the crude extract failed to show statistically significant activity at all doses of PTZ model (P>.05). Conclusion: The results of this study showed that crude extract of Moringa stenopetala exhibited anti-convulsant effect both in vitro and in vivo MES models.

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Mentha longifolia lowers blood pressure in anesthetized rats through multiple pathways

Bangladesh Journal of Pharmacology ◽

10.3329/bjp.v11i4.27340 ◽

2016 ◽

Vol 11 (4) ◽

pp. 784 ◽

Cited By ~ 2

Author(s):

Abdul Jabbar Shah ◽

Ishfaq Ali Bukhari ◽

Anwarul Hassan Gilani

Keyword(s):

Blood Pressure ◽

Crude Extract ◽

Video Clip ◽

Chloroform Fraction ◽

Response Curves ◽

Aqueous Fraction ◽

Anesthetized Rats ◽

High K ◽

Mentha Longifolia ◽

Dose Dependent

This study was aimed to investigate the effect of the extract of Mentha longifolia on blood pressure and the possible mechanisms. In anesthetized rats, the crude extract of M. longifolia and aqueous and chloroform fractions caused a dose-dependent fall in mean arterial pressure. Atropine pretreatment abolished the effect of extract and aqueous fraction but did not change that of chloroform fraction. In rabbit aortic rings, crude extract relaxed phenylephrine (1 µM) and high K+ (80 mM) pre-contractions. Chloroform fraction was more potent against high K+, similar to verapamil and caused a rightward shift in the Ca++ concentration-response curves. Aqueous fraction partially relaxed high K+ pre-contractions. In rat aortic rings, crude extract and aqueous fraction-induced endothelium-dependent atropine-sensitive vasodilator effect. Extract and fractions also relaxed high K+ precontractions. In guinea-pig atrial strips, crude extract and chloroform fraction suppressed force and rate of contractions, similar to verapamil. In conclusion, M. longifolia lowers blood pressure through Ca++ channel blockade and atropine-sensitive-NO pathway.Video Clip:<a href="https://youtube.com/v/Fz0MrZ6q2WI">Experiment using aorta:</a> 2 min 35 sec

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In Vitro α-Amylase and α-Glucosidase Inhibitory and Antioxidant Activities of the Crude Extract and Solvent Fractions of Hagenia abyssinica Leaves

BioMed Research International ◽

10.1155/2021/6652777 ◽

2021 ◽

Vol 2021 ◽

pp. 1-9

Author(s):

Zemene Demelash Kifle ◽

Simachew Gidey Debeb ◽

Yaschilal Muche Belayneh

Keyword(s):

Ethyl Acetate ◽

Crude Extract ◽

Antioxidant Activities ◽

Ethyl Acetate Fraction ◽

Maximum Activity ◽

Chloroform Fraction ◽

Aqueous Fraction ◽

Water Fraction ◽

Hagenia Abyssinica

Background. The leaves of Hagenia abyssinica have been used in the management of diabetes mellitus in Ethiopian folk medicine. Thus, this study is aimed at investigating the in vitro α-amylase and α-glucosidase inhibitory and antioxidant activities of the crude extract and solvent fractions of H. abyssinica leaves. Methods. The in vitro α-amylase and α-glucosidase inhibitory and antioxidant activities of the plant extract were assessed using 3,5-dinitrosalicylic acid (DNSA), p-nitro-phenyl-a-D glucopyranoside (p-NPG), and 1,1-diphenyl-2-picrylhydrazyl (DPPH) assays, respectively. Each value of percent inhibition of α-amylase, α-glucosidase, and DPPH scavenging effect was presented as means ± SEM ( n = 3 ). Results. The α-amylase inhibitory activity of the crude extract and solvent fractions was found to be concentration-dependent. The strongest activity was exhibited by the crude extract at the highest concentration with a percentage inhibition of 74.52% (IC50, 14.52 μg/ml) followed by water fraction 68.24% (IC50, 16.31 μg/ml), ethyl acetate fraction 61.57% (IC50, 18.73 μg/ml), and chloroform fraction 56.87% (IC50, 21.57 μg/ml) of H. abyssinica leaves. In the α-glucosidase inhibition assay, the maximum activity was exhibited by the aqueous fraction 62.54% (IC50, 11.67 μg/ml) followed by ethyl acetate fraction 54.97% (IC50, 15.89 μg/ml), crude extract 46.79% (IC50, >16.5 μg/ml), and chloroform fraction 36.44% (IC50, >16.5 μg/ml). In the antioxidant assay, the crude extract exhibited the highest antioxidant activity 86.36% (IC50, 10.25 μg/ml) followed by water fraction 78.59% (IC50, 13.86 μg/ml), ethyl acetate fraction 71.58% (IC50, 16.34 μg/ml), and chloroform fraction 63.65% (IC50, 18.83 μg/ml). Conclusion. This study has revealed that H. abyssinica leaves possess noticeable in vitro α-amylase and α-glucosidase inhibitory and antioxidant activities.

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Antiplasmodial Activity of the Crude Extract and Solvent Fractions of Stem Barks of Gardenia ternifolia in Plasmodium berghei-Infected Mice

Evidence-based Complementary and Alternative Medicine ◽

10.1155/2021/9625169 ◽

2021 ◽

Vol 2021 ◽

pp. 1-16

Author(s):

Dejen Nureye ◽

Muktar Sano ◽

Mesfin Fekadu ◽

Tadesse Duguma ◽

Eyob Tekalign

Keyword(s):

Crude Extract ◽

Plasmodium Berghei ◽

Negative Control ◽

Chloroform Fraction ◽

Oral Toxicity ◽

Aqueous Solvent ◽

Parasite Plasmodium ◽

Evolution Of Resistance

Background. The evolution of resistance to currently used malaria medicines together with the severe economic burden of malaria initiates the search for novel antimalarial drugs. Thus, the present experiment was intended to assess the in vivo antiplasmodial effect of Gardenia ternifolia based on the traditional claims and in vitro antimalarial effect of the plant. Methods. For the crude extraction of stem barks of G. ternifolia, a cold maceration method using hydromethanol as a solvent was employed. The hydroalcoholic extract was then fractionated by three solvents (chloroform, n-butanol, and aqueous solvent) with different polarity indexes. Swiss albino mice infected with the chloroquine-sensitive malaria parasite (Plasmodium berghei) were used in this study. Acute oral toxicity study was done according to standard protocols. Four-day suppressive (hydromethanolic crude extract and solvent fractions), Rane’s (crude extract), and repository (crude extract) tests were used to examine the antiplasmodial effects of the study plant. Results. The chemosuppressive study revealed that all doses of the crude extract and its fractions displayed a significant P < 0.001 inhibition of parasitemia compared with the vehicle (negative control). The crude extract’s highest dose (600 mg/kg) showed the maximum (57.84%) parasitemia suppression during the chemosuppressive test. The crude extract also produced significant P < 0.001 curative and prophylactic effects at all doses in Rane’s and repository tests compared with the negative control. In the 4-day test, the n-butanol fraction produced parasitemia suppression higher than the chloroform fraction but lower than the crude extract. Of these, water fractions demonstrated the lowest chemosuppressive effect. Anthraquinone, alkaloids, flavonoids, saponins, steroids, tannins, and terpenoids were qualitatively detected in the plant material. Conclusion. The current results showed that the hydromethanolic extract and fractions of G. ternifolia stem barks have antiplasmodial action with a high curative effect. Chloroform and n-butanol fractions were more active among the fractions, indicating that the nonpolar and semipolar constituents of the plant are responsible for the antimalarial effects.

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Evaluation of Antiulcer Activity of 80% Methanol Extract and Solvent Fractions of the Root of Croton macrostachyus Hocsht: Ex Del. (Euphorbiaceae) in Rodents

Evidence-based Complementary and Alternative Medicine ◽

10.1155/2020/2809270 ◽

2020 ◽

Vol 2020 ◽

pp. 1-11

Author(s):

Alefe Norahun Mekonnen ◽

Seyfe Asrade Atnafie ◽

Mohammedbirhan A. Wahab Atta

Keyword(s):

Peptic Ulcer ◽

Ethyl Acetate ◽

Crude Extract ◽

Antiulcer Activity ◽

Chloroform Fraction ◽

Sprague Dawley ◽

Aqueous Fraction ◽

Pylorus Ligation ◽

Croton Macrostachyus ◽

Ulcer Model

Background. Peptic ulcer disease causes significant mortality and morbidity. Plant kingdom provides a useful source for the development of new antiulcer agents. Croton macrostachyus is traditionally used to treat peptic ulcer in Ethiopia. This study aimed to evaluate the antiulcer activity of C. macrostachyus root extracts in rodents using different models. Methods. The crude extract was obtained by cold maceration in 80% methanol and fractionated with chloroform, ethyl acetate, and distilled water. The antiulcer activity was evaluated using pylorus ligation-induced ulcer model in Sprague Dawley rats and acidified ethanol-induced ulcer model in Swiss albino mice. The test groups received three doses (100, 200, and 400 mg/kg) of the crude extract and fractions for 7 days before induction of ulcer. Positive controls received omeprazole 30 mg/kg for the pylorus ligation-induced ulcer model and sucralfate 100 mg/kg for the acidified ethanol-induced ulcer model. Negative controls received vehicle (2% tween 80). Results. The crude hydromethanolic extract of C. macrostachyus showed significant (p<0.05) antiulcer activity on both pyloric ligation and HCl/ethanol-induced ulcer in rats and mice. It has antisecretary effect (p<0.001) as well. All three administered doses of chloroform fraction (p<0.05) and only higher doses of ethyl acetate fraction (p<0.05) possessed significant antiulcer activity. In contrast, the aqueous fraction did not have significant antiulcer effect at all tested doses. Conclusion. The present study demonstrated that the crude extract, chloroform, and ethyl acetate fractions possessed significant dose-dependent antiulcer activity.

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COMPARATIVE STUDY OF ANTICONVULSANT EFFECT OF THE LEAVES OF SAPINDUS EMARGINATUS AND ACORUS CALAMUS IN EXPERIMENTALLY INDUCED ANIMAL MODELS OF EPILEPSY

International Journal of Pharmacy and Pharmaceutical Sciences ◽

10.22159/ijpps.2021v13i1.39872 ◽

2021 ◽

pp. 36-39

Author(s):

PRIYADARSHINI SHOUGRAKPAM ◽

ABHISHEK BHATTACHARJEE ◽

NGANGOM GUNINDRO ◽

SANJENBAM RITA

Keyword(s):

Anticonvulsant Activity ◽

Clonic Seizure ◽

Acorus Calamus ◽

Anticonvulsant Effect ◽

Maximal Electroshock ◽

Group V ◽

Gum Acacia ◽

Group I ◽

Seizure Models ◽

Animal Models Of Epilepsy

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.

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ANTICONVULSANT ACTIVITY OF CITRUS MAXIMUS LEAVES IN EXPERIMENTAL ANIMAL MODELS

Asian Journal of Pharmaceutical and Clinical Research ◽

10.22159/ajpcr.2016.v9s3.14576 ◽

2016 ◽

Vol 9 (9) ◽

pp. 97

Author(s):

Nishanta Thakuria ◽

Swarnamoni Das ◽

Babul Dewan

Keyword(s):

Anticonvulsant Activity ◽

Albino Rats ◽

Anticonvulsant Effect ◽

Maximal Electroshock ◽

Dependent Manner ◽

Maximal Electroshock Seizure ◽

Wistar Strain ◽

Seizure Models ◽

Clonic Convulsions ◽

Dose Dependent

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.

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