Evaluation of anxiolytic and anticonvulsant potential of Mirabilis jalapa ethanolic extracts on standardized rat models

2021 ◽  
Vol 23 (09) ◽  
pp. 482-495
Author(s):  
M. Kumar ◽  
◽  
G. Thamotharan ◽  
P. Revathi ◽  
S. Shyji ◽  
...  

Anxiety and Convulsion are the most prominent, crippled and cruel neurological diseases in recent times. There are many indigenous plants have beneficial properties to treat mental disease and psychic complaints. Evaluation of anxiolytic and anticonvulsant activity of leaf and root ethanolic extracts of mirabilis jalapa in rat models were carried out using standardized experimental methods. The dried leaves and root was macerated with ethanol separately and administered the discern dose of 200 mg/k g p.o. and 400mg/kg p.o. from each extract and employed in Elevated Plus Maze test (EPM) and Open field test (OFT) with 2mg/kg i.p of Diazepam as a standard drug to assess the anxiolytic activity. Maximal electroshock induced convulsion (MES) (Phenytoin-20mg/kg i.p as a standard drug) and Pentylenetetrazol (PTZ) induced seizures analyzed where Diazepam (5mg/kg) i.p as a standard drug to assess the anticonvulsant activity. Substantial changes in all tested activities EPM, OFT in anxiety model and MES, PTZ in anticonvulsant model were observed. The results revealed that ethanol leaf extract (400 mg/kg p.o.) was more impetus due to the high amount of flavonoid, phenolic compounds, steroids, terpenoid contents possess tremendous anti-anxiety whereas the ethanol root extract (400 mg/kg p.o.) and ethanol leaf extract (400 mg/kg p.o.) produce significant anticonvulsant potential effect compared to the control and standard drug treatment group. This study suggested that the plant M. jalapa is a much more active compound consistent medicinal plant to derive a potent drug against anxiety and convulsion.

Author(s):  
Sushma V. Naidu ◽  
Harsha R. ◽  
Jyothsnya S.

Background: To evaluate the anti-convulsant activity of ethanolic extract of Moringa oleifera (Drum stick leaves) in seizure induced albino mice and to compare it with standard drug Sodium valproate.Methods: Swiss albino mice of either sex weighing around 25-30g were randomly selected and divided into four groups of six mice each. Group 1: control- treated with gum acacia. Group 2: Standard - Valproic acid 40mg/kg body weight. Group 3: T1- ethanolic extract of Moringa oleifera (150mg/kg). Group 4: T2 - ethanolic extract of Moringa oleifera (300mg/kg). All drugs were administered orally one hour prior to induction of seizure. The anticonvulsant activity was screened using maximal electroshock seizure (MES) model and pentylenetetrazole (PTZ) model.Results: Results were analysed by ANOVA followed by Bonferroni’s post hoc test. Abolition of Tonic hind limb extension was taken as the protective end point against MES induced seizures and prolongation of seizure latency in PTZ model.At both the doses the ethanolic extract of Moringa oleifera significantly (p value <0.05) reduced the duration of hind limb extension in MES test and also significantly (p value <0.05) delayed the onset of clonic seizures in PTZ induced convulsion when compared with control group.Conclusions: On comparing the percentage protection offered by Moringa oleifera leaves against both MES and PTZ model, it possesses significant anticonvulsant activity at both doses, with more efficacy at 300mg/kg BW indicating that the test drug can prove a very promising drug for treatment of epilepsy. Further studies are required for isolation and identification of the active constituent.


2020 ◽  
Vol 10 ◽  
pp. 1
Author(s):  
Abdullahi Akanji Murtala ◽  
A. Omoloye Adesina ◽  
Aderonke Aderinola Adeyinka ◽  
Eniola Wasiu Olooto

Epilepsy is the fouth most common brain disorder in the world and about 65 million of the global population are victims. Sadly, the currently available conventional drugs are riddled with numerous side effects, expensive and have not demonstrated adequate capacity in managing this disorder. Hence, the need for safer, cheaper and more effective therapy. This study is aimed at investigating the anticonvulsant activity of the ethanol leaf extract of Uvaria afzelii. Twenty-five (25) mice were randomly allotted to five different groups of five mice each. The animals were treated orally with 100, 200 and 400 mg/kg of the extract respectively and 10 ml/kg of distilled water. The standard group received diazepam (5 mg/kg, i.m). Both strychnine (4 mg/kg, i.p) and picrotoxin (5mg/kg, i.p.) were used to induce convulsion 30 minutes post administration of extract and distilled water, and 15 minutes for standard drug. The onset and duration of convulsion for each mouse were recorded. Mice that did not convulse within 30 min of strychnine and picrotoxin injection were considered protected. The extract (400 mg/kg) significantly (P<0.01) delayed the onset of convulsion with significant reduction (P<0.05) in the duration of seizures induced by picrotoxin with  20% mortality. In the strychnine-induced test, U. afzelii (200 & 400 mg/kg) significantly delayed (p<0.001, 0.0001) the onset of convulsion with mortality of about 40%. Preliminary phytochemical screening revealed the presence of tannins, alkaloids, flavonoids, phenols and saponin. The findings in this study show that the ethanol leaf extract of Uvaria afzelii possesses anticonvulsant activity.


2014 ◽  
Vol 2014 ◽  
pp. 1-9
Author(s):  
Narendra Kumar Singh ◽  
Damiki Laloo ◽  
Debapriya Garabadu ◽  
Tryambak Deo Singh ◽  
Virendra Pratap Singh

The present study was carried out to evaluate the anticonvulsant activity and probable mechanism of action of the methanol root extract from I. frutescens (MEIF) using different experimental animal models. Anticonvulsant activity of the single dose of MEIF (100, 200, and 400 mg/kg, p.o.) was evaluated in maximal electroshock- (MES-), pentylenetetrazole- (PTZ-), and isoniazid- (INH-) induced convulsions models in rats. The levels of γ-amino butyric acid (GABA), glutamate, GABA-transaminase (GABA-T) activity and oxidative stress markers were measured in pretreated rat’s brain homogenate to corroborate the mechanism of observed anticonvulsant activity. MEIF (200–400 mg/kg, p.o.) protected the animals in all the behavioral models used. Pretreatment of MEIF (200–400 mg/kg, p.o.) and diazepam (1.0 mg/kg, i.p.) to the animals in INH-induced convulsion model showed 100% and 80% protection, respectively, as well as significant restoration of GABA and glutamate level in the rat’s brain. MEIF and vigabatrin (50 mg/kg, i.p.) reduced the PTZ-induced increase in the activity of GABA-T (46%) in the brain. Further, MEIF reversed the PTZ-induced increase in lipid peroxidase (LPO) and decrease in reduced glutathione (GSH), catalase (CAT), and superoxide dismutase (SOD) activities. The findings of this study validate the anticonvulsant activity of I. frutescens.


2018 ◽  
Vol 8 (6-s) ◽  
pp. 120-124 ◽  
Author(s):  
Priya Tyagi ◽  
Satish Kumar Sharma ◽  
Pawan Kumar

Glycyrrhiza glabra Linn. is an Indian medicinal plant demonstrated to exert multiple health cures. This plant grows naturally in tropical, subtropical and temperate regions. It is traditionally used as anti-acne, anti-arthritic, anti-convulsant, anti-diabetic, anti-microbial, anti inflammatory, wound healing, anti-oxidant, anti-platelet, anti-stress and nootropic, anti-viral, diuretic and gastroprotective. The antihyperlipidemic effect of ethanolic root extracts of Glycyrrhizaglabrawas studied in wistar rats using High Fat Diet (FD) induced hyperlipidemic model, at the doses of 400 mg/kg body weight. The efficacy of extract was compared with standard drug simvastatin. The ethanolic extracts, significantly decreased the serum lipid profile level in a dose dependent manner in wistar rats. Ethanolic extracts at 400 mg/kg have shown significant antihyperlipidemic action. These results support the fact that this plant is used traditionally as antihyperlipidemic. The study will help in exploring new plant source as an antihyperlipiedemic agent which can minimize the risk and side effects as compared to that of conventional medicine.  Keywords: Glycyrrhizaglabra, Antihyperlipidemic Activity, Simvastatin, High Fat Diet (FD) induced hyperlipidemic model.


Author(s):  
Aaditya Singh ◽  
SHALINI TRIPATHI ◽  
SINGH PN

Objective: Rauvolfia tetraphylla is a plant potentially applicable in Ayurvedic and Unani System of Medicine for the treatment of various diseases. However, the anticonvulsant activity of this plant has not been reported and studied. Therefore, the ethanolic extract of leaf from the plant R. tetraphylla is used to evaluate anticonvulsant activity. Methods: Anticonvulsant activity was screened using maximal electroshock seizure (MES) model and pentylenetetrazole (PTZ)-induced seizure model in Swiss albino mice. The ethanolic extract was also evaluated for rutin and gallic acid content by high-performance thin-layer chromatography studies. Results: Rutin and gallic acid contents were found as 15.60% and 7.81%, respectively. Ethanolic leaf extract (100–800 mg/kg) significantly reduced the duration of seizures which was induced by MES. The same doses also protected animals from PTZ-induced tonic seizures. Conclusion: The study demonstrates that R. tetraphylla plant leaves have significant anticonvulsant activity.


2021 ◽  
Vol 16 (2) ◽  
pp. 85-90
Author(s):  
R.O Imade ◽  
A.P. Uchendu ◽  
A.M. Akhigbemen ◽  
M. Abah

Background: Epilepsy is one of the most common serious neurological disorders. Most antiepileptic or anticonvulsant drugs do not prevent or reverse the pathological process that underlies epilepsy, hence the continuous search for new therapeutic agents with minimal side effects and greater efficacy.Objective: The objectives of this study were to determine the acute toxicity profile and investigate the anticonvulsant activity of volatile oil of Kochia scoparia (Amaranthaceae ).Method: Volatile oil was extracted from fresh leaves of K. scoparia through hydrodistillation process, using a Clavenger-type apparatus. Acute toxicity testing was done using Lorke’s method. The anticonvulsant models used were pentylenetetrazol, strychnine and maximal electroshock. Albino mice were randomly divided into five groups (n=5). Group I (control group) was given 0.2 ml each of water orally while groups II, III and IV received 75, 150 and 300 mg/kg of the volatile oil. Group V received the standard drug solution; 30 mg/kg phenobarbitone for Maximal electroshock and 2 mg/kg diazepam for pentylenetetrazol and strychnine models. The onset of tonic leg extension, duration and protection from mortality were noted.Results: Sub acute toxicity test revealed that doses above 1000mg/kg of the volatile oil is toxic. Doses of 75, 150 and 300 mg/kg significantly (P<0.05) protected the mice against seizures with scores of 20, 20 and 40 % respectively in both Maximal electroshock and pentylenetetrazol induced convulsion models. No protection was offered in strychnine induced convulsion model; P > 0.05.Conclusion: The volatile oil of K. scoparia could be useful in the management of epilepsy.


Author(s):  
Nnama T.N ◽  
Anibueze C.I.P ◽  
Okwara B.O ◽  
Okafor M.C

The emphasis of harmful health challenges caused by preserved food or processed food is a global problem and the need to reduce its effect on the vital organs in the body has been the subject of great concern to researchers. The present study seeks to evaluate the efficacy of ethanolic extracts of Curcuma longa (turmeric) roots and Cassia occidentalis leaves on potassium induced kidney damage in albino rats. Fifty adult male rats weighing about 100g-200g classified into ten groups (I-X) were used in the study. Group1 served as control and were administered only with distilled water and rat feeds ad libitum all throughout the experiment. Group II served as negative (-ve) control and were administered 50mg/kg bodyweight of potassium bromate orally. Groups III, IV, VII and VIII received 50mg/kg bodyweight of potassium bromate for two weeks thereafter received 50mg/kg bodyweight with 500mg and 1000mg/kg body weight of ethanolic root extract of Curcuma longa and leaves extract Cassia occidentalis respectively for two weeks. Groups V, VI, and IX and X received 500mg and 1000mg/kg bodyweight of ethanolic root extract of Curcuma longa and leaves extract Cassia occidentalis for two weeks thereafter received 50mg/kg bodyweight of potassium bromate withethanolic root extract of Curcuma longa and leaves extract Cassia occidentalis respectively for two weeks. The rats at the end of 28 days were anaesthetised, blood samples were collected and the kidneys were harvested. The result of biochemical analysis revealed significant decrease in the level of biochemical parameters following administration of 500mg/ kg and 1000mg/kg body weight of Curcuma longa and Cassia occidentalis ethanolic leaf extract for curative and protective purpose when compared with group II (+ve control) that received 50mg/kg body weight of potassium bromate. Histological findings revealed restoration and protection of the extracts on the kidney architecture of male albino rats. Results obtained thus showed that oral administration of ethanolic root extracts of Curcuma longa and leaf extract of Cassia occidentalis may possess preventive and therapeutic purpose against kidney damage


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.


Author(s):  
Roopa B. ◽  
Janardhan M. ◽  
Venkata Rao Y.

Background: The objective of the study was to evaluate the anticonvulsant activity of amlodipine in albino rats.Methods: Anticonvulsant activity of amlodipine was done in three graded doses (1 mg/kg, 2 mg/kg, 4 mg/kg), and combination group with low dose of amlodipine (1 mg/kg) and standard drug (phenytoin) in maximal electroshock seizures (MES) experimental animal model.Results: Amlodipine in dose of 2, 4 mg/kg showed dose dependent significant anticonvulsant effect and combination of low dose amlodipine and low dose of standard drug also showed significant anticonvulsant effect in MES model.Conclusions: Amlodipine is having anticonvulsant activity and also potentiated the anticonvulsant effect of phenytoin in MES model. 


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