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ANTICONVULSANT ACTIVITY OF ETHANOLIC EXTRACT OF AEGLE MARMELOS (L.) CORRȆAALONE AND IN COMBINATION WITH PHENYTOIN BY MAXIMAL ELECTROSHOCK INDUCED SEIZURE (MES) IN ALBINO MICE.
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Aim: To evaluate the anticonvulsant activity of ethanolic extract of Aegle marmelos (L.) correa alone and in combination with phenytoin by
maximal electroshock (MES) induced seizure in albino mice. Method: Ethanolic extract of Aegle marmelos (L.) correa (EEAM) was prepared
using Soxhlet apparatus. The anticonvulsant activity of 2 doses of EEAM (200mg/kg and 400mg/kg), standard drug phenytoin (therapeutic dose
20mg/kg, sub therapeutic dose 10mg/kg), combination of EEAM (200mg) and phenytoin (10mg/kg) and combination of EEAM (400mg/kg) and
phenytoin 10mg/kg were evaluated by maximal electroshock induced seizure (MES) model. After 1hr of oral administration of the test drug and
standard drug, the pre-screened albino mice were subjected to MES seizures by electroconvulsiometer with a current of 45mA for 0.2 sec via
transauricular electrodes. Duration of Tonic hind limb extension (THLE) was recorded and percentage protection calculated. Results: EEAM
exhibited signicant anticonvulsant activity in the MES model at doses 200mg/kg and 400mg/kg and also in combination with phenytoin
subtherapeutic dose (10mg/kg) when compared with control group (p< 0.001). Combination of EEAM 400mg/kg and sub therapeutic dose of
phenytoin 10mg/kg exhibited similar anticonvulsant effect when compared with standard therapeutic dose of phenytoin. Conclusion: EEAM
exhibited signicant anticonvulsant activity when given alone and it also potentiates the anticonvulsant activity of sub therapeutic dose of
phenytoin when given in combination in the MES model.
Title: ANTICONVULSANT ACTIVITY OF ETHANOLIC EXTRACT OF AEGLE MARMELOS (L.) CORRȆAALONE AND IN COMBINATION WITH PHENYTOIN BY MAXIMAL ELECTROSHOCK INDUCED SEIZURE (MES) IN ALBINO MICE.
Description:
Aim: To evaluate the anticonvulsant activity of ethanolic extract of Aegle marmelos (L.
) correa alone and in combination with phenytoin by
maximal electroshock (MES) induced seizure in albino mice.
Method: Ethanolic extract of Aegle marmelos (L.
) correa (EEAM) was prepared
using Soxhlet apparatus.
The anticonvulsant activity of 2 doses of EEAM (200mg/kg and 400mg/kg), standard drug phenytoin (therapeutic dose
20mg/kg, sub therapeutic dose 10mg/kg), combination of EEAM (200mg) and phenytoin (10mg/kg) and combination of EEAM (400mg/kg) and
phenytoin 10mg/kg were evaluated by maximal electroshock induced seizure (MES) model.
After 1hr of oral administration of the test drug and
standard drug, the pre-screened albino mice were subjected to MES seizures by electroconvulsiometer with a current of 45mA for 0.
2 sec via
transauricular electrodes.
Duration of Tonic hind limb extension (THLE) was recorded and percentage protection calculated.
Results: EEAM
exhibited signicant anticonvulsant activity in the MES model at doses 200mg/kg and 400mg/kg and also in combination with phenytoin
subtherapeutic dose (10mg/kg) when compared with control group (p< 0.
001).
Combination of EEAM 400mg/kg and sub therapeutic dose of
phenytoin 10mg/kg exhibited similar anticonvulsant effect when compared with standard therapeutic dose of phenytoin.
Conclusion: EEAM
exhibited signicant anticonvulsant activity when given alone and it also potentiates the anticonvulsant activity of sub therapeutic dose of
phenytoin when given in combination in the MES model.
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