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Abdul Waheed 
M.Pharm-Pharmacology 
Department of Pharmacology 
Amity University Noida
Epileptic seizure 
 Epilepsy is a chronic brain disorder 
 characterized by tendency to recurrent seizures or fits. 
 The seizures can leads to loss of consciousness, disturbance of 
movement, muscle spasms, autonomic and mental functions. 
 At least 12 millions people in India and 65 millions of people 
worldwide are affected. 
 Epilepsy affects all the ages, races, sex, education, economic 
status and social classes across all geohraphical boundaries
 As per WHO epilepsy is one of the most common serious brain 
disorders that affects not only the individual, but also has impect 
on family and the society in general. 
 Mechanism of epilepsy is believe to be imbalance in 
neurotransmitter release i.e. abnormally increase the level of 
excitatory neurotransmitter glutamate while decrease in inhibitory 
neurotransmitter GABA. 
 Several types of epilepsy have now been linked to defective 
genes for ion channels that control the flow of ions and regulate 
neuron signalling. 
 During the seizure, neurons may fire 500 times faster than normal 
neuron.
Types of seizures 
Generalised seizures 
 Tonic - clonic 
 Tonic 
 Clonic 
 Atonic 
 Absence 
 Myoclonus 
Focal (partial) seizures 
 Simplex partial 
 Complex partial 
 Partial onset with secondary 
generalisation
Generalised tonic-clonic seizure 
(grand mal) 
 The most common seizure 
 Major epilepsy 
 Last for 1-2 min 
 symptoms: 
 Cry, loss of consciousness, fall 
 Tonic phase- generalised muscle contraction, apnoea 
 Clonic phase- rhythmic contraction of muscles, tongue 
bite, foaming, enuresis 
 Terminal sleep and gradual regaining of consciousness 
(transient confusion)
Absence 
 Cognitive dysfunction with a sudden onset 
 lasting ½ min. 
 Minor epilepsy 
 Stare, expressionless face; arrest of ongoing activity; 
generally no motor phenomena 
 Loss of consciousness 
 EEG shows characteristics 3 cycles per second spike 
and wave pattern. 
 Occurs in genetic (idiopathic) epilepsies, mostly in 
children
Myoclonic seizure 
 Sudden, quick, arrhythmic muscle contraction 
 No loss of consciousness 
 EEG: generalised polyspike and wave activity 
 Occurs in genetic (idiopathic) epilepsies 
 Not only an epileptic phenomenon- it can be the sign 
of diffuse encephalopathies
Atonic seizures 
 Akinetic epilepsy 
 Unconsciousness 
 Relaxation of all muscles due to excessive inhibitory 
discharge 
 Patient may fall
Simplex partial seizures 
 Cortical focal epilepsy 
 Last ½ - 1 min. 
 No loss of consciousness 
 Symptoms depend on area of brain involved: 
 Motor 
 Sensory 
 Autonomic 
 Psychosensory
Complex partial seizures 
 Temporal lob epilepsy 
 Origin is most often in the temporal lobe 
 A common seizure type in adulthood 
 Loss of consciousness: stare, ‘going blank’ 
 Last 1-2 min. 
 Automatisms: 
 oral automatisms 
 fiddling with the hands 
 Confused behaviour and purposeless movements
Experimental models 
 Maximal electroshock method 
50 mA for 0.2 second 
 Pentylenetetrazol (PTZ) clonic seizure 
70mg/kg 
 Chronic focal seizure 
Application of alumina cream on the motor cortex of 
monkey 
 Kindled seizure 
90mk/kg
AEDs 
Old 
 Primidon 
 Phenobarbital 
 Phenytoin 
 Clobazam 
 Clonazepam 
 Ethosuximid 
 Valproate 
 Carbamazepine 
New 
 Lamotrigine 
 Oxcarbazepine 
 Topiramate 
 Gabapentin 
 Felbamate 
 Vigabatrin 
 Levatiracetam 
 Zonisamide 
 Tiagabin
Mechanism of action of AEDs 
Inhibition of voltage gated Na, Ca 
channels 
Na: phenytoin, carbamazepine, 
oxcarbazepine, lamotrigine, 
topiramate, felbamate, zonisamide 
Ca: ethosuximid, valproate? 
lamotrigine, topiramate, zonisamide 
Potentiaton of GABA mediated 
inhibition 
phenobarbital, benzodiazepins, 
vigabatrin, tiagabine, topiramate, 
valproate, gabapentin, felbamate 
Decrease of glutamate mediated 
excitation 
felbamate, topiramate
Side effects of AEDs 
 Allergy 
 Central nervous system side effects (dose dependent) 
 drowsiness, headache 
 dizziness, dysequilibrium 
 cognitive dysfunction (memory) 
 Idiosynchratic reactions / chronic side effects 
 bone marrow suppression 
 hepatic failure 
 rash 
 weight gain, weight loss 
 tremor 
 polycystic ovary syndrome 
 visual field defect
Diagnostic tools 
 Primary diagnosis of epilepsy includes eye–witness and family 
history. 
 Electroencephalograph (ECG) is the cornerstone for diagnosis 
of epilepsy and measures the brain wave activity. 
 Neuroimaging like computed tomography (CT) scan, magnetic 
resonance imaging (MRI) and positron emission tomography 
(PET) techniques are used to diagnose abnormalities in 
structure and function of brain. 
 Video recording is also useful for the monitoring of epileptic 
events.
Myths and Facts 
 Myth: Epilepsy is because of possession by evil sprit and hence 
sorcery is the treatment. 
Fact: Neurological disorder, drugs to treat 
 Myth: Epilepsy is mental illness 
Fact: No, it’s a brain disorder 
 Myth: People with epilepsy are below normal in their intelligence 
Fact: epilepsy does not affect intelligence or memory. 
 Myth: Marriage cure epilepsy 
Fact: off course not! Medicines do. 
 Myth: Seizure can be stopped by giving a key in the hand or 
making a person to smell onion or shoe 
Fact: False, the attack stops on its own and not due to the above 
factors.
References 
 KD Tripathi, Essential of medical pharmacology, jaypee 
publication, 6th edition, p.no. 401. 
 Schmidt D, Schachter S.C.Drug treatment of epilepsy in adults. 
BMJ. 2014 Feb 28;348:g254. 
 Aristea S. Galanopoulou, Merab Kokaia, Jeffrey A. Loeb, Astrid 
Nehlig, Asla Pitkänen, Michael A. Rogawski, Kevin J. 
Staley, Vicky H. Whittemore, and F. Edward Dudek. Epilepsy 
Therapy Development: Technical and Methodological Issues in 
Studies with Animal Model. Epilepsia. Aug 2013; 54(0 4): 13–23.
Epilepsy: Diagnostics, Medications, Myths and Facts

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Epilepsy: Diagnostics, Medications, Myths and Facts

  • 1. Abdul Waheed M.Pharm-Pharmacology Department of Pharmacology Amity University Noida
  • 2. Epileptic seizure  Epilepsy is a chronic brain disorder  characterized by tendency to recurrent seizures or fits.  The seizures can leads to loss of consciousness, disturbance of movement, muscle spasms, autonomic and mental functions.  At least 12 millions people in India and 65 millions of people worldwide are affected.  Epilepsy affects all the ages, races, sex, education, economic status and social classes across all geohraphical boundaries
  • 3.  As per WHO epilepsy is one of the most common serious brain disorders that affects not only the individual, but also has impect on family and the society in general.  Mechanism of epilepsy is believe to be imbalance in neurotransmitter release i.e. abnormally increase the level of excitatory neurotransmitter glutamate while decrease in inhibitory neurotransmitter GABA.  Several types of epilepsy have now been linked to defective genes for ion channels that control the flow of ions and regulate neuron signalling.  During the seizure, neurons may fire 500 times faster than normal neuron.
  • 4. Types of seizures Generalised seizures  Tonic - clonic  Tonic  Clonic  Atonic  Absence  Myoclonus Focal (partial) seizures  Simplex partial  Complex partial  Partial onset with secondary generalisation
  • 5. Generalised tonic-clonic seizure (grand mal)  The most common seizure  Major epilepsy  Last for 1-2 min  symptoms:  Cry, loss of consciousness, fall  Tonic phase- generalised muscle contraction, apnoea  Clonic phase- rhythmic contraction of muscles, tongue bite, foaming, enuresis  Terminal sleep and gradual regaining of consciousness (transient confusion)
  • 6. Absence  Cognitive dysfunction with a sudden onset  lasting ½ min.  Minor epilepsy  Stare, expressionless face; arrest of ongoing activity; generally no motor phenomena  Loss of consciousness  EEG shows characteristics 3 cycles per second spike and wave pattern.  Occurs in genetic (idiopathic) epilepsies, mostly in children
  • 7. Myoclonic seizure  Sudden, quick, arrhythmic muscle contraction  No loss of consciousness  EEG: generalised polyspike and wave activity  Occurs in genetic (idiopathic) epilepsies  Not only an epileptic phenomenon- it can be the sign of diffuse encephalopathies
  • 8. Atonic seizures  Akinetic epilepsy  Unconsciousness  Relaxation of all muscles due to excessive inhibitory discharge  Patient may fall
  • 9. Simplex partial seizures  Cortical focal epilepsy  Last ½ - 1 min.  No loss of consciousness  Symptoms depend on area of brain involved:  Motor  Sensory  Autonomic  Psychosensory
  • 10. Complex partial seizures  Temporal lob epilepsy  Origin is most often in the temporal lobe  A common seizure type in adulthood  Loss of consciousness: stare, ‘going blank’  Last 1-2 min.  Automatisms:  oral automatisms  fiddling with the hands  Confused behaviour and purposeless movements
  • 11. Experimental models  Maximal electroshock method 50 mA for 0.2 second  Pentylenetetrazol (PTZ) clonic seizure 70mg/kg  Chronic focal seizure Application of alumina cream on the motor cortex of monkey  Kindled seizure 90mk/kg
  • 12. AEDs Old  Primidon  Phenobarbital  Phenytoin  Clobazam  Clonazepam  Ethosuximid  Valproate  Carbamazepine New  Lamotrigine  Oxcarbazepine  Topiramate  Gabapentin  Felbamate  Vigabatrin  Levatiracetam  Zonisamide  Tiagabin
  • 13. Mechanism of action of AEDs Inhibition of voltage gated Na, Ca channels Na: phenytoin, carbamazepine, oxcarbazepine, lamotrigine, topiramate, felbamate, zonisamide Ca: ethosuximid, valproate? lamotrigine, topiramate, zonisamide Potentiaton of GABA mediated inhibition phenobarbital, benzodiazepins, vigabatrin, tiagabine, topiramate, valproate, gabapentin, felbamate Decrease of glutamate mediated excitation felbamate, topiramate
  • 14. Side effects of AEDs  Allergy  Central nervous system side effects (dose dependent)  drowsiness, headache  dizziness, dysequilibrium  cognitive dysfunction (memory)  Idiosynchratic reactions / chronic side effects  bone marrow suppression  hepatic failure  rash  weight gain, weight loss  tremor  polycystic ovary syndrome  visual field defect
  • 15. Diagnostic tools  Primary diagnosis of epilepsy includes eye–witness and family history.  Electroencephalograph (ECG) is the cornerstone for diagnosis of epilepsy and measures the brain wave activity.  Neuroimaging like computed tomography (CT) scan, magnetic resonance imaging (MRI) and positron emission tomography (PET) techniques are used to diagnose abnormalities in structure and function of brain.  Video recording is also useful for the monitoring of epileptic events.
  • 16. Myths and Facts  Myth: Epilepsy is because of possession by evil sprit and hence sorcery is the treatment. Fact: Neurological disorder, drugs to treat  Myth: Epilepsy is mental illness Fact: No, it’s a brain disorder  Myth: People with epilepsy are below normal in their intelligence Fact: epilepsy does not affect intelligence or memory.  Myth: Marriage cure epilepsy Fact: off course not! Medicines do.  Myth: Seizure can be stopped by giving a key in the hand or making a person to smell onion or shoe Fact: False, the attack stops on its own and not due to the above factors.
  • 17. References  KD Tripathi, Essential of medical pharmacology, jaypee publication, 6th edition, p.no. 401.  Schmidt D, Schachter S.C.Drug treatment of epilepsy in adults. BMJ. 2014 Feb 28;348:g254.  Aristea S. Galanopoulou, Merab Kokaia, Jeffrey A. Loeb, Astrid Nehlig, Asla Pitkänen, Michael A. Rogawski, Kevin J. Staley, Vicky H. Whittemore, and F. Edward Dudek. Epilepsy Therapy Development: Technical and Methodological Issues in Studies with Animal Model. Epilepsia. Aug 2013; 54(0 4): 13–23.