Antiepileptic Drugs Department of Pharmacology Zhang Yan-mei.

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Presentation transcript:

Antiepileptic Drugs Department of Pharmacology Zhang Yan-mei

Nature of Epilepsy Epilepsy affects about 0.5% of the population. The characteristic event is the seizure, which is often associated with convulsion, but may occur in many other forms. The seizure is caused by an abnormal high- frequency discharge of a group of neurons, starting locally and spreading to a varying extent to affect other parts of the brain.

Nature of Epilepsy Seizures may be partial or generalised depending on the location and spread of the abnormal neuronal discharge. The attack may involve mainly motor, sensory or behavioural phenomena. Unconsciousness occurs when the reticular formation is involved.

Types of Epilepsy Partial seizures –The discharge begins locally, and often remains localised. Produce relatively simple symptoms without loss of consciousness. Two major categories, namely partial and generalised seizures; there is some overlap and many varieties of each.

Types of Epilepsy Generalised seizures –Involve the whole brain, including the reticular system, thus producing abnormal electrical activity throughout both hemispheres. Immediate loss of consciousness.

Nature of Epilepsy Two common forms of generalised epilepsy are the tonic-clonic fit (grand mal) and the absence seizure (petit mal). Status epilepticus is a life- threatening condition in which seizure activity is uninterrupted.

Nature of Epilepsy The neurochemical basis of the abnormal discharge is not well understood. It may be associated with enhanced excitatory amino acid transmission, impaired inhibitory transmission, or abnormal electrical properties of the affected cells. The glutamate content in areas surrounding an epileptic focus is often raised.

Nature of Epilepsy Repeated epileptic discharge can cause neuronal death (excitotoxicity). Current drug therapy is effective in % of patients.

Mechanism of Action Current antiepileptic drugs are thought to act mainly by two main mechanisms:

Mechanism of Action –Reducing electrical excitability of cell membranes, possibly through inhibition of sodium channel. –Enhancing GABA-mediated synaptic inhibition. This may be achieved by an enhanced pre- or post- synaptic action of GABA, by inhibiting GABA-transaminase, or by drugs with direct GABA-agonist properties.

Mechanism of Action A few drugs appear to act by a third mechanism, namely inhibition of T-type calcium channels. Newer drugs act by other mechanism, yet to be elucidated. Drugs that block excitatory amino acid receptors are effective in animal models, but not yet developed for clinical use.

The Major Antiepileptic Drugs The main drugs in current use are: phenytoin, carbamazepine, valproate and ethosuximide. Secondary drugs include: –Phenobarbitone: highly sedative –Various benzodiazepines (e.g. clonazepam); Diazepam used in treating status epilepticus.

Phenytoin Mechanism of Action: acts by stabilizing membranes (1)Blocking voltage-dependence Na + channel (2) Blocking voltage-dependence Ca 2+ channel (3) Inhibiting calcium-induced secretory processes, including release of hormones and neurotransmitters. (4) Inhibiting post tetanic potentiation (PTP).

PHARMACOKINETICS Because phentoin is a weak acid, its intestinal absorption is variable and plasma concentration can vary widely. Monitoring is therefore needed It is metabolized by the microsomal system and is excreted first in the bile and then in the urine.

Therapeutic uses Antiseizure: used in the treatment of grand mal epilepsy and tonic-clonic seizure disorders, not in absence seizures. Treatment on peripheral neuralgia. Antiarrhythmias

Adverse effects Gastrointestinal irritation Ataxia and diplopia. Blood dyscrasias. Gingival hyperplasia, hirsutism, increased collagen proliferation.

Adverse effects Hepatitis. Fetal malformations: fetal hydantion syndrome( 胎儿妥因综合症 ) Drug interactions: increased plasma concentrations of phenytoin can occur by concurrent administration of chloramphenicol( 氯霉素 ), isoniazid (异烟 肼), cimetidine (甲氰咪胍), dicumarol (双香豆素), et al.

Carbamazepine Derivative of tricyclic antidepressants Similar profile to that of phenytoin, but with fewer unwanted effects Effective in most forms of epilepsy (except absence seizures); particularly effective in psychomotor epilepsy; also useful in trigeminal neuralgia and mania.

Carbamazepine Strong inducing agent; therefore many drug interactions Low incidence of unwanted effects; principally sedation, ataxia, mental disturbances, water retention

Valproate Valproate is very effective against absence seizure. Mechanism: facilitate glutamic acid decarboxylase; inhibit GABA-transaminase; enhance synaptic responses. some effect on sodium channels Relatively few unwanted effects: anorexia, nausea, teratogenicity, liver damage (rare, but serious)

Ethosuximide The main drug used to treat absence seizures, may exacerbate other forms Acts by blocking T-type Ca 2+ -channels Relatively few unwanted effects, mainly nausea and anorexia. (mental disturbances)

Benzodiazepine Diazepam: preferred drugs for Status epilepticus. Nitrazepam: petit mal,especially myoclonic seizures and infantile spasms. Clonazepam: is one of the most effective in some cases of myoclonic seizures. Used in petit mal and status epilepticus

Barbiturates Phenobarbital, Luminal: is useful in the treatment of generalized tonic-clonic seizures and statue epilepticus. Mechanism:(1) block Ca 2+ currents presynaptic membrane and decrease neurotransmitter release.(2) prolong the openings of the Cl - channel in postsynaptic membrane and decrease it’s response. Adverse effects: sedation, depression, drug interaction.

Clinical Uses of Antiepileptic Drugs Tonic-clonic (grand mal) seizures: carbamazepine preferred because of low incidence of side-effects, phenytoin, valproate. Use of single drug is preferred when possible, because of risk of pharmacokinetic interactions. Partial (focal) seizures: carbamazepine, valproate; clonazepam or phenytoin are alternatives.

Clinical Uses of Antiepileptic Drugs Absence seizures (petit mal): ethosuximide or valproate. Valproate is used when absence seizures coexist with tonic-clonic seizures, since most drugs used for tonic-clonic seizures may worsen absence seizures. Myoclonic seizures: valproate or clonazepam. Status epilepticus: must be treated as an emergency, with diazepam intravenously.

Attentions Selection of an appropriate antiseizure agent Use of single drug Withdrawal Toxicity Fetal malformations