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DESCRIPTIONHere is an overview of Antipsychotics,starting from basic pathophysiology of Psychosis and Schizophrenia,breifing the Neuropharmacology and lastly introduction of drugs with special reference to side effects and clincal uses.
- 1.NEUROLEPTICS (ANTIPSYCHOTICS) Mohsin Aziz 1
2. ANTIPSYCHOTICS / NEUROLEPTICS Neuroleptic: synonym for antipsychotic drug. Antipsychotics are the drugs currently used in the prevention of psychosis. They have also been termed neuroleptics, because they suppress motor activity and emotionality. Mohsin Aziz 2 3. WHAT IS PSYCHOSIS.???? Mohsin Aziz 3 4. PSYCHOSIS Psychosis (from the Greek , psyche, "mind/soul", and -osis, "abnormal condition or derangement") refers to an abnormal condition of the mind. A syndrome of chronic disordered thinking and disturbed behavior (schizophrenia, mania, depression) The most important types of psychosis are: Schizophrenia Affective disorders (e.g. depression, mania) Organic psychoses (mental disturbances caused by head injury, alcoholism, or other kinds of organic disease). Mohsin Aziz 4 5. Mohsin Aziz 5 6. SCHIZOPHRENIA A chronic mental disorder of a type involving a breakdown in the relation between thought, emotion, and behaviour, leading to faulty perception, inappropriate actions and feelings, withdrawal from reality and personal relationships into fantasy and delusion, and a sense of mental fragmentation. The disorder is characterized by a divorcement from reality in the mind of the person (psychosis). Mohsin Aziz 6 7. SYMPTOMS POSITIVE SYMPTOMS: Delusions Hallucinations Combativeness Insomnia Mohsin Aziz 7 8. SYMPTOMS NEGATIVE SYMPTOMS: Affective Flattening (blunt) Alogia Anhedonia Amotivation Apathy Asocial Behavior Mohsin Aziz 8 9. SYMPTOMS DISORGANIZED SYMPTOMS: Disorganized thought,speech, behavior. Poor Attention. Mohsin Aziz 9 10. TYPES OF SCHIZOPHRENIA PARANOID : a person feels extremely suspicious (everyone plotting against me), persecuted (opressed), grandiose ( great), or experiences a combination of these emotions. DISORGANIZED : a person is often incoherent but may not have delusions. CATATONIC : a person is withdrawn, mute, negative and often assumes very unusual postures ( motor symptoms). RESIDUAL : a person is no longer delusion or hallucinating (psychotic), but has no motivation or interest in life. These symptoms can be most devastating. UNDIFFERENTIATED : a person meet the criteria for schizophrenia but cant be classified as a particular type. Mohsin Aziz 10 11. SCHIZOPHRENIA Mohsin Aziz 11 12. Mohsin Aziz 12 13. DOPAMENERGIC SYSTEM: There are four major pathways for the dopamenergic system in brain : I. The Nigro-Striatal Pathway. II. The Mesolimbic Pathway. III. The Mesocortical Pathway. IV. The Tuberoinfundibular Pathway. ETIOLOGY Mohsin Aziz 13 14. Mohsin Aziz 14 15. THE DOPAMINE HYPOTHESIS Schizophrenia results from excess activity of dopamine neurotransmission in Mesolimbic and Mesocortical Pathways because: All antipsychotic drugs block dopamine receptors. Stimulant drugs which act through dopamine can produce schizophrenic- like behaviors (eg.amphetamines). Levodopa, a dopamine precursor, can exacerbate schizophrenic symptoms, or occasionally elicit them in non-schizophrenic patients. Higher levels of dopamine receptors measured in brains of schizophrenics by PET. Brain [DA] increases during psychotic episodes but not during remissions. Mohsin Aziz 15 16. THE DOPAMINE HYPOTHESIS The role of dopamine in Schizophrenia is quite complex : Positive Symptoms are thought to be result of OVERACTIVITY in Mesolimbic pathway ( activating D2 receptors ). While, negative symptoms may result from a DECREASE ACTIVITY in Mesocortical pathway (D1 receptors). Nigrostriatal and Tuberoinfundibular pathways appear to be normal in Schizophrenia. Mohsin Aziz 16 17. GLUTAMATE HYPOTHESIS Glutamate : excitatory Neurotransmitter NMDA Receptors : Ionotropic Glutamate Receptors It is observed that NMDA hypofunction on one hand Decrease DA in Mesocortical Pathway so Increase Negative Symptoms And on the other hand Increase DA in Mesolimbic Pathway , hence, Increase Positive Symptoms. Evidence : NMDA rec Antagonists (Phencyclidine,ketamine) produce both Positive and Negative Psychotic Symptoms. Mohsin Aziz 17 18. SEROTONINE HYPOTHESIS Many effective antipsychotic drugs, in addition to blocking dopamine receptors, also act as 5-HT-receptor antagonists. Many 'atypical antipsychotic drugs produce fewer extrapyramidal side effects than dopamine-selective compounds, as they also combine with 5-HT2A-receptors. Whether 5-HT2A-receptor blockade accounts directly for their antipsychotic effects, or merely reduces undesirable side effects associated with D2-receptor antagonists, remains controversial. Mohsin Aziz 18 19. CLASSIFICATION OF ANTIPSYCHOTIC DRUGS Typical antipsychotics Phenothiazines e.g. chlorpromazine, fluphenazine, thioridazine Butyrophenones e.g. haloperidol, droperidol Thioxanthines e.g. chlorprotixen, thiothixene Atypical antipsychotics Clozapine Risperidone Sulpiride Sertindole Seroquel Olanzapine Quetiapine. Mohsin Aziz 19 20. CLASSIFICATION Distinction between typical and atypical groups is not clearly defined, but rests on: Incidence of extrapyramidal side-effects (less in atypical group) Efficacy in treatment-resistant group of patients Efficacy against negative symptoms. Mohsin Aziz 20 21. DRUG TARGETS Dopamine receptors: D1, D2, D3, D4, D5 Serotonin receptors: 5- HT-1A, 2A, 3, 6, 7 Norepinephrine: -1 & - 2 Muscarinic acetylcholine: mACh-1 & 4 Histamine: H-1 & 2 Dopamine, norepinephrine & serotonin transporters NMDA-glutamate receptor Haloperidol Clozapine Risperidone Olanzapine Quetiapine Ziprasidone 5HT2A D2 D1 Alpha 1 Musc H1 5HT1A (agonist) Casey 1994 Atypical Antipsychotics In Vivo Binding Affinities Mohsin Aziz 21 22. MECHANISM OF ACTION There are many type of DA-receptors (see upper). The antipsychotic drugs probably owe their therapeutic effects mainly to blockade of D2 receptors. The main groups, phenothiazines, thioxanthines and butyrophenones, show preference for D2 over D1 receptors; some newer agents (e.g. remoxipride) are highly selective for D2 receptors, whereas clozapine is relatively non-selective between D1 and D2, but has high affinity for D4. Most striatal neurons have D1 responses and most accumbens neurons have D2 responses. Mohsin Aziz 22 23. MECHANISM OF ACTION Daily treatment with neuroleptics for several weeks produces a reversible cessation of firing of midbrain DA neurons. These inactivated neurons are said to be in a state of depolarization block. The time antipsychotics take for the clinical response to be manifested is thought to correlate with this delayed induction of depolarization blockade of mesolimbic DA neurons. DA-ergic blockade in basal ganglia (nigrostristal pathway) appears to cause the extrapyramidal symptoms, while that in tubero- hypophyseal pathway induces endocrine disorders, and in central trigger zone - is responsible for antiemetic action. Mohsin Aziz 23 24. EFFECTS OF ANTIPSYCHOPTIC DRUGS 1.Central Nervous System : In a psychotic patients they reduce irrational behaviour, agitation and aggressiveness and controls psychotic symptoms. Disturbed thought and behaviour are gradually normalised, anxiety is relieved. Hyperactivity, hallucinations and delusions are suppressed. All phenothiazines, thioxanthenes and butyrophenones have the same antipsychotic efficacy, but potency differs . Chlorpromazine, triflupromazine, thioridazine have low potency, produce more sedation and cause greater potentiation of hypnotics, opioids etc. The sedative effect is produced immediately while antipsychotic effect takes weeks to develop. Moreover, tolerance develops to the sedative but not to the antipsychotic effect. Mohsin Aziz 24 25. EFFECTS OF ANTIPSYCHOPTIC DRUGS antiemetic effect : inhibit chemoreceptor trigger zone or directly depress the medullary vomiting center. temperature-regulating effect : produce hypothermia 2. Autonomic Nervous System : Neuroleptics have varying degrees of --adrenergic blocking activity clorpromazine=triflupromazine>thioridazine> fluphenazine>haloperidol>trifluoperazine>clozapine>pimozide. anticholinergic property of neurolrptics is weak and may be graded as thiridazine>chlorpromazine>triflupromazine>trifluoperazine=haloperido l The phenothiazines have weak H1- antihistaminic and anti-5-HT action as well. Mohsin Aziz 25 26. EFFECTS OF ANTIPSYCHOPTIC DRUGS 3.Local anaesthetic Chlorpromazine : potent a local anaesthetic. However, not used because of its irritant action. 4.Cerebrovascular system Produce hypotension (primarily postural) by -adrenergic blocked. High doses of chlorpromazine : produce ECG changes QT prolongation and suppression of T wave. 5.Endocrine system Increase prolactin : which may result in galactorrhea and gynecomastia. They reduce gonadotropin secretion but amenorrhea and infertility occur only occasionally. ACTH release in response to stress is diminish. Decreased release of ADH may result in an increase in urine volume. Mohsin Aziz 26 27. TYPE MANIFESTATIONS MECHANISM Autonomic nervous system Dry mouth, loss of accommodation; difficulty urinating, constipation Muscarinic blockade Orthostatic hypotension, impotence, failure to ejaculate Alpha adrenergic blockade Central nervous system Parkinsons syndrome; akathisia, dystonia Dopamine receptor blockade Tardive dyskinesia Dopamine receptor supersensitivity Toxic confusional state Muscarinic blockade Endocrine system Galactorrhea; amenorrhea; infertility, impotence Hyperprolactinemia secondary to dopamine receptor blockade Mohsin Aziz 27 28. Mohsin Aziz 28 29. UNWANTED EFFECTS 1.Extrapyramidal reactions include a) Parkinsonism : usually of mild degree responds to anticholinergic drugs or amantadine. b) Akathisia : is a subjective sense of restlessness usually (inability to sit) accompanied by mild to moderate motor hyperactivity, usually responds to -adrenergic receptor antagonists, anticholinergics, antihistamines or amantadine. Mohsin Aziz 29 30. UNWANTED EFFECTS Acu