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- 1.Antipsychotic Drugs Chapter 29OBJECTIVES1. Describe the dopamine hypothesis of schizophrenia. 2. List the major receptors blocked by antipsychotic drugs. 3. Describe the pharmacodynamics of older antipsychotic drugs and relate these characteristics to their clinical uses. 4. Identify the main characteristics and clinical uses of newer atypical antipsychotic drugs. 5. List the major adverse effects of the antipsychotic drugs.
2. Significance of antipsychotics/neuroleptics Introduction of chlorpromazine in 1952 led by the end of the 1950s to emptying psychiatric hospitals back into community, with mixed results The successful treatment of a psychiatric disorder with a drug led to a search for biological mechanisms and development of biological psychiatry 3. Negative Symptoms - AsAffect Flattening Found in about 2/3 of schizophrenic patients Often suggests a poor prognosis Alogia The failure to respond to questions or comments Can also take the form of slow or delayedresponses Avolition Inactivity or early loss of interest in ongoing activity Anhedonia -inability to derive pleasure 4. Dysbindin (??, located pre and post synaptically, glutamate neurotransmission?) COMT(catechol-o-methyl transferase) Neuregulin1 (transmembrane protein many isoforms) Disc1 (neuronal migration, maturation, neurite outgrowth) 5. Antipsychotics (Neuroleptics) The Dopamine Hypothesis3. Antipsychotic drugs block D2 dopaminereceptors 4. Drugs that increase dopaminergic activityproduce or exacerbate schizophrenia 5. Dopamine receptor density is increased inschizophrenia patients 6. PET shows increased D2 receptor density 7. Successful treatment of schizophreniachanges HVA in CSF of patients 6. Correlation between potency ofdopamine blocking drugs andclinical effectsPotency measured asAbility of drug to displace 3H-labeledselective D1 or D2 antagonists fromreceptor (Y-axis)Ability of drug to control symptoms ofschizophrenia 7. Pharmacological effects A. Effects on dopamine systems i. Mesolimbic/ mesocorticalii. Nigrostriataliii. TuberoinfundibularG. Dopamine receptors and their effects i. D1/D5ii. D2/D3/D4 family 8. Antipsychotics Chemical types b) Phenothiazines c) Thioxanthenes d) Butyrophenones e) Miscellaneous structuresTypical antipsychotics Atypical antipsychotics 9. CLOZAPINE: AN EXAMPLE OF AN ATYPICAL NEUROLEPTIC Clozapine (sold as Clozaril, Leponex, Fazaclo; Gen-Clozapine in Canada) was the first of the atypical antipsychotics to be developed. It was approved by the United States Food and Drug Administration (FDA) in 1989 and is the only FDA-approved medication indicated for treatment-resistant schizophrenia and for reducing the risk of suicidal behaviour in patients with schizophrenia. [dubious discuss]Clozapine has been shown to be superior in efficacy in treating schizophrenia. Were it not for its side effects it would be first line treatment; however the rare but potentially lethal side effects of agranulocytosis and myocarditis relegate it to third- line use. Furthermore it may rarely lower seizure threshold, cause hepatic dysfunction, weight gain and be associated with type II diabetes. More common side effects are predominantly anticholinergic in nature, with dry mouth, sedation and constipation. It is also a strong antagonist at different subtypes of adrenergic, cholinergic, histaminergic and serotonergic receptors.Safer use of clozapine requires weekly blood monitoring for around five months followed by four weekly testing thereafter. Echocardiograms are recommended every 6 months to exclude cardiac damage. 10. Charlton BG. If 'atypical' neuroleptics did not exist, it wouldn't be necessary to invent them: perverse incentives in drug development, research, marketing and clinical practice. Medical Hypotheses. 2005; 6: 1005-9. There is now ample evidence to suggest that neuroleptics (aka. anti-psychotics and major tranquillizers) are dangerous drugs, and patients exposure to them should be minimized wherever possible. This clinical imperative applies whether neuroleptics are of the traditional type or atypical variety, albeit for different reasons since the traditional agents are neurotoxic while atypicals are mainly metabolic poisons. Usage of traditional neuroleptics seems indeed to be declining progressively, but the opposite seems to be happening for atypicals, and new indications for these drugs are being promoted. Yet the atypical neuroleptics are a category of pharmaceuticals which are close to being un-necessary since there are safer, cheaper and pleasanter substitutes such as benzodiazepines and the sedative antihistamines (eg. promethazine). In terms of therapeutic value, it therefore seems likely that 'atypicals' are merely an unusually dangerous way of sedating patients. In therapeutic terms these drugs therefore represent a significant backward step. Rationally, the atypicals should now be dropped and replaced with safer sedatives. Potential neuroleptic- substitutes which already exist would include benzodiazepines and sedative antihistamines such as promethazine [4,8]. 11. Clozapine is generally referred to as an "atypical" neuroleptic. What is the difference between "atypical" and "typical" neuroleptics (such as haloperidol)? There is no rigorous line between typical andatypical neurolepticsbut Atypicals have less tendency to producemotor side effects Atypicals produce effects on negativesymptoms of schizophrenia May have effects in therapy-resistantpatients 12. Pharmacological effects A. Effects on dopamine systems i. Mesolimbic/ mesocorticalii. Nigrostriataliii. TuberoinfundibularG. Dopamine receptors and their effects i. D1/D5ii. D2/D3/D4 family 13. Adverse pharmacological effectsa) Behavioural Effects (pseudodepression, akinesia, confusion)b) Neurological Effects (parkinsonism, akathisia, dystonia, tardive dyskinesia)c) Autonomic Effects (orthostatic hypotension, impaired ejaculation)d) Metabolic and Endocrine Effects (weight gain, hyperprolactinemia, loss of libedo, impotence)e) Toxic or allergic effects (agranulocytosis, choleostatic jaundice, clozapine) 14. Adverse pharmacological effects Ocular complications (thioridazine only) Cardiac toxicity (Thioridazine T waveabnormality) Neuroleptic Malignant Syndrome (lifethreatening, marked muscle rigidity,sweating, fever, autonomic instability, bloodpressure, heart rate, muscle breakdown,CV collapse, arrhythmias mortality = 5-12% 15. Pharmacological effects A. Effects on dopamine systems i. Mesolimbic/ mesocorticalii. Nigrostriataliii. TuberoinfundibularG. Dopamine receptors and their effects i. D1/D5ii. D2/D3/D4 family 16. Drug Combinations Combining antipsychotic drugs confounds evaluation of the efficacy of the drugs being used. Use of combinations, however, is widespread, with more emerging experimental data supporting it. Tricyclic antidepressants or, more often, SSRIs may be used with antipsychotics for clear symptoms of depression complicating schizophrenia. Lithium or valproic acid is sometimes added to antipsychotic agents with benefit to patients who do not respond to the latter drugs alone. Clozapine plus lamotrigine developed here in Psychiatry. It is uncertain whether such instances represent misdiagnosed cases of mania or schizoaffective disorder. Sedative drugs may be added for relief of anxiety or insomnia not controlled by antipsychotics.