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PSYC650 Psychopharmacology Antipsychotics And Sedative-Hypnotics How many people with Sz respond well to classical antipsychotics? A little over 80% Roughly 50% About 35% Respond marginally Around 15% Do not respond at all 10 15 % 5% nd ro u bo ut 3 A ou R A gh ly r8 50 % 0% 25% 25% 25% 25% ov e tle lit A 1. 2. 3. 4. Psychopathology Refresher • Positive Symptoms – Classical Antipsychotics • Negative Symptoms – Atypical Antipsychotics • The Dopamine Hypothesis Mechanisms of Action • Classicals are usually D2 and D2-like receptor antagonists • Atypicals antagonize D2-like receptors plus some 5-HTa action – LSD – The serotonin hypothesis of negative symptoms Some Pharmacokinetics • Long half-lives, so a 1ce daily dose usually suffices – Often at night to capitalize on sedating effects • Elders Beware: – Mostly metabolized in liver – Can induce tachycardia – Anticholinergic reactions Other General ADRs • Lowers seizure threshold • Can induce parkinsonian symptoms – Especially Haldol – Can be rectified with anticholinergic drugs • Beware…exacerbation of cholinergic ADRs • Monitor for dry mouth, disorientation, agitation, confusion, etc. • If too bad may need to provide a cholinergic agonist (physostigmine) http://www.youtube.com/watch?v=OVAUDAn7Tco&f eature=related http://www.youtube.com/watch?v=0E7x1mPa3iM&NR=1 Extrapyramidal Side Effects • About 30% of people who take classical antipsychotics – – – – – – – Akathisia (fidgety) Dyskenisia (impaired voluntary movement) Dystonia (muscle spasms in head and neck) Oculogyric crisis (fixed eyeballs) Torticullis (tilted head) Hypersalivation Parkisnonian symptoms Tardive Dyskinesia Tardis • Sometimes irreversible • Anticholiergics sometimes given to prevent EPS can exacerbate tardis Phenothiazines • Early 1950’s • Aliphilactics – Largactil (chlorpromazine—Thorazine) – Fewer ADR but lower in potency • Anticholinergic, TD, EPS, menstrual changes, weight gain • Piperazines – EPS, TD, sometimes anticholinergic, weight changes, orthostatic hypotension, abnormal lactation – prochlorperazine (Compazine) • Excellent antiemetic – Fluphenazine (Prolixin) • Can do shots 1ce-2ce per month Phenothiazines-Piperidines • Includes thioridazine (Mellaril) – Similar to aliphiliactics but less sedating and has fewer EPS – Anticholinergic, weight changes, menstrual, lactation, orthostatic hypotension – Long term-high dose: Lens opacity & Retinal pigmentation (esp bad with Mellaril) Butyrophenones • Droperidol (Inapsine), haloperidol (Haldol) • Similar to phenothiazines, but faster with less ACH • Haldol can be injected as a long-term depot bound substance • Droperidol is effective as an antiemetic – Often given for nasuea associated with anasthesia • EPS, blood disorders, lactation and menstrual difficulties, postural hypotension, sedation, TD Atypicals • Clozapine (Clozaril), olanzapine (Zyprexa), risperidone (Risperdal) • Treatment-resistant clients • Negative symptoms • Fewer ADRs – Anticholinergic, antihistaminic – Serotonin-related symptoms (10-40% patients): constipation, drowsiness, headache, hypersaliation, hypotension, tachycardia – Neutropenia (2% patients) decrease in neutrophil count in blood. Increases susceptibility to bacterial and fungal infections • Fatal! Sedative Hypnotics Uses… • • • • • Depresses CNS Anxiety Sleep disturbances Not for depression-associated anxiety If on stimulant, wait for stimulant effects to wear off – “Wide awake drunk” Dreaming of Drugs • Some sedative hypnotics suppress REM, others suppress N-REM • May be desirable to prescribe a drug that suppresses the stage at which another disorder ‘strikes’ – N-REM: Night terrors – REM: Nocturnal angina • Beware REM rebound Barbiturates • Lots of legends around name – St. Barbara’s day 1903 – “Barbara’s Urates” • Over 2,500 barb’s synthesized and 50 marketed • Now about 10 are “going strong” – Benzo’s knocked them out of the market • Better marketed • Lower abuse potential • Higher TI Barbituarates: Pharmacokinetics and Pharmacodynamics • Vary in potency, depending on lipid solubility – Most lipophilic is thiopental (Pentothal) • Metabolized in liver – Enzyme induction • Probably GABA-ergic – – – – Barb’s bind to receptor near GABA receptor Causes retention of GABA Increases influx of ClInhibiting transmission Barbiturates: ADRs • CNS depression – Normal and transient – Slow breathing, low BP • OD: Respiratory depression, coma, kidney failure, cardiovascular collapse, death • Little use other than sedation – Tolerance can occur in as little as 2 weeks • Sometimes therapeutic adjunct • Paradoxical effect on elderly and young • Can cause insomnia – More frequent and intense dreaming – Angina – Exacerbates gastric ulcers Benzodiazepines • • • • • • • • About a zillion of them Chlordiazepoxide (Librium): prototypic Lorazepam (Ativan) Clonazepam (Klonopin) Diazepam (valium) Alprazolam (xanax) Estazolam (ProSom) Triazolam (Halcion) Mechanism of Action • Probably GABA • Largely in amygdala and thalamus – Probably via Cl- channels Benzo ADRs • • • • • • • • • • Best anxiolytics, buts… REM suppression at high doses Short acting benzo’s may have rebound insomnia Amnestic effects Confusion Motor coordination Disorientation Lethargy Oversedation Some reports of tachycardia Benzo Dependence • Withdrawal comes in 3 phases: 1. Rebound anxiety and insomnia – could last several days, depending on T-1/2 – Starts 1-4 days after drug removal 2. Anxiety, difficulty concentrating, headache, irritability, sleep problems – Lasts about 1-3 weeks 3. Anxiety – May last several months Benzoverdose • May have to administer a BZ antagonist – Flumazenil – T-1/2 of 1 hour • Need to be careful to monitor and readminister as needed • Watch for withdrawal as well Miscellaneous: Chloral Hydrate • • • • • • Knock out drops Quite a few interactions Active metabolite trichloroethanol Tolerance OD potential Severe nausea (take with meals to prevent vomiting) Miscellaneous Others • Buspirone – Only mildly sedating – Serotonergic • Methqualone – High abuse potential – Once thought to be an aphrodesiac T A -H 10 it, 5 hi b In it, G hi b In at e ci lit Fa AB ,5 -H T BA ,G A at e ci lit Fa 1. 2. 3. 4. Benzodiazepines __________ binding at the _____________ receptor Facilitate, GABA 25% 25% 25% 25% Facilitate, 5-HT Inhibit, GABA Inhibit, 5-HT ne s ia ni sm dy s ki ns o ve rd i Ta Pa rk i ka A ys to n th is i ia a Dystonia Akathisia Parkinsonism Tardive dyskinesia D 1. 2. 3. 4. Your patient on Haldol seems agitated, and when he’s not pacing he’s rocking back and forth. 25% 25% 25% 25% What’s most likely? 10