Chlorpromazine chemical structure
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Thorazine

Chlorpromazine was the first antipsychotic drug, used during the 1950s and 1960s. Used as chlorpromazine hydrochloride and sold under the tradenames Largactil® and Thorazine®, it has sedative, hypotensive and antiemetic properties as well as anticholinergic and antidopaminergic effects. It has also anxiolytic (alleviation of anxiety) properties. Today, chlorpromazine is considered a typical antipsychotic. more...

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Chemistry

Chlorpromazine is derived from phenothiazine, its chemical name is 2-chloro-10- phenothiazine monohydrochloride and its molecular formula is C17H19ClN2S•HCl. Chlorpromazine has an aliphatic side chain, typical for low to middle potency neuroleptics. The oral bioavailability is estimated to be 30% to 50% due to extensive first pass metabolization in the liver. Its elemination-halflife is 16 to 30 hours. It has many active metabolites (approx. 75 different ones) with greatly varying halflives and own pharmacological profiles. The CYP-450 isoenzymes 1A2 and 2D6 are needed for metabolization of chlorpromazine and the subtype 2D6 is inhibited by chlorpromazine (NB: possible interactions with other drugs).

Mechanism of action

Central

Chlorpromazine acts as an antagonist (blocking agent) on different postsysnaptic receptors -on dopaminergic-receptors (subtypes D1, D2, D3 and D4 - different antipsychotic properties on productive and unproductive symptoms), on serotonergic-receptors (5-HT1 and 5-HT2, with anxiolytic, antidepressive and antiaggressive properties as well as an attenuation of extrapypramidal side-effects, but also leading to weight gain, fall in blood pressure, sedation and ejaculation difficulties), on histaminergic-receptors (H1-receptors, sedation, antiemesis, vertigo, fall in blood pressure and weight gain), alpha1/alpha2-receptors (antisympathomimetic properties, lowering of blood pressure, reflex tachycardia, vertigo, sedation, hypersalivation and incontinence as well as sexual dysfunction, but may also attenuate pseudoparkinsonism - controversial) and finally on muscarinic (cholinergic) M1/M2-receptors (causing anticholinergic symptoms like dry mouth, blurred vision, obstipation, difficulty/inability to urinate, sinus tachycardia, ECG-changes and loss of memory, but the anticholinergic action may attenuate extrapyramidal side-effects).

Additionally, Chlorpromazine is a weak presynaptic inhibitor of Dopamine reuptake, which may lead to (mild) antidepressive and antiparkinsonian effects. This action could also account for psychomotor agitation and amplification of psychosis (very rarely noted in clinical use).

Peripheral

Antagonist to H1-receptors (antiallergic effects), H2-recptors (reduction of forming of gastric juice), M1/M2-receptors (dry mouth, reduction in forming of gastric juice) and some 5-HT receptors (different antiallergic/gastrointestinal actions).

Because it acts on so many receptors, chlorpromazine is often referred to as 'dirty drug', whereas the atypical neuroleptic amisulpride e.g. acts only on central D2/D3-receptors and is therefore a 'clean drug'. This distinction expresses no valuation of the drugs.

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Drugs minimally effective for neuropsychiatric symptoms of dementia
From Journal of Family Practice, 5/1/05 by K.M. Sink

Sink KM, Holden KF, Yaffe K. Pharmacological treatment of neuropsychiatric symptoms of dementia. A review of the evidence. JAMA 2005; 293:596-608.

* Clinical Question

How useful are the various pharmacologic agents in the management of neuropsychiatric symptoms of dementia?

* Bottom Line

Pharmacologic agents are minimally, if at all, effective in managing the neuropsychiatric symptoms of dementia. The atypical antipsychotics olanzapine (Zyprexa) and risperidone (Risperdal) are the most effective, but these agents may increase the risk of stroke. The decision to use any of these drugs must be made on the basis of individual circumstances. (LOE=1a-)

Study Design Systematic review

Setting Various (guideline)

Synopsis

Every week it seems as if somebody publishes Neuropsychiatric symptoms of dementia--such as agitation, aggression, delusions, hallucinations, and wandering--increase caregiver stress and lead to an increased risk of hospitalization and nursing home placement. To evaluate the value of various pharmacologic agents in treating these symptoms, the investigators systematically reviewed the English-language literature using Medline, the Cochrane Database of Systematic Reviews, and a manual search of relevant bibliographies. They included only doubleblind placebo-controlled randomized trials or meta-analyses of drug trials of patients with dementia that used measured outcomes, including neuropsychiatric symptoms.

Two authors independently evaluated the quality of each trial and a third served as the final arbitrator when consensus was not reached. From an initial 78 articles reviewed, only 25 randomized controlled trials and 4 meta-analyses met the inclusion criteria. The investigators do not discuss the possibility of publication bias but report informally on the homogeneity of the results.

The atypical antipsychotics, including olanzapine and risperidone, showed modest benefit in reducing agitation/aggression, hallucinations, and delusions. However, the atypical antipsychotics may increase the risk of stroke. There is no clear evidence that typical antipsychotics, such as haloperidol (Haldol), thioridazine (Mellaril), thiothixene (Navane), and chlorpromazine (Thorazine) were useful for treating any neuropsychiatric symptoms. Haloperidol may be slightly useful for reducing aggression, but the adverse effects may outweigh the benefits.

There is no evidence that 1 typical antipsychotic is more efficacious than any other. Trials investigating the use of serotonergic antidepressants reported no efficacy for treating neuro-psychiatric symptoms other than depression, with the exception of i industry-sponsored trial of citalopram (Celexa), which reported a 10-point reduction (out of 168 points) in agitation compared with placebo.

Mood stabilizers (eg, valproate [Depakote] and carbamazepine [Tegretol]) were ineffective.

The available evidence on cholinesterase inhibitors (eg, galantamine [Reminyl], donepezil [Aricept], rivastigmine [Exelon]) shows a small benefit (summary estimate of 1.72-point improvement vs placebo on a scale of 0 to 120). Most of the statistically significant difference was driven by 2 studies on a drug never approved for use by the Food and Drug Administration in the United States because of toxicities.

Memantine (Namenda) may be of some benefit, but the evidence is mixed and unlikely to be clinically significant.

COPYRIGHT 2005 Dowden Health Media, Inc.
COPYRIGHT 2005 Gale Group

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