Sulpiride

Sulpiride

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Systematic (IUPAC) name
(±)-5-(aminosulfonyl)-N-[(1-ethylpyrrolidin-2-yl)methyl]-2-methoxybenzamide
Clinical data
Routes of administration	Oral
Legal status
Legal status	℞ (Prescription only)
Pharmacokinetic data
Bioavailability	25–35%
Biological half-life	7 hours
Identifiers
CAS Number	15676-16-1
ATC code	N05AL01 (WHO) N05AL07
PubChem	CID 5355
DrugBank	APRD00032
Chemical data
Formula	C15H23N3O4S
Molar mass	341.427 g/mol[[]]
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Sulpiride (sold as Meresa, Bosnyl, Dogmatil, Eglonyl, Modal) is an atypical antipsychotic drug used mainly in the treatment of psychosis (e.g. schizophrenia) and depression. It is a substituted benzamide. Sulpiride is more commonly used in Europe and Japan. Levosulpiride is its purified levo- isomer and is sold in India for similar purpose. So far it has not been approved in the United States and Canada. The drug has strong chemical and clinical similarities to the related antipsychotic amisulpride.

Uses and dosage

• Productive psychosis: treatment with rather high doses—in excess of 600 mg daily
• Long-term treatment of negative (unproductive) psychosis: in moderate doses (approx. 600 mg daily)
• Treatment of depression and vertigo: in low to moderate doses (50 to 200 mg daily)
• Levosulpiride has also been promoted as a gastroprokinetic agent

Pharmacology

Pharmacokinetics

Sulpiride is absorbed slowly from the gastrointestinal tract. Its oral bioavailability is only 25 to 35% with marked interindividual differences. The peak plasma concentration is reached 4.5 hours after oral dosing. The usual half-life is 6 to 8 hours. Ninety-two percent is excreted unchanged in the urine. Sulpiride is usually given in 2 or 3 divided doses.

Pharmacodynamics

Sulpiride is a selective antagonist at dopamine D₂ and D₃ receptors. This action dominates in doses exceeding 600 mg daily. In doses of 600 to 1,600 mg sulpiride shows mild sedating and antipsychotic activity. Its antipsychotic potency compared to chlorpromazine is only 0.2 (1/5). In low doses (in particular 50 to 200 mg daily) its prominent feature is antagonism of presynaptic inhibitory dopamine receptors accounting for some antidepressant activity and a stimulating effect. Therefore, it is in these doses used as a second line antidepressant. Additionally, it alleviates vertigo.

The benzamide neuroleptics (including sulpiride, amisulpride, and sultopride) have been shown to activate the endogenous gamma-hydroxybutyrate receptor in vivo at therapeutic concentrations. Sulpiride was found in one study in rats to upregulate GHB receptors. GHB has neuroleptic properties and it is believed binding to this receptor may contribute to the effects of these neuroleptics.

Side effects

Sulpiride has fewer extrapyramidal side effects (dystonia, parkinsonism, tardive dyskinesia, and akathisia) than many of the older antipsychotic medications. Most of these do not seem to occur in a dose related manner. Other side effects occur infrequently (hypotension, rarely long-QT syndrome, dry mouth, sweating, nausea, activation or sedation, insomnia, allergic rash or pruritus). Isolated cases of the potentially life-threatening NMS (neuroleptic malignant syndrome) have been reported. Sulpiride should not be taken after 4 p.m. in order to avoid insomnia. The foremost problem with sulpiride is a strong stimulation of prolactin-secretion; whether this may contribute to the development of breast-cancer in women is currently not known.

• Levodopa : Sulpiride and levodopa have antagonistic effects.
• Alcohol : Sedation and hypotension may be potentiated.
• Antihypertensive agents : Hypotension may be potentiated (risk of postural collapse).
• Other central depressants : Increased sedation with negative impact on the capacity to drive or operate machinery.

Overdose

Sulpiride has a relatively low order of acute toxicity. Substantial amounts may cause severe but reversible dystonic crises with torticollis, protrusion of the tongue, and/or trismus. In some cases all the classical symptoms typical of severe Parkinson's Disease may be noted; in others, over-sedation/coma may occur. The treatment is largely symptomatic. Some or all extrapyramidal reactions may respond to the application of anticholinergic drugs such as biperiden or benztropine. All patients should be closely monitored for signs of long-QT syndrome and severe arrhythmias.

Contraindications and cautions

• Hypersensitivity to sulpiride
• Pre-existing breast cancer or other prolactin-dependent tumors
• Phaeochromocytoma
• Intoxication with other centrally active drugs
• Concomitant use of levodopa
• Caution : Pre-existing Parkinson's Disease
• Caution : Patients below 18 years of age (insufficient clinical data)
• Caution : Pre-existing severe heart disease/bradycardia, or hypokalemia (predisposing to long QT syndrome and severe arrhythmias)
• Caution : Patients with pre-existing epilepsy. Anticonvulsant therapy should be maintained.

Pregnancy and lactation

• Pregnancy: Animal studies did not reveal any embryotoxicity or fetotoxicity, nor did limited human experience. Due to insufficient human data, pregnant women should be treated with sulpiride only if strictly indicated. Additionally, the newborns of treated women should be monitored, because isolated cases of extrapyramidal side effects have been reported.
• Lactation: Sulpiride is found in the milk of lactating women. Since the consequences are unclear, women should not breastfeed during treatment.

See also

• Typical antipsychotic
• Benzamide

References

ar:سلبيريد ru:Сульпирид