Levosulpiride

Last updated
Levosulpiride
Levosulpiride.svg
Clinical data
Trade names Dislep, Sulpepta, others
Other namesL-Sulpiride; S-(–)-Sulpiride; RV-12309
Routes of
administration 		Oral
ATC code
Identifiers
  • N-[[(2S)-1-ethylpyrrolidin-2-yl]methyl]-2-methoxy-5-sulfamoylbenzamide
CAS Number
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
Formula C15H23N3O4S
Molar mass 341.43 g·mol−1
3D model (JSmol)
  • CCN1CCC[C@H]1CNC(=O)C2=C(C=CC(=C2)S(=O)(=O)N)OC
  • InChI=1S/C15H23N3O4S/c1-3-18-8-4-5-11(18)10-17-15(19)13-9-12(23(16,20)21)6-7-14(13)22-2/h6-7,9,11H,3-5,8,10H2,1-2H3,(H,17,19)(H2,16,20,21)/t11-/m0/s1
  • Key:BGRJTUBHPOOWDU-NSHDSACASA-N
   (verify)

Levosulpiride, sold under the brand names Dislep and Sulpepta among others, is a dopamine antagonist medication which is used in the treatment of psychotic disorders like schizophrenia, major depressive disorder, nausea and vomiting, and gastroparesis. [1] [2] [3] [4] It is taken by mouth.

Contents

It is a selective antagonist of the dopamine D2 receptor and an agonist of the serotonin 5-HT4 receptor. [4] [5] Chemically, it is a benzamide and the (S)-(−)-enantiomer of sulpiride. [4]

Levosulpiride is marketed widely throughout the world, including in Europe, South Korea, Latin America, India, and Pakistan. [2] It is not available in the United States or the United Kingdom. [2]

Medical uses

Levosulpiride is used in the treatment of: [3] [1]

Levosulpiride is not currently licensed for treatment of premature ejaculation in the United Kingdom or other European countries. [8]

Side effects

Side effects of levosulpiride include amenorrhea, gynecomastia, galactorrhea, changes in libido, and neuroleptic malignant syndrome. [9] In the United States, as of 2013 only one case of adverse reaction to levosulpiride had been recorded on the FDA Adverse Event Reporting System Database. [8] A case of rapid-onset resistant dystonia caused by low-dose levosulpiride was reported in India. [10]

Pharmacology

Pharmacodynamics

Levosulpiride is a selective dopamine D2 receptor antagonist. [4] The drug has also been found to act as a moderate agonist of the serotonin 5-HT4 receptor. [5] It is said to have antipsychotic, antidepressant, antiemetic, and gastroprokinetic effects. [4]

Chemistry

Levosulpiride is a substituted benzamide derivative. [4] It is the levorotatory enantiomer of sulpiride. [4] Other benzamide derivatives include amisulpride, metoclopramide, tiapride, sultopride, and veralipride, among others.

References

  1. 1 2 "Levosulpiride". AdisInsight. 24 October 2021. Retrieved 22 October 2024.
  2. 1 2 3 "Levosulpiride (International database)". Drugs.com. 6 October 2024. Retrieved 22 October 2024.
  3. 1 2 Mucci A, Nolfe G, Maj M (February 1995). "Levosulpiride: a review of its clinical use in psychiatry". Pharmacol Res. 31 (2): 95–101. doi:10.1016/1043-6618(95)80053-0. PMID   7596960.
  4. 1 2 3 4 5 6 7 Rossi F, Forgione A (February 1995). "Pharmacotoxicological aspects of levosulpiride". Pharmacol Res. 31 (2): 81–94. doi:10.1016/1043-6618(95)80052-2. PMID   7596959.
  5. 1 2 Tonini M, De Giorgio R, Spelta V, Bassotti G, Di Nucci A, Anselmi L, Balestra B, De Ponti F (April 2003). "5-HT4 receptors contribute to the motor stimulating effect of levosulpiride in the guinea-pig gastrointestinal tract". Dig Liver Dis. 35 (4): 244–250. doi:10.1016/s1590-8658(03)00061-6. PMID   12801035.
  6. ↑ Arshad A, Irfan M, Inam M, Hussain NH, Ismail SB (2022). "Levosulpiride for Premature Ejaculation: A Systematic Review and Meta-Analysis". Am J Mens Health. 16 (5) 15579883221124832. doi:10.1177/15579883221124832. PMC   9515538 . PMID   36154321.
  7. ↑ Greco E, Polonio-Balbi P, Speranza JC (August 2002). "Levosulpiride: a new solution for premature ejaculation?". Int J Impot Res. 14 (4): 308–309. doi:10.1038/sj.ijir.3900901. PMID   12152121.
  8. 1 2 Poluzzi E, Raschi E, Koci A, Moretti U, Spina E, Behr ER, et al. (June 2013). "Antipsychotics and torsadogenic risk: signals emerging from the US FDA Adverse Event Reporting System database". Drug Safety. 36 (6): 467–79. doi:10.1007/s40264-013-0032-z. PMC   3664739 . PMID   23553446.
  9. ↑ "Levosulpiride drug information". DrugsUpdate India.
  10. ↑ Naskar S, Nath K (January 2007). "Rapid onset resistant dystonia with low dose of Levosulpiride". British Journal of Psychiatry. 190 (1): 81. doi: 10.1192/bjp.190.1.81a .
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