Amineptine

From Wikipedia, the free encyclopedia
Jump to: navigation, search
Amineptine
Amineptine.svg
Clinical data
Trade names Survector
Routes of
administration		 Oral
ATC code N06AA19 (WHO)
Legal status
Legal status
Pharmacokinetic data
Metabolism Hepatic
Biological half-life 48 mins (original drug)
2.5 hours (metabolites)[1]
Excretion Renal
Identifiers
CAS Number 57574-09-1 YesY
PubChem (CID) 34870
DrugBank DB04836 YesY
ChemSpider 32091 YesY
UNII 27T1I13L6G YesY
KEGG D07335 YesY
ChEBI CHEBI:32499 YesY
ChEMBL CHEMBL418995 YesY
ECHA InfoCard 100.055.271
Chemical and physical data
Formula C22H28NO2
Molar mass 338.4653 g/mol
3D model (Jmol) Interactive image
  (verify)

Amineptine was developed by the French Society of Medical research in the 1960s.[2] Under the trade-names (Survector, Maneon, Directim, Neolior, Provector, Viaspera) amineptine was used as an atypical tricyclic antidepressant (TCA) that selectively inhibits the reuptake of dopamine[3] and to a lesser extent norepinephrine, in turn producing an antidepressant effect.[4]

Introduced in France in 1978 by the pharmaceutical company Servier[5] and marketed under the trade name Survector, amineptine soon gained a reputation for abuse due to its short-lived, but pleasant, stimulant effect experienced by some patients. (This is to be distinguished from its antidepressant effect, which appears in approximately seven days after commencing treatment.)

After its release into the European market, cases of hepatotoxicity emerged, some serious. This, along with the potential for abuse, led to the suspension of the French marketing authorization for Survector in 1999.[6]

Amineptine was never approved by the U.S. Food and Drug Administration (FDA) for marketing in the United States, meaning that it is not legal to market or sell amineptine for any medical uses in the US.

Therapeutic indications[edit]

Approved[edit]

Amineptine was approved in France for severe clinical depression of endogenous origin in 1978.[7]

Unapproved/off-label/investigational[edit]

Parkinson's Disease, amotivational syndromes, ADHD (Attention Deficit Hyperactivity Disorder)

Mechanism of action[edit]

Amineptine inhibits the reuptake of dopamine and, to a lesser extent, of norepinephrine. There is also some evidence that amineptine additionally acts to selectively induce the presynaptic release of dopamine.[8][9] In addition to its catecholaminergic actions, amineptine is a very weak anticholinergic and antihistamine.

Side effects[edit]

Dermatological[edit]

Severe acne due to amineptine was first reported in 1988 by various authors—Grupper, Thioly-Bensoussan, Vexiau, Fiet, Puissant, Gourmel, Teillac, Levigne, to name a few—simultaneously[10][11][12][13][14] in the same issue of Annales de dermatologie et de vénéréologie and in the 12 March 1988 issue of The Lancet.[15] A year later, Dr Martin-Ortega and colleagues in Barcelona, Spain reported a case of "acneiform eruption" in a 54-year-old woman whose intake of amineptine was described as "excessive."[16] One year after that, Vexiau and colleagues reported six women, one of whom never admitted to using amineptine, getting severe acne concentrated in the face, back and thorax, the severity of which varied with the dosage.[17] Most of them were treated unsuccessfully with isotretinoin (Accutane) for about 18 months; two of the three that discontinued amineptine experienced a reduction in cutaneous symptoms, with the least affected patient going into remission.[17]

Psychiatric[edit]

Psychomotor excitation can very rarely occur with this drug.

Cardiovascular[edit]

Very rarely:

Hepatic[edit]

Amineptine can rarely cause hepatitis, of the cytolytic, cholestatic varieties.[18] Amineptine-induced hepatitis, which is sometimes preceded by a rash, is believed to be due to an allergic reaction.[19] It resolves upon discontinuation of the offending drug.[18] The risk of getting this may or may not be genetically determined.[20]

Additionally, amineptine is known to rarely elevate transaminases, alkaline phosphatase, and bilirubin.[21]

Mixed hepatitis, which is very rare, generally occurs between the 15th and 30th day of treatment. Often preceded by sometimes intense abdominal pains, nausea, vomiting or a rash, the jaundice is variable. Hepatitis is either of mixed type or with cholestatic prevalence. The evolution was, in all the cases, favorable to the discontinuation of the drug. The mechanism is discussed (immunoallergic and/or toxic).[22]

In circa 1994 Spain, there was a case associating acute pancreatitis and mixed hepatitis, after three weeks of treatment.[23]

Lazaros and colleagues at the Western Attica General Hospital in Athens, Greece reported two cases of drug induced hepatitis 18 and 15 days of treatment.[24]

One case of cytolytic hepatitis occurred after ingestion of only one tablet.[25]

Gastrointestinal[edit]

  • Acute pancreatitis (very rare) A case associating acute pancreatitis and mixed hepatitis after three weeks of treatment.[23]

Immunological[edit]

In 1989, Sgro and colleagues at the Centre de Pharmacovigilance[26] in Dijon reported a case of anaphylactic shock in a woman who had been taking amineptine.[27]

Withdrawal[edit]

Pharmacodependence is very common with amineptine compared to other antidepressants.[28] A variety of psychological symptoms can occur during withdrawal from amineptine,[29] such as anxiety and agitation.[30]

Effects on the fetus[edit]

  • Lacking information in humans
  • Non-teratogenic in rodents

Abuse and dependence[edit]

The risk of addiction is low, but exists nonetheless. Between 1978 and 1988, there were 186 cases of amineptine addiction reported to the French Regional Centres of Pharmacovigilance; an analysis of 155 of those cases found that they were predominantly female, and that two-thirds of cases had known risk factors for addiction.[31] However, a 1981 study of known opiate addicts and schizophrenia patients found no drug addiction in any of the subjects.[32] In a 1990 study of eight amineptine dependence cases, the gradual withdrawal of amineptine could be achieved without problems in six people; in two others, anxiety, psychomotor agitation, and/or bulimia appeared.[33]

Precautions for use[edit]

Warnings and precautions before taking amineptine:[34]

Contraindications[edit]

See also[edit]

References[edit]

  1. ^ Lachatre G, Piva C, Riche C, et al. (1989). "Single-dose pharmacokinetics of amineptine and of its main metabolite in healthy young adults". Fundamental & Clinical Pharmacology. 3 (1): 19–26. doi:10.1111/j.1472-8206.1989.tb00026.x. PMID 2714729. 
  2. ^ DE Patent 2011806 - NEW TRICYCLIC DERIVATIVES AND PROCESS FOR THEIR MANUFACTURE
  3. ^ Vaugeois JM, Corera AT, Deslandes A, Costentin J (June 1999). "Although chemically related to amineptine, the antidepressant tianeptine is not a dopamine uptake inhibitor". Pharmacology, Biochemistry, and Behavior. 63 (2): 285–90. doi:10.1016/S0091-3057(98)00242-1. PMID 10371658. 
  4. ^ Dunlop, B.; Nemeroff, C. (2007). "The role of dopamine in the pathophysiology of depression". Archives of General Psychiatry. 64 (3): 327–337. doi:10.1001/archpsyc.64.3.327. PMID 17339521. 
  5. ^ Sittig, Marshall (1 April 1988) [1979]. Pharmaceutical Manufacturing Encyclopedia (2nd ed.). Park Ridge, New Jersey, United States American: William Andrew Publishing/Noyes Publications. ISBN 0-8155-1144-2. Archived from the original on 23 October 2005. Retrieved 29 October 2005. [page needed]
  6. ^ "Docket No. 02N-0101". U.S. Food and Drug Administration. 2002-04-09. Retrieved 2014-01-30. 
  7. ^ Doctissimo (2005). "SURVECTOR - Amineptine" (in French). Retrieved 27 October 2005. 
  8. ^ J. K. Aronson (2009). Meyler's Side Effects of Psychiatric Drugs. Elsevier. pp. 29–. ISBN 978-0-444-53266-4. 
  9. ^ Ceci, A.; Garattini, S.; Gobbi, M.; Mennini, T. (1986). "Effect of long term amineptine treatment on pre- and postsynaptic mechanisms in rat brain". British Journal of Pharmacology. 88 (1): 269–275. doi:10.1111/j.1476-5381.1986.tb09495.x. ISSN 0007-1188. PMC 1917102Freely accessible. PMID 3708219. 
  10. ^ Grupper C (1988). "[New iatrogenic acne: acne caused by amineptin (Survector)]". Annales de dermatologie et de vénéréologie (in French). 115 (11): 1174–6. PMID 2977079. 
  11. ^ Thioly-Bensoussan D, Charpentier A, Triller R, et al. (1988). "[Iatrogenic acne caused by amineptin (Survector). Apropos of 8 cases]". Annales de dermatologie et de vénéréologie (in French). 115 (11): 1177–80. PMID 2977080. 
  12. ^ Vexiau P, Gourmel B, Husson C, et al. (1988). "[Severe lesions of acne type induced by chronic amineptin poisoning: apropos of 6 cases]". Annales de dermatologie et de vénéréologie (in French). 115 (11): 1180–2. PMID 2977081. 
  13. ^ Teillac D, Weber MJ, Lowenstein W, de Prost Y (1988). "[Acne caused by Survector]". Annales de dermatologie et de vénéréologie (in French). 115 (11): 1183–4. PMID 2977082. 
  14. ^ Lévigne V, Faisant M, Mourier C, et al. (1988). "[Monstrous acne in the adult. Inducer role of Survector?]". Annales de dermatologie et de vénéréologie (in French). 115 (11): 1184–5. PMID 2977083. 
  15. ^ Vexiau P, Gourmel B, Julien R, et al. (March 1988). "Severe acne-like lesions caused by amineptine overdose". Lancet. 1 (8585): 585. doi:10.1016/S0140-6736(88)91373-6. PMID 2894512. 
  16. ^ Martín-Ortega E, Zamora E, Herrero C, Palou J (1989). "[Acneiform eruption induced by amineptin (Survector)]". Medicina Cutánea Ibero-latino-americana (in Spanish). 17 (6): 414–6. PMID 2534534. 
  17. ^ a b Vexiau P, Gourmel B, Castot A, et al. (1990). "Severe acne due to chronic amineptine overdose". Archives of Dermatological Research. 282 (2): 103–7. doi:10.1007/BF00493467. PMID 2141246. 
  18. ^ a b Bories P, Pomier-Layrargues G, Chotard JP, et al. (December 1980). "[Amineptine-induced cholestatic hepatitis. 5 cases (author's transl)]". La Nouvelle Presse Médicale (in French). 9 (48): 3689–92. PMID 7454584. 
  19. ^ Pessayre D, Larrey D (April 1988). "Acute and chronic drug-induced hepatitis". Baillière's Clinical Gastroenterology. 2 (2): 385–422. doi:10.1016/0950-3528(88)90009-7. PMID 3044468. 
  20. ^ Larrey D, Pageaux GP (1997). "Genetic predisposition to drug-induced hepatotoxicity". Journal of Hepatology. 26 (Suppl 2): 12–21. doi:10.1016/S0168-8278(97)80492-8. PMID 9204405. 
  21. ^ "Questions au Professeur Daniel Dhumeaux" [Drug-induced liver disorders. Questions for Professor Daniel Dhumeaux]. Gastroentérologie Clinique et Biologique (in French). 23 (8–9): 917–20. 1999. PMID 10533145. 
  22. ^ Concours Med 1982; 104:5733-5734[verification needed]
  23. ^ a b Sebastián Domingo JJ, Simón Marco MA, Uribarrena Echebarría R (March 1994). "Hepatic and pancreatic injury associated with amineptine therapy". Journal of Clinical Gastroenterology. 18 (2): 168–9. doi:10.1097/00004836-199403000-00023. PMID 8189020. 
  24. ^ Lazaros GA, Stavrinos C, Papatheodoridis GV, Delladetsima JK, Toliopoulos A, Tassopoulos NC (1996). "Amineptine induced liver injury. Report of two cases and brief review of the literature". Hepato-gastroenterology. 43 (10): 1015–9. PMID 8884331. 
  25. ^ Jonville AP, Dutertre JP, Autret E (1992). "[Immediate acute hepatic cytolysis after the administration of a single amineptin tablet]". Gastroentérologie Clinique et Biologique (in French). 16 (4): 368. PMID 1397859. 
  26. ^ centres-pharmacovigilance.net Archived 8 February 2012 at the Wayback Machine.
  27. ^ Sgro C, Lacroix S, Waldner A, Lacroix M, Ferrut O, Bureau A (1989). "[Anaphylactic shock caused by amineptine. Report of a case]". La Revue De Médecine Interne (in French). 10 (5): 461–2. doi:10.1016/s0248-8663(89)80054-2. PMID 2488491. 
  28. ^ Blayac, JP.; Hillaire-Buys, D.; Peyrière, H. (1997). "[Pharmacovigilance of new antidepressants: evaluation of neuro-psychobehavioral disorders]". Therapie. 52 (2): 117–22. PMID 9231505. 
  29. ^ Castot, A.; Benzaken, C.; Wagniart, F.; Efthymiou, ML. (1990). "[Amineptin abuse. Analysis of 155 cases. An evaluation of the official cooperative survey of the Regional Centers of Pharmacovigilance]". Therapie. 45 (5): 399–405. PMID 2260032. 
  30. ^ Bertschy, G.; Luxembourger, I.; Bizouard, P.; Vandel, S.; Allers, G.; Volmat, R. (1990). "[Amineptin dependence. Detection of patients at risk. Report of 8 cases]". Encephale. 16 (5): 405–9. PMID 2265603. 
  31. ^ Castot A, Benzaken C, Wagniart F, Efthymiou ML (1990). "[Amineptin abuse. Analysis of 155 cases. An evaluation of the official cooperative survey of the Regional Centers of Pharmacovigilance]". Thérapie (in French). 45 (5): 399–405. PMID 2260032. 
  32. ^ Deniker P, Lôo H, Zarifian E, et al. (1981). "[Amineptine and amotival syndrome (author's transl)]". L'Encéphale (in French). 7 (1): 59–64. PMID 7227285. 
  33. ^ Bertschy G, Luxembourger I, Bizouard P, Vandel S, Allers G, Volmat R (1990). "[Amineptin dependence. Detection of patients at risk. Report of 8 cases]". L'Encéphale (in French). 16 (5): 405–9. PMID 2265603. 
  34. ^ Amineptine Medication - Uses, Side Effects and Precautions of Amineptine. Health-care-information.org. Retrieved on September 28, 2013
Retrieved from "https://en.wikipedia.org/w/index.php?title=Amineptine&oldid=755365921"