Английская Википедия:Alpidem

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Шаблон:Short description Шаблон:Cs1 config Шаблон:Infobox drug Alpidem, sold under the brand name Ananxyl, is a nonbenzodiazepine anxiolytic medication which was briefly used to treat anxiety disorders but is no longer marketed.[1] It was previously marketed in France, but was discontinued due to liver toxicity.[1] Alpidem is taken by mouth.[2]

Side effects of alpidem include sedation, fatigue, dizziness, and headache, among others.[1][3][4] It has much less to no impact on cognition, memory, and psychomotor function relative to benzodiazepines.[1][5] Similarly, no rebound anxiety or withdrawal symptoms have been observed with alpidem.[1][3] Rarely, alpidem can cause serious liver toxicity, including liver failure and death.[1] Alpidem is a nonbenzodiazepine of the imidazopyridine family, structurally related to the Z-drug zolpidem,[2] and acts as a GABAA receptor positive allosteric modulator of the benzodiazepine site of the receptor complex.[1] In contrast to zolpidem however, alpidem has anxiolytic effects rather than sedative or hypnotic effects at normal therapeutic doses.[1]

Alpidem was first described by 1982[6][7] and was introduced for medical use in France in 1991.[1][8][9] It was also under development for use in other countries in the 1990s, but development was discontinued and the drug was never marketed in any other country.[8][9] Alpidem was withdrawn from the market in France in 1993 due to liver toxicity.[10][11][12][13][1]

Шаблон:TOC limit

Medical uses

Alpidem was approved for the treatment of generalized anxiety disorder and possibly also other anxiety problems.[1][14][8] By 1990, 17Шаблон:Nbspclinical studies including more than 1,500Шаблон:Nbsppatients had been conducted in Europe studying alpidem for the treatment of anxiety.[3][1] In clinical trials, alpidem demonstrated effectiveness in the treatment of chronic and situational anxiety, including stress-related anxiety, generalized anxiety, and adjustment disorder (situational depression) with anxiety.[3][14] It also showed preliminary effectiveness in institutionalized individuals with chronic psychosis and high anxiety levels.[3][15] The effectiveness of alpidem for panic disorder, on the other hand, is understudied and uncertain.[14][16]

The anxiolytic effects of alpidem are described as rapid, robust, and maintained in the long-term.[1][3] For situational anxiety, the anxiolytic effects of alpidem onset within 1.5 to 2Шаблон:Nbsphours, whereas for chronic anxiety disorders the effects onset within 3 to 5Шаблон:Nbspdays in most cases.[3] No indications of tolerance to its anxiolytic effects or need for dose increases have been observed.[3] In people with anxiety taking alpidem, improvement in mood and sleep have also been found.[4]

The anxiolytic effectiveness of alpidem, for example measured by reductions on the Hamilton Anxiety Rating Scale (HAM-A), was superior to placebo and comparable or equivalent to that of benzodiazepines including diazepam (10–15Шаблон:Nbspmg/day), lorazepam (1–6Шаблон:Nbspmg/day), and clorazepate (30Шаблон:Nbspmg/day) in directly comparative randomized controlled trials.[1][3][4][14] Alpidem has also been directly compared with buspirone (20–30Шаблон:Nbspmg/day) for generalized anxiety disorder.[17] Relative to buspirone, it was found to produce more rapid improvement, to have significantly greater effectiveness, and to have fewer side effects and a lower discontinuation rate.[17]

The recommended dose of alpidem was 75 to 150Шаблон:Nbspmg total per day, given in single doses of 25 to 75Шаблон:Nbspmg two to three times per day.[1][18][19]

Available forms

Alpidem was provided in the form of 50-mg oral tablets.[20]

Side effects

Alpidem is described as well-tolerated.[3] Side effects include sedation (6–8%; dose-dependent), fatigue (3–4%), dizziness (3–4%), and headache (2–3%), among others.[1] It is reported to have minimal sedative effects and to have virtually no negative effects on cognition, memory, and psychomotor function at therapeutic doses.[1][3][4] However, some impairment of vigilance and psychomotor function has been reported at high doses (100–200Шаблон:Nbspmg).[1][3] In addition, driving ability has been studied with alpidem and has been found to be impaired.[21][22] The central side effects of alpidem were found to be no worse in elderly people than in young adults.[1][23]

Alpidem does not alter sleep architecture as measured by electroencephalography.[3] In laboratory tests, 0.9% of patients treated with alpidem showed alterations.[3] No adverse effects on cardiovascular or respiratory function were seen in clinical trials.[3]

No rebound anxiety or withdrawal symptoms have been observed with alpidem after abrupt discontinuation following 4Шаблон:Nbspweeks to 6–12Шаблон:Nbspmonths of treatment.[1][3][4] Conversely, substantial withdrawal symptoms, including rebound anxiety, were observed with lorazepam.[4]

The side effects of alpidem are described as quite different from those of benzodiazepines.[1] In directly comparative trials, alpidem produced similar anxiolytic effects with less fatigue, asthenia, depressive mood, and psychomotor impairment than benzodiazepines, while rates of somnolence and drowsiness were comparable to benzodiazepines but described as milder in severity.[3][4] Whereas benzodiazepines commonly produce dizziness, muscle weakness, fatigue, and sleepiness as side effects, these are not prominent adverse effects with doses of alpidem that have similar anxiolytic effectiveness.[1] The lack of withdrawal or rebound symptoms with alpidem upon discontinuation is also in contrast to benzodiazepines.[3] In addition, alpidem significantly antagonized the amnestic effects of lorazepam and showed similar trends for other cognitive measures in a clinical study in which the two drugs were combined and assessed for interaction.[1][24]

Following marketing authorization in France, several cases of severe liver toxicity were reported in people taking alpidem.[1][25] This resulted in one death and several cases of liver transplantation.[1][25][26] As a result, alpidem was soon withdrawn from the market.[1] The liver toxicity of alpidem was subsequently characterized in preclinical research.[27][28][29][19] It may be related to interactions of alpidem with the translocator protein (TSPO), which is present in high amounts in the liver and which may mediate toxic effects in this tissue.[28][29][17][19]

Overdose

Little information is available on overdose with alpidem.[3] Doses of as high as 300Шаблон:Nbspmg/day, which is 2 to 4Шаблон:Nbsptimes the recommended total daily dose, were assessed in clinical trials.[3][1][30]

Interactions

Alpidem may interact with alcohol, but to a lesser extent than benzodiazepines.[4]

Pharmacology

Pharmacodynamics

Alpidem is a GABAA receptor positive allosteric modulator (GABAkine),[31] specifically acting as an agonist of the benzodiazepine site of the receptor complex (formerly known as the central benzodiazepine receptor (CBR)).[1] In addition to its affinity for the benzodiazepine site of the GABAA receptor (Ki = 1–28Шаблон:NbspnM), alpidem has similarly high affinity for the translocator protein (TSPO) (formerly the peripheral benzodiazepine receptor (PBR)) (Ki = 0.5–7Шаблон:NbspnM).[32][33][34][35][36] Alpidem shows more than 500-fold selectivity for α1 subunit-containing GABAA receptors over α5 subunit-containing GABAA receptors[1] and 80-fold selectivity for α1 subunit-containing GABAA receptors over α3 subunit-containing GABAA receptors.[37] However, alpidem has also been described as potently modulating α1, α2, and α3 subunit-containing GABAA receptors with no effect on α5 subunit-containing GABAA receptors.[38] Findings appear to be mixed on whether alpidem is a partial agonist or a full agonist of the benzodiazepine site of the GABAA receptor.[1] In animals, alpidem has anxiolytic-like effects in some but not all models, weak anticonvulsant effects, and weak or no sedative, amnesic, ataxic, or muscle relaxant effects.[1][5][39][30] High doses of alpidem antagonize the sedative and muscle relaxant effects of diazepam in animals.[39] Flumazenil has been shown to antagonize the anxiolytic and anticonvulsant effects of alpidem in animals.[5] Besides acting directly via the GABAA receptor, interactions with the TSPO might also contribute to the anxiolytic effects of alpidem.[40][32][41][38] This protein mediates promotion of neurosteroidogenesis in the brain, for instance of allopregnanolone.[40][32][41]

Alpidem is structurally related to zolpidem, and both alpidem and zolpidem are GABAA receptor positive allosteric modulators of the benzodiazepine site with preference for α1 subunit-containing receptors.[1][14] Both alpidem and zolpidem have very low affinity for α5 subunit-containing GABAA receptors, in contrast to benzodiazepines.[42][43] Similarly, both alpidem and zolpidem are selective for γ2 subunit-containing GABAA receptors, with very low affinity for γ1 and γ3 subunit-containing GABAA receptors, in contrast to other Z-drugs and to diazepam.[44] Alpidem has very high affinity for the TSPO, while zolpidem has very low affinity for this protein.[14][45][46] The affinity of alpidem for the TSPO (also previously known as the ω3 receptor)[47] was once the highest of any drug known.[45] Although benzodiazepines like diazepam are also known to bind to the TSPO, the affinity of alpidem for this protein is at least 3,000-fold higher in comparison.[45] Whereas zolpidem shows hypnotic and sedative effects and is used to treat insomnia, alpidem shows mainly anxiolytic effects and is used to treat anxiety disorders.[1][14] Alpidem was developed before the widespread use of recombinant GABAA receptors.[1] Hence, its pharmacological profile at the GABAA receptors, including its profile at different subpopulations of these receptors, has never been fully characterized.[1]

The pharmacodynamic mechanisms underlying the anxioselective (anxiolytic-selective) profile of alpidem as a GABAA receptor positive allosteric modulator are unclear.[1][48] In any case, subtype selectivity for different populations of GABAA receptors, partial agonism of the benzodiazepine site of the GABAA receptor, and/or interactions with the TSPO may potentially all be involved.[1][45][5][49][39][50][51] Although anxioselective profiles have been observed for many GABAA receptor positive allosteric modulators in preclinical research, alpidem is the only GABAA receptor positive allosteric modulator for which anxioselective effects have been unambiguously demonstrated in human clinical trials.[1] Ocinaplon has also shown preliminary signs of an anxioselective profile in clinical studies, but development of this agent was discontinued in late-stage trials due to findings of elevated liver enzymes in a small subset of patients.[1] GABAA receptor positive allosteric modulators with selectivity for α2 and α3 subunit-containing GABAA receptors over α1 subunit-containing GABAA receptors, for instance adipiplon, L-838,417, and darigabat—among others, have been and are under investigation as potential anxioselective agents.[1][31][52] However, no such drugs have yet completed clinical development or been marketed for medical use.[31][52][48][38] Despite many developmental failures, alpidem serves as a potential proof of concept that anxioselective GABAA receptor positive allosteric modulators may be possible.[1][48][38] However, if interactions with the TSPO are key to the anxiolytic effects of alpidem, then this may not actually be the case.[41]

Pharmacokinetics

Absorption

Alpidem is taken via oral administration.[2] The absorption of alpidem is rapid and it reaches peak levels after 1.0 to 2.5Шаблон:Nbsphours.[2] Its overall bioavailability is estimated to be approximately 32 to 35%, but no precise value for absolute bioavailability has been determined.[2][3] Absorption of alpidem as indicated by peak and area-under-the-curve levels is linear across a dose range of 25 to 100Шаблон:Nbspmg.[2] Food increases the bioavailability of alpidem by 15 to 20%.[2]

Distribution

Alpidem is a highly lipophilic compound and in animals is extensively distributed into lipid-rich tissues.[2] Similarly, alpidem has been shown to cross the blood–brain barrier in animals, and showed a brain/plasma ratio of about 2.0 to 2.5 following systemic administration.[2] This is related to significantly slower efflux of alpidem from the brain than entry.[2] The active metabolites of alpidem are also brain-penetrant, although occur in the brain at levels lower than those of alpidem.[2] Alpidem may be concentrated more in lipid-rich white matter brain structures than grey matter structures.[2] In humans, the volume of distribution of alpidem is large at 8.7Шаблон:NbspL•kg−1.[2] The plasma protein binding of alpidem is 99.4%, with similar isolated fractions bound to albumin (97.0%) and α1-acid glycoprotein (97.3%).[2] The free fraction of alpidem is slightly higher in people with cirrhosis (0.86 ± 0.06%) and renal failure (0.72 ± 0.03%) relative to normal individuals (0.61 ± 0.05%).[2]

Metabolism

Alpidem is extensively metabolized, including by hydroxylation, dealkylation, and conjugation.[2] Many metabolites of alpidem have been identified, and some of these metabolites may contribute to its pharmacological activity.[2]

Elimination

Alpidem is eliminated mainly in feces, with less than 0.1% excreted in urine.[2] A majority of alpidem is eliminated within 48 to 72Шаблон:Nbsphours following oral dosing.[2] Only trace amounts of unchanged alpidem are found in feces and urine.[2] The metabolites of alpidem are excreted mainly in via the bile in feces, with less than 5% eliminated via urine.[2]

The elimination half-life of alpidem was mean 18.8 ± 0.8Шаблон:Nbsphours (range 7 to 44Шаблон:Nbsphours) following a single 50-mg oral dose given to young individuals.[2] In elderly individuals, a trend toward a longer half-life was observed (22.6 ± 2.3Шаблон:Nbsphours).[2] Conversely, in children age 8 to 12Шаблон:Nbspyears, the half-life of alpidem was considerably reduced (11.4 ± 1.9Шаблон:Nbsphours).[2] The half-lives of alpidem and its metabolites are significantly prolonged in people with hepatic impairment.[2] Conversely, the half-lives of alpidem and its metabolites were unchanged in people with different stages of renal impairment, though plasma concentrations were significantly increased.[2] The clearance of alpidem was estimated to be 0.86 ± 0.04Шаблон:NbspL•h−1•kg−1 in healthy individuals.[2]

Chemistry

Alpidem is a nonbenzodiazepine, and hence is not structurally related to benzodiazepines.[2][53] It is a member of the imidazopyridine group of compounds.[2][14] Alpidem is structurally related to the Z-drug zolpidem, which is also an imidazopyridine.[2][14]

History

Alpidem was developed by Synthélabo Recherche (subsequently Sanofi-Synthélabo and now Sanofi-Aventis).[4][9] It was developed under the code name SL 80.0342 and was first described in the literature by 1982.[54][6][7][8] Alpidem was introduced for medical use in France in 1991.[1][8][9] It was also undergoing development in the 1990s for use in other countries such as the United States and other European countries like Germany, the Netherlands, and Spain.[8] The drug reached phase 3 clinical trials in these countries.[8] However, development in the United States was halted in 1992 due to "divergent results".[55][8] All development in other countries was discontinued by 1999.[8] Alpidem was withdrawn from the market in France in 1993 due to liver toxicity.[10][11][12][13][1] It was never marketed in any other country.[8][54][9]

Society and culture

Names

Alpidem is the generic name of the drug and its Шаблон:Abbrlink, Шаблон:Abbrlink, Шаблон:Abbrlink, and Шаблон:Abbrlink.[6][54] The developmental code name of alpidem was SL 80.0342.[54][8] Alpidem was previously marketed under the brand name Ananxyl.[6][54]

Availability

Alpidem was previously marketed in France, but is no longer available in any country.[1][8][9]

See also

References

Шаблон:Reflist

Further reading

Шаблон:Refbegin

Шаблон:Refend

External links

Шаблон:Anxiolytics Шаблон:GABAA receptor positive allosteric modulators Шаблон:Translocator protein modulators

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Разное

  1. ↑ 1,00 1,01 1,02 1,03 1,04 1,05 1,06 1,07 1,08 1,09 1,10 1,11 1,12 1,13 1,14 1,15 1,16 1,17 1,18 1,19 1,20 1,21 1,22 1,23 1,24 1,25 1,26 1,27 1,28 1,29 1,30 1,31 1,32 1,33 1,34 1,35 1,36 1,37 1,38 1,39 1,40 1,41 1,42 1,43 Шаблон:Cite journal
  2. ↑ 2,00 2,01 2,02 2,03 2,04 2,05 2,06 2,07 2,08 2,09 2,10 2,11 2,12 2,13 2,14 2,15 2,16 2,17 2,18 2,19 2,20 2,21 2,22 2,23 2,24 2,25 2,26 2,27 2,28 2,29 Шаблон:Cite journal
  3. ↑ 3,00 3,01 3,02 3,03 3,04 3,05 3,06 3,07 3,08 3,09 3,10 3,11 3,12 3,13 3,14 3,15 3,16 3,17 3,18 3,19 3,20 Шаблон:Cite journal
  4. ↑ 4,0 4,1 4,2 4,3 4,4 4,5 4,6 4,7 4,8 Шаблон:Cite journal
  5. ↑ 5,0 5,1 5,2 5,3 Шаблон:Cite journal
  6. ↑ 6,0 6,1 6,2 6,3 Шаблон:Cite book
  7. ↑ 7,0 7,1 Шаблон:Cite journal
  8. ↑ 8,00 8,01 8,02 8,03 8,04 8,05 8,06 8,07 8,08 8,09 8,10 8,11 Шаблон:Cite web
  9. ↑ 9,0 9,1 9,2 9,3 9,4 9,5 Шаблон:Cite web
  10. ↑ 10,0 10,1 Шаблон:Cite journal
  11. ↑ 11,0 11,1 Шаблон:Cite web
  12. ↑ 12,0 12,1 Шаблон:Cite news
  13. ↑ 13,0 13,1 WHO Drug Information Vol. 8, No. 2, 1994, page 64
  14. ↑ 14,0 14,1 14,2 14,3 14,4 14,5 14,6 14,7 14,8 Шаблон:Cite journal
  15. ↑ Шаблон:Cite journal
  16. ↑ Шаблон:Cite journal
  17. ↑ 17,0 17,1 17,2 Шаблон:Cite journal
  18. ↑ Шаблон:Cite book
  19. ↑ 19,0 19,1 19,2 Шаблон:Cite web
  20. ↑ Шаблон:Cite journal
  21. ↑ Шаблон:Cite journal
  22. ↑ Шаблон:Cite journal
  23. ↑ Шаблон:Cite journal
  24. ↑ Шаблон:Cite journal
  25. ↑ 25,0 25,1 Шаблон:Cite journal
  26. ↑ Шаблон:Cite journal
  27. ↑ Шаблон:Cite journal
  28. ↑ 28,0 28,1 Шаблон:Cite book
  29. ↑ 29,0 29,1 Шаблон:Cite journal
  30. ↑ 30,0 30,1 Шаблон:Cite journal
  31. ↑ 31,0 31,1 31,2 Шаблон:Cite journal
  32. ↑ 32,0 32,1 32,2 Шаблон:Cite journal
  33. ↑ Шаблон:Cite book
  34. ↑ Шаблон:Cite book
  35. ↑ Шаблон:Cite journal
  36. ↑ Шаблон:Cite journal
  37. ↑ Шаблон:Cite journal
  38. ↑ 38,0 38,1 38,2 38,3 Шаблон:Cite journal
  39. ↑ 39,0 39,1 39,2 Шаблон:Cite journal
  40. ↑ 40,0 40,1 Шаблон:Cite journal
  41. ↑ 41,0 41,1 41,2 Шаблон:Cite journal
  42. ↑ Шаблон:Cite journal
  43. ↑ Шаблон:Cite journal
  44. ↑ Шаблон:Cite journal
  45. ↑ 45,0 45,1 45,2 45,3 Шаблон:Cite journal
  46. ↑ Шаблон:Cite journal
  47. ↑ Шаблон:Cite journal
  48. ↑ 48,0 48,1 48,2 Шаблон:Cite journal
  49. ↑ Шаблон:Cite journal
  50. ↑ Шаблон:Cite journal
  51. ↑ Шаблон:Cite journal
  52. ↑ 52,0 52,1 Шаблон:Cite journal
  53. ↑ Шаблон:Cite journal
  54. ↑ 54,0 54,1 54,2 54,3 54,4 Шаблон:Cite book
  55. ↑ Шаблон:Cite web
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