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Tetrabenazine



Tetrabenazine
Systematic (IUPAC) name
1,3,4,6,7,11b-Hexahydro- 9,10-dimethoxy-3- (2-methylpropyl)- 2H-benzo[a]quinoline; Ro-1-9569
Identifiers
CAS number 58-46-8
ATC code N05AK01
PubChem 6018
Chemical data
Formula C19H27NO3 
Mol. mass 317.427
Pharmacokinetic data
Bioavailability  ?
Metabolism  ?
Half life  ?
Excretion  ?
Therapeutic considerations
Pregnancy cat.

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Legal status

Orphan drug

Routes tablets: 25 mg

Tetrabenazine is a drug for the symptomatical treatment of hyperkinetic movement disorder and is marketed under the trade names Nitoman® in Canada and Xenazine® in New Zealand and some parts of Europe, and is also available in the USA as an orphan drug. On December 6, 2007 an advisory committee to the U.S. Food and Drug Administration (FDA) voted unanimously to recommend the approval of tetrabenazine, which would be the first drug approved in the United States to treat chorea associated with Huntington disease (HD). The compound is known since the 1950s. Tetrabenazine works mainly as a VMAT-inhibitor[1] and as such promotes the early metabolic degradation of the neurotransmitter dopamine.

Contents

Common uses

Tetrabenazine is used as a treatment, but not a cure for hyperkinetic disorders[2] such as:

Side effects

Because tetrabenazine is closely related to the antipsychotics, many of its side effects are similar. Some of these include:

  • Akathisia (aka "restless pacing" - an inability to keep still, with intense anxiety when forced to do so)
  • Depression - the most common side effect, reported in roughly 15% of those who take the medication
  • Dizziness/drowsiness
  • Parkinsonism

Unlike many of the antipychotics, tetrabenazine is not known to cause Tardive dyskinesia, and in fact can be an effective treatment for the antipsychotic-induced movement disorder.

Warnings

  • Because of the relatively high incidence of depression, it has been recommended that people with a history of depression avoid taking tetrabenazine. Research into this is ongoing however, and this warning may be dropped in the future.
  • The concomitant intake of MAO inhibitors is contraindicated.

References

  1. ^ Guangrong Zheng et al. (2006): "Vesicular Monoamine Transporter 2: Role as a Novel Target for Drug Development", AAPSJ. Fulltext
  2. ^ Jankovic J, Beach J (1997). "Long-term effects of tetrabenazine in hyperkinetic movement disorders.". Neurology 48 (2): 358-62. PMID 9040721.
 
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Tetrabenazine". A list of authors is available in Wikipedia.
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