Valproic acid: Difference between revisions

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imported>Howard C. Berkowitz
(Uses in mood disorder and neurogenic pain; side effect of tremor)
imported>Paul Wormer
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{{subpages}}
{{subpages}}
'''Valproic acid''' is a medication that is "a [[fatty acid]] with anticonvulsant properties used in the treatment of [[epilepsy]]; the sodium salt is used in treating [[mood disorders]]. It also is used for [[neurogenic pain]].
{{Chem infobox
|align=right
|image=[[Image:Valproic acid.jpg|center|thumb|175px]]
|width=175px
|molname=valproic acid
|synonyms=Abbott-44089; 2-Propylpentanoic acid; 2-Propylvaleric acid; di-n-dipropylacetic acid
|molformula= C<sub>8</sub>H<sub>16</sub>O<sub>2</sub>
|molmass= 144.2
|uses=anticonvulsant
|properties=fatty acid derivative
|hazards= hepatotoxicity, birth defects, pancreatitis
|iupac=
|casnumber= 99-66-1
}}
'''Valproic acid''' is a medication that is "a [[fatty acid]] with anticonvulsant properties used in the treatment of [[epilepsy]]; the sodium salt is used in treating [[mood disorders]]. It also is used for [[neurogenic pain]]. It is a colorless to pale yellow liquid that is slightly soluble in water (1.2 mg/mL) but fully soluble in [[acetone]], [[chloroform]], [[ether (chemistry)|ether]] and [[methanol]].
 


The mechanisms of its therapeutic actions are not well understood. It may act by increasing [[gamma-aminobutyric acid]] levels in the [[brain]] or by altering the properties of voltage dependent sodium channels."<ref>{{MeSH}}</ref>
The mechanisms of its therapeutic actions are not well understood. It may act by increasing [[gamma-aminobutyric acid]] levels in the [[brain]] or by altering the properties of voltage dependent sodium channels."<ref>{{MeSH}}</ref>
== Side effects ==
== Side effects ==
Valproic acid causes [[carnitine]] deficiency. All patients under valproate therapy should have their carnitine status monitored. Since available tests are not reliable indicators of carnitine status in tissues, prophylactic carnitine therapy can be considered. Intravenous carnitine is markedly
Valproic acid causes [[carnitine]] deficiency. All patients under valproate therapy should have their carnitine status monitored. Since available tests are not reliable indicators of carnitine status in tissues, prophylactic carnitine therapy can be considered. Intravenous carnitine is markedly
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Benign hand tremor is not infrequent as a side effect, and can be suppressed, if there are no contraindications to their use, with [[beta-adrenergic antagonist]]s.
Benign hand tremor is not infrequent as a side effect, and can be suppressed, if there are no contraindications to their use, with [[beta-adrenergic antagonist]]s.
==External links==


== Metabolism ==
Valproic acid is metabolized principally by beta and omega oxidation in the liver.  Although more than 10 metabolites of valproic acid have been identified in human blood and urine, only [[2-propyl 2-pentanoic acid]] has been shown to accumulate in the brain and is 1.3 times more potent than its parent compound and it contributes
significantly to the anti-convulsant effect of chronically administered valproic acid.<ref>{{cite web|url=http://www.inchem.org/documents/pims/pharm/pim551.htm#PartTitle:3.%20%20PHYSICO-CHEMICAL%20PROPERTIES|accessdate=2008-06-29|title=International Programme on Chemical Safety's INCHEM}}</ref>


{{DailyMed}}
== Brand names ==
{{col-begin}}
{{col-break|width=33%}}
* Byk®
* Convulex®
* Convulexette®
* Depakene®
* Depakin®
* Depakine®
* Depamide®
* Deparkine®
{{col-break|width=33%}}
* Epilim®
* Epival®
* Ergenyl®
* Gerot®
* Mylproin®
* Leptilan®
* Leptilen®
{{col-break|width=33%}}
* Logical®
* Promonta®
* Valcote®
* Propymal®
* Orfilept®
* Orfiril®
* Vistora®
{{col-end}}


==External links==
{{CZMed}}


==References==
==References==
<references/>
<references/>

Latest revision as of 08:04, 2 September 2008

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Valproic acid.jpg
valproic acid
IUPAC name:
Synonyms: Abbott-44089; 2-Propylpentanoic acid; 2-Propylvaleric acid; di-n-dipropylacetic acid
Formula: C8H16O2

 Uses: anticonvulsant

 Properties: fatty acid derivative

 Hazards: hepatotoxicity, birth defects, pancreatitis

Mass (g/mol): CAS #:
144.2 99-66-1


Valproic acid is a medication that is "a fatty acid with anticonvulsant properties used in the treatment of epilepsy; the sodium salt is used in treating mood disorders. It also is used for neurogenic pain. It is a colorless to pale yellow liquid that is slightly soluble in water (1.2 mg/mL) but fully soluble in acetone, chloroform, ether and methanol.


The mechanisms of its therapeutic actions are not well understood. It may act by increasing gamma-aminobutyric acid levels in the brain or by altering the properties of voltage dependent sodium channels."[1]

Side effects

Valproic acid causes carnitine deficiency. All patients under valproate therapy should have their carnitine status monitored. Since available tests are not reliable indicators of carnitine status in tissues, prophylactic carnitine therapy can be considered. Intravenous carnitine is markedly superior to oral; oral acetylcarnitine may be advantageously used as well, if the underlying disorder allows it.

Benign hand tremor is not infrequent as a side effect, and can be suppressed, if there are no contraindications to their use, with beta-adrenergic antagonists.

Metabolism

Valproic acid is metabolized principally by beta and omega oxidation in the liver. Although more than 10 metabolites of valproic acid have been identified in human blood and urine, only 2-propyl 2-pentanoic acid has been shown to accumulate in the brain and is 1.3 times more potent than its parent compound and it contributes significantly to the anti-convulsant effect of chronically administered valproic acid.[2]

Brand names

  • Byk®
  • Convulex®
  • Convulexette®
  • Depakene®
  • Depakin®
  • Depakine®
  • Depamide®
  • Deparkine®

  • Epilim®
  • Epival®
  • Ergenyl®
  • Gerot®
  • Mylproin®
  • Leptilan®
  • Leptilen®

  • Logical®
  • Promonta®
  • Valcote®
  • Propymal®
  • Orfilept®
  • Orfiril®
  • Vistora®

External links

The most up-to-date information about Valproic acid and other drugs can be found at the following sites.


References