Licarbazepine: Difference between revisions
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'''Licarbazepine''' is a [[voltage-gated sodium channel]] | '''Licarbazepine''' is a [[voltage-gated sodium channel]] blocker with [[anticonvulsant]] and [[mood stabilizer|mood-stabilizing]] effects. It is structurally and pharmacologically related to [[oxcarbazepine]], a second-generation anticonvulsant used primarily in the management of [[epilepsy]] and [[bipolar disorder]]. | ||
== | == Pharmacology == | ||
Licarbazepine is an active metabolite of oxcarbazepine, which itself is a prodrug that exerts its therapeutic effects only after metabolism. Upon administration, oxcarbazepine undergoes reduction in the liver, resulting in the formation of licarbazepine and eslicarbazepine, its (S)-isomer. These metabolites are responsible for the anticonvulsant activity by blocking voltage-gated sodium channels, thereby stabilizing neuronal membranes and preventing excessive repetitive neuronal firing. | |||
=== Mechanism of Action === | |||
Licarbazepine primarily exerts its effects by: | |||
* Blocking voltage-gated sodium channels ([[VGSC]]) in the central nervous system, reducing hyperexcitability in neurons. | |||
* Modulating excitatory neurotransmission, leading to decreased seizure activity and mood stabilization. | |||
* Inhibiting repetitive firing of neurons, which plays a critical role in preventing seizures and stabilizing mood in individuals with bipolar disorder. | |||
== Isomeric Forms == | |||
Licarbazepine exists in two isomeric forms: | |||
* (S)-(+)-licarbazepine, commonly known as [[eslicarbazepine]], which is an active metabolite of [[eslicarbazepine acetate]]. | |||
* (R)-(-)-licarbazepine, which has less clinical significance compared to its (S)-isomer. | |||
Both oxcarbazepine and eslicarbazepine acetate function as prodrugs, meaning they must be metabolized in vivo to their active forms (licarbazepine and eslicarbazepine, respectively) to exert therapeutic effects. | |||
== Clinical Uses == | |||
Licarbazepine is not available as a standalone medication but is the active component in the treatment of: | |||
* [[Focal seizures]] (partial-onset seizures) in patients with [[epilepsy]]. | |||
* [[Bipolar disorder]], where it has mood-stabilizing effects similar to [[carbamazepine]] and [[lamotrigine]]. | |||
* Neuropathic pain, including [[trigeminal neuralgia]] and [[diabetic neuropathy]]. | |||
== Metabolism and Excretion == | |||
* Liver metabolism: Oxcarbazepine undergoes hepatic metabolism to form licarbazepine. | |||
* Renal excretion: The majority of the active metabolite is excreted unchanged in the urine. | |||
== Adverse Effects == | |||
Since licarbazepine is an active metabolite of oxcarbazepine, it shares similar side effects, including: | |||
* Dizziness and drowsiness | |||
* Hyponatremia (low blood sodium levels) | |||
* Fatigue and headache | |||
* Gastrointestinal disturbances (nausea, vomiting) | |||
* Skin rashes, including hypersensitivity reactions similar to [[carbamazepine]] (e.g., Stevens-Johnson syndrome) | |||
* Double vision (diplopia) and blurred vision | |||
== Related Compounds == | |||
Licarbazepine is closely related to: | |||
* [[Carbamazepine]] – The first-generation anticonvulsant from which oxcarbazepine was derived. | |||
* [[Oxcarbazepine]] – A second-generation carbamazepine derivative and prodrug of licarbazepine. | |||
* [[Eslicarbazepine]] – The (S)-isomer of licarbazepine, which is also an active metabolite of eslicarbazepine acetate. | |||
== See Also == | |||
* [[Voltage-gated sodium channels]] | |||
* [[Anticonvulsant]] | |||
* [[Mood stabilizer]] | |||
* [[Carbamazepine]] | |||
* [[Oxcarbazepine]] | |||
* [[Eslicarbazepine acetate]] | |||
* [[Epilepsy]] | |||
* [[Bipolar disorder]] | |||
{{Anticonvulsants}} | {{Anticonvulsants}} | ||
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{{Channel blockers}} | {{Channel blockers}} | ||
{{Tricyclics}} | {{Tricyclics}} | ||
{{stub}} | |||
[[Category:Anticonvulsants]] | [[Category:Anticonvulsants]] | ||
[[Category:Mood stabilizers]] | [[Category:Mood stabilizers]] | ||
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[[Category:Ureas]] | [[Category:Ureas]] | ||
{{anticonvulsant-stub}} | {{anticonvulsant-stub}} | ||
Latest revision as of 22:03, 19 March 2025

Licarbazepine is a voltage-gated sodium channel blocker with anticonvulsant and mood-stabilizing effects. It is structurally and pharmacologically related to oxcarbazepine, a second-generation anticonvulsant used primarily in the management of epilepsy and bipolar disorder.
Pharmacology[edit]
Licarbazepine is an active metabolite of oxcarbazepine, which itself is a prodrug that exerts its therapeutic effects only after metabolism. Upon administration, oxcarbazepine undergoes reduction in the liver, resulting in the formation of licarbazepine and eslicarbazepine, its (S)-isomer. These metabolites are responsible for the anticonvulsant activity by blocking voltage-gated sodium channels, thereby stabilizing neuronal membranes and preventing excessive repetitive neuronal firing.
Mechanism of Action[edit]
Licarbazepine primarily exerts its effects by:
- Blocking voltage-gated sodium channels (VGSC) in the central nervous system, reducing hyperexcitability in neurons.
- Modulating excitatory neurotransmission, leading to decreased seizure activity and mood stabilization.
- Inhibiting repetitive firing of neurons, which plays a critical role in preventing seizures and stabilizing mood in individuals with bipolar disorder.
Isomeric Forms[edit]
Licarbazepine exists in two isomeric forms:
- (S)-(+)-licarbazepine, commonly known as eslicarbazepine, which is an active metabolite of eslicarbazepine acetate.
- (R)-(-)-licarbazepine, which has less clinical significance compared to its (S)-isomer.
Both oxcarbazepine and eslicarbazepine acetate function as prodrugs, meaning they must be metabolized in vivo to their active forms (licarbazepine and eslicarbazepine, respectively) to exert therapeutic effects.
Clinical Uses[edit]
Licarbazepine is not available as a standalone medication but is the active component in the treatment of:
- Focal seizures (partial-onset seizures) in patients with epilepsy.
- Bipolar disorder, where it has mood-stabilizing effects similar to carbamazepine and lamotrigine.
- Neuropathic pain, including trigeminal neuralgia and diabetic neuropathy.
Metabolism and Excretion[edit]
- Liver metabolism: Oxcarbazepine undergoes hepatic metabolism to form licarbazepine.
- Renal excretion: The majority of the active metabolite is excreted unchanged in the urine.
Adverse Effects[edit]
Since licarbazepine is an active metabolite of oxcarbazepine, it shares similar side effects, including:
- Dizziness and drowsiness
- Hyponatremia (low blood sodium levels)
- Fatigue and headache
- Gastrointestinal disturbances (nausea, vomiting)
- Skin rashes, including hypersensitivity reactions similar to carbamazepine (e.g., Stevens-Johnson syndrome)
- Double vision (diplopia) and blurred vision
Related Compounds[edit]
Licarbazepine is closely related to:
- Carbamazepine – The first-generation anticonvulsant from which oxcarbazepine was derived.
- Oxcarbazepine – A second-generation carbamazepine derivative and prodrug of licarbazepine.
- Eslicarbazepine – The (S)-isomer of licarbazepine, which is also an active metabolite of eslicarbazepine acetate.
See Also[edit]
- Voltage-gated sodium channels
- Anticonvulsant
- Mood stabilizer
- Carbamazepine
- Oxcarbazepine
- Eslicarbazepine acetate
- Epilepsy
- Bipolar disorder
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| Neuropathic pain and fibromyalgia pharmacotherapies | ||||||
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| Tricyclics | ||||||||||
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