2003
DOI: 10.1517/13543784.12.4.663
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Pregabalin: a new anxiolytic

Abstract: Pregabalin (S-[+]-3-isobutylgaba) was designed as a lipophilic GABA (gamma-aminobutyric acid) analogue substituted at the 3'-position in order to facilitate diffusion across the blood-brain barrier. It was originally developed as an anticonvulsant agent, however it has been shown to be effective in the treatment of several disorders including hyperalgesia and behavioural disorders. Although its exact mode of action remains unclear, pregabalin interacts with the same binding site and has a similar pharmacologic… Show more

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Cited by 302 publications
(38 citation statements)
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“…10,17 When studied in non-humans pregabalin appears to be 3 to 10 times more potent as an anticonvulsant than gabapentin. 18,19 Pregabalin is 2 to 4 times more potent as an analgesic than gabapentin. 18,19 Pregabalin is 6 times more potent than gabapentin in binding affinity.…”
Section: 6mentioning
confidence: 99%
See 1 more Smart Citation
“…10,17 When studied in non-humans pregabalin appears to be 3 to 10 times more potent as an anticonvulsant than gabapentin. 18,19 Pregabalin is 2 to 4 times more potent as an analgesic than gabapentin. 18,19 Pregabalin is 6 times more potent than gabapentin in binding affinity.…”
Section: 6mentioning
confidence: 99%
“…18,19 Pregabalin is 2 to 4 times more potent as an analgesic than gabapentin. 18,19 Pregabalin is 6 times more potent than gabapentin in binding affinity. 20 We choose 900 mg of gabapentin to 300mg of pregabalin.…”
Section: 6mentioning
confidence: 99%
“…This is prompted by multiple reports involving gabapentin, pregabalin and tiagabin among others. 53,54 While these medications are less dependency forming than benzodiazepines they are also less effective. Some newer agents such as pregabaline seem to have more antianxiety properties, but this remains to be documented in large controlled clinical trials.…”
Section: Pharmacologicalmentioning
confidence: 99%
“…3 It has also got anxiolytic property. 11,12 Pregabalin has been recommended in a dose 75 mg to 600 mg/day for treatment of epilepsy and central neuropathic pain. It has linear pharmacokinetic profile across the therapeutic range with fewer side effects, most common being dizziness and somnolence, having no effect on arterial pressure or heart rate.…”
Section: Discussionmentioning
confidence: 99%