Literature DB >> 7693432

Gabapentin. A review of its pharmacological properties and clinical potential in epilepsy.

Karen L Goa1, Eugene M Sorkin1.   

Abstract

Gabapentin is an antiepileptic drug with an unknown mechanism of action apparently dissimilar to that of other antiepileptic agents, and possessing some desirable pharmacokinetic traits. The drug is not protein bound, is not metabolised and does not induce liver enzymes, diminishing the likelihood of drug interactions with other antiepileptic agents and drugs such as oral contraceptives. Although gabapentin is a structural analogue of the neurotransmitter gamma-aminobutyric acid (GABA), which does not cross the blood-brain barrier, gabapentin penetrates into the CNS and its activity is seemingly distinct from GABA-related effects. Present clinical evaluation is largely restricted to proof of efficacy trials of gabapentin as add-on therapy in patients with partial epilepsy resistant to conventional treatment. Gabapentin (usually 600 to 1800 mg/day) provides notable benefit, reducing seizure frequency by > or = 50% in 18 to 28% of patients with refractory partial seizures, as shown in 3 double-blind, placebo-controlled trials. Overall, seizure frequency decreased by 18 to 32% during 3-month treatment periods. Patients with complex partial seizures, and partial seizures secondarily generalised, are particularly likely to respond to gabapentin. Current experience with the drug in other seizure types, and as monotherapy, is limited. Mild adverse events, commonly somnolence, fatigue, ataxia and dizziness, have been reported in about 75% of gabapentin recipients. While the drug has been well tolerated when administered to a few patients for periods of up to 5 years, its long term tolerability profile has yet to be fully expounded. Thus, with its favourable pharmacokinetic profile, and efficacy in some refractory patients, gabapentin is poised to fill a niche as an adjunct to the treatment of partial epilepsy. Promising results obtained thus far warrant further work to clarify its long term tolerability, its possible efficacy in other seizure types, its position relative to other agents and its use as monotherapy. In the meantime, gabapentin is likely to provide a much-needed option in a therapeutic area requiring complex management.

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Year:  1993        PMID: 7693432     DOI: 10.2165/00003495-199346030-00007

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  22 in total

1.  Determination of gabapentin in plasma and urine by capillary column gas chromatography.

Authors:  W D Hooper; M C Kavanagh; R G Dickinson
Journal:  J Chromatogr       Date:  1990-07-13

Review 2.  Antiepileptic medications in development.

Authors:  N M Graves; I E Leppik
Journal:  DICP       Date:  1991-09

3.  Determination of gabapentin in plasma and urine by high-performance liquid chromatography and pre-column labelling for ultraviolet detection.

Authors:  H Hengy; E U Kölle
Journal:  J Chromatogr       Date:  1985-06-14

4.  Lack of a pharmacokinetic interaction between phenobarbitone and gabapentin.

Authors:  W D Hooper; M C Kavanagh; G K Herkes; M J Eadie
Journal:  Br J Clin Pharmacol       Date:  1991-02       Impact factor: 4.335

5.  Gabapentin as add-on therapy in refractory partial epilepsy: a double-blind, placebo-controlled, parallel-group study. The US Gabapentin Study Group No. 5.

Authors: 
Journal:  Neurology       Date:  1993-11       Impact factor: 9.910

6.  Gabapentin decreases monoamine release without affecting acetylcholine release in the brain.

Authors:  E Schlicker; W Reimann; M Göthert
Journal:  Arzneimittelforschung       Date:  1985

7.  Selected CSF biochemistry and gabapentin concentrations in the CSF and plasma in patients with partial seizures after a single oral dose of gabapentin.

Authors:  E Ben-Menachem; L I Persson; T Hedner
Journal:  Epilepsy Res       Date:  1992-03       Impact factor: 3.045

8.  Characterisation of [3H]gabapentin binding to a novel site in rat brain: homogenate binding studies.

Authors:  N Suman-Chauhan; L Webdale; D R Hill; G N Woodruff
Journal:  Eur J Pharmacol       Date:  1993-02-15       Impact factor: 4.432

9.  Potent and stereospecific anticonvulsant activity of 3-isobutyl GABA relates to in vitro binding at a novel site labeled by tritiated gabapentin.

Authors:  C P Taylor; M G Vartanian; P W Yuen; C Bigge; N Suman-Chauhan; D R Hill
Journal:  Epilepsy Res       Date:  1993-01       Impact factor: 3.045

10.  Comparison of gabapentin with other antiepileptic and GABAergic drugs.

Authors:  T Kondo; G H Fromm; B Schmidt
Journal:  Epilepsy Res       Date:  1991-04       Impact factor: 3.045

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  48 in total

1.  Bioavailability prediction based on molecular structure for a diverse series of drugs.

Authors:  Joseph V Turner; Desmond J Maddalena; Snezana Agatonovic-Kustrin
Journal:  Pharm Res       Date:  2004-01       Impact factor: 4.200

Review 2.  Management of focal-onset seizures: an update on drug treatment.

Authors:  Svein I Johannessen; Elinor Ben-Menachem
Journal:  Drugs       Date:  2006       Impact factor: 9.546

Review 3.  Recent advances in the development of treatments for alcohol and cocaine dependence: focus on topiramate and other modulators of GABA or glutamate function.

Authors:  Bankole A Johnson
Journal:  CNS Drugs       Date:  2005       Impact factor: 5.749

4.  Not another gabapentin mechanism!

Authors:  Graeme J Sills
Journal:  Epilepsy Curr       Date:  2005 Mar-Apr       Impact factor: 7.500

Review 5.  Alteration of thyroid hormone homeostasis by antiepileptic drugs in humans: involvement of glucuronosyltransferase induction.

Authors:  M Strolin Benedetti; R Whomsley; E Baltes; F Tonner
Journal:  Eur J Clin Pharmacol       Date:  2005-11-24       Impact factor: 2.953

Review 6.  Drug treatment of epilepsy in the 1990s. Achievements and new developments.

Authors:  A Sabers; L Gram
Journal:  Drugs       Date:  1996-10       Impact factor: 9.546

7.  Effectiveness of preanesthetic administration of gabapentin on sedative action during intravenous sedation with propofol.

Authors:  Rumiko Hosokawa; Shinichi Ito; Jun Hirokawa; Yu Oshima; Takeshi Yokoyama
Journal:  J Anesth       Date:  2018-09-20       Impact factor: 2.078

Review 8.  Benefits and risks of pharmacological treatments for essential tremor.

Authors:  Kelly E Lyons; Rajesh Pahwa; Cynthia L Comella; Mahmood S Eisa; Rodger J Elble; Stanley Fahn; Joseph Jankovic; Jorge L Juncos; William C Koller; William G Ondo; Kapil D Sethi; Matthew B Stern; Caroline M Tanner; Ron Tintner; Ray L Watts
Journal:  Drug Saf       Date:  2003       Impact factor: 5.606

Review 9.  Drug dosage in the elderly. Is it rational?

Authors:  K Turnheim
Journal:  Drugs Aging       Date:  1998-11       Impact factor: 3.923

10.  Gabapentin adjunctive to risperidone or olanzapine in partially responsive schizophrenia: an open-label pilot study.

Authors:  Adel Gabriel
Journal:  Neuropsychiatr Dis Treat       Date:  2010-10-29       Impact factor: 2.570

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