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Basic mechanisms of gabitril (tiagabine) and future potential developments.
- Source :
-
Epilepsia [Epilepsia] 1999; Vol. 40 Suppl 9, pp. S2-6. - Publication Year :
- 1999
-
Abstract
- Gabitril (tiagabine) is a potent selective inhibitor of the principal neuronal gamma-aminobutyric acid (GABA) transporter (GAT-1) in the cortex and hippocampus. By slowing the reuptake of synaptically-released GABA, it prolongs inhibitory postsynaptic potentials. In animal models of epilepsy, tiagabine is particularly effective against kindled (limbic) seizures and against reflexly-induced generalized convulsive seizures. These data are predictive of its efficacy in complex partial seizures in humans. Possible clinical applications outside the field of epilepsy include bipolar disorder and pain.
- Subjects :
- Animals
Anticonvulsants therapeutic use
Bipolar Disorder drug therapy
Carrier Proteins drug effects
Epilepsy metabolism
Epilepsy physiopathology
GABA Antagonists pharmacology
GABA Antagonists therapeutic use
GABA Plasma Membrane Transport Proteins
Humans
Kindling, Neurologic drug effects
Kindling, Neurologic physiology
Limbic System drug effects
Limbic System physiology
Membrane Proteins drug effects
Mice
Nipecotic Acids therapeutic use
Pain drug therapy
Rats
Tiagabine
gamma-Aminobutyric Acid metabolism
Anticonvulsants pharmacology
Epilepsy drug therapy
Membrane Transport Proteins
Nipecotic Acids pharmacology
Organic Anion Transporters
Subjects
Details
- Language :
- English
- ISSN :
- 0013-9580
- Volume :
- 40 Suppl 9
- Database :
- MEDLINE
- Journal :
- Epilepsia
- Publication Type :
- Academic Journal
- Accession number :
- 10612355
- Full Text :
- https://doi.org/10.1111/j.1528-1157.1999.tb02087.x