Abstract
Gabitril (tiagabine) is a potent selective inhibitor of the principal neuronal γ-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 palatal seizures in humans. Possible clinical applications outside the field of epilepsy include bipolar disorder and pain.
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Meldrum, B. S., & Chapman, A. G. (1999). Basic mechanisms of gabitril (tiagabine) and future potential developments. In Epilepsia (Vol. 40). Lippincott Williams and Wilkins. https://doi.org/10.1111/j.1528-1157.1999.tb02087.x
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