Volume 42, Issue 4 pp. 543-548

Topiramate Rapidly Raises Brain GABA in Epilepsy Patients

Ognen A. C. Petroff

Ognen A. C. Petroff

Departments of Neurology and

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Fahmeed Hyder

Fahmeed Hyder

Diagnostic Radiology, Yale University, New Haven, Connecticut, U.S.A.

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Douglas L. Rothman

Douglas L. Rothman

Diagnostic Radiology, Yale University, New Haven, Connecticut, U.S.A.

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Richard H. Mattson

Richard H. Mattson

Departments of Neurology and

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First published: 20 December 2001
Citations: 70
Address correspondence and reprint requests to Dr. O. A. C. Petroff at Department of Neurology, Yale University, 333 Cedar Street, New Haven, CT 06520-8018, U.S.A.

Abstract

Summary: Purpose: The short- and long-term pharmacodynamic effects of topiramate (TPM) on brain γ-aminobutyric acid (GABA) metabolism were studied in patients with complex partial seizures.

Methods: In vivo measurements of GABA, homocarnosine, and pyrrolidinone were made of a 14-cc volume in the occipital cortex using 1H spectroscopy with a 2.1-Tesla magnetic resonance spectrometer and an 8-cm surface coil. Fifteen patients (four men) were studied serially after the first, oral dose (100 mg) of TPM.

Results: The first dose of TPM increased brain GABA within 1 h. Within 4 h, GABA was increased by 0.9 mM (95% CI, 0.7–1.1). Brain GABA remained elevated for ≥24 h. Pyrrolidinone and homocarnosine increased slowly during the first day. Daily TPM therapy (median, 300 mg; range, 200–500) increased GABA (0.3 mM; 95% CI, 0.1–0.5), homocarnosine (0.4 mM; 95% CI, 0.3–0.5), and pyrrolidinone (0.15 mM; 95% CI, 0.10–0.19), compared with levels before TPM. There was no dose response evident with daily TPM doses of 200–500 mg.

Conclusions: TPM promptly elevates brain GABA and presumably offers partial protection against further seizures within hours of the first oral dose. Patients may expect to experience the effects of increased homocarnosine and pyrrolidinone within 24 h.

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