Mu‐opiate receptors measured by positron emission tomography are increased in temporal lobe epilepsy

J. James Frost, Helen S. Mayberg, Robert S. Fisher, Kenneth H. Douglass, Robert F. Dannals, Jonathan M. Links, Alan A. Wilson, Hayden T. Ravert, Arthur E. Rosenbaum, Solomon H. Snyder, Henry N. Wagner

Research output: Contribution to journalArticlepeer-review

Abstract

Neurochemical studies in animal models of epilepsy have demonstrated the importance of multiple neurotransmitters and their receptors in mediating seizures. The role of opiate receptors and endogenous opioid peptides in seizure mechanisms is well developed and is the basis for measuring opiate receptors in patients with epilepsy. Patients with complex partial seizures due to unilateral temporal seizure foci were studied by positron emission tomography using 11C‐carfentanil to measure mu‐opiate receptors and 18F‐fluoro‐deoxy‐D‐glucose to measure glucose utilization. Opiate receptor binding is greater in the temporal neocortex on the side of the electrical focus than on the opposite side. Modeling studies indicate that the increase in binding is due to an increase in affinity or the number of unoccupied receptors. No significant asymmetry of 11C‐carfentanil binding was detected in the amygdala or hippocampus. Glucose utilization correlated inversely with 11C‐carfentanil binding in the temporal neocortex. Increased opiate receptors in the temporal neocortex may represent a tonic anticonvulsant system that limits the spread of electrical activity from other temporal lobe structures.

Original languageEnglish (US)
Pages (from-to)231-237
Number of pages7
JournalAnnals of neurology
Volume23
Issue number3
DOIs
StatePublished - Mar 1988

ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology

Fingerprint Dive into the research topics of 'Mu‐opiate receptors measured by positron emission tomography are increased in temporal lobe epilepsy'. Together they form a unique fingerprint.

Cite this