QUANTIFICATION OF OPIATE RECEPTORS IN 2 PATIENTS WITH MESIOBASAL TEMPORAL-LOBE EPILEPSY, BEFORE AND AFTER SELECTIVE AMYGDALO-HIPPOCAMPECTOMY, USING POSITRON EMISSION TOMOGRAPHY

被引:26
作者
BARTENSTEIN, PA
PREVETT, MC
DUNCAN, JS
HAJEK, M
WIESER, HG
机构
[1] HAMMERSMITH HOSP,MRC,CYCLOTRON UNIT,LONDON W12 0HS,ENGLAND
[2] UNIV LONDON,INST NEUROL,DEPT CLIN NEUROL,LONDON WC1N 3BG,ENGLAND
[3] UNIV MUNSTER,NUKL MED KLIN & POLIKLIN,W-4400 MUNSTER,GERMANY
[4] UNIV SPITAL ZURICH,NEUROL KLIN & POLIKLIN,CH-8091 ZURICH,SWITZERLAND
基金
英国惠康基金;
关键词
OPIATE RECEPTORS; PET; AMYGDALO-HIPPOCAMPECTOMY;
D O I
10.1016/0920-1211(94)90004-3
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Using PET, reduced glucose metabolism (rCMRglu) and increased binding of the mu opiate receptor ligand C-11-carfentanil have been demonstrated in lateral temporal cortex overlying mesial temporal epileptic foci. Binding of the non-specific opiate receptor ligand C-11-diprenorphine (DPN) to lateral temporal cortex has not shown consistent asymmetries. We measured rCMRglu with F-18-FDG and binding of C-11-diprenorphine in two patients with temporal lobe epilepsy (TLE) before and 5 months after selective amygdalo-hippocampectomy (both patients were seizure-free post-operatively). Pre-operatively, in both patients rCMRglu was decreased in mesial temporal lobe (MTL) (asymmetry index AI = -9.1 and 9.0) ipsilateral to the EEG focus. A more marked reduction was seen in ipsilateral lateral temporal cortex (LTC) (AI = -32.0 and 18.9). DPN binding was reduced in MTL and LTC (AI MTL = -9.3 and 16.2; AI LTC = -8.0 and 5.5) ipsilateral to the focus, but was within 2 SD of the normal range. Post-operatively, the reduction of rCMRglu in LTC was accentuated in one patient and decreased in the other (AI = -23.1 and 45.7) while there was a further reduction of DPN binding in LTC in both patients (AI = -27.8 and 9.8). These preliminary results in only two patients are compatible with downregulation of opiate receptors in LTC after removal of the epileptic focus or post-operative neuronal dysfunction.
引用
收藏
页码:119 / 125
页数:7
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