Lloyd K G, Bossi L, Morselli P L, Munari C, Rougier M, Loiseau H
Adv Neurol. 1986;44:1033-44.
Although animal models consistently indicate that gamma-amino-butyric acid (GABA) synaptic function (GABA levels, synthesis, uptake and/or receptors) is decreased in seizure states, there is little evidence to date in support of such a hypothesis for human epilepsy. This chapter presents the results of an in-depth study of the activity of the GABA-synthesizing enzyme L-glutamic acid decarboxylase (GAD) in brain tissue removed during neurosurgical resection for intractable epilepsy. The tissue studied is unique in that identified (by stereo EEG) foci were excised (rather than large blocks of tissue containing mixtures of foci and nonepileptic material) and compared with nonepileptic (stereo EEG and morphological definitions) tissue from the same patients. In patients in which there was no indication of a tumor, GAD activity in the foci was low in more than 50% of the patients examined. Furthermore, when the population distribution of GAD was compared in epileptic versus nonepileptic tissue fragments from all patients, the peak distribution of epileptic tissue fragments occurred at much lower GAD activities than for the nonepileptic fragments (0-20 versus 41-80 nmol CO2/mg protein X hr, respectively). A small subgroup of epileptic fragments occurred with a normal GAD distribution, indicating that the presence of an epileptic focus was not invariably associated with low GAD activity. When the low levels of GABA "A" binding sites in these epileptic tissue fragments are taken into consideration in combination with the low GAD levels, then it can be estimated that 60 to 70% of the present patient population had deficient GABAergic transmission in epileptic foci as compared to nonepileptic brain tissue from the same patients. It follows that the GABA hypothesis of human epilepsy is not an exclusive or unitary hypothesis, and some patients appear to have normally functioning GABA synapses (as assessed biochemically) in epileptogenic areas. Thus, other neurotransmitter and neurohumoral systems certainly play a role in the epileptic process.
尽管动物模型一直表明,在癫痫发作状态下γ-氨基丁酸(GABA)的突触功能(GABA水平、合成、摄取和/或受体)会降低,但迄今为止,几乎没有证据支持人类癫痫存在这样的假说。本章介绍了一项深入研究的结果,该研究针对难治性癫痫患者在神经外科手术切除过程中获取的脑组织中GABA合成酶L-谷氨酸脱羧酶(GAD)的活性展开。所研究的组织具有独特性,即切除了经立体脑电图确定的病灶(而非包含病灶和非癫痫组织混合物的大块组织),并与同一患者的非癫痫组织(根据立体脑电图和形态学定义)进行比较。在无肿瘤迹象的患者中,超过50%接受检查的患者病灶中的GAD活性较低。此外,当比较所有患者癫痫组织碎片与非癫痫组织碎片中GAD的总体分布时,癫痫组织碎片的峰值分布出现在比非癫痫碎片低得多的GAD活性水平上(分别为0 - 20与41 - 80 nmol CO2/毫克蛋白×小时)。一小部分癫痫组织碎片的GAD分布正常,这表明癫痫病灶的存在并非总是与低GAD活性相关。当结合这些癫痫组织碎片中低水平的GABA“A”结合位点以及低GAD水平来考虑时,可以估计,与同一患者的非癫痫脑组织相比,目前60%至70%的患者癫痫病灶中存在GABA能传递缺陷。由此可见,人类癫痫的GABA假说并非唯一或单一的假说,一些患者在致痫区域似乎具有正常功能的GABA突触(根据生化评估)。因此,其他神经递质和神经体液系统肯定在癫痫过程中发挥作用。