Sisodiya S M, Lint W R, Harding B N, Squier M V, Thom M
University Department of Clinical Neurology, Institute of Neurology, University College London, UK.
Novartis Found Symp. 2002;243:167-74; discussion 174-9, 180-5. doi: 10.1002/0470846356.ch12.
The basis of drug resistance in human epilepsy is not understood. Parallels with resistance in cancer suggest that drug resistance proteins may have a role. To examine this possibility, we have studied human brain tissue containing pathologies capable of causing refractory epilepsy. Using immunohistochemistry for P glycoprotein (Pgp) and multidrug resistance-associated protein 1 (MRP1), we examined both pathological tissue and control tissue. We demonstrate expression of Pgp and MRP1 in glia from cases of malformation of cortical development studied both before and after the onset of epilepsy, as well as in cases of hippocampal sclerosis and dysembryoplastic neuroepithelial tumours. In one particular type of malformation, we also demonstrate that dysplastic neurons express MRP1. The pattern of immunolabelling suggests overexpression is concentrated particularly around vessels in most of the pathologies. The timing shows that expression may be constitutive in some pathologies. These findings suggest that drug resistance proteins may contribute to drug resistance in refractory epilepsy.
人类癫痫耐药性的基础尚不清楚。与癌症耐药性的相似之处表明,耐药蛋白可能起作用。为了研究这种可能性,我们研究了含有能够导致难治性癫痫的病理组织的人脑组织。通过对P糖蛋白(Pgp)和多药耐药相关蛋白1(MRP1)进行免疫组织化学,我们检查了病理组织和对照组织。我们证明,在癫痫发作前后研究的皮质发育畸形病例的胶质细胞中,以及在海马硬化和胚胎发育不良性神经上皮肿瘤病例中,Pgp和MRP1均有表达。在一种特定类型的畸形中,我们还证明发育异常的神经元表达MRP1。免疫标记模式表明,在大多数病理情况下,过表达尤其集中在血管周围。时间显示,在某些病理情况下,表达可能是组成性的。这些发现表明,耐药蛋白可能导致难治性癫痫的耐药性。