Yu Nian, Zhang Yan-Fang, Zhang Kang, Cheng Yong-Fei, Ma Hai-Yan, Di Qing
Department of Neurology, Nanjing Medical University, Affiliated Nanjing Brain Hospital, 210029, Nanjing, China.
Neurochem Res. 2017 Aug;42(8):2167-2177. doi: 10.1007/s11064-017-2224-x. Epub 2017 Mar 16.
Drug-resistance epilepsy (DRE) is attributed to the brain P-glycoprotein (P-gp) overexpression. We previously reported that nuclear factor-kappa B (NF-κB) played a critical role in regulating P-gp expression at the brain of the acute seizure rats. This study was extended further to investigate the interaction effect of NF-κB and pregnane X receptor (PXR) on P-gp expression at the brain of chronic epileptic rats treated with carbamazepine (CBZ). The chronic epileptic models were induced by the micro-injection of kainic acid (KA) into rats' hippocampus. Subsequently, the successful models were treated with different intervention agents of CBZ; PMA(a non-specific PXR activity inhibitor) or PDTC(a specific NF-κB activity inhibitor) respectively. The expression levels of P-gp and its encoded gene mdr1a/b were significantly up-regulated on the brain of KA-induced chronic epilepsy rats or the epilepsy rats treated with CBZ for 1 week, meanwhile with a high expression of PXR. The treatment of PMA dramatically reduced both PXR and P-gp expressions at the protein and mRNA levels in the chronic epilepsy brain. By compared to the epilepsy model group, the P-gp expression was not markedly attenuated by the inhibition of NF-κB activity with PDTC treatment, nevertheless with a decrease of NF-κB expression in this intervention group. Higher levels of proinflammatory cytokines(IL-1β, IL-6, TNF-α) were found both in the brain tissue and the serum in the epilepsy rats of each group. There was a declined trend of the pro-inflammatory cytokines expression of the PDTC treatment group but with no statistical significance. This study demonstrates for the first time that P-gp up-regulation is due to increase PXR expression in the chronic phase of epilepsy, differently from that NF-κB signaling may induce the P-gp expression in the acute seizure phase. Our results offer insights into the mechanism underlying the development of DRE using or not using CBZ treatment.
耐药性癫痫(DRE)归因于脑P-糖蛋白(P-gp)的过表达。我们之前报道过核因子-κB(NF-κB)在调节急性癫痫发作大鼠脑内P-gp表达中起关键作用。本研究进一步扩展,以探讨NF-κB与孕烷X受体(PXR)对卡马西平(CBZ)治疗的慢性癫痫大鼠脑内P-gp表达的相互作用。通过向大鼠海马体微量注射 kainic acid(KA)诱导慢性癫痫模型。随后,成功的模型分别用不同的干预剂CBZ、PMA(一种非特异性PXR活性抑制剂)或PDTC(一种特异性NF-κB活性抑制剂)进行治疗。KA诱导的慢性癫痫大鼠或用CBZ治疗1周的癫痫大鼠脑内,P-gp及其编码基因mdr1a/b的表达水平显著上调,同时PXR表达也很高。PMA处理显著降低了慢性癫痫脑内PXR和P-gp在蛋白质和mRNA水平的表达。与癫痫模型组相比,PDTC处理抑制NF-κB活性并未显著减弱P-gp表达,不过该干预组中NF-κB表达有所下降。在每组癫痫大鼠的脑组织和血清中均发现促炎细胞因子(IL-1β、IL-6、TNF-α)水平较高。PDTC治疗组促炎细胞因子表达有下降趋势,但无统计学意义。本研究首次表明,癫痫慢性期P-gp上调是由于PXR表达增加,这与NF-κB信号在急性发作期可能诱导P-gp表达不同。我们的结果为使用或不使用CBZ治疗的DRE发生机制提供了见解。